Scientist I - Analytical R&D

Thermo Fisher Scientific•Florence, SC

1d•Onsite

About The Position

The Scientist I conducts laboratory work to ensure products are tested according to operating procedures and that work is carried out efficiently and safely. The role applies judgment when adapting or modifying assignments and performs routine analyses in an analytical chemistry laboratory. It includes testing raw materials, samples, stability samples, production intermediates, and active pharmaceutical ingredients, as well as method development and qualification activities. The Scientist I supports internal development and manufacturing operations and makes detailed observations, reviews results, and documents and communicates findings. The position is based in Florence, South Carolina, and has a standard Monday–Friday schedule, 8 a.m.–5 p.m., with flexibility required. Work takes place in a laboratory and cleanroom environment, with adherence to GMP and safety standards. The role may involve hazardous or toxic materials, strong odors, and required personal protective equipment. Cleanroom restrictions include no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, or facial hair. The role requires a bachelor’s degree in chemistry or a related field; new graduates are considered. One or more years of laboratory experience and experience with analytical instrumentation are preferred. Candidates must pass a comprehensive background check, including drug screening. The position requires physical activity including standing, walking, stooping, kneeling, and crouching, as well as handling light-to-medium weights. The company provides competitive wages, benefits, role-related equipment, and required personal protective equipment.

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.
Good 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 oral and written interpersonal and 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 test reliability determination, analysis of variance, and correlation techniques.
Ability to lift 40 pounds without assistance.
Ability to stand, walk, stoop, kneel, and crouch periodically for prolonged periods; manipulate light-to-medium weights; use arm, hand, and finger dexterity for tasks including prolonged grasping and typing; and use visual, speaking, hearing, sitting, and reaching abilities for prolonged periods.

Nice To Haves

One or more years of laboratory experience, preferably in a GLP or GMP/cGMP environment.
One or more years 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

Maintain housekeeping standards and a clean, safe work environment, including work areas, instrumentation, and testing materials.
Comply with cGMP, OSHA, safety regulations, SOPs, and laboratory procedures.
Perform cGMP procedures, lab 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 the guidance of a scientist.
Conduct 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/or traditional wet chemistry.
Recognize and report 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 prescribed 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 support functional, technical, and operational excellence and team effectiveness.
Work on multiple projects simultaneously and communicate results to customers, clients, and colleagues.