Would you like to receive the latest vacancies in your e-mail box? Create a job alert based on your keyword(s) and preferences.
QA Specialist - Document Verification
Are you looking for a QA-position in the pharmaceutical biotech industry? Then this is the position for you! Apply immediately if you have experience with reviewing GMP-documentation.
Job
Job description
You will be part of a large QA team, focus on batch records, final product labels, and logbooks. You review production and QC records, preparing them for QP release, and initiate investigations of deviations with senior QA officers. We are looking for a candidate that already has some experience with QA and GMP-Batch Record Review. If this sounds interesting, contact us immediately to discuss more details and your suitability.
Responsibilities
- Batch record verification
- Final product label verification
- Review related GMP documentation
- Identify out of specifications and deviations
- Initiate investigations and CAPA
- Prepare for release by QP
- Work under GMP guidelines
Benefits
Benefits
- Temporary position, 1 year contract
- Fulltime position (40 hours per week)
- Salary range: €3500,- - €4400,- gross per month
- Location: Amsterdam area
- Vacancy number / Vacaturenummer; 24801
Company profile
Profile
- Bachelor's degree in a relevant field
- At least 2 years of GMP-experience in a QA-team
- You speak English on a professional level
- Willing to work weekends occasionally
