Stage Support Opérationnel PMS - Formulation - Lyophilisation H/F

Business Introduction We manufacture and supply reliable, high-quality medicines and vaccines to meet patients’ needs and drive our performance.
Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it’s vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply.
We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. Stage Support Opérationnel PMS - Formulation - Lyophilisation H/F Position Summary Join our team at GSK as a Stage Support Opérationnel in PMS, focusing on formulation and lyophilisation. You will work closely with experienced colleagues to support daily production activities and improve processes. This role is designed for someone eager to learn, take initiative, and contribute to the delivery of high-quality vaccines. At GSK, you will grow your skills in an innovative and inclusive environment united by the mission to unite science, technology, and talent to get ahead of disease together. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Support the production team in formulation and lyophilisation operations to ensure smooth workflows. - Assist in monitoring equipment performance and material availability for production schedules. - Contribute to identifying potential improvements in process efficiency, quality, and timelines. - Participate in documentation updates and data recording related to production activities. - Collaborate with cross-functional teams including quality, maintenance, and supply to support continuous improvement. - Help ensure compliance with safety, quality, and regulatory standards during all operational tasks. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Currently enrolled in a Master’s program in pharmacy, chemical engineering, biotechnology, or related scientific field. - Strong interest in pharmaceutical manufacturing, particularly formulation and freeze-drying (lyophilisation) processes. - Good knowledge of Microsoft Office tools (Excel, Word, PowerPoint). - Ability to communicate clearly in French; good understanding of written English is a plus. - Proactive, rigorous, and able to work both independently and as part of a team. - Commitment to safety, quality, and integrity. Preferred Qualification If you have the following characteristics, it would be a plus: - Previous internship or academic project experience in a pharmaceutical or biotech production environment. - Familiarity with production planning, validation processes, or quality control fundamentals. - Knowledge of GMP (Good Manufacturing Practices) concepts. - Analytical mindset with attention to detail. - Effective interpersonal skills and openness to feedback. - Ability to adapt quickly in a dynamic, fast-paced environment. Work Arrangement This position is based on-site at our Saint-Amand-les-Eaux production site in France. Regular presence at the site is required to work closely with operational teams and fully benefit from hands-on learning opportunities. If you are ready to develop your skills in a meaningful role and contribute to improving health worldwide, apply now. We look forward to welcoming you to our team.

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This is a temporary internship/apprenticeship opportunity focused on professional development. Any reimbursement, scholarship, allowance, or financial support will be provided in accordance with applicable local laws, regulations, and GSK site policies. More detailed information will be provided during the recruitment process.Il s’agit d’une opportunité de stage/alternance temporaire axée sur le développement professionnel. Tout remboursement, bourse, indemnité ou soutien financier sera accordé conformément aux lois et réglementations locales applicables, ainsi qu’aux politiques du site GSK. Des informations plus détaillées seront fournies au cours du processus de recrutement.

Why GSK?

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

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on Fr-diversity.recruitment@gsk.com​

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GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

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