Total 134 job vacancies by 1001 Amgen Inc.

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Process Development Senior Scientist

Live

What you will do

Let’s do this! Let’s change the world! In this vital role you will be responsible for the development, scale-up, and transfer of both upstream and downstream processes for early clinical manufacturing of therapeutic molecules. The programs develop a wide range of biological molecules including mAbs, BiTEs, bispecifics, conjugations, and other novel modalities ranging from early molecule assessments with Research to IND enabling GMP manufacturing supplies for clinical studies.

• Develop processes amenable to cGMP operation and lead deliveries of drug substance in a cGMP manufacturing environment in both internal and external capacity for batch and continuous processes
• Applying technical and platform knowledge to design studies for the development of cell culture or purification processes
• Provides significant contributions to drug substance development teams (e.g., product, process development and product quality teams) by providing drug substance updates, documentation, data interpretation, technical recommendations, etc.
• Develop and apply automation to enhance the agility of the platform model
• Independently authors technical reports, regulatory filings, patents, peer reviewed publications and actively participate in scientific conferences
• Serves as a technical authority and keeps current in relevant literature and related technology with a record of successful application of said technology complying to current and emerging regulatory requirements (FDA, EMA, ICH, etc)
• Works cross-functionally to author CMC regulatory documents and documentation in support of Amgen’s regulatory filings
• Conveys information and makes recommendations on scientific issues to senior management
• Provides mentoring and expertise to less-experienced staff

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a Scientist with these qualifications.

Basic Qualifications:

• Bachelor’s degree and 5 years of life sciences experience OR
• Master’s degree and 3 years of life sciences experience OR
• Doctorate degree PhD OR PharmD OR MD

Preferred Qualifications:

• Ph.D. in Chemical Engineering, Biochemistry, Biotechnology, Bioengineering, Biomedical engineering, or Bioprocessing discipline or relevant experience in the pharmaceutical or related industry
• Experience in bioreactor process development or cell line development.
• Experience with metabolomics analysis methods.
• Scientific understanding of current bioreactor technologies, as well as the ability to explore and develop new approaches to further advance innovative bioreactor technologies
• Understanding of protein characteristics and critical attributes so as to direct bioreactor development and product/process control strategies
• Independently uncovering and resolving issues associated with cell culture and harvest and implementation of scientific projects
• Strong technical communication skills, both written and verbal, to interact effectively and appropriately with all stakeholders and document learned information, improvements, and value generated
• Motivated self-starter with excellent interpersonal and organizational skills
• Leadership experience of progressively increased scope and a demonstrated ability to inspire and lead a group of scientists to deliver on complex and challenging objectives in defined timelines
• Demonstrated eminence in the scientific community through a sustained record of peer reviewed publications
• Demonstrated success working with diverse team members in a dynamic, cross-functional environment
• Familiarity with design of experiments and statistical analysis of data
• Knowledge of license application and the drug development process
• Exposure to cGMP manufacturing and CMC components of regulatory submissions

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

Principal Scientist - Clinical Pharmacology

Live

What you will do

Let’s do this. Let’s change the world. Amgen Clinical Pharmacology Modeling and Simulation (CPMS) is seeking a Principal Scientist in our Thousand Oaks, CA location. As part of the Clinical Pharmacology, Modeling and Simulation department, the Modeling and Simulation. The Principal Scientist will support Amgen clinical development and translational sciences programs across multiple therapeutic areas with emphasis on oncology.

Key responsibilities include:

• Building pharmacostatistical models to support Population Pharmacokinetics/Pharmacodynamic (PKPD) and exposure-response analyses using relevant state of the art modeling and simulation techniques.
• Training in binary and categorical and binary data analyses, time-to-event (hazard) models, Poisson models, MCMC and Bayesian methods as applied to exposure-response analyses and Population PK and PKPD analysis.
• Perform meta-analysis using proprietary and/or literature data.
• Participate in cross-functional project teams and provide scientific input for dose selection, early and late phase study designs using modeling and simulation inputs.
• Contribute to clinical pharmacology strategy for the program(s) and implement project plans.
• Generate modeling reports and contribute to the summary documents for regulatory submissions.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a scientist with these qualifications.

Basic Qualifications:

Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 2 years of Pharmacokinetics/Pharmacodynamic or statistical modeling experience

Or

Master s degree and 5 years of Pharmacokinetics/Pharmacodynamic or statistical modeling experience

Or

Bachelor s degree and 7 years of Pharmacokinetics/Pharmacodynamic or statistical modeling experience

Preferred Qualifications:

• PhD in Pharmacometrics, Pharmaceutical sciences, Applied Statistics/Mathematics, Biostatistics, and/or Engineering or related fields with equivalent professional degrees (e. g. MD, PharmD) with 3+ years of PK/PD or statistical modeling experience.
• 3+ years industry or relevant academic experience in pharmacometric analyses, data science, and/or applied biostatistics of small molecules and/or biologics.
• Proficiency in modeling software (e. g. NONMEM, R/S-Plus, STAN, Python, SAS, MATLAB)

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Environmental, Health, Safety and Sustainability Manager

Live

What you will do

Let’s do this! Let’s change the world!

The Environment, Health, Safety and Sustainability (EHSS) Manager will drive world class EHSS performance across the site in a diverse biotech/pharma environment. The role will be responsible for the execution of key EHSS processes including:

• Continuous EHS improvement of manufacturing across site

• Trending and interpretation of EHS information and provide data intelligence and actions

• Provide EHSS support for the manufacturing and facilities and engineering operations at the Thousand Oaks, CA site

• Provide subject matter expertise for several EHSS programs including industrial safety, environment and environmental sustainability

Primary responsibilities include:

• Provide EHSS Support for building startup

• Conduct Pre-Start Up Safety Reviews (PSSRs) and Operational Readiness Reviews (ORR) for equipment start up.

• Partner with manufacturing, facilities, engineering and/or warehouse operations to advance their safety culture and manage EHSS risks

• Provide EHSS leadership and guidance to key partners

• Collect/Analyze performance metrics and establish annual action plans to drive continuous improvement.

• Establish and complete risk assessment plans for clients to ensure all risks are proactively addressed and control systems are implemented and maintained

• Ensure all changes with potential EHSS impact are assessed and controls are established prior to implementation

• Establish safe work procedures for hazardous work

• Conduct regular inspections of the work areas

• Monitor incident trends and assist management in conducting incident investigations

• Conduct regular EHSS management reviews with functional leadership

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an employee with these qualifications.

Basic Qualifications:

Doctorate degree

OR

Master’s degree and 3 years of EHSS experience within a cGMP manufacturing environment

Or

Bachelor’s degree and 5 years of EHSS experience within a cGMP manufacturing environment

Or

Associate’s degree and 10 years of EHSS experience within a cGMP manufacturing environment

Or

High school diploma / GED and 12 years of EHSS experience within a cGMP manufacturing environment

Preferred Qualifications:

• Degree in safety, industrial hygiene, chemical engineering, mechanical engineering, chemistry, biology or other life science areas

• Applied knowledge and understanding of EHS and process safety practices, engineering principles, regulatory standards, and requirements in context of business activities

• Ability to take responsibility for several projects / initiatives at one time with an emphasis on quality and organization

• Demonstrated EHSS leadership supporting manufacturing or laboratory environments. Demonstrated ability to lead diverse teams and influence management

• 5 – 7 years of experience in the pharmaceutical/biotech industry implementing industrial and safety programs

• Certified Industrial Hygienist (CIH) and/or Certified Safety Professional (CSP)

• Strong communication and presentation skills, action oriented, self-starting, program development and project management

• Strong technical writing skills

• Proficient in Microsoft Office and other computer software systems

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The annual base salary range for this opportunity in the U.S. is $99,533 - $122,280.

In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

• Stock-based long-term incentives

• Award-winning time-off plans and bi-annual company-wide shutdowns

• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Data Scientist

Live

What you will do

Let’s do this. Let’s change the world. In this vital role you will use data science and artificial intelligence technology and their knowledge of medical device development and design control to create and improve Combination products and processes. The candidate will have a key role in creating sophisticated tools using AI and automation technologies for combination product lifecycle. This position also requires data engineering skills to handle and optimize the incoming data, ensuring high-quality data integration and analysis. While also working closely with the product development and engineering teams to understand existing business processes, engineer the future while ensuring compliance with regulatory standards.

• Convert and standardize data from different sources into data products that conform to information models that match business data domains.
• Help Design, develop, test, and automate reliable, observable, high-performance data pipelines that instantiate data in both graph and relational forms.
• Design, prototype, and evaluate AI solutions that automate prompt engineering for various natural language processing tasks.
• Use Gen AI tools to extract relevant information from different sources of technical documents, such as manuals, specifications, or reports.
• Analyze and structure the extracted information into semantic graphs that capture the relations and attributes of the entities and concepts in the documents.
• Manage delivery of a continuous, iterative flow of Combination product data products and improvements to meet business needs.
• Collaborate with Technical teams to shape how the data can drive value for Combination Products business problems.
• Accelerate Combination product introduction by providing innovative solutions to design control results.
• Design and develop data visualization solutions to communicate complex data insights to various stakeholders and support data-driven decision making for Combination products.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The [vital attribute] professional we seek is a [type of person] with these qualifications.

Basic Qualifications:

• High school diploma/GED and 12 years of Engineering experience OR
• Associate's degree and 10 years of Engineering experience OR
• Bachelor's Degree and 5 years of Engineering experience OR
• Master's Degree and 3 years of Engineering experience OR
• Doctorate Degree

Preferred Qualifications:

• M.S. or Ph. D. in engineering, Mechanical, Biomedical or Chemical
• a minimum of 3 years of experience in Medical Device or combination products
• at minimum of 3 years of experience in data analytics and using data and statistical methods
• Experience with querying languages and databases, such as SQL, Python, and MongoDB
• Experience with natural language processing and machine learning, such as NLTK, TensorFlow, PyTorch, or GPT-3
• Proficiency in visualization tools like Spotfire and Tableau
• Experience with AWS services, such as S3, Redshift, Bedrock, or SageMaker
• Experience with leading technical teams, including setting priorities and leveling resources
• Knowledge of device regulatory requirements, medical device development and engineering, and design controls.
• Experience in developing and implementing design plans, protocols, reports, and risk assessments for medical devices
• Working knowledge of medical device and combination product regulations and standards such as 21 CFR Part 4,21 CFR 820, ISO 13485, and ISO 14971
• Experience with change controls, deviations, CAPA Experience with Medical Device or Combination products
• Understanding of the six sigma process, applying statistical tools to solve statistical problems
• Excellent written and verbal communication skills together with demonstrated ability to work in a highly matrixed team environment

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Process Development Senior Scientist - Drug Substance Technologies

Synthetics

Live

What you will do

Amgen is seeking a talented Process Development Senior Scientist with experience in peptide chemistry to join our Drug Substance Technologies - Synthetics (DSTS) group in Cambridge, MA. Amgen’s DSTS group within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets. Process chemists within our team bring together their training in synthetic and bioorganic chemistry to invent efficient and sustainable manufacturing processes to support drug substance manufacturing from early to late-stage development. The successful candidate will be a highly motivated and team-oriented individual with a strong background in peptide chemistry with a proven track record of scientific innovation and achievement.

Key Responsibilities:

• Support the development of sustainable and cost-effective processes to manufacture synthetic and hybrid drug substances
• Advance enabling technologies to accelerate pharmaceutical development and to improve sustainability and process efficiency
• Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers
• Ensure process performance through process understanding, modeling and characterization
• Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
• Work cross-functionally to deliver regulatory documents and support regulatory filings
• Serve as a technical expert and keep current in the field of peptide synthesis and manufacturing
• Work effectively in a multi-disciplinary team of chemists, engineers, and attribute scientists
• Work independently in advancing projects and studies within required deadlines.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The self-starter professional we seek is a scientist with these qualifications.

Basic Qualifications:

Doctorate degree in Chemistry Biochemistry/Chemical Biology completed by December 2024

OR

Master’s degree in Chemistry or Biochemistry/Chemical Biology and 4 years of industry experience

Or

Bachelor’s degree in Chemistry or Biochemistry/Chemical Biology and 6 years of industry experience

Preferred Qualifications:

• Ph.D. in organic chemistry or biochemistry/chemical biology with a specialization in peptide/protein synthesis, protein engineering, peptide modification or conjugation chemistry
• Post-doctoral experience in an academic laboratory or pharmaceutical/biotech industry
• Track record of peer-reviewed publications and research presentations
• Demonstrated ability to work within a dynamic and interdisciplinary environment to achieve results
• Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on complex projects
• A research summary included with CV is strongly encouraged

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Process Development Senior Associate – Drug Substance Technologies Synthetics

Live

What you will do

Amgen is currently seeking a talented Process Development Senior Associate to join our Drug Substance Technologies - Synthetics (DSTS) group in Cambridge, MA. Amgen’s DSTS group within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets. Senior Associates in our team collaborate with chemists, process engineers, and attribute scientists to support drug substance manufacturing from early to late-stage development. The successful candidate will be a highly motivated and team-oriented individual with prior lab-based research experience in organic chemistry or biochemistry/chemical biology.

Key Responsibilities:

• Work within a drug substance team comprised of chemists, engineers, and attribute scientists to solve technical problems
• Contribute to the invention of synthetic routes and development of safe, robust, and cost-effective processes to manufacture synthetic and hybrid drug substances
• Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers
• Support process characterization activities, including process understanding and modeling
• Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
• Works regularly with a supervisor to advance projects within required deadlines.
• Work cross-functionally to deliver regulatory documents and support regulatory filings
• Follows good laboratory documentation practices and standard operating procedures

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The scientific professional we seek will possess these qualifications.

Basic Qualifications:

Master’s degree Chemistry or Biochemistry/Chemical Biology completed by June 2024

OR

Bachelor’s degree in Chemistry or Biochemistry/Chemical Biology and 2 years of industry experience

Or

Associate’s degree in Chemistry or Biochemistry/Chemical Biology and 4 years of industry experience

Or

High school diploma / GED and 6 years of industry experience

Preferred Qualifications:

• M.S. in organic chemistry or biochemistry/chemical biology with a specialization in synthetic methodology, total synthesis, peptide/protein chemistry, oligonucleotide chemistry, or synthetic/conjugation chemistry
• Prior research experience in the biopharmaceutical or pharmaceutical industry
• Demonstrated ability to work in a chemistry laboratory with minimal supervision
• Ability to independently collect and interpret analytical results (NMR, HPLC, MS, IR, Raman, etc)
• Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on projects
• A research summary included with CV is strongly encouraged

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Process Development Associate – Drug Substance Technologies Synthetics

Live

What you will do

Amgen is currently seeking a talented Process Development Associate to join our Drug Substance Technologies - Synthetics (DSTS) group in Cambridge, MA. Amgen’s DSTS group within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets. Associates in our team collaborate with chemists, process engineers, and attribute scientists to support drug substance manufacturing from early to late-stage development. The successful candidate will be a highly motivated and team-oriented individual with prior lab-based research experience in organic chemistry or biochemistry/chemical biology.

Key Responsibilities:

• Follows established procedures to perform assignments with detailed instructions on the process and expectations
• Works routinely with a supervisor to advance projects within required deadlines.
• Support the development of safe, robust, and cost-effective processes to manufacture synthetic and hybrid drug substances
• Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers
• Support process characterization activities, including process understanding and modeling
• Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, etc.
• Follows good laboratory documentation practices and standard operating procedures

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The scientific professional we seek will possess these qualifications.

Basic Qualifications:

Bachelor’s degree in Chemistry or Biochemistry/Chemical Biology completed by June 2024

OR

Associate’s degree Chemistry or Biochemistry/Chemical Biology and 2 years of industry experience

Or

High school diploma / GED and 4 years of industry experience

Preferred Qualifications:

• Bachelor degree in organic chemistry or biochemistry/chemical biology with undergraduate research experience in synthetic methodology, total synthesis, peptide/protein chemistry, oligonucleotide chemistry, or synthetic/conjugation chemistry
• Demonstrated ability to work in a chemistry laboratory with minimal supervision and familiarity with analytical techniques such as NMR, HPLC, MS, IR, Raman, etc.
• Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on projects

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Live

What you will do

Let’s do this. Let’s change the world. This position will report to the Sr. F&E Manager and be responsible for providing technical and administrative leadership to a group of responsible for planning, scheduling, troubleshooting, repairing, maintaining and improving the reliability of GMP and non-GMP equipment at Amgen Thousand Oaks (TO). Managerial responsibilities include: establishing strategy, objectives, and goals for the team, improving team performance and achievement of key metrics/milestones, supervising and technically developing direct reports, and supporting Amgen’s continuous improvement culture.

Specific responsibilities include:

Strategic / Managerial

• Meet regularly with key clients to find opportunities and establish the strategic direction for the Maintenance Team.
• Establish annual team goals and track progress / communicate to GMP F&E leadership team
• Develop staff through annual Career Development Planning and acting as a role model
• Improve team performance by conducting regular 1:1 meetings and using Maxmizing Amgen’s Performance (MAP) process : regular coaching, mid-year and end of year reviews, compensation planning, and talent management planning
• Promote Operational Excellence and Safety through purposeful presence on the floor (Regular job task walk-through with staff members)
• As a member of the extended leadership team, partner with maintenance managers to improve Maintenance support
• Provide Subject Matter Expertise to triage and resolve issues related to Maintenance process non-conformances

Technical

• Leverage knowledge of GMP F&E Process, Mechanical and Utility systems and instrumentation to develop team capabilities in diagnosis and troubleshooting of issues
• Manage lifecycle assessment and recommend replacement / upgrades as required to ensure high reliability
• Maintain awareness of relevant industry and regulatory trends for calibration /instrumentation and maintenance
• Provide input for responses to regulatory inspections or internal audits relating to instrument calibrations or maintenance programs

Logistical / Administrative

• Manage staff resources and work schedules (vacations, on-call rotation, etc.) to ensure adequate staff coverage and meet required PM calibration dates
• Ensure that staff maintain required training qualifications and are cross-trained to support multiple GMP buildings as needed
• Coordinate resources to support capital projects and work activities during maintenance shutdowns
• Manage department budget and expenses
• May require second or third shift work

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an employee with these qualifications.

Basic Qualifications:

Doctorate degree

Or

Master’s degree and 2 years of maintenance and/or operations/manufacturing experience

Or

Bachelor’s degree and 4years of maintenance and/or operations/manufacturing experience

Or

Associate’s degree and 10 years of maintenance and/or operations/manufacturing experience

Or

High school diploma / GED and 12 years of maintenance and/or operations/manufacturing experience

Preferred Qualifications:

• Bachelor’s degree in life science, technical or aligned field of study
• 6+ years of relevant work experience in operations/manufacturing environment
• 3+ years of experience with regulated environments (i.e. cGMP, OSHA, EPA)
• Managerial experience directly managing people and/or leadership experience leading teams
• Experience working with ATO GMP F&E clients and systems (Bulk Manufacturing, Filling and Packaging, Supply Chain, Quality Labs, Small Molecule Manufacturing)
• In-depth technical knowledge of GMP instrumentation
• Experience supporting GMP capital project execution and verification activities
• Demonstrated leadership attributes as an individual contributor (e.g., leadership of initiatives or participation on network level or continuous improvement teams)
• Demonstrated proficiency in process improvement methodologies
• Leverage a strong background in GMP Maintenance combined with excellent leadership and communication skills (written and verbal)
• Ability to support multiple clients and prioritize resources against competing objectives

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Regulatory Labeling Manager

Live

What you will do

Let’s do this. Let’s change the world. As part of Global Labeling (GL), and under the supervision of the Therapeutic Area Lead, the Regulatory Labeling Manager is responsible for supporting the facilitation and management of the end-to-end labeling processes for the pre- & post-marketed products over the product's life cycle. In this vital role you will author, enable internal governance reviews and manage the development of the Target Product Label, Core Labeling documents and USPI in accordance with Amgen Labeling Processes for assigned therapeutic area(s).

Principal responsibilities include:

• Authors and maintains core company labeling documents (including Core Data Sheet, Core Patient Information Leaflet, and Core Instructions for Use) in support of global marketing applications and variations.
• Leads the cross-functional Labeling team as a Labeling Strategy subject matter expert for the creation and update of labeling - for alignment and communication of labeling text at product launch.
• Authors US labeling documents (including USPI, Medication Guide, PPI, IFU) for the initial Marketing Authorization Application and updates for new indications, efficacy data, product quality changes and safety related topics. Presents to cross-functional and executive level management to obtain endorsement, as appropriate, for the proposed core document and US labeling text.
• Leads cross-functional teams (Labeling Working Group) to align on the proposed core document and US labeling text.
• Provides strategic guidance on labeling regulations, requirements, competitor labeling, and labeling trends across the organization.
• Provides consultation to internal and/or external experts on the creation of high quality core labeling documents and manages the dossier annotations within the documents
• Provides strategic labeling advice for major regions and works with cross functional teams to ensure that the implementation of global regulatory labeling plans are aligned with global regulatory strategies
• Reviews and approves deviations from core labeling; ensures deviations from labeling procedures and policies are addressed appropriately.
• Supports preparation of responses to labeling-related Health Authority queries
• Incorporates feedback from HF studies into the cIFU (e.g., with incorporation of participants output during the formative/summative studies into the labeling) and associated combination product labeling
• Supports the continuous improvement of initiatives across the End to End labeling process.
• Supports creation of target product labeling.
• Manages the review and approval of core DHCP letters
• Regulatory Labeling core member/SME on product-specific Global Regulatory Teams (GRT).

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.

Basic Qualifications:

Doctorate degree

Or

Master’s degree and 2 years of related experience

Or

Bachelor’s degree and 4 years of related experience

Or

Associate’s degree and 10 years of related experience

Or

High school diploma / GED and 12 years of related experience

Preferred Qualifications:

• Demonstrated experience in authoring, developing, and updating Pharmaceutical or Biotechnology product prescribing information labeling
• Degree in pharmaceuticals, life science or medicine
• Knowledge of prescribing information labeling development within various Therapeutic Areas
• Knowledge of FDA, or EMA, or other international regulations for prescribing information labeling with understanding the impact of emerging trends and their implications for Amgen
• Project Management experience, experience managing individual and group projects of moderate complexity
• Strong collaboration, presentation, communication, interpersonal, and leadership skills
• Experience working in a Veeva-based RIM Regulatory Management system

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

Director, Induced Proximity Platform - Large Molecule Modalities

Live

What you will do

Let’s do this. Let’s change the world. In this vital role you will be a part of Amgen’s Induced Proximity Platform team. We are seeking an accomplished Director to lead our efforts to discover the next generation of novel large molecule induced proximity therapeutics. In this position you will lead a research team in the Induced Proximity Platform at the cutting edge of drug discovery to enable both platform technology development and enablement of pipeline programs. As a skilled organizational leader, this individual should be an efficient manager, a strong team builder and a collaborator who will provide robust organizational and scientific leadership consistent with Amgen’s culture of innovation and teamwork.

Responsibilities:

• Supervise a group engaged in developing platform technology for large molecule Induced Proximity modalities
• Contribute to the development and implementation of the research strategy in the Induced Proximity Platform, with a specific focus towards large molecules
• Deliver programs into our pipeline focused on induced proximity with large molecules
• Develop effective cross functional relationships with colleagues in therapeutic areas, including Oncology, Inflammation, Cardiometabolic, and Large Molecule Discovery

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Scientific professional we seek is ambitious collaborative leader with these qualifications.

Basic Qualifications:

Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable] and 5 years of relevant industry experience

Or

Master’s degree and 8 years of relevant industry experience

Or

Bachelor’s degree and 10 years of relevant industry experience

Preferred Qualifications:

• A proven track record of scientific innovation and accomplishment in large molecule induced proximity modalities, as demonstrated by a strong publication record, patent submissions, and presentations at leading conferences.
• A deep understanding of ubiquitin biology, protein trafficking, protein degradation, proximity based therapeutics, and large molecule formats
• Demonstrated experience in advancing novel drug discovery programs from hit finding to preclinical evaluation
• An understanding of the emerging technologies being directed at hard to drug targets
• Strong written/verbal communication and interpersonal skills
• Experience in leading, mentoring and developing the careers of a diverse and talented team
• An ability to build strong and productive relationships with peers and cross functional partners

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Contracts and Development Manufacturing Manager

Live

What you will do

Let’s do this! Let’s change the world!

Amgen is seeking a Manager to join the Amgen Contract Development and Manufacturing (ACDM) Organization. The location can be based out of either Thousand Oaks, CA or Cambridge, MA office and may exist in a virtual setting. The ACDM Manager will oversee contract test labs to deliver on Amgen’s pipeline and commercial products. The ACDM Manager will be responsible to ensure multiple Amgen programs meet critical timelines at external partner analytical and manufacturing sites.

Job Responsibilities include:

• Project leadership for analytical testing of pipeline and commercial drug product and drug substance programs. Primary focus will be to manage delivery of analytical work packages (method validation, method transfer, release testing, stability testing) on time to support pipeline and commercial programs.

• Supplier relationship management, including reporting of metrics and monitoring performance to continuously improve efficiency and effectiveness of suppliers.

• Ensuring programs meet compliance, speed, quality, and cost targets through strong scientific and technical understanding of the programs and drug product development.

• Identification of project optimization opportunities (timeline, budget, technical execution), prioritization of a rolling portfolio of projects.

• External vendor evaluation and selection.

• Self-starter who can manage multiple assignments.

• Building and maintaining strong partnerships with internal and external functions to increase overall effectiveness and success of programs.

• Ability to lead highly matrixed teams.

• Presentation of analyses and recommendations to Senior Management.

• This position will require occasional domestic and international travel.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The management professional we seek is a collaborative cross-functional leader with these qualifications.

Basic Qualifications

• Doctorate degree OR

• Master’s degree and 2 years of experience OR

• Bachelor’s degree and 4 years of experience OR

• Associate’s degree and 8 years of experience OR

• High school diploma / GED and 10 years of experience

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

• Stock-based long-term incentives

• Award-winning time-off plans and bi-annual company-wide shutdowns

• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

You’ve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role.

Senior Mechanical Engineer

Live

What you will do

Let’s do this! Let’s change the world! In this vital role you will be responsible for ensuring execution of a safe, compliant, effective, efficient, and cost appropriate engineering & design programs. The Engineering Technical Authority (ETA) within Amgen Corporate Engineering leads the design effort for critical projects and provides technical expertise across Amgen’s global operations network. This position is part of the ETA organization that includes Process Systems, Facilities and Utilities, Site Project Engineering, Maintenance and Metrology functions. The Senior Engineer will be part of the implementation of capital projects design and delivery teams, among other responsibilities, and will work with the Global Engineering Services Team.

This position is primarily responsible for the engineering & design of both new and existing biotech manufacturing, laboratory facility, general offices, and cold storage projects. It is a technical role that leads and facilitates the engineering and design of HVAC and related systems for biotech manufacturing, laboratory, and general building projects. The engineer is responsible for ensuring compliance with regulatory, quality, and cost standards, as well as providing technical guidance and specifications to optimize the performance and sustainability of Amgen's assets. The engineer will also coordinate with other engineering fields, consultants, contractors, and key collaborators to deliver safe, effective, and efficient solutions for capital projects and network support. The engineer will have strong leadership, communication, analytical, and technical skills, as well as knowledge of industry trends and best practices.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a strong collaborator with these qualifications.

Basic Qualifications:

• Doctorate degree OR
• Master’s degree and 2 years of Maintenance or Engineering experience OR
• Bachelor’s degree and 4 years of Maintenance or Engineering experience OR
• Associate’s degree and 8 years of Maintenance or Engineering experience OR
• High school diploma / GED and 10 years of Maintenance or Engineering experience

Preferred Qualifications:

• Bachelor’s Degree in Engineering.
• Engineering Professional License.
• 6+ years’ experience in engineering or maintenance or related function within the biotechnology and/or pharmaceutical and/or Medical Device industry.
• 5+ years’ experience and track record of ensuring compliance in a highly regulated environment.
• Familiar with and understand current Good Manufacturing Practices, HVAC and Building Mechanical Systems with demonstrated experience with load calculations, air handling systems, hydronic systems, plumbing systems, fire protection systems, airflow diagrams, A&IDs, and Building Mechanical System P&IDs.
• Proven success applying these to cGMP manufacturing and laboratory facilities.
• Ability to apply knowledge of ductwork and piping sizing, design, installation, and commissioning, cold storage refrigeration systems.
• Experience in system and equipment sizing, selection, specification, operation, commissioning, and troubleshooting, including air handlers, fans, coils, humidifiers, filters and filtration, terminal devices, refrigeration equipment, compressors, chillers, pumps, cooling towers, boilers, fume hoods and biosafety cabinets, HVAC control system design and function, code requirements.

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

Process Development Senior Principal Scientist – Peptide Chemistry (Synthetics)

Live

What you will do

Let’s do this. Let’s change the world. Amgen is seeking a dedicated Process Development Senior Principal Scientist with industry experience in peptide synthesis and manufacturing to join our Drug Substance Technologies - Synthetics (DSTS) group in Cambridge, MA. Amgen’s DSTS group within Process Development (PD) is responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's portfolio of synthetic and hybrid assets. The Senior Principal Scientist role will include leading a multidisciplinary team of chemists and chemical engineers in the development of efficient and sustainable manufacturing processes for peptide synthesis and purification, driving technology innovation in the areas of chemical and microbial recombinant peptide production technologies, and providing technical expertise as well as developing and mentoring staff within the organization. The successful candidate for this role will be a people-centered leader with expertise in peptide process development and manufacturing with a consistent track record of scientific innovation and leadership within the pharmaceutical industry.

Key Responsibilities:

• Lead a multidisciplinary project team in the development of sustainable and cost-effective processes for peptide manufacturing
• Drive technology innovation in the areas of chemical and microbial recombinant peptide production technologies
• Support cGMP manufacturing and technology transfer to large-scale peptide production facilities
• Develop strategies to ensure process performance through process understanding, modeling and characterization
• Guide successful completion of project deliverables and ensure timelines are met
• Work multi-functionally to deliver regulatory documents and support regulatory filings
• Serve as a technical expert and keep current in the field of peptide synthesis and manufacturing
• Coach and provide career and scientific / technical advice to colleagues within the organization

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The scientific professional we seek will possess these qualifications.

Basic Qualifications:

Doctorate degree PhD OR PharmD OR MD in Chemistry, Chemical Engineering, or Biochemistry/Chemical Biology and 3 years of industry experience

Or

Master’s degree in Chemistry, Chemical Engineering, or Biochemistry/Chemical Biology and 6 years of industry experience

Or

Bachelor’s degree n Chemistry, Chemical Engineering, or Biochemistry/Chemical Biology and 6 years of industry experience

Preferred Qualifications:

• 6+ years in the pharmaceutical industry with expertise in peptide process development and manufacturing (solid-phase peptide synthesis, liquid-phase peptide synthesis, site-selective peptide modification, semisynthetic approaches, chemoenzymatic peptide synthesis)
• Ability to work within a dynamic and interdisciplinary environment to achieve results
• People-centered leadership skills in building strong teams through mutual trust and respect and exhibits Amgen leadership attributes of inspire, accelerate, integrate, and adapt
• Track record of publications, patents and presentations

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans and bi-annual company-wide shutdowns
• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

Environment, Health, Safety and Sustainability (EHSS) Senior Manager

Live

What you will do

Let’s do this! Let’s change the world! In this vital role, you will provide world class EHSS Environmental Management leadership and client support across Amgen’s growing network. This role will work with an empowered team to lead global environmental compliance programs and support the development of innovative and compliant solutions.

The successful candidate will:

• Support Amgen’s expanding business by assuring innovative, compliant, and efficient facility design, execution, and operational readiness.

• Actively participate in Capital Project Engineering assessments and conceptual design process.

• Apply a “Plan, Do, Check, Act” management systems approach to monitor and continually improve environmental program network performance.

• Serve as a global program manager and subject matter expert in designated environmental programs including water quality, air quality, waste management, and hazardous material transportation.

• Apply your environmental compliance expertise to the network to provide guidance, support the business, and manage complex challenges.

Primary responsibilities include:

• Implement global environmental management systems to assure compliance with all country, state, and local regulatory requirements and authorizations.

• Liaise with regulatory agency representatives and other external parties.

• Support Engineering teams by completing compliance assessments, effluent modeling, and review of treatment system designs.

• Investigate environmental incidents and assure robust corrective and preventive actions are implemented.

• Provide environmental expertise to risk assessments of new and existing systems and processes.

• Prepare EHSS governance dashboards and provide guidance and expertise to functional leadership.

• Evaluate the impact of changes in the regulatory landscape upon Amgen operations and lead the development of compliance plans and processes.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The experienced professional we seek is a strong leader with these qualifications.

Basic Qualifications:

• High school diploma / GED and 12 years of EHSS or Engineering experience OR

• Associate degree and 10 years of EHSS or Engineering experience OR

• Bachelor’s degree and 6 years of EHSS or Engineering experience OR

• Master’s degree and 4 years of EHSS or Engineering experience OR

• Doctorate degree and 2 years of EHSS or Engineering experience

Preferred Qualifications:

• Advanced Engineering or Environmental Management degree in related field and 10 years of experience in the pharmaceutical/biotech industry leading EHSS programs.

• Advanced relevant EHSS Certifications such as Certified Hazardous Materials Manager, Certified Environmental Professional, Board Certified Environmental Engineer.

• Demonstrated success in managing Environmental Compliance programs, with expertise in wastewater management and treatment system design.

• Strong leadership and communication skills.

• Demonstrated success with maturing programs and processes with a continuous improvement mindset.

• Proficient in Microsoft Office and EHS management system software solutions.

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

• Stock-based long-term incentives

• Award-winning time-off plans and bi-annual company-wide shutdowns

• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

Career Category

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of.

Oncology Advocacy Relations Senior Manager (Open)

Live

What you will do

Let’s do this! Let’s change the world! In this vital role, the Oncology Senior Manager of Advocacy Relations at Amgen is responsible for building and leading long-term relationships with global advocacy groups and contributes to elevating Amgen as a trusted partner of choice for patients and patient organizations. They may support educational campaigns, integrate the patient voice across a product’s lifecycle, elevate individual patient stories, and champion equitable access to improve the health outcomes for patients living with cancer.

The following are key responsibilities and elements of the role:

• Builds and maintains long term, substantive relationships with patient groups, professional associations and other key stakeholders based on values of trust, respect and transparency

• Develops aligned advocacy strategy plans with internal functions to ensure One Amgen voice and priorities are incorporated into engagement plans

• Drives high-quality initiatives around shared goals including improving patient empowerment, shared decision making, and bringing novel therapies to the patients who need them.

• Supports patient groups to advocate for patients to receive guideline appropriate cancer screening and treatment

• Mobilizes patient groups to advocate for equitable patient access to appropriate treatments

• Brings the voice of patients and advocates to address patient unmet needs and drive patient focused solutions in the design and development of our clinical development programs

• Creates engagement opportunities for patients and their caregivers to share their stories and experiences across the organization

• Works cross-functionally as a strong partner and collaborator with global and US teams including Marketing, Medical, Value and Access, Government Affairs and Corporate Affairs

• Coordinates Amgen’s engagement strategies with stakeholders at Medical Congresses

• Identifies and understands the drivers behind the official positions, priorities, and networks of influence of key patient and professional associations and advocacy groups to advise Amgen’s business strategies

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Advocacy professional we seek will have these qualifications.

Basic Qualifications:

Doctorate degree and 2 years of advocacy, policy, marketing, or medical experience

Or

Master’s degree and 4 years of advocacy, policy, marketing, or medical experience

Or

Bachelor’s degree and 6 years of advocacy, policy, marketing, or medical experience

Or

Associate’s degree and 10 years of advocacy, policy, marketing, or medical experience

Or

High school diploma / GED and 12 years of advocacy, policy, marketing, or medical experience

Preferred Qualifications:

• 5+ years of experience with oncology patient advocacy groups and/or professional (medical) associations.

• 3+ years of experience working for global pharmaceutical companies as a liaison with patient advocacy groups and/or professional associations.

• Sensitivity to diverse groups of people both internal and external with the ability to manage many different opinions and perspectives, including tolerance for ambiguity.

• Demonstrated reputation internally and externally as a well-respected, dynamic team-player.

• Empathic and hardworking individual with the ability to build meaningful connections with stakeholders.

• Previous experience leading the development of professional medical society and patient advocacy strategies for pharmaceutical organizations.

• Previous experience as relationship manager for professional medical associations and patient advocacy groups.

• Demonstrated understanding of key external and internal trends affecting patient and consumer engagement; solid understanding and experience in new forms of patient/consumer interactions such as social media and patient online communities.

• Previous experience communicating the value of innovation and addressing access barriers to care.

• Previous experience communicating complex health policy access issues to patient advocates

• Demonstrated ability to adapt relationship style to external partner’s preferences and comfort levels

• Previous experience in government affairs.

• Outstanding verbal and written communications skills and an ability to adapt one’s approach to a challenge, as well as excellent interpersonal skills.

• Ability to assimilate complex medical knowledge and communicate to non-medical audiences.

• Capable of handling shifting priorities in a constantly evolving environment.

• Understands the pharma/biotech business model, regulatory process & compliance guidelines.

• Experience with product (drug) launches.

Thrive

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for our teammates’ professional and personal growth and well-being.

Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities including:

• Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan

• Stock-based long-term incentives

• Award-winning time-off plans and bi-annual company-wide shutdowns

• Flexible work models, including remote work arrangements, where possible

Apply now

for a career that defies imagination

Objects in your future are closer than they appear. Join us.

careers.amgen.com

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range