Batch Record Reviewer
Vor 2 Tagen
About the Role
We are searching for a Batch Record Reviewer with experience in GMP regulated manufacturing to support daily production activities at our site in Valais. The role focuses on the accurate review of completed production batch records, close collaboration with QA and Operations, and the maintenance of documentation systems to ensure smooth and compliant manufacturing processes.
This position is ideal for someone who works with precision, enjoys structured tasks, and understands the importance of timely documentation review in a GMP environment.
Responsibilities:
- Review manufacturing documents such as batch records and cleaning protocols in line with internal procedures
- Transfer and verify data in electronic and paper based control systems
- Prepare and maintain production relevant documents and controlled copies
- Support Operations and QA in daily review meetings
- Maintain documentation lists such as KPI and issuance lists
- Create production certificates after batch completion
- Check labels and support document distribution and collection
- Ensure correct archiving of process relevant documents
- Provide additional administrative support to Operations when required
- Ensure compliance with cGMP and internal procedures in all activities
Requirements:
- Experience in a GMP regulated pharmaceutical environment
- Completed vocational training or equivalent education
- Very strong German skills in spoken and written form
- English is an advantage
- Good understanding of GMP requirements and documentation standards
- Proficiency with MS Office and standard IT tools
- High attention to detail and ability to follow written procedures precisely
- Ability to organise daily tasks and deliver on time
- Team oriented structured reliable and flexible work style
Preferred Skills:
- Previous experience in batch record review
- Understanding of production workflows in pharma or biotech
- Familiarity with document control and archiving processes
What We Offer:
An opportunity to support compliant pharmaceutical manufacturing in a dynamic environment
A collaborative team that values precision and continuous improvement
A role with clear impact on product release and operational efficiency
Long term career development within GMP operations.
