Consultant, Regulatory Specialist, Tissue Bank / Pharmaceutical. Summary. Our client, an Innovative Medical Device company, has engaged GForce Life Sciences to provide a Regulatory Specialist. This position will report to a Manager within the Regulatory department. This individual will play a crucial role in ensuring compliance with regulatory requirements governing tissue banking operations. They are responsible for submitting state licensing fi...
Summary. Our client, a biochemistry analytical company, has engaged GForce Life Sciences to provide a staff analytical scientist. . This position will report to the Director of Process Technology. The Staff Analytical Scientist is a key position that will help develop various analytical tools for complex biological assays. A variety of qualitative and quantitative chromatographic (LC), and electrophoretic (CE) analyses are the key underpinning of...
The Project Physician tasks may include. Contribute to writing and reviewing of study related documents such as: protocols, protocol amendments, informed consent forms, statistical analysis plans, clinical study reports, and other similar documents. Contribute to writing and reviewing medical monitoring plans and other plans for clinical trials, internal or between Pharmaceutical Development & Commercialization, Inc. and a CRO. Serve as the prima...
Consultant, Staff Engineer, Controls Automation. Summary. Our client, a global Fortune 500 Medical Technology Company. . has engaged GForce Life Sciences to provide a Staff Engineer, Controls Automation. . This position will report to a Sr Manager in Engineering within the. . R&D. . department. This individual will be responsible for managing End-to-End Automation Projects/Programs. This position requires the ability to do manage and push large p...
Consultant, SME, Validation Engineer. Summary. Our client, a growing medical device manufacturer, requires a SME validation engineer to join their team. This individual will perform process validations and qualifications of new/existing equipment and processes in a medical device environment. Focus on validations will be to document the processes and equipment to current regulatory standards and requirements. Duties / Expectations of Role. This i...
