
Clean Utilities Validation Engineer-gmp/pharma
3 days ago
PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.
With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.
This focus, and our people's experience in delivering consistent quality results for our clients over the past 20 years has been key to our success to date.
We are currently looking for **CQV Engineers with Clean Utilities Experience **to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.
Key Attributes/Responsibilities:
- Provide knowledge, competency and governance to sustain the qualified status of engineering services operations.
- First line support to quality/compliance-related events (e.g. deviation, CAPA, requalification, alarms, etc.
- Own FMECA’s, reliability and efficiency initiatives, and optimization of all maintenance plans including spare part planning.
- Manage external activities such as Service Contract management or regulatory Inspections
- Manage business-related responsibilities such as adherence to the personal training plan and ownership of all equipment-related processes
- Accountable for all clean utility systems, including clean utility equipment and surrounding environment infrastructure linked to functionality and performance
- Experienced in Commissioning & Qualification, technical documentation and managing audits for clean utility systems (e.g. SFDA, EMA, PMDA and HSA).
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