Analytical R&D Scientist II

2 months ago


Greenville, United States Thermo Fisher Scientific Full time
and Requirements: Validate test methods for pharmaceutical raw materials and finished products by using analytical techniques such as HPLC, GC, LC/MS, dissolution, spectroscopy, and compendial testing. Recognize and report out-of-specification or unexpected results, contributing to problem-solving and troubleshooting efforts. Write deviations, OOS, CAPA, Change Controls, SOP, and specification documents to ensure regulatory compliance. Develop validation, verification, and transfer protocols and implement them. Conduct instrument calibrations/verifications as required. Record and report analysis results, interpret data, and make recommendations based on findings. Research and assist with the implementation of new methods and processes to enhance operations. Manage projects, ensuring deliverables are met and next steps are identified. Collaborate with internal teams to meet project objectives and client expectations. Contribute to talent acceleration by training and mentoring Junior Scientists. Maintain compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Ability to function in a rapidly changing environment and balance multiple priorities.

Qualifications:

Bachelor's Degree in Chemistry, Biochemistry, Molecular Biology, or a related physical/biological science field, or equivalent experience. 3+ years of method development/validation experience (or 2+ years experience with a Master's degree). Strong experience with HPLC. Experience with EMPOWER preferred.

Join our team and be part of Thermo Fisher Scientific Inc., a company dedicated to making the world healthier, cleaner, and safer. As an equal opportunity employer, we value diversity and strive to build an inclusive and collaborative work environment. We are committed to providing reasonable accommodations for applicants with disabilities during the job application process.



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