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QC Scientist

Job in Florence, Florence County, South Carolina, 29506, USA
Listing for: ThermoFisher Scientific
Full Time position
Listed on 2026-01-24
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager
Job Description & How to Apply Below
Position: QC Scientist I

Work Schedule

Other

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Overview

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Job Description

Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will perform chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments, you’ll conduct testing of raw materials, in-process samples, finished products, and stability samples.

Our collaborative environment provides opportunities for continuous learning and career growth as you help deliver vital therapies to patients.

Responsibilities

The role involves performing chemical, physical, and microbiological analyses in support of manufacturing operations, conducting testing of raw materials, in-process samples, finished products, and stability samples, and ensuring compliance with GMP and data integrity through standard procedures in collaboration with cross-functional teams.

Qualifications
  • Bachelor’s degree required, no prior experience required
  • Preferred Fields of Study:
    Chemistry, Biology, Biochemistry or related scientific field
  • Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods
  • Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards
  • Strong attention to detail with ability to follow standard procedures and maintain data integrity
  • Excellent problem-solving skills and logical approach to scientific challenges
  • Proficient computer skills including Microsoft Office and laboratory information systems
  • Strong written and verbal communication abilities
  • Ability to work both independently and collaboratively in a dynamic environment
  • Physical requirements include standing/walking for extended periods, lifting up to 50 lbs, and manual dexterity
  • Must be able to work in cleanroom environments wearing required PPE
  • Ability to work various shifts including nights, weekends, and holidays as needed
  • Experience in pharmaceutical/regulated environment preferred but not required

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

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