Job Description
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 have been key to our success to date. We are currently looking for
CQV Doc Prep Lead
to join us permanently to help us deliver various projects in the Life Sciences Industry. Key Responsibilities: Develop and review CQV lifecycle documents, including URS, DQ summaries (as applicable), IQ, OQ, and PQ protocols and reports Author validation protocols and reports in accordance with site procedures and regulatory expectations Ensure proper document formatting, version control, and traceability throughout the do...
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 have been key to our success to date. We are currently looking for
CQV Doc Prep Lead
to join us permanently to help us deliver various projects in the Life Sciences Industry. Key Responsibilities: Develop and review CQV lifecycle documents, including URS, DQ summaries (as applicable), IQ, OQ, and PQ protocols and reports Author validation protocols and reports in accordance with site procedures and regulatory expectations Ensure proper document formatting, version control, and traceability throughout the do...