Offers “Gsk”

Expires soon Gsk

QC Supervisor

  • CDD
  • Wavre (Nivelles)
  • Procurement

Job description



Your Responsibilities :
- You write analytical method validation protocols and reports, by the use of appropriate statistical tools
- You integrate the validation results to the release activities.
- You define experimental plan for analytical method development.
- You write supporting documentation and follow the team planning for testing activities

Key Responsibilities:

- You manage a team of QC technicians and establish the planning and priorities with the team. You provide technical experience and expertise to the staff. You assure the training of people in accordance with GSK policies and standards and motivate employees toward operational excellence and respect of Good Manufacturing Practices.

- You follow the quality system for laboratory and documentation activities, follow up of trend analysis if required,…
- Timings respect : You ensure the follow up of activities, analyse the data and transmit them
- Critical raw data analysis
- You are responsible for a few analytical project in parallel

- You guarantee good communication within the team and with the management.

- You guarantee the application and maintenance of the c'GMP (e.g.: SOP, Documentation, Audits, training, method validation).
- You ensure the efficiency of Quality Control (quality, delay, results interpretation, KPI) and release results of tests conducted in your laboratory.
- You ensure the success of methods validation with the impacted team
- You proactively propose testing improvement in the frame of your laboratory and guarantee the appropriate review of the scientific knowledge in your field.
- You manage critical deviation and investigation.

*LI-GSK

Why You?

Basic qualifications:
- Scientific university certificate or equivalent scientific background.
- Practical and theoretical knowledge in the domain of laboratory activity (eg. Biochemistry, Physicochemistry, ). Knowledge in Physicochimical techniques (HPLC, GC, AAS, IR, NIR, UV-Vis., KF and other basic analytical method).
- You have at least 2 years of experience in the area, preferably within R&D, GIO/Q or similar roles in Pharma industry. - cGMP knowledge

Preferred qualifications:
- You are client oriented
- You show autonomy et proactivity
- You demonstrate scientific rigor and writing skils
- You have good communication skills
- You are fluent in English.

If you require a reasonable adjustment to the application/selection process to enable you to demonstrate your ability to perform the job requirements you will have the opportunity to let us know what specific assistance you require. This will help us to make suitable arrangements to support you throughout our selection process.

Why GSK? :
GSK is a science-led global healthcare company with a special purpose: to help people do more, feel better, live longer.

We have 3 global businesses that research, develop and manufacture innovative pharmaceutical medicines, vaccines and consumer healthcare products.

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.

Our 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.

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.

At GSK we value diversity and treat all candidates equally. We aim to create an inclusive workplace where all employees feel engaged, supportive of one another, and know their work makes an important contribution.

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

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