Job Description

We are recruiting for a motivated professional C&Q Lead to join a leading CDMO and pharmaceutical manufacturer based near Basel for an initial 6 month contract with a chance to be extended for further. In this role, you will be responsible for leading a team of CQV engineers undertaking tasks relating to lyophilization equipment within a GMP setting.Your ResponsibilitiesLead and coordinate C&Q activities across the organizationServe as the interface between Engineering, Quality, Production, and external partnersManage the creation, review, and approval of C&Q documentation (URS, DQ, IQ, OQ, PQ)Ensure strict compliance with regulatory requirements and internal SOPsLead C&Q teams or coordinate external service providers effectivelyWhat We’re Looking ForStrong background in Commissioning & Qualification within regulated industriesExcellent organizational and communication skills to manage multiple stakeholdersAbility to lead teams and coordinate external service providersExperience with Lyophilization is preferred but not essential.German language skills are essential

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