Scientist II - R&D Manufacturing - Days

Thermo Fisher Scientific•Cincinnati, OH

About The Position

As an R&D/Manufacturing Scientist II at Thermo Fisher Scientific’s Oral Solid Dose site in Cincinnati, you will perform complex analytical testing and contribute to analytical method validation in support of pharmaceutical development and manufacturing. You will help coordinate daily laboratory activities, support investigations, and mentor junior scientists. The site provides drug development and commercial manufacturing services and specializes in advanced dosage forms, including controlled- and sustained-release products, osmotic release dosage forms using laser drilling, liquid-filled hard capsules, controlled substances, and abuse-deterrent technologies. The role involves testing pharmaceutical raw materials, finished products, and stability samples; validating analytical methods; processing and documenting data; and maintaining instruments and laboratory areas. Work is conducted in a laboratory and cleanroom environment under applicable SOP, GMP, GLP, and safety requirements. The position follows a standard Monday–Friday schedule, with flexibility to work shifts, including nights, weekends, or holidays, as needed.

Requirements

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 to 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 personal protective equipment.
Flexibility to work shifts, including nights, weekends, or holidays, as needed.

Nice To Haves

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

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 methods for strength, impurities, identity, dissolution, and other quality attributes using HPLC, GC, spectroscopy, or quantitative analysis, as applicable.
Verify and process analytical data.
Maintain and troubleshoot analytical instruments as needed.
Assist the supervisor with planning and scheduling, 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.

Benefits

Medical, dental, and vision benefits effective Day 1.
Paid time off and holidays.
401(k) company match up to 6% after one year.
Tuition reimbursement, eligible after 90 days.
Employee referral bonus.
Employee discount program.
Recognition program.
Charitable gift matching.
Company-paid parental leave.
Vital role equipment, including a computer, monitor, keyboard, and mouse.
Personal protective equipment, including lab coats, safety glasses, and safety shoes.