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QA Reviewer
Join a leading Biotechnology and Pharmaceutical Contract Manufacturing company in Amsterdam as a QA Reviewer!
You'll play a central role in managing all documentation for the Quality Assurance Department, and acting as the main contact for operational tasks, overseeing progress across various departments.
Job
Key Responsibilities:
You'll be responsible for all the documentation to and from the QA Department, monitoring progress, and acting as the point of contact for all operational tasks across various departments. This includes:
- Review and approval of batch manufacturing
- Review and approval of QC testing records
- Prepare the lot package for batch disposition
- Support the back office during client audits
Profile
Qualifications:
- HBO or BSc degree in Life Sciences Chemistry, (Micro)Biology, or Pharmaceutical Sciences;
- At least one year of working experience in a GMP environment
- MS Office (Word, Excel, PowerPoint) experience;
- Knowledge of TrackWise is a plus;
- Proficient in English, both verbal and written, Dutch is preferred;
- Clear and open communication, organizational and planning skills;
- Hands-on, quality-oriented, problem-solving, proactive behavior, flexibility.
Benefits
Offer:
- Salary: Up to 64.000€ per year
- Job Type: Full-Time 32-40h, On-site
- Location: Amsterdam, On-site
- Holiday and commute allowance
- 30 vacation days
- Long term career growth and training opportunities
Company profile
Our customer is a dynamic CDMO in Amsterdam area - specialising in contract manufacturing of therapeutic proteins, vaccines, Live Microbial Products as drug substance and drug product. With over 20 years of experience producing microbial derived proteins and vaccines, they are a world-leading partner when it comes to development and manufacturing.
Contact
Interested? Apply now!
We want to hear from you, so click on "Easy Apply" to submit your CV or reach out to:
Mah Rukh Chohdri - Recruitment Consultant at Grafton Recruitment Netherlands
