Current jobs related to Regulatory Affairs and Quality Assurance Specialist - Portage - Rose International

  • Regulatory Affairs Specialist

    4 weeks ago

    Portage, Michigan, United States Kelly Science, Engineering, Technology & Telecom Full time

    Regulatory Affairs and Quality Assurance SpecialistThis is an exciting opportunity to join our team at Kelly Science, Engineering, Technology & Telecom as a Regulatory Affairs and Quality Assurance Specialist.Key Responsibilities:Coordinate and prepare document packages for regulatory submissions from all areas of the organization.Collect all materials...

  • Regulatory Affairs Specialist

    4 weeks ago

    Portage, Michigan, United States Ledgent Technology Full time

    Job Title: Regulatory Affairs SpecialistRoth Staffing is seeking a highly skilled Regulatory Affairs Specialist to join our team within the medical technologies industry.Key Responsibilities:Coordinate and prepare document packages for regulatory submissions from various areas of the organization.Collect and submit data from customers for auditable...

  • Regulatory Affairs Specialist

    1 month ago

    Portage, Michigan, United States Comrise Full time

    Job Title: Labeling and Regulatory Affairs SpecialistThis is an 18-month contract position with a high possibility of extension.Key Responsibilities:Execute complex tasks associated with support of medical device labeling development and maintenance.Pull data from our quality system to upload IFUs to our eIFU website.Work with partners regarding supplemental...

  • Regulatory Affairs Specialist

    2 months ago

    Portage, Michigan, United States Ledgent Technology Full time

    Job Summary:Ledgent Technology is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our organization, you will be responsible for coordinating and preparing document packages for regulatory submissions from various areas of the company.Key Responsibilities:Collect and compile all necessary materials for regulatory...

  • Regulatory Affairs Specialist

    4 weeks ago

    Portage, Michigan, United States The Judge Group Full time

    Job Title: Specialist, RAQAWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at The Judge Group.Job Summary:The successful candidate will be responsible for providing regulatory support to our clients in the medical device industry. This includes collecting and submitting data from customers for auditable records, coordinating...

  • Regulatory Affairs Specialist

    4 weeks ago

    Portage, Michigan, United States The Judge Group Full time

    Job Title: Specialist, RAQAWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at The Judge Group.Job Summary:The successful candidate will be responsible for providing regulatory support to our clients in the medical device industry. This includes collecting and submitting data from customers for auditable records, coordinating...

  • Regulatory Affairs Specialist

    4 weeks ago

    Portage, Michigan, United States The Judge Group Full time

    Job Title: Specialist, RAQAWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at The Judge Group.Job Summary:The successful candidate will be responsible for providing regulatory support to our clients in the medical device industry. This includes collecting and submitting data from customers for auditable records, coordinating...

  • Regulatory Affairs Specialist

    1 month ago

    Portage, Michigan, United States The Judge Group Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at The Judge Group. As a key member of our Product Field Action team, you will play a critical role in ensuring compliance with regulatory requirements.Key ResponsibilitiesCollect and submit data from customers for auditable recordsCoordinate and prepare document...

  • Regulatory Affairs Specialist

    2 months ago

    Portage, Michigan, United States The Judge Group Full time

    Job Summary:The Judge Group is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our organization, you will be responsible for ensuring compliance with regulatory requirements and guidelines in the medical device industry.Key Responsibilities:Collect and submit data from customers for auditable recordsCoordinate and...

  • Senior Regulatory Affairs Specialist

    2 weeks ago

    Portage, Michigan, United States Stryker Full time

    Job SummaryWe are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team at Stryker. As a key member of our Acute Care business unit, you will be responsible for maintaining global market access by analyzing the impact of device modifications and emerging regulatory intelligence.Key Responsibilities:Evaluate device modifications and...

  • Regulatory Affairs Specialist

    1 month ago

    Portage, Michigan, United States Ledgent Technology Full time

    Job SummaryRoth Staffing is seeking a highly skilled RAQA Specialist to join our team within the medical technologies industry. As a key member of our team, you will be responsible for coordinating and preparing document packages for regulatory submissions, ensuring compliance with industry regulations and standards.Key ResponsibilitiesCollect and compile...

  • Senior Regulatory Affairs Specialist

    1 week ago

    Portage, Michigan, United States Stryker Full time

    We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Stryker. As a key member of our Acute Care business unit, you will play a critical role in maintaining global market access by analyzing the impact of device modifications and emerging regulatory intelligence.Key Responsibilities:Evaluate device modifications and take...

  • Regulatory Affairs Specialist

    1 month ago

    Portage, Michigan, United States GForce Life Sciences Full time

    GForce Life Sciences is seeking a highly skilled Regulatory Submissions Coordinator to join our team. As a key member of our regulatory affairs department, you will be responsible for coordinating and preparing document packages for regulatory submissions across all organizational areas. Your role will involve collecting all necessary materials for...

  • Labeling and Regulatory Affairs Specialist

    1 month ago

    Portage, United States Comrise Full time

    **** This is an 18-month contract position with a high possibility of extension ***POSITION: Labeling and Regulatory Affairs SpecialistLOCATION: 1941 Stryker Way Portage, MIDURATION: 18-month contract positionWORK SET-UP: OnsitePAY: $24 to $26/hour in W2OverviewThis role executes several complex tasks associated with support of medical device labeling...

  • Labeling and Regulatory Affairs Specialist

    1 month ago

    Portage, United States Comrise Full time

    **** This is an 18-month contract position with a high possibility of extension ***POSITION: Labeling and Regulatory Affairs SpecialistLOCATION: 1941 Stryker Way Portage, MIDURATION: 18-month contract positionWORK SET-UP: OnsitePAY: $24 to $26/hour in W2OverviewThis role executes several complex tasks associated with support of medical device labeling...

  • Quality Assurance Specialist

    1 month ago

    Portage, Indiana, United States Ursitti Enterprises LLC Full time

    Job Title: Quality Assurance SpecialistUrsitti Enterprises LLC is seeking a highly skilled Quality Assurance Specialist to join our team.Job Summary:We are looking for a detail-oriented and organized Quality Assurance Specialist to perform AQL testing and sampling on finished products. The ideal candidate will have a strong understanding of AQL procedures...

  • Advanced Quality Assurance Specialist

    1 month ago

    Portage, Indiana, United States Ursitti Enterprises LLC Full time

    Job SummaryUrsitti Enterprises LLC is seeking an experienced Advanced Quality Assurance Specialist to join our team at our Portage facility. As a key member of our quality assurance team, you will be responsible for leading the development, implementation, and maintenance of quality systems that support manufacturing operations.Key Responsibilities:Provide...

  • Regulatory Affairs Specialist

    2 months ago

    Portage, United States GForce Life Sciences Full time

    Job Title: Regulatory Submissions CoordinatorJob Description:As a Regulatory Submissions Coordinator, you will be responsible for coordinating and preparing document packages for regulatory submissions across all organizational areas. Your role will involve collecting all necessary materials for submissions, license renewals, and annual registrations....

  • Quality Assurance Specialist

    2 weeks ago

    Portage, Indiana, United States Ursitti Enterprises LLC Full time

    Job OverviewUrsitti Enterprises LLC is seeking a highly skilled Quality Assurance Specialist to join their team.This part-time position will be based at the Portage facility and will involve performing AQL attribute testing and required sampling on finished products.The ideal candidate will have a strong understanding of AQL procedures and guidelines, as...

  • Quality Assurance Specialist

    6 days ago

    Portage, Michigan, United States Chili's Grill & Bar Full time

    Quality Assurance Specialist At Chili's Grill & Bar, we're committed to delivering the best experience to every Guest, every day. As a Quality Assurance Specialist, you'll play a crucial role in ensuring that our food meets the highest standards of quality and taste. Responsibilities:Prepare and present food to company standards and specificationsEnsure food...

Regulatory Affairs and Quality Assurance Specialist

2 months ago

Portage, United States Rose International Full time

Co-ordinates and prepares document packages for regulatory submissions from all areas of the organization.

Collects and submits data from customers for auditable records.

Collects all materials required in submissions, license renewal, and annual registrations.

Keeps abreast of regulatory procedures and changes. May interact with regulatory agencies.

Works on problems of complex scope where data analysis requires evaluation of specific factors.

Utilizes independent judgment within broad parameters to determine an appropriate solution.

May determine methods and procedures on new projects and may provide guidance to other lower-level staff.

This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision.

Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.

Job requires an understanding and application of procedures and concepts of own discipline.

The job requires the ability to make judgements based on practice and previous experience.

  • **Only those lawfully authorized to work in the designated country associated with the position will be considered.**

  • **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**

Benefits:

For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.

California Pay Equity:

For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.

If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.

Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).