Responsible for the supervision of the team members within QC Microbiology laboratory. Includes scheduling of work assignments based on department priorities, review of analytical data and documents generated by team members, coaching, and managing the development and performance evaluation of direct reports to align with business function. Responsible for creating and su

Manage team of Operational Quality professionals (24/7) to support production activities and shop floor presence Ensure Operational Quality schedules and activities support batch record review and batch disposition needs Review and approve deviation reports, corrective actions, to support GMP decisions and material disposition. Review and approve SOPs, batch records, form

Manage team of Operational Quality professionals (24/7) to support production activities and shop floor presence Ensure Operational Quality schedules and activities support batch record review and batch disposition needs Review and approve deviation reports, corrective actions, to support GMP decisions and material disposition. Review and approve SOPs, batch records, form

Site Name USA District of Columbia Washington Dc Posted Date May 1 2024 Location On site at the Washington, DC office. Relocation assistance will not be provided. The Manager, Public Policy role is a key member of the US Public Policy team. The Manager will work closely with Policy Directors as a thought partner on reimbursement and federal prescription drug policy issues

Site Name USA Maryland Rockville, Marietta PA, Upper Merion Posted Date May 1 2024 GSK is currently looking for an Engineering Design Manager to join our team. This role will manage the front end engineering of large and/or complex capital projects of value > $10m. Front end engineering includes determining business objectives, identifying process technology and delivery

Site Name USA Maryland Rockville, USA Pennsylvania Upper Providence Posted Date Apr 30 2024 Are you looking for a highly visible role where you can ensure the development and execution of appropriate strategies across all stages of the product life cycle consistent with the Vaccines Development Strategy/Integrated Asset Plan (IAP)? If so, this role could be an exciting op

Site Name Belgium Rixensart, Italy Siena, UK London Brentford, USA Maryland Rockville Posted Date Apr 30 2024 Job purpose As the Head of Vaccines (Vx) CMC Project and Portfolio Management you are accountable for all operational aspects of Vx CMC project and portfolio delivery internally and externally including budget, risk, resourcing, planning, reporting and strategic c

Participate in key technical activities, including product Lifecycle Management (Technical Risk Assessment, Product Control Strategies, Continued Process Verification, Process Robustness Assessment). Participate in site evaluation of New Product Introduction and Technical Transfer to other sites/third party manufacturers. Manage projects or activities associated with the

Lead all site related engineering and maintenance activities. Additionally, serves on the Site Leadership Team and provides leadership and direction across cross functional groups and serves as site Process Safety Champion. Lead facility compliance to Global Engineering Standards and EH&S requirements. Champion for energy reduction and key sustainability activities for bi

Job Description Are you energized by a challenging role in biology, where scientific demand is driving team growth? If so, this Scientist role would be a great opportunity to consider. As a Scientist, you will be contributing to various studies and be responsible for delivering pre clinical and clinical data analysis. This role will provide YOU the opportunity to lead key

To ensure EHS is consistently at the top of the site agenda, driving improvement every day To ensure sustainable, competitive business advantage through leadership and excellence in Environment, Health, and Safety. To provide professional and specialist advice and support to the site to ensure the business remains legally compliant as a minimum. In so doing to identify re

Site Name USA Maryland Rockville Posted Date Apr 15 2024 The Rockville Biopharm site exists to produce and deliver biopharmaceutical drug substance of the highest quality in a safe, compliant, reliable and cost effective manner for our patients. Our vision is to be wholly entrusted to make innovative, high quality medicines by leveraging the best talent and technology, on

Within the Analytical Development US, Expert Scientist, Mass Spec and Spectrophotometry (Biophysical Characterization) will serve as Subject Matter Expert (SME) in LC MS and biophysical analysis of vaccine antigens. The scientist will be responsible for characterizing antigens and their interactions using Mass Spec and an array of biophysical and traditional protein chemi

Site Name USA Maryland Rockville, USA Pennsylvania Upper Providence Posted Date Apr 11 2024 Are you looking for a regulatory leadership role where you can build advocacy and accelerate product development and licensure on a global scale, but with a focus on US? If so, this Director, Global Regulatory Affairs, Vaccines role could be an exciting opportunity to explore. As a

Site Name USA Pennsylvania King of Prussia, USA Maryland Rockville Posted Date Apr 11 2024 Are you energized by a impactful role that allows you to drive technology transfer, process performance qualification and commercialization for the drug substance manufacturing process for our innovative large molecule portfolio? If so, our MSAT drug substance lead role could be an