Batch Record Reviewer

Agap2 is an European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.

As a consultant, you will have to support our clients in the realization of their projects on site by bringing your expertise and your skills.

You are agile and eager to adapt to different work environments that will fuel your curiosity of seeing what’s behind closed doors of the biggest projects of our client’s portfolio.

As a Batch Record Reviewer, you will be handling the following tasks, pharma and biotech manufacturing activities:

• Review and approve production batch records to ensure compliance with GMP (Good Manufacturing Practices) and Standard Operating Procedures (SOPs).
• Identify and document deviations from procedures and specifications.
• Collaborate with production, quality control, and quality assurance teams to resolve issues and implement Corrective and Preventive Actions (CAPA).
• Participate in the continuous improvement of quality control processes and systems.
• Maintain accurate and complete documentation of all batch record review activities.

• At least 1 experience in Batch record review for pharma/biotech