Senior Advisor External QA, Open to flexibility

Location
Ware, Hertfordshire
Salary
£Competitive
Posted
06 Sep 2017
Closes
18 Sep 2017
Ref
WD136056
Contract Type
Permanent

Senior Advisor External QA, Open to flexibility

GlaxoSmithKline (GSK) is one of the world's leading research-based pharmaceutical companies. Our powerful combination of skills and resources provide the platform for delivering strong growth and the platform for responding quickly to the rapidly changing global healthcare environment. We are a science-led global healthcare company that researches and develops a broad range of innovative products in three primary areas of Pharmaceuticals, Vaccines and Consumer Healthcare. We have a significant global presence with commercial operations in more than 150 markets, a network of 86 manufacturing sites in 36 countries and large R&D centres in the UK, USA, Spain, Belgium and China.

An opportunity has arisen to join External QA in the UK as a Senior Advisor. External QA is part of Preclinical Quality Assurance in Global Quality Assurance that provides QA support to PDS, Dermatology Unit and GSK's third party partners. External QA is a global team based in UK, US & Shanghai. The role will work closely with and assist all the External QA Managers in their support of the activities related to third parties globally. The successful candidate will have a critical role in ensuring quality and compliance of Investigational Medicinal Products used worldwide. In addition the job holder will have the opportunity to further develop existing expertise and to gain experience within an R&D environment.

The successful candidate will be involved with a diverse range of activities including:

  • Assessment by Audit (on site and remote) of third party suppliers to GSK as part of the PCQA auditor pool.
  • Review of documentation (batch and analytical records) and recommend release for Intermediates, API and a range of dosage form batches and finished clinical trial packs of Investigational Medicinal Products in accordance with GMP/GSK requirements.
  • Assessment of Quality Deviations, customer complaints and vendor complaints and make recommendations for corrective and preventative actions, and follow up on the implementation of those recommendations.
  • Initiation and maintenance of quality agreements with third party suppliers & contractors including management of the review of quality agreements
  • Assist in the support of oversight of analytical laboratories including the review of technical agreements.
  • Assist in scheduling assessments for new/existing suppliers/contractors and associated Vendor Management activities.
  • Assist in the tracking and chasing of CAPAs associated with third party assessments.
  • Provide advice and support to business partner areas relating to quality matters and process improvement.

Closing date for applications: Monday 18th September 2017

Thank you for your interest in this opportunity.

You may apply for this position online by selecting the 'Apply' button.

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