Specialist Quality Contracts & Release

Basic qualifications:

  • University Degree in Sciences : Pharmacist (preferred), Bio Engineer or equivalent
  • Good knowledge of GMP. At least 10 years professional experience from which at least 5 years in a GMP environment related to pharmaceutical production with preference to aseptic

Preferred qualifications:

  • Ability to create and maintain networks and build relationships transversally across the GSK network.
  • Creative approach to problem solving


Job Purpose:

  • Management of Quality Contracts within GSK organization, including:
  • Management of the team in charge of the creation/review of Quality Contracts
  • Maintaining a robust and compliant system for creation/review of Quality Contracts
  • Support to the Local Release System Owner (His or her Line Mgr)

Key Responsibilities:

  • Management of the team in charge of the creation/review of Quality Contracts
  • Review and negociate Quality Contracts with other GSK manufacturing entities or Local Operating Companies
  • Review and negociate Quality Contracts with Contract Manufacturing Organizations, outside GSK
  • Manage and ensure communication/implementation of GSK Roles and Responsibilities wtih GSK stakeholders
  • Develop and manage KPI for Quality Contracts activity
  • Participate to release system related activities as support to the local Release System Owner (His/her Line Mgr)

Our Offer:

At GSK we provide a supportive working environment, and a range of development challenges and opportunities. We also offer competitive benefits and compensation packages designed to attract and to retain the very best. GSK is proud to promote an open culture, encouraging people to be themselves and giving their ideas a chance to flourish. GSK is an equal opportunity employer.

The Department:

Global Quality Departments is responsible for setting up all global rules and regulations to ensure GSK vaccine products are manufactured, tested, released and distributed in compliance with regulatory requirements.

The QA Belgium departments manage all product quality related activities in industrial operations in Belgium, including regulatory compliance. The scope covers any action that potentially impacts final product quality. The QA Belgium department is also responsible for the release of final products made in Belgium and abroad.

Quality for Research & Development in partnership with R&D teams promotes quality and enables them ensuring activities of Research & Development are delivered in a compliant and sustainable way, in order to guarantee patient safety, company and regulators satisfaction, as well as successful product pipeline delivery.

Our Company:

GSK is one of the world's leading research-based pharmaceutical and healthcare companies – is committed to improving the quality of human life by enabling people to do more, feel better and live longer.

GSK Vaccines is one of the world's leading vaccine companies, with a comprehensive portfolio of 39 vaccines for infants, adolescents and adults and 15 more in development. We have more than 16,000 people working worldwide to deliver nearly 2 (1.9) million vaccines every day to people in around 90% (172) of the world's countries.

For further information, please visit www.gsk.com.

  • LI-GSK

Contact information:

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

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