The Stability Coordinator, reporting to the QC Manager, will be responsible for maintaining the stability program of Cambrex High Point (CHP) customer products. This role will ensure the stability program meets the expectations of all regulatory agencies and remains compliant with applicable Company SOPs and regulatory guidance’s. This position will be required to work well with cross functional teams and will be the key point of contact for the CHP stability program.
BS or MS in Chemistry (or closely related discipline). Strong comprehension and facility in quantitative/qualitative analytical Chemistry. A minimum of at least 4-6 years of strongly relevant background in GMP/QC-compliant analytical testing in a pharmaceutical laboratory environment.
PI240092512
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