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Quality Assurance Compliance Officer - Audit

Reference Number: 925336 | Salary: Competitive | Location: Wiltshire, United Kingdom | Division: Scientific Permanent


Quality Assurance Compliance Officer

Biopharma

Wiltshire

Competitive Salary

The opportunity

A superb opportunity has arisen to join a growing and successful biopharmaceutical company as a quality assurance compliance officer. This is a supplier focussed role so you will be responsible for organising, planning and performing internal and supplier audits and ensure that supplier relationships are maintained at all time. This is a great opportunity to join a fast growing and well respected company.

The company

A leading and growing biopharmaceutical manufacturer, our client has their own product portfolio as well as operating as a contract manufacturer. With approximately 300 people in the business, they are continuing to expand across all of the business functions.

Main duties and responsibilities

  • Organise, plan and perform internal and supplier audits
  • Identify, initiate and progress Supplier Complaints to satisfactory closure
  • Ensure supplier questionnaires are completed in a timely manner
  • Update supplier monitoring database and spread sheets
  • Carry out relevant GMP training
  • Produce Quality Technical Agreements for the supply of goods and services from critical suppliers

Knowledge and experience

  • 2-3 years’ experience in operating quality management systems in a GMP QA environment
  • GMP auditing experience
  • Working knowledge of GMP and other GxP’s
  • Experience of producing accurate documents, procedures and reports in a timely fashion
  • Practical experience in a GMP Biopharmaceutical manufacturing environment would be beneficial
  • Experience of training/troubleshooting small groups of staff would be beneficial

 

Harris Lord is acting as an employment agency for this role


Contact: Mark Bux-Ryan

Keywords: GMP/Quality/QA/audit/supplier/technical file/GxP/BSE/TSE/


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