We need you to have:

• Awareness of the relevant quality standards: GLP, GMP or GCP.
• Communications skills with the ability to clearly report findings, results and messages
• Quality related or analytical background which includes some specialist knowledge within a relevant area
• Awareness of quality related topics in the Chemical and Pharmaceutical Industry
• The ability to effectively time-manage personal workload and work on multiple jobs as training allows.
• Good comprehension skills with the ability to check analytical information and ensure the report reflects the raw data.
• Checking/ auditing of analytical results, under supervision, with the ability to make suggestions for solutions to known issues.
  

ABOUT THE OPPORTUNITY

As part of the Analytical Process Review, a numerical review is performed to include verifying that any derived numbers are correct by checking the derivation using the raw data and method calculations. This review also includes verifying the transcription of data into spreadsheets, software or elsewhere and assists with ensuring compliance to all relevant current national and international quality standards and customer requirements.

Whilst being supervised, to assist the Head of Quality in the overall implementation of the Quality Team functions necessary for maintenance of the quality management systems and related activities and play a key part in supporting the business to consistently deliver accurate and compliant work whilst exceeding our Clients expectations.

• Checking GLP, GCP and GMP raw data, under supervision, to verify that relevant analytical processes have been followed accurately and in accordance with relevant test methods and procedures to improve the quality of test results.
• Verifying, under supervision, that any derived numbers are correct by checking the derivation using the raw data and method calculations. This review also includes verifying the transcription of data into spreadsheets, software or elsewhere and assists with ensuring compliance to all relevant current national and international quality standards and customer requirements.
• Checking audit trails, with guidance, whether electronic or hybrid systems employed.
• Accurately report, with guidance, relevant anomalies to study personnel.
• Check GLP, GCP and GMP certificates and reports, under supervision, to ensure that they are internally consistent and accurately and completely reflect the raw data.
• Ability to work, with guidance, generating audit reports.
• Ability to checking technical data but will require assistance.
  

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 Intertek Pharmaceutical Services Manchester (IPSM), Blackley Manchester

We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.

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