Manufacturing Asset Specialist

PerkinElmer’s OneSource team seeks a Manufacturing Asset Specialist to work on a customer site in Schachen, supporting the company’s laboratory‑solutions business that blends science with purpose. The role sits within the OneSource service offering and follows a hybrid‑working model. The specialist will handle the review and approval of documentation linked to calibration, maintenance and repair activities, and will authorize the release of assets once work is completed. Daily tasks include close collaboration with internal and external calibration and maintenance engineers to resolve any GDocP documentation gaps, processing changes, deviations and CAPA items related to equipment upkeep, and contributing to investigations as part of cross‑functional teams. In addition, the position requires maintaining and updating asset records in the customer’s calibration and maintenance databases (CCMS/CMMS) and performing the administrative release of successful entries. Candidates need three to five years of experience in a (bio‑)pharma environment, preferably in quality, validation or compliance, and should have worked as an operator process specialist. A bachelor’s degree in life sciences, quality or a comparable field is preferred, along with solid knowledge of cGMP and validation rules; familiarity with GMP, GLP, GDocP, pharmacopeial standards and related regulations is advantageous. Strong written and spoken English is required, while German proficiency is highly valued. The role calls for a customer‑service mindset, meticulous attention to technical detail, and the ability to work both independently and within a team while adhering to FDA, EU and SwissMedic guidelines. PerkinElmer emphasizes career growth and offers opportunities to develop expertise while contributing to impactful scientific work.