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’For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to [Cambridge, UK] . The location of this role will therefore subsequently change to [Cambridge, UK] in accordance with timelines to be se

The Quality Control Microbiology Associate Director is responsible for planning and prioritizing resource allocation in Upper Merion Biopharma quality control microbiology laboratory to meet testing requirements for product release, raw material, utility, in-process, etc. Oversee the operation of QC

Le Laboratoire GSK recherche un Contrôleur de stock H/F dans le cadre d’un CDD jusqu’au 31 décembre 2027 au sein de l’équipe Logistique & Services Clients. Le poste est rattaché au site industriel d’Evreux (27). Responsabilités clés Contrôleur de stock Gérer la précision des stocks et les activités

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

This role is part of a dynamic operations team delivering vital medicines to patients globally. The Production Manager upholds GSK Values and Expectations, working collaboratively with colleagues and support groups. Reporting to the Value Stream Lead and Site Leadership, they are responsible for ens

Position Summary The Global Medical Affairs Director, Oncology (Multiple Myeloma) role provides strategic global medical affairs leadership for an assigned oncology asset or portfolio. The role holder will set and deliver the long-term disease and medicine strategy, lead integrated global medical pl