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

As an Expert Scientist in the High Parametric Flow Cytometry & Immunomonitoring Team, you will be responsible for leading and performing immune monitoring activities on human clinical trial samples, ensuring business needs are supported and technology platforms advanced. Details ( Your Responsibilities ) This role will provide YOU the opportunity to lead key activities an

Site Name Belgium Rixensart, Italy Siena, UK London Brentford, USA Maryland Rockville Posted Date Apr 23 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

As a Scientist in the High Parametric Flow Cytometry & Immunomonitoring Team, you will be responsible for performing immune monitoring activities on human clinical trial samples, ensuring business needs and technology platforms are supported. Key Responsibilities This role will provide YOU the opportunity to lead key activities and to progress YOUR career. These responsib

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

Procedures Operates in compliance with relevant Standard Operating Procedures and cGMP practices and updates and reviews department procedures, SOP's, WI's, and training documents with guidance. Receives training on Production Planning processes as needed. In SAP, responsible for ensuring purchase orders are placed on time and monitored to maintain appropriate inventory l

Site Name USA Maryland Rockville Posted Date Mar 14 2024 This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following Basic understanding and knowledge of the following areas and ability to perform the activity with some supervisory guidance Follow appropriate standard operating procedures

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 Italy Siena, Cambridge Park Drive, GSK House, Rockville Vaccines, Warsaw Cirrus, Wavre Posted Date Apr 17 2024 Position summary The Executive Director, Safety Evaluation & Risk Management (SERM) Head is accountable to lead SERM (Safety Evaluation & Risk Management) medical and scientific staff and define and drive the strategy and vision of clinical safety and p

Management (timely reporting & effectiveness) of KPI's through Inspection readiness and Site Quality Council Oversight of the lead investigator qualification plan Provides deviation and CAPA related data for Periodic Product Review Review and approve deviation reports, corrective actions to support GMP decisions and material disposition. Leading DRB to assess active inves

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