QC – Supervisor (CDD 1an)

In order to reinforce our team, we are looking for a QC Supervisor for a 1 year contract.

• You participate in adequate validation/qualification (design and follow-up of execution) of (in-process) analytical methods using appropriate statistical tools, in line with projects timelines

• You participate in the analytical methods transfer from ARD and to other quality control departments

• You write technical documents (SOPs, validation protocols and reports)

• You ensure (in-process) analytical support to process scale-up, to industrialization bulks and formulation groups, to process evaluation and validation and ensures the testing of development and phase 3 clinical lots

• You assist the QC product coordinator by providing all analytical relevant information generated in his/her team

• You are a representant of his/her activities in internal teams (ex: staff, transfer meetings)

• You guarantee the compliance to cGMP/QA rules in his/her laboratory team (SOP, Documentation, Audits, training, method validation)

• You participate in deviations management in his/her laboratory team

• You ensure contact and collaboration with maintenance, QA, R&D, RA, production, QCss, purchasing, ...

• You proactively propose testing improvement in the frame of his/her laboratory

• You share know-how with others (Coaches technicians and assures their evolution) in his/her competency domain and proactively supports others to develop

• You participate in the replies to auditor’s requests during inspections

• You gather information requested by RA

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

• Master’s in sciences linked to Microbiology/Biotechnology/Vaccines development (Bioengineer, University’s degree in Microbiology, Biology, Biotechnology, Pharmacology, ...) or equivalent experience acquired though professional experience.

• 2 to 3 years of experience in similar function in the pharmaceutical or biological sector

• Demonstrated practical knowledge and competency in in general microbiology and associated pharma industry testing (Detection of Bioburden, Sterility test, Disinfectant efficacy, Detection of Mycoplasma, …) with a focus on the endotoxin test and LER effect

• Fluent in French and good level of spoken and written English beyond scientific English

• cGMP and regulatory constraints knowledge

• Rigorous, proactive, organized, resilient, autonomous

• Ability to work on several projects/subjects in the same time

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

• PhD is a plus

• Good knowledge in microbiology test validation principles. Rapid Microbiology methods is a plus

• Li-GSK

Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork in a culture of Innovation, Performance and Trust.

GSK Vaccines – Our Vaccines business has a broad portfolio and innovative pipeline of vaccines to protect people of all ages. We deliver over two million vaccine doses per day to people living in over 160 countries.

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

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

If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.

Our goal is to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing.

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