Total 30 Quality Assurance / Control job vacancies in Green Forest Plant - Green Forest, Arkansas

Duties may include, but are not limited to:

-Prepares for compliance survey (audit) of an education and training program by examining and reviewing various informational sources.
-Examines education records for enrolled students and ascertains enrollment data and award actions.
-Verifies institution has provided appropriate forms for compliance with Equal Opportunity Laws, Conflicting Interest and other documents required for State Approving Agency (SAA) program approval of Veteran education benefits.
-Conducts investigations and evaluations pertaining to compliance with provisions of Title VI of the Civil Rights Act of 1964 and Title IX of the Education Amendments of 1972, Section 404 of the Rehabilitation Act of 1973 and the Age Discrimination Act of 1975. Interviews students and school administrators or employees during the course of investigation to substantiate or refute allegations.
-Completes assigned Targeted Risked Based Reviews (TRBR) and Risk-Based Surveys (RBS)
-Conducts entrance and exit-briefings at educational and or training establishments, delineating results of survey findings with School Certifying Officials.
-Prepares compliance survey report which indicates whether discrepancies found on a prior survey have or have not been corrected, report any discrepancy found on the current survey, and explains what additional action, if any, is required.
-Records payment discrepancies to include direct overpayments or underpayments made to the educational institution on behalf of a GI Bill beneficiary.
-Refers institution approval and payment discrepancies for action, as appropriate, to other VA personnel, and/or other regulatory agency and provides recommendations in cases of egregious or negligent reporting errors or possible fraud.
-Assists with liaison visits to educational institutions and training establishments. Aids in the preparation and dissemination of necessary compliance information, conducts face to face training, addresses deficiencies found during a compliance survey, and presents at school conferences and workshops advising school officials about VA regulations and directives. Other duties as assigned.

Work Schedule: 8:00 a.m. to 4:30 p.m. Monday through Friday
Telework: Eligible
Virtual: This is NOT a virtual position
Position Description Numbers: 38799A, 38798A
Relocation/Recruitment Incentives: Not Authorized
Financial Disclosure Report: Not Required
Compressed/Flexible: Available for highly qualified candidates.
Must have a Valid Drivers License: Yes
Physical Requirements: The work is primarily sedentary. Some physical effort may be required such as walking, standing, bending, reaching, and carrying of office and event materials.
Promotion Potential: GS-11

Starting at $51,332 Per Year (GS 9-11)

Financial Institution Interns will be assigned to the Division of Depositor and Consumer Protection (DCP).  Interns will work directly on teams with experienced FDIC employees to evaluate FIDC-insured institutions' compliance with fair lending and consumer protection laws and regulations.  These teams are responsible for assessing financial institutions to determine whether they are maintaining effective controls and procedures, managing their institutions effectively, and complying with all applicable laws and regulations, including those relating to consumer protection, privacy, community reinvestment, and fair lending.

Under the direction and supervision of an Examiner or a higher grade team member, the incumbent will participate in and/or independently perform the following:

Assesses the adequacy and determines the strength of the Compliance Management System (senior management oversight; compliance program, including the elements of policies, monitoring, and training; and audit procedures) to ensure ongoing compliance as related to the particular regulation under review.  Conducts reviews and assessments of the following: 

• Examine initial disclosures, periodic statements, advertisements, and other information to evaluate procedures and reviews for compliance with applicable regulations.
• Examine closed-end non-real estate credit transactions for compliance with applicable regulations.
• Review the Home Mortgage Disclosure Act loan application register for accuracy and assesses the bank's overall reporting procedures.
• Review adverse action notices for compliance, and to gain a cursory exposure to applicable lending-related regulations.
• Examine a sample of residential, consumer, commercial and/or agricultural files to determine compliance with consumer laws and regulations.

Reviews applicable regulations and examination manual to become informed about the Community Reinvestment Act (CRA).

Participates in discussing the overall examination process including evaluating the bank's Compliance Management System (senior management oversight; compliance program, including the elements of policies, monitoring, and training; and audit procedures).  Asks questions to gain clarification and understanding of examination policies and procedures.

• Observes the interactions between the FDIC and Bank personnel.
• Responds to questions from other examiners regarding his/her section of the Report of Examination.
• Reviews the CRA of an institution and participates in discussion for assigning its rating.
• Prepares a summary of each performance factor describing why rating was assigned.
• With the assistance of an experience examiner, participates in meetings as appropriate.
• After the meeting, asks questions and discusses exam findings with the examiner-in-charge or higher graded team member.

Starting at $51,262 Per Year (CG 04)

• Designs/implements/maintains a risk-based surveillance program and assessment plan associated with the quality assurance provisions of contracts.
• Identifies opportunities for process improvements by analyzing data.
• As a member of a multi-functional or technical team, implements the overall Quality Program for diverse products and services to support the U.S. Government’s acquisition at one or more supplier facilities.
• Ensures contractor compliance with design, manufacturing, repair, overhaul, and modernization requirements.
• Independently audits/surveys contractor processes to ensure compliance with customer/contractual requirements.
• Investigates customer complaints/concerns about contractor quality performance and processes which impact user satisfaction, then provides data about the complaints.
• Provides technical support to DCMA team members, assisting with analyzing contractual issues, and determining the best course of action to support the contractor and customers.

Starting at $72,553 Per Year (GS 11)

You will be able to find a full Job description and Person Specification attached within the supporting documents or please click Apply now to view in Trac Main Responsibilities Planning and Design Responsible for planning & prioritising own workload. Improvement and Monitoring The post holder will be expected to trouble-shoot and diagnose faults on the complex equipment The post holder, will be responsible for ensuring that all equipment and processes are maintained in a validated state, reporting deficiencies to their manager. The post holder will be responsible for the calibration, validation of critical test kits and equipment The post holder may be requested to prepare Operating Procedures The post holder will be expected to follow all policies/procedures and SOPs identified as a requirement of their job role. This will involve reading and understanding relevant polices and being trained to SOPs. The post holder will be expected to support and participate in the production of peer reviewed publications, including posters, abstracts and presentations. Communications The post holder will be required to demonstrate effective communication and team working skills with colleagues in their own team/department, staff in other departments of the WBS and external customers. Examples of this will include the taking and passing on of accurate messages to person(s) who need to know, providing information when requested, participating fully within the team. The post holder will be required to communicate both verbally and in written format with internal colleagues and external customer hospitals as directed by the Head of Quality Assurance Laboratory to ensure the service requirements are met. Clinical and Scientific The post holder will be required to perform specialist technical and scientific procedures in the four sections of the Quality Assurance Laboratory. The post holder will be required to possess a BSc Hons in Biomedical Sciences or other honours degree approved by the Institute of Biomedical Science (IBMS) for registration with the Health and Care Professions Council (HCPC). The post holder must be a registered BMS with the HCPC. If registration qualification has been achieved through the IBMS Registration Portfolio the post holder will be required to complete or have attained the IBMS specialist portfolio in Transfusion Science and GMP as a pre-requisite for a specialist BMS post. This typically requires at least 2 years post graduate study to diploma level. The post holder will be required to participate in the Continuing Professional Development (CPD) The post holder is required to have a thorough working knowledge of the requirements of external regulatory requirements to which the WBS must comply. These will include MHRA/BSQR, UKAS. The post holder will be required to have a thorough understanding of the principles of Good Manufacturing Practice (GMP) and its role in WBS quality systems. The post holder will be required to demonstrate an awareness of all relevant guidelines to which the WBS must adhere. These will include UK Guidelines for Transfusion Services (Red Book), Council of Europe Guidelines, and relevant BSH Guidelines. The post holder will be responsible for the preparation of samples and testing on specialised automated equipment. Interpret diagnostic test results and refer any out of control or abnormal results to the senior staff within Quality Assurance Laboratory for subsequent referral onto the medical staff of FBC results that may indicate the need for a clinical referral. Ensures that all specialist equipment is maintained in a calibrated state by the use of appropriate control and reference samples, thus ensuring that any patient results or quality monitoring samples can be reliably reported. Finance and Budget Responsible for the safe use of expensive and highly complex equipment, Responsible for maintaining stocks of disposable and recyclable items and ordering from stores to agreed financial limits. Maintenance of adequate stock levels of both in-house prepared and commercial reagents. Assist with evaluation and validation of equipment and processes being introduced at the Welsh Blood Service (WBS). Assist Section Leaders in the maintenance of chemical and reagent stock and ensure safe disposal of samples and waste. Assist in the management of COSHH. Management, Leadership and/or Training The post holder will be required to prioritise their own work and the work of their colleagues once they have been deemed competent to do so. Examples of this will include the prioritisation of routine work against research activities, or the prioritisation of calibration activities that are scheduled against validation activities following the failure of GMP critical equipment. The post holder will be expected on occasions to work and report autonomously within defined laboratory procedures e.g. CD34+ and on-call Digital and Information Assist the HOD or section leader in the collection of quality control data for Statistical Process Control/Monitoring and enter test results onto the appropriate computer software packages to maintain and improve the Quality Systems. Identify any problems and initiate appropriate agreed corrective action. The postholder will be required to create statistical reports Perform regular data back-up Qualifications and Knowledge Experience Essential BSc Hons in Biomedical Sciences (accredited by IBMS) for HCPC registration Registered with HCPC IBMS Specialist Portfolio in Transfusion Science (or equivalent qualification where appropriate or evidence of working towards completion) Participating in a CPD scheme Knowledge of Regulatory requirements i.e. MHRA, CPA and ISO Knowledge of UK Guidelines for Transfusion Services (Red Book) and relevant BSQR, BSH & Council of Europe Guidelines Essential Previous employment as a registered BMS whilst completing Specialist Portfolio Previous experience of quality control, sampling analysing and reporting data metrics Desirable Previous experience of QA Previous experience of root cause analysis and investigation techniques Previous Experience of change management Skills and Attributes Other Ability to communicate effectively both orally and in written format Ability to work effectively as part of a team Generic Laboratory skills e.g. pipetting, microscopy etc. Planning & Organising skills Good interpersonal skills Practical approach to problem solving Presentation skills Data graphics and Analytics Desirable (but not essential): Welsh Speaker (Level 1) or willingness to work towards An interest in the field of Blood transfusion & GMP, Enthusiasm for the career applied for

Material Quality Engineer / Manager

Temple Mills (London)

£200 per day PAYE / £249 per day Umbrella (based on experience)

6 month contract (Project 12 months)

Inside IR35

Job Spec:

Monitor control and generate Key Performance Indicators on the repair loop quality and performance. Update and KPI the repair reports database. Implement and maintain a closer link between the train performance and the repaired materials. Control that the outgoing materials have a clear failure description attached and a serial number. Control and challenge the suppliers on the quality of the repair reports that they provide and ensure that the scope of the repairs meet the required needs. Monitor and flag endangering consumption trends. Quarantine and return to good stock materials based on work orders data and data generated by the trains (i.e. defect codes). Analyze and close non conformance of materials previously repaired. Schedule on-train testing of parts if required.

Functions:
* Control and challenge the failure description of outgoing materials and the information in the repair reports from OEMs
* Work reports and train data checks to review defective components (quarantine and return to good stock materials. Est: 10% of the volume)
* Link between performance and materials: Monitor materials involved in performance incidents.
* Schedule on-train testing if required
* Monitor Consumption Trends (USD reduction proactive approach)
* Root cause analysis and rectification for NCMs
* Update and KPI the repair report database.
* KPI the improvements on all these areas

Qualifications and Experience

• Rolling Stock related technical background.
• Minimum 3-5 years of depot work or Maintenance Engineer Level 3.
• Experience in depot work environment.
• IT skills (user level).
• Experience in Excel.
• Experience in BI tools (desirable).
• Experience in stores processes (desirable).

Siemens supports applications from a diverse talent pool. We welcome the opportunity to discuss flexibility requirements. If you require any reasonable adjustments to be made to enable you to participate in the recruitment process, please contact us on 0161 233 7603

RBoniface

Since 1978, Rullion has been securing exceptional candidates for a range of clients; from large well-known brands, to SMEs and start-ups. As a family-owned business, Rullion's approach is credible and honest, focused on building long-lasting relationships with both clients and candidates.

Rullion is a forward-thinking recruitment company that specialises in providing a wide range of talent consultancy services to a diverse client base; from small start-ups to large household names.

Rullion celebrates and supports diversity and is committed to ensuring equal opportunities for both employees and applicants.

Relocation Assistance Eligible:

Yes

Referral Payout Eligible:

Yes

Continue growing with our family. 

Our team members make it happen. If you want to continue to grow in a new role internally and see a position that looks right for you, we encourage you to apply!

Thanks for your commitment to Tyson Foods. 

Management Level:

M3

SUMMARY:

The Associate Director Food Safety and Quality Assurance (FSQA) position is responsible for ensuring products and processes meet the highest standards of compliance for food safety and quality within Tyson Facilities.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Work with Plant FSQA managers to ensure FSQA policies and procedures are adhered to and to lend technical expertise when needed
• Investigate product complaints to determine cause and help determine solutions and interface directly with the customer
• Direct the continued development and implementation of new programs and/or procedures at individual plant locations
• Interacting with appropriate governmental regulatory agencies such as USDA and FSIS.
• Collaborate with appropriate departments within Tyson Sales, Marketing, Engineering, Operations, Research and Development, and Scheduling and internal/external customers on quality and food safety related issues
• Update, develop and maintain corporate FSQA programs and procedures
• FSQA training and development
• Conduct plant audits reviews to provide overview of plant systems associated with regulatory food safety and product quality concerns; data review and analysis
• Other responsibilities as they are assigned or as the need arises.

REQUIREMENTS:

• Education: Bachelor’s degree in a technical or science related field OR equivalent experience in food safety and quality assurance
• Experience: 8 plus years of food safety quality assurance operations experience
• Computer Skills: Basic computer skills including proficiency in MS Office Suite, experience with ERP/SAP, product specification management, product develop applications
• Communication Skills: Excellent verbal and written communication skills
• Supervisory: Position will have direct reports at multiple locations
• Travel: Extensive travel to the location in which this role supports. Minimum 12 trips per year.

Work Shift:

1ST SHIFT (United States of America)

Tyson is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will be considered without regard to race, national origin, color, religion, age, genetics, sex, sexual orientation, gender identity, disability or veteran status.

We provide our team members and their families with paid time off; 401(k) plans; affordable health, life, dental, vision and prescription drug benefits; and more.

Relocation Assistance Eligible:

Yes

Referral Payout Eligible:

No

Continue growing with our family. 

Our team members make it happen. If you want to continue to grow in a new role internally and see a position that looks right for you, we encourage you to apply!

Thanks for your commitment to Tyson Foods. 

Management Level:

M2

To feed a changing world, it takes an incredible team. From the cutting board to the board room, every Tyson Foods team member plays an important role in our success. That’s where you come in. We are hiring immediately for a Food Safety Quality Assurance General Manager role.

Setting the table for your success:

At Tyson Foods, our team members’ health and wellness is very important to us. We believe in helping our team members thrive inside and outside of the workplace. That’s why we’re committed to providing a holistic benefits package that provides support for you and your family.

We invest in our team members and their success by providing resources like BENEFITS ON DAY ONE OF EMPLOYMENT and FREE EDUCATION!

Benefits include: medical/Rx, dental, and vision coverage; 9 paid holidays; 4 weeks paid vacation upon hire, plus earned time off; 401(k) with employer match; stock purchase program; and product purchase program.  We also offer CAREER GROWTH and much more!

SUMMARY: This location is part of our Prepared Foods Division and manufactures bacon! The Food Safety Quality Assurance General Manager is responsible for the daily management of all activities of the FSQA department to include food safety programs specification adherence and product quality for products within their assigned facility. In addition, the FSQA Manager will oversee all special projects as assigned, departmental budgets, turnover and safety.

RESPONSIBILITIES:

Production Oversight:

• Manage daily production practices, including the reception of raw materials.
• Ensure pre-operational and operational sanitation standards are met.

Quality Assurance:

• Oversee finished product quality and Food Safety Systems.
• Implement and enforce Tyson FSQA policies and procedures.
• Monitor verification and documentation for compliance with government regulations.

Program Development:

• Develop, implement, and maintain HACCP, HARPC, SOP, GMP, and SSOP programs.

Product Conformity:

• Ensure finished products align with customer specifications and label requirements.
• Report product issues and audit results to relevant stakeholders.

Customer Interaction:

• Interact with customers and their agents for product showings, plant tours, and audits.
• Address initial product runs and respond to quality-related customer complaints.

Microbiological Monitoring:

• Monitor microbiological results and conduct bacterial swabs.
• Generate shelf-life environmental graphs.

Research and Development:

• Conduct research and development activities to enhance food safety and quality.

Team Management:

• Select, train, and manage FSQA Supervisors and Technicians.
• Facilitate both Food Safety and Foreign Material teams at the plant.

Audit Management:

• Complete required internal, regulatory, and customer audits.

Inventory Control:

• Manage Hold Release inventories at the plant level in SAP.

REQUIREMENTS:

• Education: Requires broad knowledge in general professional or technical field. This knowledge is normally acquired through a bachelor s degree in an academic field directly related and essential to the job.
• Experience: Minimum 3 years of prior industry experience to fully grasp regulatory, production and manufacturing concepts preferred.  Experience with FDA and USDA regulated products.  SAP Experience a plus. 
• Computer Skills:  Standard computer skills required; generating spreadsheets and developing templates for use by plant management and corporate FSQA, sales and operations.
• Communication Skills: Excellent communication skills required, both written and verbal, demonstrating the proven ability to correspond with all levels - line team members to corporate management.
• Special Skills: Must have good problem identification and problem-solving skills. Must be able to work independently yet interact with many different facets within the organization and be the plant liaison to USDA.  HACCP Certified, PCQI Certified and SQF Certified preferred.
• Supervisory: Manage crewing labor and attendance of the FSQA department.
• Travel: 3-5 plus trips per year.

Work Shift:

1ST SHIFT (United States of America)

Tyson is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will be considered without regard to race, national origin, color, religion, age, genetics, sex, sexual orientation, gender identity, disability or veteran status.

We provide our team members and their families with paid time off; 401(k) plans; affordable health, life, dental, vision and prescription drug benefits; and more.

Are you ready for what’s next?  

Come explore opportunities within Brunswick, a global marine leader committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond.  Brunswick believes “Next Never Rests™,” and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation. 

Sea Ray Tellico Operation

Vonore, TN

Job Opening: Quality Engineer

Position Overview: The Quality Engineer (QE) role is responsible to pro-actively support development, implementation, and continuous improvement of the Tellico quality management system to ensure a consistently high level of performance within the facility and market segments that we participate.  The scope of the role will include activities spanning supplier quality, internal process control, and customer feedback.  The Quality Engineer will be accountable to help drive continuous improvement through the facility by analyzing quality data, prioritizing opportunities and leading improvement activities throughout the entire operations.

Roles and Responsibilities:

• Pro-actively facilitate the development of Quality Systems to provide consistent inspection and testing to meet company standards of good sound visual quality and functional reliability.
• This role will support both internal and external quality processes.
• Improve processes to reduce common cause variability and eliminate special cause by following Problem Solving techniques such as Six Sigma (DMAIC).
• Use of structured quality improvement tools including six sigma tools is required.
• Ensure appropriate collection of quality data, analyze the data for trends, identify corrective action opportunities, and drive corrective action activities.
• Interpret basic technical drawings including characteristics such as views, title blocks, dimensioning, tolerancing, etc. Interpret specification requirements in relation to product and process characteristics.
• Assist in the development, maintenance and reporting of quality measurements and analysis. Helps determine the adequacy and accuracy of quality standards. Where standards are not available, coordinates their development.
• Promote and ensure quality activities in manufacturing and support functions to assure that Quality Metrics improve.
• Facilitate and train employee groups on process improvement and waste elimination techniques.
• Lead teams in applying structured problem-solving methodology and tools to eliminate waste.
• Some common tools required to use are: Process Map, Pareto Chart, Trend Chart, Fishbone Diagram, 5-Why Analysis, Histogram, SPC, FMEA, 5S, Correlation Analysis, Error-proofing, and Control Plans.
• Investigate, analyze, and benchmark industry practices for process validation assessments.
• Accurately maintain company records and documents in accordance with policies and procedures.
• Actively support and lead our Corrective Action processes.
• Perform special assignments as required.

EDUCATION REQUIREMENTS:

• Bachelor’s degree in a related engineering field required although consideration will be given to individuals with commensurate marine experience

• Must be willing to complete additional advanced education/training courses as required.

PREFERRED QUALIFICATIONS/SKILLS:

• At least 3-5 years in a Quality or Manufacturing Engineering position required. Preferred time spent working in the marine industry.
• Hold a Six Sigma Green Belt or Black Belt or ability to acquire.
• ASQ Certified Quality Engineer certification (or equivalent) or ability to acquire.
• Must have working knowledge of CAR methodology, computer literate, root cause analysis, be able to apply inspection data for process control, process capability assessment, ISO quality systems, and SPC.
• Microsoft Word, Excel, PowerPoint, Project, Visio. Statistical software.
• Thorough knowledge of statistical process control, teaching skills, blueprint analysis, quality concepts, basic and advanced quality tools, and problem-solving techniques.
• Ability to lead, teach and motivate a team.
• Able to work a flexible work schedule when required.
• Organizational skills necessary to successfully manage multiple projects simultaneously.
• Ability to get along with diverse personalities while remaining tactful, professional, and flexible.
• Good written and oral communication to communicate with all levels of the organization.

Next is Now!  
We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and inspiration. Therefore, we encourage people from all backgrounds to apply to our positions. Please let us know if you require accommodations during the interview process. 

Equal Opportunity Employer: Minorities/Women/Protected Veterans/Disabled

EEO is The Law - click here for more information

Brunswick and Workday Privacy Policies

Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: hrsharedservices@brunswick.com or 866-278-6942.

All job offers will come to you via the candidate portal you create when applying through a posted position through https:///www.brunswick.com/careers.  If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at 866-278-6942 or HRSharedServices@brunswick.com.

#Brunswick Corporation - Sea Ray

Relocation Assistance Eligible:

No

Referral Payout Eligible:

No

Continue growing with our family. 

Our team members make it happen. If you want to continue to grow in a new role internally and see a position that looks right for you, we encourage you to apply!

Thanks for your commitment to Tyson Foods. 

Management Level:

P4

SUMMARY: As a part of Corporate Accounting this position is responsible for maintaining various elements of the Internal Control Environment for the Company and ensuring all risks both key and non-key are appropriately mitigated.

 

Responsibilities include but are not limited to the following:

• Developing, organizing, planning, and maintaining global Sarbanes-Oxley SOX documentation for various processes.
• Ensuring an adequate internal control environment exists and is operating effectively and efficiently to mitigate the risk of financial misstatement.
• Identifying and assessing business and operational risks on a continuous basis.
• Identifying internal controls to mitigate identified risks proactively.
• Identifying changes in the Company’s organization or strategy, acquisitions, divestitures, etc. and effectively communicating recommendations as to the impact these changes would have on ICFR, control-self assessment, process sub- certification process, and related software tools.
• The team member may also be responsible for understanding, maintaining, and developing IT controls that support the SOX documentation.

 

Additionally, this role will be involved in the effort to implement all necessary changes to the control environment and related documentation, as they are deemed necessary. The team member will need to be able to proactively develop and communicate intelligent viable scalable solutions when controls are deemed deficient, inefficient, or ineffective in addressing risks. Execute oversight and support in designing, planning, and administering global Sarbanes-Oxley SOX control self- assessment process, as well as, quarterly certification process. Facilitate education on the Company’s global SOX procedures including the control-self assessment, sub-certification processes, and related software tools to all business units and applicable team members. This position will be recognized as a subject matter expert on controls, SOX, and ICFR including keeping current and up to speed with new changes or proposed PCAOB, COSO, or other related regulatory changes as well as segregation of duties SOD issues and their impact on ICFR.

 

This position will also be responsible for other supplementary activities that support management’s ability to assert on the effectiveness of the control environment. Coordinating with Auditing Services and external audit firm to enhance efforts across groups to ensure compliance with SOX regulations and reporting requirements; monitoring segregation of duties SOD conflicts within the general ledger system and across all other SOX relevant applications; evaluating IS service requests for potential ICFR implications; and other duties and ad-hoc requests as deemed necessary.

 

REQUIREMENTS:

Education: Bachelor’s degree in an academic field directly related and essential to this job Business, Accounting, or Finance degree preferred. Master’s degree is a plus.

Experience: 2 plus years of progressive experience in financial accounting, internal controls audit, or comparable experience or advanced degree, professional certification with 1 plus years of progressive experience preferred. Public accounting experience a plus. Project Management experience a plus.  Experience working with auditors is a plus. Experience working with IT General Controls is a plus.

Computer Skills: Strong computer skills including Microsoft Office tools e.g. Word Excel PowerPoint Visio Power BI etc. Knowledge of SAP and Tyson legacy systems is a plus.

Communication Skills: Strong written and verbal communication skills.

Special Skills: Certified Public Accountant or Certified Internal Auditor preferred but not required.

Supervisory: NA

Travel: Limited to a few domestic trips per year.

Work Shift:

1ST SHIFT (United States of America)

Tyson is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will be considered without regard to race, national origin, color, religion, age, genetics, sex, sexual orientation, gender identity, disability or veteran status.

We provide our team members and their families with paid time off; 401(k) plans; affordable health, life, dental, vision and prescription drug benefits; and more.

Ihre Aufgabe

• Wahrnehmen der Product Center Verantwortlichkeiten für die Produktgrupp ‚PD-Lösungen‘
• Überwachungsaktivitäten der übergeordneten Produktqualität (über alle Standorte z.B. mittels globaler Besprechungen)
• Aufbereitung von Daten zu spezifischen Qualitätsereignissen
• Koordinieren der Kommunikation mit den internen und externen Interessenvertretern im Fall eines Qualitätsereignisses
• Aufbereiten von Reklamationsstatistiken (z.B. zur Unterstützung von PMS Aktivitäten)
• Mitarbeit an der globalen Harmonisierung von qualitätsbezogenen Prozessen und Testmethoden
• Schnittstelle zu den Qualitätseinheiten der relevanten Werke, zum Value Stream sowie anderen unternehmensweiten Funktionen
• Unterstützung der regulatorischen Funktionen zur Wahrung der Produktqualität/-konformität
• Unterstützung CAPA Management im Bereich Product Center Sterile Fluids
• Management globaler Änderungsprojekte mit regulatorischem Hintergrund

 

Ihr Profil

• Abgeschlossenes Studium (mind. Bachelor) im technischen oder naturwissenschaftlichen Bereich
• Erfahrung in einem Regulatory Affairs- oder Qualitätsumfeld im Arzneimittelbereich oder im medizinischen Bereich wünschenswert
• Kenntnisse im Bereich von Medizinprodukte- und Arzneimittelregelwerken (MDD, MDR, GMP, etc.) sowie Qualitätsmanagement- und Risikomanagementstandards (z. B. ISO13485, ISO14971, FDA 21 CDR §820, etc.) wünschenswert
• Sehr gute Englischkenntnisse in Wort und Schrift
• Sorgfalt, Eigeninitiative, Teamfähigkeit und Kommunikationsstärke runden Ihr Profil ab

Are you ready for what’s next?  

Come explore opportunities within Brunswick, a global marine leader committed to challenging conventions and innovating next-generation technologies that transform experiences on the water and beyond.  Brunswick believes “Next Never Rests™,” and we offer a variety of exciting careers and growth opportunities within united teams defining the future of marine recreation. 

Summary of Position: This 3rd shift position works with the V6/V8/V10 outboard assembly product lines and reports to the Quality Engineering Manager.  The main role of this position will be to maintain quality assurance procedures, practices, and standard evaluation methods, that will ensure product quality and integrity, and will minimize process variation.

Primary Duties and Responsibilities:

• Work individually or collaboratively to reduce manufacturing process or product variation, using laboratory instruments and equipment, along with root cause corrective action methods
• Lead or assist in formal problem-solving projects including completion of corrective action requests
• Look up engineering drawings on computers, read and understand tolerances and key product features
• Perform basic dimensional inspections of parts utilizing calipers, micrometers, and other hand-held gauges
• Recommend design changes or improvements in production methods through FMEA or other methods as appropriate
• Work with engineers, technicians, and operators to assist with training as required
• Support manufacturing's non-conforming material process as required, and identify scrap reduction opportunities
• Organize and assist in resolving quality spills, including part sorts, containment activities, and creating quality alerts
• Create visual aids to support operator instructions
• Perform internal process, product, and ISO audits as directed, to ensure assembly conformance to requirements
• Contribute to deviations, FMEAs, and other quality documents in the quality management system
• Clearly communicate quality standards on the production line and in toolbox meetings
• Clearly communicate quality concerns immediately to managers, supervisors, process techs, and operators
• Document quality issues through shift notes and hand off meetings
• Commitment to health and safety (both in the office, laboratory, and in the plant)

Knowledge, Skill and Ability Requirements:

• Possess a mechanical aptitude with the ability to reason through problems and suggest workable solutions
• Must be detail oriented, with the ability to pay very close attention to specifications
• Ability to perform basic mathematical calculations and basic statistics
• Proficient knowledge of PC software including Word, Excel, and Power Point
• Working knowledge of pertinent manufacturing assembly techniques
• Working knowledge of inspection techniques, metrology methods, and print tolerances
• Working proficiency in the use of inspection equipment such as micrometers, gauges, fixtures, etc.
• Possess both verbal and written communication skills to effectively present data and information to management
• Ability to guide supervision in making proper decisions relative to product and process control issues
• Self-motivated with the ability to learn and lead by example, utilizing a good work ethic and a positive attitude
• Excellent organizational, time management, communication, and follow-up skills
• Ability to perform duties independently, consulting supervisor for only occasional exceptions
• Ability to be flexible and able to manage diverse and/or changing priorities and assignments
• Ability to lead, work with, and instruct others in related job functions
• Willingness to work extended hours and weekends, per schedule and as needed

Education and Experience Requirements:

• High School diploma or GED required
• Associate degree or equivalent post high school combination of experience and relevant technical training
• Three or more years of experience with complex assembly operations in a manufacturing setting

Preferred Certifications:

• ASQ – Certified Quality Auditor, Quality Inspector, or Quality Technician is desired
• LSS Green Belt Certification desired

Preferred Qualifications:

• Associate’s or bachelor’s degree in manufacturing, engineering, science, or related field
• Demonstrated history of problem-solving skills and root cause analysis
• Ability to conduct mathematical calculations of moderate complexity
• Ability to organize data, perform statistical process analyses, and draw meaningful conclusions
• Ability to read and understand GD&T (Geometric Dimensioning and Tolerancing)
• Strong computer skills including knowledge of software such as Power BI and Power Apps
• Knowledge of manufacturing execution systems such as PINpoint or Rockwell Automation
• Knowledge of S.P.C. techniques
• Knowledge of quality tools including Process Mapping, PFMEA, Validation Studies, MSA, and Control Plans
• Experience in Lean Manufacturing and 5S
• Bilingual - ability to speak both English and Spanish

Next is Now!  
We value growth and development, recognizing that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. Diversity of experience and skills combined with passion is a key to innovation and inspiration. Therefore, we encourage people from all backgrounds to apply to our positions. Please let us know if you require accommodations during the interview process. 

Equal Opportunity Employer: Minorities/Women/Protected Veterans/Disabled

EEO is The Law - click here for more information

Brunswick and Workday Privacy Policies

Brunswick does not accept applications, inquiries or solicitations from unapproved staffing agencies or vendors. For help, please contact our support team at: hrsharedservices@brunswick.com or 866-278-6942.

All job offers will come to you via the candidate portal you create when applying through a posted position through https:///www.brunswick.com/careers.  If you are ever unsure about what is being required of you during the application process or its source, please contact HR Shared Services at 866-278-6942 or HRSharedServices@brunswick.com.

#Brunswick Corporation - Mercury Marine

Relocation Assistance Eligible:

Yes

Referral Payout Eligible:

No

Continue growing with our family. 

Our team members make it happen. If you want to continue to grow in a new role internally and see a position that looks right for you, we encourage you to apply!

Thanks for your commitment to Tyson Foods. 

Management Level:

M2

Please be sure to submit a resume in a Word or .pdf format.

SUMMARY: This position is responsible for the daily management of all activities of the FSQA department to include food safety programs specification adherence and product quality for products within their assigned facility. In addition, the FSQA Manager will oversee all special projects as assigned, departmental budgets, turnover and safety. 

Essential Duties & Responsibilities Include:

• Daily oversight of production practices including raw material receiving requirements; pre-operational and operational sanitation; finished product quality and Food Safety Systems; ensuring all Tyson FSQA policies and procedures are followed
• Monitoring verification and documentation associated with adherence to government regulations
• Developing, implementing and maintaining the HACCP, PCQI, SOP, GMP and SSOP based programs
• Ensuring finished product conforms to customer product and label specifications
• Report product issues and audit results to plant and corporate FSQA, plant management, corporate sales and/or operations
• Interacting with customers and their agents for product showings, plant tours and audits; visits to customer facilities
• Initial product runs and investigation response to quality related customer complaints
• Monitoring microbiological results; conducting bacterial swabs and generating shelf-life environmental graphs
• Performing research and development activities
• Responsible for implementing and maintaining food safety and quality programs and for the selecting, training and managing of FSQA Supervisors and FSQA Technicians
• Facilitating both the Food Safety and Foreign Material teams at the plant
• Completing required internal, regulatory, and customer audits
• Managing Hold Release inventories at plant level in SAP.

REQUIREMENTS:

Education: Bachelor’s degree or higher in food safety, animal science, natural science, or a related technical field, or equivalent job experience essential to the role.

Experience: 5+ years of industry experience, with 8+ years preferred. Experience with USDA regulated products is preferred, and SAP experience is a plus.

Computer Skills: Proficient in standard computer skills, including spreadsheet generation and template development for effective communication with plant management, corporate FSQA, sales, and operations.

Communication Skills: Exceptional written and verbal communication skills, demonstrating the ability to correspond effectively with team members at all levels, from the production line to corporate management.

Special Skills: Strong problem identification and problem-solving skills. Ability to work independently while effectively collaborating with various facets within the organization and serving as the plant liaison to USDA. HACCP Certified, GFSI Certified, and PCQI Certified are preferred.

Supervisory Skills: 2+ years of direct supervisory experience, with 5+ years preferred.

Travel: Occasional travel, approximately 2-5 trips per year.

Position Specific Requirements:

• Internal applicants should either upload a resume to their application in Workday OR complete their application fully showing current and past work experience OR make sure their Career Profile in Workday is up to date and complete.
• Must reside in the United States to be considered.
• Sponsorship is not available for this position.

Internal disqualifiers are the following:

• No more than 4 attendance points for locations on an 8 point policy
• No written warnings in the past six (6) months
• No suspensions on record for the last 12 months

Work Shift:

1ST SHIFT (United States of America)

Tyson is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will be considered without regard to race, national origin, color, religion, age, genetics, sex, sexual orientation, gender identity, disability or veteran status.

We provide our team members and their families with paid time off; 401(k) plans; affordable health, life, dental, vision and prescription drug benefits; and more.

Location: Remote UK, United Kingdom

Thales people architect identity management and data protection solutions at the heart of digital security. Business and governments rely on us to bring trust to the billons of digital interactions they have with people. Our technologies and services help banks exchange funds, people cross borders, energy become smarter and much more. More than 30,000 organizations already rely on us to verify the identities of people and things, grant access to digital services, analyze vast quantities of information and encrypt data to make the connected world more secure.

Together we offer fantastic opportunities for committed employees to learn and develop their career with us. At Thales UK, we research, develop, and supply technology and services that impact the lives of millions of people each day to make life better, and keep us safer. We innovate across five major industries; Aerospace, Defence, Ground Transportation, Security and Space. Your health and well-being matters to us and that’s why we offer you the flexibility to do what’s important to you; whether that’s part time hours, job sharing, home working, or the ability to flex your start and finish times. Where possible, we support a working pattern that suits your lifestyle and helps you reach your ambitions.

Cyber Security Assurance Manager

We have a brand new role for a Cyber Assurance Manager to join our growing Cyber Competency Centre, providing Thales UK business units with Cyber Security expertise.

Reporting to the UK Head of Cyber and the assigned domain Technical Director for the assurance of through-life cybersecurity engineering activities relating to products and solutions within the domain:

Key responsibilities:

• Participating in key technical reviews for all bids and projects within the scope of their assignment.
• Verifying that cybersecurity risks have been identified, assessed and managed within bids and projects in agreement with the delegated authorities for engineering security risk approval in Thales UK.
• Reviewing the principle security artefacts and security deliverables (as defined within the Cybersecurity Management Plan) and advising the security practitioners on the artefact’s completeness and fitness for purpose.
• Maintaining sector based specific knowledge in their area of responsibility.
   
• Overseeing the continued (cyber) assurance activities of products and solutions within the scope of their assignment. This should include all relevant phases of DDQS and in-service assurance.
• Articulating the cybersecurity risks of products and solutions, and the assessment of potential/proposed risk management options.
• Supporting the cybersecurity assurance aspects of product policy and road mapping
• Supporting Business Unit leadership’s cybersecurity transformation, including general cybersecurity upskilling and knowledge transfer within domain
• Assist customers in the routine development of Operational Technology (OT) security practices

Location: Can be flexible on Base location (Reading, Crawley, Bristol, Ebbw Vale, Cheadle, Doncaster, Home Start) ; Circa. 40% remote but will need to be flexible to travel around the numerous Thales & Customer facilities/locations.

What we are looking for:

• A background with Cyber Security Engineering
• Operated in multi stakeholder environments with the ability to influence to ensure right outcomes are reached.
• Experience of guiding complex projects through security risks and mitigation activities
• Have worked with external partners and accreditation bodies
• Experience of applying cybersecurity to OT, IOT and/or embedded environments.
• Ability to apply secure by design approach through engineering lifecycle and in service.
• Understand where and how key cybersecurity technologies are applied, the fundamentals behind the technology and the ability to assess suitability of candidate products.
• Ability to articulate (and distinguish between) cyber security and cyber resilience approaches.

Desirable:

• CISSP Accreditation

• CCP Architect

• SABSA Chartered Security Arch – Foundation & Practitioner

• IEng/CEng

YOUR CAREER AT THALES
Future opportunities will allow you to discover other domains or sites. You will be able to evolve and grow your competences in different areas:

Room and attention to personal development
Build your talents in another domain of Thales Group, discovering new products, new customers, new country or go to a more complex Solution
Choose between a technical expertise or a leadership path
Build an international career within a leading Engineering Group

#LI-SW1

In line with Thales' Baseline Security requirements, candidates will be asked to provide evidence of identity, eligibility to work in the UK and employment and/or education history for up to three years. Some vacancies may require full Security Clearance which can require further evidence to be provided. For further details of the evidence required to apply for Baseline and Security Clearance please refer to the Defence Business Services National Security Vetting (DBS NSV) Agency.

At Thales we provide CAREERS and not only jobs. With Thales employing 80,000 employees in 68 countries our mobility policy enables thousands of employees each year to develop their careers at home and abroad, in their existing areas of expertise or by branching out into new fields. Together we believe that embracing flexibility is a smarter way of working.

Thales UK is committed to providing an inclusive and barrier-free recruitment process. We will provide reasonable adjustments and support to ensure neuro-diverse applicants or those with a disability or long-term condition can be their best during the recruitment process. To request an adjustment, if you need this job advert in an alternative format or if you have any questions about the recruitment process, please contact Resourcing Ops for mid to senior roles, or the Early Careers Team for graduate and apprentice roles.

Great journeys start here, apply now!

This role combines the Design Quality Assurance and the Product Center Manager role. In your role as Design Quality Assurance Expert (m/f/d) you will be working as a part of product development team on new product development or on design changes to ensure product quality and reliability, minimize risk to users and patients. In addition, the Product Center Manager's responsibilities are added to this position, which includes post-market surveillance tasks and ensuring regulatory compliance. This ensures that the entire life cycle of the product can be managed and controlled.

Your assignments

Design Control

• Ensure that all design control deliverables comply with applicable regulatory requirements and design control processes
• Guide engineering and other teams and ensure that design control requirements are being met in an effective manner to achieve quality by design, including those for design verification, validation, specification and procedure development, risk management, and design review
• Provide input to design and manufacturing engineering project DHF deliverables including material specifications, drawings, inspection procedures, and manufacturing procedures, to ensure that the resulting products can be adequately manufactured and tested. Review DHF files for accuracy and completeness and provide guidance on FDA compliance and procedures
• Work independently on high visibility new product development projects; including projects involving multiple technologies and design sites
• Create processes and process improvements to ensure consistent implementation of internal requirements and external regulations and standards

Product Conformity

• Main contact for medical devices marked with the CE-mark with a focus on non-active medical devices for Peritoneal Dialysis
• Ensure that Technical Files are complete and up to date and that essential requirements are met

Post Market Surveillance

• Analyze PMS data and if needed initiate required activities

NC/CAPA

• Acts as a Quality Approver for design control related topics and as a Quality Assignee for system related topics

Your profile

• Bachelor or master’s degree in engineering or a similar technical field required, such as medical technology or a technical apprenticeship with further training to be a technician, along with relevant professional experience
• Several years related experience or an advanced degree without experience
• Advanced knowledge of Design Control and Risk Management standards (e.g, ISO13485, IEC 60601 and ISO 14971)
• Advanced knowledge of medical device regulations (e.g. MDR 745/2017, 21CFR820.30, NMPA-Regulation)
• Experience with product or design and development or quality engineering of sterile disposables utilizing various plastic processes such as injection molding and extruding
• Deep understanding of Design Controls and solid engineering expertise that enables them to guide engineering teams
• Experienced with development of design input and traceability through verification and validation V&V activities
• Excellent presentation and communication skills, high engagement on achieving targets and ability to communicate technical information to non-technical audiences
• Willingness to travel national and international
• Fluent in written and spoken English and German

Relocation Assistance Eligible:

No

Referral Payout Eligible:

No

Continue growing with our family. 

Our team members make it happen. If you want to continue to grow in a new role internally and see a position that looks right for you, we encourage you to apply!

Thanks for your commitment to Tyson Foods. 

Management Level:

P5

Job Purpose/Summary:

We are seeking an experienced Senior Manager in Global Ethics & Compliance, with a focus on Global Training and Awareness, to join our team. This role will have strategic responsibility for developing and implementing an effective risk based global ethics and compliance training program that promotes a culture of integrity and compliance with both internal policies and external regulations. The ideal candidate will be a strategic thinker with a strong background in ethics and compliance, and a proven track record in designing and delivering engaging training, communication, and brand programs. This role reports directly to the Managing Director of Global Compliance.

Essential Duties and Responsibilities:

• Develop and implement a comprehensive Global Ethics & Compliance training strategy that aligns with the company's values, policies, and regulatory requirements.
• Design and deliver engaging and effective training materials and programs, utilizing a variety of formats including e-learning, webinars, workshops, and in-person sessions.
• Collaborate with key stakeholders across the organization to assess training needs, and customize programs to address specific risks, roles, regions, and business needs.
• Monitor and evaluate the effectiveness of the ethics and compliance training program, making adjustments as needed to ensure continuous improvement.
• Stay abreast of global compliance regulations and trends to ensure training content is current, relevant, and effective in mitigating risks.
• Develop and implement a brand strategy to foster a positive culture of ethics and compliance throughout the organization, promoting awareness and understanding of ethical standards and compliance obligations.
• Prepare and present reports to senior management and the board on the progress and effectiveness of the training programs.
• Collaborate with the Legal and HR departments to ensure alignment of the ethics and compliance training with overall company policies and procedures.

Requirements:

Work Shift:

1ST SHIFT (United States of America)

Tyson is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will be considered without regard to race, national origin, color, religion, age, genetics, sex, sexual orientation, gender identity, disability or veteran status.

We provide our team members and their families with paid time off; 401(k) plans; affordable health, life, dental, vision and prescription drug benefits; and more.