Specialist, Analytical Instrument Validation (On-site)
USA - New Jersey - Rahwayonsitemid$96K – $151K
Posted today · via Workday
About this role
Job Description The Pharmaceutical Analysis & Digital Technologies (PADT) External Capabilities, Validation, and Compliance (ECVC) department of our company Research Laboratories Division is seeking applicants for a Validation Specialist position available at either the Rahway, New Jersey research facilities. The Analytical Instrument Validation Specialist will work as part of the integrated Validation and Compliance team and drive a culture of quality and operational excellence across the global Development Sciences & Clinical Supply (DSCS) network. The Analytical Instrument Validation Specialist role oversees and/or supports the validation of novel computerized analytical instrumentation within the GMP environment for multiple sites (Pennsylvania, New Jersey, and Schachen, CH).…
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This role is based in USA - New Jersey - Rahway. We weight your proximity and willingness to relocate.
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