Superviseur QC - Deviation Writer

Basic qualifications:

  • Master of Sciences (Biochemistry), Pharmacist, bio-engineer, microbiologist
  • Experience in pharmaceutical industry
  • Experience in Deviation management

Preferred qualifications:

  • Knowledge of good manufacturing practices and deviation system
  • Good analytical and writing skills
  • Critical review of technical data
  • Ability to investigate and ask questions on the shopfloor
  • Ability to work in multidisciplinary team
  • Autonomous, rigorous, structured and systematic
  • Fluent in French – Business knowledge of English
  • Knowledge of SAP System

Details:

Job Purpose:

  • Deviation writer within CQC, responsible for deviation management

Key Responsibilities:

  • Manage deviation in a quality control team
  • Initiate and describe the deviation in SAP system
  • Investigate deviation to identify root-cause (operator interviews, 5Why's, 6M, gemba tour,…)
  • Define preventive and corrective actions
  • Complete deviation in SAP system and collect appendix
  • Ensure deviation closure on time

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 Dapertment:

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.

Contact information:

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

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