Scientist II - Analytical R&D

Thermo Fisher Scientific•Florence, SC

1d•Onsite

About The Position

The Scientist II conducts laboratory work to ensure products are tested according to operating procedures and that work is performed efficiently and safely. The role uses judgment to adapt and modify assignments and provides routine and non-routine analytical chemistry testing following standard practices. Testing covers raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification. The position supports internal development and manufacturing operations and requires detailed observation, review, documentation, and communication of results to internal teams and external clients. The role is based in Florence, South Carolina, with a standard Monday–Friday schedule of 8:00 a.m.–5:00 p.m.; flexibility is required. Work takes place in a laboratory and cleanroom environment and requires adherence to GMP, OSHA, safety, BOP, and SOP requirements. The position includes operating and calibrating laboratory instruments, independently conducting experiments, reviewing data, investigating unexpected or out-of-specification results, preparing technical and regulatory documents, and training employees on analytical techniques. The role requires a chemistry or related bachelor's degree. Five or more years of laboratory and analytical-instrument experience are preferred, particularly in GLP or GMP/cGMP environments. The position involves physical activity such as standing, walking, stooping, kneeling, and crouching, as well as lifting and carrying items. PPE is required, and cleanroom restrictions apply.

Requirements

Bachelor’s degree in chemistry or a related field.
Must be able to pass a comprehensive background check, including drug screening.
Extensive knowledge of chemistry, analytical instrumental technologies, qualitative and quantitative chemical analysis, pharmaceutical quality and regulatory requirements, pharmaceutical GMPs, and descriptive organic chemistry.
Proficiency with HPLC, GC, LC/MS, and dissolution techniques.
Good problem-solving skills and a logical approach to scientific problems.
Good interpersonal and oral and written communication skills, including presentation skills.
Ability to read, analyze, and interpret technical procedures and governmental regulations.
Ability to write standard operating procedures, simple protocols, and reports.
Ability to respond to common inquiries or complaints from customers or regulatory agencies.
Ability to apply mathematical operations to tasks such as determining test reliability and applying analysis of variance and correlation techniques.
Strong proficiency in Microsoft Office Suite, including Word, Excel, and PowerPoint.
Ability to work on multiple projects simultaneously.
Ability to stand, walk, stoop, kneel, and crouch periodically for prolonged periods; lift, carry, and move light to medium weights; use arm, hand, and finger dexterity; and sit, reach, talk, hear, and use a keyboard, monitor, and equipment for prolonged periods.
Ability to lift 40 pounds without assistance.
Adherence to cleanroom restrictions on hair products, jewelry, makeup, nail polish, perfume, exposed piercings, and facial hair.

Nice To Haves

Five or more years of laboratory experience, preferably in a GLP or GMP/cGMP environment.
Five or more years of experience with analytical instrumentation such as HPLC, GC, CE, ICP, and dissolution apparatus.
Equivalent combinations of education, training, and relevant work experience may be considered.

Responsibilities

Maintain housekeeping standards and a clean, safe work environment, including work areas, instrumentation, and testing materials.
Comply with cGMP, OSHA, safety regulations, BOPs, and SOPs, and perform applicable laboratory procedures.
Perform daily instrument calibrations and verifications and conduct weekly or monthly inspections of safety equipment.
Assemble and operate bench-scale laboratory equipment and independently conduct experiments.
Conduct routine and non-routine chemical testing and method development or qualification for pharmaceutical raw materials, in-process samples, and active pharmaceutical ingredient samples using internally developed and compendial methods.
Perform developmental and validated test methods using HPLC, GC, spectroscopy, GC/MS, LC/MS, and traditional wet-chemical testing; train other employees on these techniques.
Review data collected by other employees and provide thoughtful technical review.
Recognize, report, and investigate out-of-specification or unexpected results and non-routine analytical or product problems.
Document testing and results clearly and accurately and record and report analyses according to laboratory procedures and systems.
Assist in preparing regulatory documents and communications with outside agencies, clients, and colleagues at other corporate sites.
Write and review analytical methods, validation protocols, validation reports, and SOPs as needed.
Solve problems related to chemical procedures and support internal development and manufacturing operations.
Communicate work results internally and externally to clients.
Work on multiple projects simultaneously and contribute to functional, technical, and operational excellence and team effectiveness.

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 eligibility after 90 days.
Employee referral bonus.
Employee discount program.
Recognition program.
Charitable gift matching.
Company-paid parental leave.
Company-provided role equipment, including computer, monitor, keyboard, and mouse.
Company-provided personal protective equipment, including lab coats, safety glasses, and safety shoes.