Exciting opportunity to join a major greenfield biopharmaceutical facility during the commissioning phase, supporting the validation of a state‑of‑the‑art aseptic manufacturing site.
Responsibilities
Lead execution of cleaning validation protocols (IQ/OQ/PQ) for process equipment and manufacturing systems.
Develop and maintain cleaning validation documentation, including protocols, reports and risk assessments.
Support commissioning and qualification activities across the manufacturing facility.
Work cross‑functionally with engineering, quality and manufacturing teams during start‑up activities.
Requirements
Degree in Engineering, Chemistry, Pharmaceutical Science or related discipline.
3+ years’ cleaning validation experience within GMP pharmaceutical or biopharma environments.
Experience working on start‑up, commissioning or large capital projects desirable.
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