R&D Mfg Scientist II - Analytical Development

Thermo Fisher Scientific•Greenville, NC

2d•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Position Summary: Provides routine analyses in a biochemistry environment within defined procedures and practices. Performs analytical methods for moderately sophisticated testing on samples, stability, and production intermediates to support process development and/or manufacturing operations. May research and implement new methods and technologies to improve operations. Makes detailed observations and reviews, documents, and communicates test results.

Requirements

Bachelor Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological science field minimally required with 3+ years related experience, or
Master’s degree, 1+ year related pharmaceutical industry experience strongly preferred.
Experience with HPLC and Dissolution.
Experience performing method development and validation, chemical tests with chromatographic, spectroscopic, or other analytical techniques preferred
Experience with EMPOWER preferred.
Equivalent combinations of education, training, and meaningful work experience will be considered.
Good knowledge and understanding of chemistry and analytical instrumental technologies.
Good knowledge of qualitative and quantitative chemical or microbiological analysis.
Awareness of quality and regulatory requirements in the pharmaceutical industry
Strong interpersonal and communications skills, written and oral
Ability to read, analyze, and interpret technical procedures and governmental regulations.
Excellent organization and planning skills.
Strong attention to detail and ability to implement to standard procedures.
Ability to design and complete tasks and studies based on the deliverables.
Ability to accurately detail work and write reports.

Responsibilities

Lead the validation of test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, potency, and dissolution by HPLC, GC, dissolution, spectroscopy, and traditional quantitative analysis, using HPLC, GC, LC/MS, and compendial testing.
Recognize and report out-of-specification or unexpected results and non-routine analytical and product problems.
Write deviations, OOS, CAPA, Change Controls, SOP and specification documents.
Perform daily instrument calibrations/verifications as required.
Write and complete validation protocols in accordance with regulatory guidelines
Review and interpret analytical test results; make recommendations based on data
Run projects at the broad task level under supervision, ensuring deliverables are met and next steps are clearly identified.
Participate in meetings/teleconferences with clients. Develop methods and processes that meet or exceed the expectations from clients and provide innovation.
Conducts routine tasks and sample analyses to support process development.
Performs all duties in compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines. Maintains the compliance status required by company and facility standards.