A global life sciences organisation is seeking an experienced QA Compliance Expert to ensure excellence in GMP Self-Inspection activities, data integrity, and quality project deployment at the Neuchâtel facility. This role reports to the Head of Quality Compliance and Systems and requires strong expertise in GMP compliance, internal audits, and quality systems. The QA Compliance Expert will partner with cross-functional teams across Production, Quality Control, Warehouse, and Engineering/Maintenance to maintain and enhance inspection readiness, continuous improvement, and compliance alignment.The QA Compliance Expert will also act as the local Data Integrity Champion, support internal and external audits, and serve as a back-up to the Head of Quality Compliance and Systems when needed.Essential RequirementsUniversity degree in a technical/scientific discipline such as Biochemistry, Chemistry, Engineering, or equivalentMinimum 7 years of experience in the biotechnology and/or pharmaceutical industryStrong knowledge of GMP and data integrity principles (Good Data and Documentation Practices - GDDP)Proven experience in creating, reviewing, and revising Standard Operating Procedures (SOPs) and technical documentsExperience supporting regulatory inspections and auditsFamiliarity with risk management tools and methodologies (e.g., FMEA, root cause analysis)Proficiency in French and English (minimum B2 level)Proficiency with electronic quality management systems (e.g., Veeva Vault, TrackWise)Strong skills in Microsoft Office (Word, Excel, PowerPoint, SharePoint) and data analysis/reporting tools, including Power BIAbility to coach and support cross-functional teams on inspection readiness and compliance topicsDemonstrated experience in leading continuous improvement initiativesPreferred RequirementsPrior experience in a biologics or complex pharmaceutical production environmentExperience benchmarking practices across sites or facilitiesProven ability to coordinate operational activities within a compliance teamPracticalitiesStart Date: ASAPLocation: Neuchâtel, SwitzerlandContract Type: 6 months (extensions expected)Team: Collaborates with Quality Compliance and Systems DepartmentLeadership: Acts as back-up for Head of Quality Compliance and Systems when neededScope: Site-level responsibility with alignment across global biologics networkInterested? Send your CV to Miguel Gomes at m.gomes@panda-int.com or call +31 (0)20 2044 502 / +41 (0)44 5514 407 to discuss the opportunity.
