

New · posted Nov 3
Thermo Fisher Scientific · Pharmaceuticals
QC Scientist I
- Florence, SC
- On-site
- Full-time
- Associate & Specialist
The role
Discover impactful work
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.
Shift Schedule: 12hr day shift position. 7 AM - 7 PM
2 days on, 2 days off and every other weekend, 12hr shift
What you need
Keys to Success
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
- Experience with microbiological testing, environmental monitoring, and aseptic techniques
- 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
Skills named in this posting
What you'll do
Day in the Life
- Conduct day-to-day testing activities including chemical, physical, and microbiological analyses of raw materials, in-process samples, finished products, and stability samples
- Complete accurate documentation and reporting duties in compliance with GMP standards and regulatory requirements
- Collaborate with other departments including Manufacturing, Quality Assurance, and Research & Development to support production goals and quality objectives
- Perform equipment maintenance and calibration tasks to ensure analytical instruments remain in proper working condition
- Participate in investigation and troubleshooting activities to identify root causes of out-of-specification results or testing anomalies
- Support training responsibilities including onboarding new team members and sharing technical expertise with colleagues
Pay
Thermo Fisher Scientific didn't publish pay for this role
See what similar roles pay on Regulatory Jobs, or try the salary calculator.
· Benefits & Total Rewards | Thermo Fisher Scientific
· Medical, Dental, & Vision benefits-effective Day 1
· Paid Time Off & Designated Paid Holidays
· Retirement Savings Plan
· Tuition Reimbursement
Where you'll work
Florence, SCOn-siteOpen in Maps (opens in a new tab)
More jobs in Florence, SCWorking conditions
12 hr shift/days
Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

From the posting
About Thermo Fisher
OTHER
· Relocation assistance is NOT provided
· Must be legally authorized to work in the United States now or in the future, without sponsorship
· Must be able to pass a comprehensive background check, which includes a drug screening
Job intelligence
The context around this role
Live data · November 3, 2026
Salary intelligence
How the pay compares
Associate & Specialist roles in the US136 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $48,000 | $63,000 | $80,000 |
Comparisons: the base pay employers published on open Quality Control roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Control
The general path across 355 open Quality Control roles on Regulatory Jobs, with the titles they carry most. Not Thermo Fisher's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 23 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Lab testing and methods7
- Collaboration and leadership5
- GMP and compliance3
- Documentation and SOPs3
- Data and digital systems2
- Investigations and CAPA1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticals
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- FDAFDA OOS guidance(official source, opens in a new tab)Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Thermo Fisher on Regulatory Jobs
- 119
- Open roles
- 106
- Distinct roles
- 50
- Locations
By discipline
- Quality76 64%
- Clinical37 31%
- Regulatory6 5%
By level
- Senior & Principal51 43%
- Associate & Specialist36 30%
- Manager26 22%
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QC Scientist I at Thermo Fisher
Applications close November 7.

