Scientist II - R&D Manufacturing - Days

Thermo Fisher Scientific•Cincinnati, OH

6d•Onsite

About The Position

The Scientist II will perform complex analytical testing and contribute to analytical method validation in support of pharmaceutical development and manufacturing at Thermo Fisher Scientific’s Oral Solid Dose site in Cincinnati. The role also helps coordinate daily laboratory activities, supports investigations, and mentors junior scientists. The position performs chemical and physical testing of pharmaceutical raw materials, finished products, and stability samples using internally developed and compendial methods. It participates in validation of methods for strength, impurities, identity, dissolution, and other quality attributes using applicable analytical techniques. The Scientist II verifies and processes analytical data, maintains and troubleshoots instruments, documents and communicates testing and results, and maintains organized laboratory work areas and materials. The role follows applicable SOP, GMP, GLP, and safety requirements. Work takes place in a laboratory and cleanroom environment and may involve hazardous or toxic materials, strong odors, and required PPE. The standard schedule is Monday through Friday, with flexibility to work shifts, including nights, weekends, or holidays, as needed.

Requirements

Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, including drug screening.
Bachelor’s degree required, preferably in Chemistry; equivalent combinations of education, training, and relevant work experience may be considered.
Advanced knowledge of chemistry, analytical instrumentation, and qualitative and quantitative chemical analysis.
Strong understanding of pharmaceutical quality and regulatory requirements, including GMP.
Advanced proficiency with HPLC, GC, LC/MS, and dissolution techniques, including method development and validation.
Strong problem-solving, organizational, leadership, presentation, and communication skills.
Ability to interpret technical procedures and regulations and write SOPs or policy manuals.
Ability to stand and walk for extended periods, perform laboratory tasks requiring manual dexterity, and lift up to 50 pounds.
Ability to work in cleanroom environments while wearing required PPE.

Nice To Haves

An advanced degree is preferred.
Three years of experience in the pharmaceutical industry, analytical development, or quality control is preferred.

Responsibilities

Perform complex chemical and physical testing of pharmaceutical raw materials, finished products, and stability samples using internally developed and compendial methods.
Participate in validation of analytical methods for strength, impurities, identity, dissolution, and other quality attributes using applicable techniques.
Verify and process analytical data.
Maintain and troubleshoot analytical instruments as needed.
Assist the supervisor with planning and scheduling laboratory work, investigations, and representing the team in meetings.
Mentor junior scientists as needed.
Document and communicate testing and results accurately in accordance with laboratory procedures and systems.
Maintain organized work areas, instruments, and testing materials.
Follow applicable SOP, GMP, GLP, and safety requirements.