Superviseur Qc Lab (Environmental & Aseptic monitoring)
• University degree with scientific orientation (Bio engineering, Biology, Biotechnology, Microbiology,…) or equivalent experience
• At least 3-5 years experience in the pharmaceutical or biological field including microbiology and aseptic experiences.
• People management experience with ability to lead a team of 5-10 technicians
• High c’GMP knowledge in is field
• Autonomous and achievements oriented. Excellent customer orientation.
• Analytical and critical mind with a pragmatic approach
• Good knowledge of written and spoken French and English
See Basic Qualifications
GlaxoSmithKline Biologicals (GSK Biologicals), the vaccine division of the GSK Group, is a global vaccine research, development and production company, at the cutting edge of innovation in the fight against the most deadly infections and diseases. Headquartered in Belgium, GSK Biologicals employs over 11,000 people worldwide, of which 7,000 in its three Belgian sites: Rixensart, Wavre and Gembloux. GSK Biologicals’ global production network is in the midst of becoming the largest in the entire vaccines industry; 15 production sites strategically positioned around the world manufacture, formulate, fill, pack, check and deliver over a billion doses of about 30 different vaccines.
Job Purpose
Provides support to GSK-Bio Belgian sites for the operations under her/his responsibility across the network of : manufacturing BU’s, QC, QA, Global QA and Validation, using technical and personal mastery, to ensure that all aseptic & Environmental Monitoring processes , confidently deliver products to patients with the highest sterility assurance level at an appropriate cost.
Raises and maintains the status of quality in her/his team and enables a company to promote itself as one that provides quality goods and services.
Responsibilities
- Supervises a team of 5 to 14 laboratory technicians
- Maintain and develop the performance and expertise of your team.
- Develop and stimulate your team and ensure appropriate resources (plan, prioritize and control laboratory activity).
- Guarantees good communication within the team and with the management.
- Leadership skills with team spirit. You are results-oriented, flexible and act as a team-player.
- Recognized as an Expert field of Environment Monitoring and Aseptic Practices (inside and outside GSKBio), provides Expert support to Manufacturing BU’s , QA, Global QA, Validation.
- Assures that adequate facilities contamination control practices monitoring tools are provided to the manufacturing to guarantee the best environmental monitoring indicators levels.
- Challenges technical and scientific aspects of facilities design and aseptic principles with Technical Services, QA, Manufacturing, etc
- Approves Scientific and technical reports (test procedure, validation report, scientific report, deviation reports…).
- Guarantees the application and maintenance of the cGMP (standard procedures, , audits, training, method validation)
- Replies to auditor’s requests during inspections and support the manufacturing during GMP inspection.
- Assures the adequate treatment of all EM deviations with QA GMP Stream and Building Managers.
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.
Thank you for taking the time and effort to apply for this role. Please note that we will only contact you again if you are invited to interview. 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.
Contact information:
You may apply for this position online by selecting the Apply now button.
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