Über
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.
Remember to check your CV before applying Also, ensure you read through all the requirements related to this role.
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. xcfaprz
- Experience working on start‑up, commissioning or large capital projects desirable.
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Sprachkenntnisse
- English
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