Batch Record Reviewer

Batch Record Reviewer | Pharmaceutical Manufacturing | GMP Documentation & Quality SupportCompany DescriptionA leading pharmaceutical manufacturing site committed to maintaining the highest standards of quality and compliance in all production activities. The company ensures its manufacturing operations adhere to cGMP principles and regulatory requirements, fostering collaboration between Production, QA, and operational teams to continuously improve efficiency and quality.Job DescriptionAs a Batch Record Reviewer, you will be responsible for the timely and independent review of production batch records and related manufacturing documentation. You will collaborate closely with QA and Operations to ensure accuracy, compliance, and completeness of production records. In addition, you will provide documentation support to the production and project teams, contributing to the efficient organization and archiving of process-related documents.Key Responsibilities:Perform independent and timely review of manufacturing documentation (e.g., batch records, cleaning records) according to internal proceduresMaintain and update operational document lists (e.g., KPI and issue logs) in coordination with the equipment and operations teamsSupport documentation management for project teams (e.g., preparation, collection, and verification of documents and labels)Create production summaries following completion of manufacturing batchesMaintain controlled copies of SOPs and ensure correct distribution within operationsManage and archive process-related documentation in compliance with internal guidelinesParticipate in review meetings with QA and production teamsProvide general administrative support, such as preparing presentations, ordering office supplies, and archiving documentsEssential Requirements:Completed vocational training and professional experience in a pharmaceutical or GMP-regulated environmentStrong understanding of cGMP regulations and documentation requirementsExcellent command of German (spoken and written); English proficiency is an advantageProficient in Microsoft Office applicationsAccurate and detail-oriented work style, following defined proceduresStrong organizational and time management skills to ensure on-time completion of tasksFlexible, communicative, and a strong team playerAdditional Insights:Location: Visp, SwitzerlandDepartment: Operations / Quality SupportInterested? Please send your CV to Miguel Gomes at m.gomes@panda-int.com or reach out directly at +31 20 20 44 502.