PES is an international services companyproviding 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 ourmultinational clients.

This focus, and our people's experience indelivering consistent quality results for our clients over the past 20 years has been key to our success to date.

We are currently looking for a Pharma cGMP Auditors to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.

Key Attributes/Responsibilities

• GxP regulations (GMP, GDP, GLP, GCP as applicable)

• Quality Management Systems (QMS) and compliance frameworks

• Regulatory requirements at both local and international levels (e.g. EU GMP, FDA, WHO,PIC/S, local authorities)

• Conducting supplier audits, internal audits, and external audits

• Risk-based auditing approaches, CAPA management, and audit reporting

• Strong understanding of quality systems, documentation, data integrity, and validation principles

We are currently looking for candidates in Singapore

If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Sruthi Srikanth(careers@pes-international.com).

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