Batch Record Reviewer

Batch Documentation Reviewer (Clinical Packaging)

Pharmaceutical / Clinical Manufacturing

Role

The Batch Documentation Reviewer is responsible for reviewing clinical packaging batch documentation to ensure accuracy, completeness, and compliance with GMP and internal procedures. The role supports quality assurance by verifying operator documentation, supporting deviation investigations, and contributing to complaint handling. This is a highly structured, administrative role with a high volume of repetitive batch record checks.

Non-Negotiable Skills, Qualifications, and Experience

• Bachelor’s degree or equivalent (university level)

• Fluent in English (spoken and written)

• Fluent in Dutch (spoken and written)

• Availability to work 100% onsite, 5 days per week

• Ability to work day shift

• Ability to work in a highly repetitive, documentation-focused administrative role

Essential Skills, Qualifications, and Experience

• Knowledge of cGMP principles

• Experience reviewing or handling GMP-regulated documentation

• Experience working according to SOPs and regulated procedures

• Experience with digital systems for documentation review (e.g. MES, SAP, or similar)

• Experience supporting deviation investigations or documentation follow-up

• Experience collaborating with QA, operations, or technical teams in a regulated environment

Desirable Skills, Qualifications, and Experience

• Experience in clinical packaging environments

• Experience with TrackWise or other deviation management systems

• Knowledge of safety, hygiene, and environmental regulations

• Prior experience in complaint handling (internal or external)
  Experience working in pharmaceutical manufacturing or packaging operations

Interested? Apply now or send your CV to f.chauca@panda-int.com