QC Scientist I

Thermo Fisher Scientific • Florence, SC

1d

About The Position

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

This is a 12-hour day-shift position, 7 AM–7 PM, on a schedule of two days on, two days off, and every other weekend. The role works in a laboratory and cleanroom environment and involves required PPE and work with hazardous or toxic materials. Physical requirements include extended periods of standing and walking, lifting up to 50 pounds, and manual dexterity. Candidates must be able to work various shifts, including nights, weekends, and holidays, as needed.

A bachelor's degree is required; prior experience is not required. The preferred fields of study are Chemistry, Biology, Biochemistry, or a related scientific field. Pharmaceutical or regulated-environment experience is preferred but not required. Applicants must be legally authorized to work in the United States now or in the future without sponsorship, and must pass a comprehensive background check, including drug screening. Relocation assistance is not provided.

Requirements

• Bachelor's degree.
• 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 and ability to follow standard procedures and maintain data integrity.
• 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 pounds, and perform tasks requiring manual dexterity.
• Ability to work in cleanroom environments while wearing required PPE.
• Ability to work various shifts, including nights, weekends, and holidays, as needed.
• Legal authorization to work in the United States now or in the future without sponsorship.
• Ability to pass a comprehensive background check, including drug screening.

Nice To Haves

• Preferred field of study: Chemistry, Biology, Biochemistry, or a related scientific field.
• Experience in a pharmaceutical or regulated environment.

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