Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing scientific expertise and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients Bioscience Biopharmaceuticals Custom manufacturing Biotechnology Life science ingredients Nutrition Microbial Control Agriculture Materials Science Personal Care and cell and gene therapy.
Job Title: QA Documentation Specialist I
Location: Portsmouth NH 03801 - Remote
Duration: 6 Months
Job Type: Contract
Work Type: Onsite
Shift: Monday to Friday from 08:00 AM to 05:00 PM
Summary
We are looking for a motivated and detail-oriented Quality Systems Support Specialist to join our Vacaville CA team. The role focuses on supporting Quality System Management through document control activities and PQS integration ensuring full compliance with cGMP and global regulatory requirements.
Responsibilities
- Support implementation execution and maintenance of PQS integration and Quality Documents in Veeva for the Vacaville site.
- Collaborate with the Quality Document Control group to complete workflows manage document gating and coordinate document change processes to minimize operational impact.
- Initiate and manage documents in Veeva Quality Docs.
- Format and edit controlled documents.
- Track and log source document requests.
- Ensure all activities comply with cGMP and global quality requirements.
- Maintain a high level of inspection readiness at all times.
Required Skills
- 1 3 years of experience in Quality within the pharmaceutical or biopharmaceutical industry (supplier quality experience preferred).
- Strong ability to collaborate within diverse cross-functional teams.
- Experience with Veeva Quality Document Management System and Microsoft Teams.
- Technical writing experience.
TekWissen Group is an equal opportunity employer supporting workforce diversity.
Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing scientific expert...
Overview:
TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing scientific expertise and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients Bioscience Biopharmaceuticals Custom manufacturing Biotechnology Life science ingredients Nutrition Microbial Control Agriculture Materials Science Personal Care and cell and gene therapy.
Job Title: QA Documentation Specialist I
Location: Portsmouth NH 03801 - Remote
Duration: 6 Months
Job Type: Contract
Work Type: Onsite
Shift: Monday to Friday from 08:00 AM to 05:00 PM
Summary
We are looking for a motivated and detail-oriented Quality Systems Support Specialist to join our Vacaville CA team. The role focuses on supporting Quality System Management through document control activities and PQS integration ensuring full compliance with cGMP and global regulatory requirements.
Responsibilities
- Support implementation execution and maintenance of PQS integration and Quality Documents in Veeva for the Vacaville site.
- Collaborate with the Quality Document Control group to complete workflows manage document gating and coordinate document change processes to minimize operational impact.
- Initiate and manage documents in Veeva Quality Docs.
- Format and edit controlled documents.
- Track and log source document requests.
- Ensure all activities comply with cGMP and global quality requirements.
- Maintain a high level of inspection readiness at all times.
Required Skills
- 1 3 years of experience in Quality within the pharmaceutical or biopharmaceutical industry (supplier quality experience preferred).
- Strong ability to collaborate within diverse cross-functional teams.
- Experience with Veeva Quality Document Management System and Microsoft Teams.
- Technical writing experience.
TekWissen Group is an equal opportunity employer supporting workforce diversity.
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