Site Name USA Pennsylvania Upper Providence, Durham Blackwell Street, USA Maryland Rockville Posted Date May 13 2024 Are you energized by a role that drives efficiency in patents and intellectual property? Do you want to work with teams developing medicines and technologies to make a difference in patients' lives? If so, a Patent Counsel role with GSK could be an ideal op

Procedures Ensures compliance with relevant Standard Operating Procedures and cGMP Participates in cross functional project teams, leads department problem solve teams. Facilitate communication with vendors to ensure timely delivery of orders Indirect PO creation & placement based on Business Owner requirements Indirect PO management Facilitating invoice approvals & conta

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 Washington DC, USA Delaware Dover , USA Delaware Wilmington, USA Maryland Baltimore, USA New Jersey Newark, USA New Jersey New Jersey City, USA Ohio Cleveland, USA Ohio Columbus , USA Ohio Dayton, USA Pennsylvania Philadelphia, USA Pennsylvania Pittsburgh, USA Virginia Richmond, USA West Virginia Charleston , USA West Virginia Morgantown Posted Date May 13 2024

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

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 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 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

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

Lead engineering projects as assigned to meet technical, budget and schedule goals. Lead in the evaluation, selection, and implementation of new equipment or modifications to existing systems with consideration to new processing technologies or strategies. This may include assessing an economic, environmental, quality, conservation, or productivity impact while generating

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

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

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

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