Thermo Fisher Scientific R&D/Mfg Scientist III in Greenville, North Carolina
Investigates, creates, and validates new scientific methodologies used to control raw materials, production intermediates, and final products on a diverse scope of projects. May be involved in pre-clinical, clinical, and/or post-marketing stages of drug development. Works on technical/scientific project activities to execute strategies and technical solutions that meet client needs and expectations. Participates in technical discussions with clients.
Engages in creation of processes and equipment design for clinical, scale up, and/or registration batches, including technology transfer of projects to and from clients. Evaluates and contributes to the design of manufacturing processes and supports problem solving as necessary with independent judgement. Typically works in a specific scientific area, such as analytical development, cell culture, purification, process validation, formulations, and/or
manufacturing technical support. Makes decisions that require choosing between multiple options or may develop new options to resolve moderately complex problems. This is typically the hiring level for a PhD with no related experience.
Contributes to development of pieces of scientific strategy.
Contributes to development of realistic proposals and timelines. Participates in and may lead relevant meetings/teleconferences with clients.
Develops methods and processes that meet or exceed the expectations from clients and provide innovation as necessary.
Researches industry practices and processes and applies to innovative development internally and for client products. Presents research internally and to clients.
Leads projects with minimal supervision; may lead projects, including managing project timelines and deliverables.
Contributes to creation of new methodologies and processes.
Analyzes problems related to the conduct of experiments.
Liaises with internal scientific, analytical, and laboratory functional areas to meet project and team objectives.
Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices and Safety guidelines. Maintains the necessary compliance status required by company and facility standards.
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