Supervisor QA MPU Rota

Basic qualifications:

  • Scientific university degree (Pharmacist, Engineer or equivalent)
  • Ideally a first experience in a Pharmaceutical/Bio/Medical device environment or equivalent
  • Good knowledge of English

Preferred qualifications:

  • Knowledge of GMP regulated environment


Job Purpose:

Develops, assures and maintains the quality of the product and processes for operations

− Standard procedures

− Quality audits/review

− Key Performance Indicators (KPIs)

Key Responsibilities:

Masters the key QA activities related to production and validation, project activities in his/her area of responsibility

  • Ensures batches of the intermediate product related to the area of responsibility are released in a timely manner
  • Ensures deviations, complaints, change controls, OOS investigation, maintenance and calibration plans are reviewed and handled in a timely manner
  • Represents QA (decision responsibility) in all meetings related to the area of responsibility (staff meetings, deviation, CAPA, RPC follow-up meetings, ICG project, …)
  • Ensures critical topics are adequately escalated to higher management
  • Is the preferred front line spokesperson during inspection for the subject of expertise as well as for all operational aspects belonging to the area of responsibility Leads local and/or transversal improvement projects to ensure the compliance level is maintained in line with cGMP and GSK standard requirements
  • Understands technical/production complex problems and evaluates potential impact on product quality
  • Assesses quality review files and draws adequate conclusions
  • Provides QA expertise support to new product introduction projects and related validations

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:

Once our pioneering treatments have been developed, they are manufactured to the highest standards and distributed across the regions that need them most. Accomplishing this as efficiently and quickly as possible can quite literally be a matter of life and death. So it's no wonder that more than 70% of our talented workforce is based within Global Industrial Operations - the essential business unit that manufactures and manages the entire vaccine supply process, from customer order to product dispatch on a global scale.

As the name suggests, it operates in a multi-national context across more than 17 sites around the world, working closely in tandem with colleagues from a variety of disciplines and professions.

The department is structured in operating units that focus on various aspects of the manufacturing and supply process. These include Industrialisation (overseeing the transfer of production from R&D to a commercial level), Supply Chain Management and Technical Services.

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

  • LI-GSK

Contact information:

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

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