Scientist I - Analytical R&D

Thermo Fisher Scientific•Florence, SC

6d•Onsite

About The Position

The Scientist I conducts laboratory work to ensure products are tested according to operating procedures and that work is performed efficiently and safely. The role provides routine analyses in an analytical chemistry laboratory, using standard practices, and performs assigned analytical methods on raw materials, samples, stability samples, production intermediates, and active pharmaceutical ingredients (APIs). It also supports method development and qualification, internal development, and manufacturing operations. The Scientist makes detailed observations, reviews and documents testing, and communicates results. The role is based in Florence, South Carolina, on a standard Monday–Friday schedule, with stated hours of 8:00 a.m.–5:00 p.m. and a need for flexibility. Work takes place in a laboratory and cleanroom environment and involves adherence to GMP and safety standards, PPE, strong odors, and hazardous or toxic materials. The position requires lifting and other physical activity as described in the posting. The Scientist maintains housekeeping and a clean, safe work area; follows cGMP, OSHA, safety regulations, SOPs, and laboratory procedures; performs instrument calibrations and verifications; inspects safety equipment; and conducts routine chemical testing and method development or qualification. Testing may use HPLC, GC, spectroscopy, GC/MS, LC/MS, and traditional wet chemistry. The role identifies and reports unexpected or out-of-specification results, documents and reports analyses, contributes to regulatory documents and communications, and may assist with analytical methods, validation protocols and reports, and SOPs. A bachelor’s degree in chemistry or a related field is required, and new graduates are considered. Laboratory and analytical-instrument experience are preferred. Candidates must be able to pass a comprehensive background check, including drug screening. The posting offers competitive wages and an excellent benefits package.

Requirements

Bachelor’s degree in chemistry or a related field.
Must pass a comprehensive background check, including drug screening.
Good knowledge and understanding of chemistry and analytical instrumental technologies.
Knowledge of qualitative and quantitative chemical or microbiological analysis.
Knowledge of pharmaceutical-industry quality and regulatory requirements, including pharmaceutical GMPs and descriptive organic chemistry.
Problem-solving skills and a logical approach to scientific problems.
Proficiency with HPLC, GC, LC/MS, and dissolution techniques.
Good interpersonal and oral and written communication skills.
Presentation skills for communicating information to customers, clients, and other employees.
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, including determination of test reliability, analysis of variance, and correlation techniques.
Ability to work on multiple projects simultaneously.
Ability to lift 40 pounds without assistance.
Ability to meet the stated physical requirements, including standing, walking, stooping, kneeling, crouching, manipulating light to medium weights, and using hands and arms for prolonged periods.

Nice To Haves

At least 1 year of laboratory experience, preferably in a GLP or GMP/cGMP environment.
At least 1 year of experience with analytical instrumentation such as HPLC, GC, CE, ICP, and dissolution apparatus.
Equivalent combinations of education, training, and meaningful work experience may be considered.

Responsibilities

Conduct laboratory testing of products in accordance with operating procedures and perform work efficiently and safely.
Perform routine analytical chemistry analyses and assigned testing on raw materials, samples, stability samples, production intermediates, and APIs.
Support method development and qualification, internal development, and manufacturing operations.
Maintain housekeeping standards and a clean, safe work area, including instrumentation and testing materials.
Comply with cGMP, OSHA, safety regulations, SOPs, and laboratory procedures.
Perform cGMP procedures, laboratory procedures, BOPs, and SOPs.
Perform daily instrument calibrations or verifications as needed and inspect safety equipment weekly or monthly.
Assemble and operate bench-scale laboratory equipment and conduct experiments under a scientist’s guidance.
Conduct routine chemical testing and method development or qualification using internally developed and compendial methods.
Use developmental and validated test methods, including HPLC, GC, spectroscopy, GC/MS, LC/MS, and traditional wet chemical testing.
Recognize and report out-of-specification results, unexpected results, and non-routine analytical or product problems.
Document testing and results clearly and accurately, and record and report analyses in accordance with laboratory procedures and systems.
Assist with regulatory documents and communications with outside agencies, clients, and colleagues at other corporate sites.
Contribute information to analytical methods, validation protocols, validation reports, and SOPs as needed.
Solve problems related to chemical procedures 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 1 year.
Tuition reimbursement, eligible after 90 days.
Employee referral bonus.
Employee discount program.
Recognition program.
Charitable gift matching.
Company-paid parental leave.
Computer, monitor, keyboard, mouse, and role-specific equipment provided.
Personal protective equipment provided, including lab coats, safety glasses, and safety shoes.