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Quality Assurance Engineer – Neuenburg | JobRevolt

Über den Job

An international pharmaceutical company based in Neuchâtel is looking for a QA Specialist to join its Quality Assurance team. This role focuses on QA Vendor Oversight, ensuring that products manufactured by external partners comply with GMP requirements and global quality standards. You will act as a key quality contact for contract manufacturers, supporting batch release activities, investigations, change controls, supplier quality management, and compliance initiatives.

Aufgaben

Manage Quality Assurance activities related to external manufacturing partners and CMOs
Maintain strong working relationships with contractors and quality representatives
Lead discussions on quality topics including deviations, change controls, complaints, OOS investigations, and CAPAs
Review and approve quality documentation, validation protocols, validation reports, investigations, and change controls
Prepare and review Batch Release Packages to support final product disposition
Support product release activities while ensuring GMP and regulatory compliance
Manage and assess change controls, including QA approval and impact evaluation
Support complaint investigations and vendor-related quality issues
Review Process Validation and Technology Transfer documentation
Participate in Annual Product Quality Reviews (APQR/PQR)
Draft, review, and manage Quality Agreements with external partners
Participate in supplier audits, self-inspections, and regulatory inspections
Maintain quality metrics, trend analyses, and quality databases
Contribute to the continuous improvement of Quality Systems
Author and review SOPs, work instructions, and quality procedures
Support GMP and GDP compliance activities across the organization

Profil

Bachelor's or Master's degree in Pharmacy, Biotechnology, Chemistry, Life Sciences, or related field
1 to 4 years of experience in Quality Assurance within a GMP-regulated pharmaceutical or biotechnology environment
Fluent German and English (written and spoken) is mandatory
Good understanding of GMP, GDP, and pharmaceutical quality standards

Rahmenbedingungen

Location: Neuchâtel, Switzerland
Contract type: Temporary – 1 year
Work model: Hybrid (50% remote)
Required languages: Fluent German and English, French not required
Work permit: Valid Swiss work permit or Swiss nationality required

Quality Assurance Engineer

Über den Job

Über den Job

Aufgaben

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Rahmenbedingungen

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