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Job Description
Title: Scientist - Microbiology
Location: New Brunswick, NJ
100% onsite position
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale! Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner.
Within our Analytical Services team, we have a functional service provider solution, which is a partnership that allows our customers to benefit from the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.
A Day in the Life:
Responsible for working with stakeholders from development, clinical, commercial, and manufacturing organizations to develop phase appropriate Container Closure Integrity Test (CCIT) and microbiological methods. This is a laboratory-based position and includes, but is not limited to, performing testing to assist in the development and validation of CCIT and microbiological methods in support of aseptic manufacturing of clinical drug products, executing assays for technology transfer to commercial sites, and new technology evaluation/implementation. Responsibilities include executing CCI and microbiological methods within the laboratory, supporting device development and manufacturing groups to evaluate and implement rapid, non-destructive technologies to facilitate testing and manufacture of vials, syringes, and devices, and providing data to interdisciplinary development teams in support of product development plans. Additional responsibilities may include the development of phase appropriate microbiological methods (bioburden, endotoxin, and rapid sterility).
Keys to Success
Education:
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