Site Name UK Hertfordshire Stevenage, USA Pennsylvania Upper Providence Posted Date Apr 26 2024 At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and tech

Site Name USA Pennsylvania Upper Providence Posted Date Apr 26 2024 This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include the following Act as a Subject Matter Expert (SME) in developing, validating and transferring analytical methods for quantitation of binding and biological activities to support biopha

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SHIFT Day (United States of America) Seeking Breakthrough Makers Children's Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will inspire you to pursue passions, develop expertise, and drive innovation. At CHOP, your experience is valued; your voice is heard; and your contributions make a

Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. Analyze specimens using approved testing procedures. Review and release test results. Follow CLIA, HIPAA, OSH

The Regulatory Affairs Specialist drafts, submits and gains clearance for 510(k) submissions, and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products. This position entails development of FDA submissions, requires working knowledge of products under review and of relevant regulations and guidance documents. This i

Coordinates and prepares document packages for regulatory submissions for new and mature products, ensuring compliance with local and regional registration requirements. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitor

Knoll is looking for a specialist to work in the facilities department. This individual will work first shift and be part of an interdisciplinary team charged with general upkeep and maintenance of a site containing both manufacturing and corporate offices. The successful candidate will have experience working in industrial settings and must be self driven to provide a hi

Promote and ensure safe work in the Teslin R&D labs, including the operation of mechanical equipment, handling of chemicals, execution of experiments, preparation of samples, characterization and performance testing of materials, etc. Learn and apply the key chemical concepts of the Teslin technology to accelerate the development of new Teslin capabilities and products. L

Coordinate the experimental work to meet project goals and timeline Communicate and share knowledge within the team and with collaborators Interact with global development labs, research team, marketing team, production team and customers to guide projects forward Use Sigma logic methodology for design of experiment and data analysis Provide support to customer and produc

Promote and ensure safe work in the Silica Pilot Plant, including the operation of equipment, handling of chemicals, etc. Learn and apply the necessary chemical concepts of precipitated silica technology to accelerate the development and scale up of new silica products. Collaborate with Silica R&D and Technical Service to translate new silica development opportunities and

Duties Conduct analyses of the quality and performance of HHS health and human services programs. Develop and conduct policy and program analyses to identify and understand the needs and preferences of HHS health and human services beneficiary programs and the populations they serve. Develop clearly written and concise issue papers and talking points for senior staff when

Adhere to an IRB approved protocol Participate in the creation and design of query development workflows Support and coordinate Query Fulfillment activities conducted within the Coordinating Center Screen, recruit and enroll patients/research participants Maintain study source documents Report adverse events Understand good clinical practice (GCP) and regulatory complianc