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C&Q/Validation Engineer- Downstream Process Equipment- Pharmaceuticals project

Salary undisclosed

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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-Downstream Process to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.

Key Responsibilities:

  • 3+ years of experience in CQV for downstream biopharmaceutical processes
  • Lead and execute CQV activities for downstream processes, including filtration, chromatography, ultrafiltration/diafiltration, and other purification steps.
  • Develop and implement CQV protocols (IQ/OQ/PQ) for downstream equipment and systems.
  • Troubleshoot and resolve equipment issues during the Commissioning phases.
  • Perform risk assessments (FMEA, HAZOP) and support deviation investigations and CAPA implementation.
  • Working knowledge of automation and data integrity compliance (21 CFR Part 11).

We will only consider candidates with prior commissioning and qualification experience in process equipment.

If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony ([email protected]).

If you would like to find out about the latest Jobs and Projects we are involved in then do follow us on LinkedIn: https://www.linkedin.com/company/processengineeringspecialists/mycompany/

PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

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-Downstream Process to join us on a permanent basis to help us deliver various projects in the Life Sciences Industry.

Key Responsibilities:

  • 3+ years of experience in CQV for downstream biopharmaceutical processes
  • Lead and execute CQV activities for downstream processes, including filtration, chromatography, ultrafiltration/diafiltration, and other purification steps.
  • Develop and implement CQV protocols (IQ/OQ/PQ) for downstream equipment and systems.
  • Troubleshoot and resolve equipment issues during the Commissioning phases.
  • Perform risk assessments (FMEA, HAZOP) and support deviation investigations and CAPA implementation.
  • Working knowledge of automation and data integrity compliance (21 CFR Part 11).

We will only consider candidates with prior commissioning and qualification experience in process equipment.

If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony ([email protected]).

If you would like to find out about the latest Jobs and Projects we are involved in then do follow us on LinkedIn: https://www.linkedin.com/company/processengineeringspecialists/mycompany/

PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.