QC Scientist I

Thermo Fisher Scientific • Florence, SC

3d

About The Position

Join Thermo Fisher Scientific as a QC Scientist I and contribute to quality control testing that supports the safety and efficacy of pharmaceutical products. The role performs chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Testing covers raw materials, in-process samples, finished products, and stability samples using analytical instruments.

This is a 12-hour day-shift position from 7 AM to 7 PM, following a schedule of two days on, two days off, and every other weekend. The work takes place in a laboratory and cleanroom setting and involves required PPE and work with hazardous or toxic materials.

The position requires a bachelor's degree, but no prior experience. Candidates must be legally authorized to work in the United States without sponsorship and pass a comprehensive background check, including drug screening. Relocation assistance is not provided.

Requirements

• Bachelor's degree required; no prior experience required.
• Proficiency with analytical techniques, including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods.
• Strong attention to detail and ability to follow standard procedures and maintain data integrity.
• Excellent problem-solving skills and a logical approach to scientific challenges.
• Proficient computer skills, including Microsoft Office and laboratory information systems.
• Strong written and verbal communication abilities.
• Ability to work independently and collaboratively in a dynamic environment.
• Ability to stand and walk for extended periods, lift up to 50 lbs, and use manual dexterity.
• Ability to work in cleanroom environments while wearing required PPE.
• Ability to work various shifts, including nights, weekends, and holidays as needed.
• Legally authorized to work in the United States now or in the future without sponsorship.
• Must pass a comprehensive background check, including drug screening.

Nice To Haves

• Preferred fields of study include Chemistry, Biology, Biochemistry, or a related scientific field.
• Experience with microbiological testing, environmental monitoring, and aseptic techniques.
• Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards.
• Experience in a pharmaceutical or regulated environment; preferred but not required.

Responsibilities

• Conduct chemical, physical, and microbiological testing of raw materials, in-process samples, finished products, and stability samples.
• Complete accurate documentation and reporting in compliance with GMP standards and regulatory requirements.
• Collaborate with Manufacturing, Quality Assurance, and Research & Development to support production goals and quality objectives.
• Perform equipment maintenance and calibration to keep analytical instruments in proper working condition.
• Participate in investigations and troubleshooting to identify root causes of out-of-specification results or testing anomalies.
• Support training, including onboarding new team members and sharing technical expertise with colleagues.

Benefits

• Medical, dental, and vision benefits effective Day 1.
• Paid time off and designated paid holidays.
• Retirement savings plan.
• Tuition reimbursement.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level