include some of the following... Enterprise leadership driving enterprise initiatives, shaping the site's strategic direction, and creating a strong shadow of the leader across 600+ team members. Direct the transfer of drug substance biopharmaceutical production processes and technologies from R&D, third party clients, or MSAT labs to/from Rockville Biopharm. Accountable

Job Description Are you motivated by a challenging role in biology, where scientific demand is driving team growth? If so, this Expert Scienti role would be a great opportunity to consider. The goal of this Expert Scientist position will be focused on devising and executing experiments in the areas of RNA vaccine discovery and research with a focus on understanding and mo

You act as essential partner for project technical teams (e.g. Technical Development Leader, functions heads and representatives, …) or other stakeholder groups and provide statistical expertise in all aspects of Technical Research & Development (Product, Process and Analytical Development and commercialization) bringing the added value of data driven decisions. Yo

Site Name USA Maryland Rockville Posted Date Apr 8 2024 Are you energized by a scientific leadership role that allows you to enhance and improve processes across biologics manufacturing? If so, this Biologics Virus Clearance Validation Leader role could be an ideal opportunity to explore. As a Biologics Virus Clearance Validation Leader, you will be responsible for techni

Site Name Rockville Biopharm Posted Date Apr 8 2024 Are you energized by a scientific leadership role that allows you to enhance and improve processes across biopharmaceutical manufacturing? If so, this Biologics Process Validation Leader role could be an ideal opportunity to explore. As a Biologics Process Validation Leader, you will be responsible for technical leadersh

Site Name USA Pennsylvania Upper Providence, Durham Blackwell Street, GSK House, Rockville Biopharm, Stevenage, UK Hertfordshire Ware, Waltham, Zug House Posted Date Feb 22 2024 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportuni

Site Name USA Maryland Rockville, USA Pennsylvania Upper Providence Posted Date Feb 20 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

Is a SME for specific tasks required by the team Leads and/or serves on team projects as needed Reviews testing results as needed Writes, reviews, and approves microbiological lab investigations, deviations, change controls, protocols, reports. Writes, updates, reviews, and approves Laboratory Standard Operating Procedures, Work Instructions, and References. Assures that

Site Name USA Maryland Rockville, Marietta PA, Upper Merion Posted Date Apr 2 2024 GSK is currently looking for a Project Design Lead to join our 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 strategies, pr

Site Name USA Maryland Rockville Posted Date Nov 13 2023 Join the GSK 's Bio pharm Manufacturing Associate Apprentice Program US , 202 4 Help us get ahead of disease together GSK Apprenticeships are full time entry level opportunities that offer high school graduates and community college students the opportunity to begin their career while studying towards their associat

Job Description Do you have experience in all aspects of a Regulatory Affairs project, supporting technical/ CMC, clinical, nonclinical and procedural aspects of strategy and submissions, but are looking to take this to the next level, supporting a best in class vaccine as we expand into new markets and maintain current licenses ? As part of the Global Regulatory Affairs

Job Description Are you a subject matter expert in technical / CMC and procedural aspects of Global Regulatory Affairs, driven to provide in depth input into asset specific regulatory strategy on a global scale for clinical/labelling or technical/NC or procedural aspects? Are you driven to provide robust regulatory advice and plans to various project teams and advisory bo

The Manager of Production is responsible for the production biotechnology platforms operating on a 24hour/7day basis. The job duties require a high level of technical knowledge combined with a sense of urgency and responsibility to meet delivery schedules. Responsible for the preparation of bulk biopharmaceutical drug substance to meet all quality standards for GSK, FDA a