Associate Scientist

**Site Name**: Belgium-Wavre
**Posted Date**: Nov 7 2024
**Job Purpose**:
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**Key Responsibilities**:

- You will plan and execute lab activities in the GMP and non-GMP environments (at the Rixensart and Wavre sites) using Size-Exclusion Chromatography (SEC-(U)HPLC), Dynamic Light Scattering (DLS), Static Light Scattering (SLS) and Analytical Ultracentrifugation (AUC).
- You will provide support and technical advice to lab technicians and participate in planning activities.
- You will participate in lab organization and maintenance, e.g., ordering reagents and following up on instrument maintenance/repair in collaboration with the lab support team.
- You will participate in method development according to Quality by Design (QbD) principles in a phase-appropriate manner.
- You will work on providing fit-for-purpose analytical methods in interaction with Analytical Product Leaders & Subteams (APL & AST), as well as Industrialization Leaders (AIL).
- You will interpret and report results after an extensive check of the raw data quality and participate in double-checking results.
- You will be involved in generating appropriate analytical documentation, including procedures, protocols, and reports (development, technical, qualification, validation).
- You will present results in internal meetings (within the team, to ASTs, etc.).
- You will interact with other Technical R&D (TRD) departments (Drug Substance, Drug Product, Statistics team), Preclinical, Regulatory, and GIO/QC organizations.

**Why you?**:
**Basic Qualifications**:

- We are looking for professionals with the following required skills:_
- A Bachelor’s or Master’s degree in Chemistry, Biochemistry, Biophysics, Biology, Bioengineering, Chemical Engineering, Pharmacy, or a related field is a key requirement for this role.
- Strong experience in working in a GMP environment.
- Experience in Dynamic Light Scattering (DLS) and liquid chromatography ((U)HPLC). Analytical Ultracentrifugation (AUC) knowledge or experience is a plus.
- Awareness of Quality by Design (QbD) principles.
- Knowledge of method qualification/validation principles.
- Sound scientific methodology and thinking, autonomy, commitment to solving problems and bringing innovative solutions to the team.
- Communication skills (oral & writing), ability to engage the team; open-minded, result
- and quality-oriented.
- The native language of the team is French; English fluency is an asset.

LI-GSK

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.

**Why GSK?**

**Uniting science, technology and talent to get ahead of disease together.**

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

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