QA Auditor

**We need you to have**:

- BSc / MSc/ PhD in Chemistry (or related scientific discipline)
- A sound working knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards
- Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry
- Quality Assurance background which includes some specialist knowledge within a defined area
- Good experience of auditing documents with technical support or guidance across multiple projects
- Excellent attention to detail
- Impressive written and verbal communication

**ABOUT THE OPPORTUNITY**

You will provide general support to Quality Assurance activities relating to GLP, GMP, GCP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved.
- Responsible for auditing GLP, GCP and GMP plans, raw data, study procedures and related facilities to ensure compliance with current relevant regulatory requirements and internal consistency,
- Identify and report any areas of non-compliance to both study and facility management.
- Liaise with key stakeholders, providing them with accurate information and progress reports on a consistent basis.

**WHAT WE OFFER**

Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
- Competitive salary/benefits
- Development and career opportunities around the Globe
- Working in a highly motivated team and dynamic working environment

In this opportunity you’ll be joining our Chemical and pharma team, based at Manchester

Intertek operates a preferred supplier arrangement and we do not accept unsolicited approaches from agencies.