Similar posts
Batch records reviewer
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
Ensure every batch tells a compliant story-join the team that keeps production records precise and audit-ready.
À±½·ÊÓÆµ is seeking a BRR for a contract role at our client's facility. In this position, you will focus on reviewing production batch records, ensuring adherence to internal standards, and working closely with compliance and operational teams. This role also involves supporting general administrative tasks within the operation, such as document archiving and preparation of presentations.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Conduct timely and independent reviews of production batch records, cleaning protocols, and related documentation in accordance with internal procedures.
- Maintain and update operational document lists, including KPIs and output lists, while supporting the equipment and operations teams.
- Provide general document support for project teams, including preparing, collecting, and verifying documents and labels.
- Create production certificates upon batch completion.
- Manage controlled copies of operational work instructions and ensure their accuracy.
- Archive process-relevant documents from operations.
Key Skills and Requirements:
- Experience in a pharmaceutical environment and completed vocational training.
- Proficiency in German (spoken and written); English skills are advantageous.
- Understanding of current Good Manufacturing Practices (cGMP) regulations.
- Strong IT skills, particularly in MS Office.
- Detail-oriented with the ability to follow established procedures and maintain accuracy.
- Organizational skills to manage daily tasks and ensure timely completion.
- Flexible, communicative, and a team player.
For more information, please contact Will Hitchcock.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.
À±½·ÊÓÆµ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. À±½·ÊÓÆµ is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy/
Related jobs
Highly Competitive
Basel, Switzerland
Shape the future of oral drug delivery-join a leading pharma team as a Formulation Scientist bridging innovation and GMP production.
Highly Competitive
Neuchâtel, Switzerland
Step into the heart of Swiss pharma as a Junior QC Analyst-where your precision, French fluency, and GMP expertise ensure quality from sample to solution.
US$75000 - US$85000 per annum
Birmingham, USA
Are you passionate about quality and precision? Join our client as Quality Manager and help ensure top-tier standards every day.
US$50.00 - US$66.00 per hour
Indiana, USA
Engineer compliance and innovation-join a leading consultancy in Indianapolis to drive CQV excellence in aseptic manufacturing.
US$27 - US$34 per hour
Norton, USA
Be the backbone of innovation and join a leading pharmaceutical company to help keep life-changing science moving forward!
Highly Competitive
Geel, Belgium
Drive innovation in cancer treatment-join as a Senior QC Analyst and ensure excellence in every atom of Ac-225!