QC Scientist I

Work Schedule

Environmental Conditions

Job Description

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

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

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

Excellent Benefits

·         Benefits & Total Rewards | Thermo Fisher Scientific

·         Medical, Dental, & Vision benefits-effective Day 1

·         Paid Time Off & Designated Paid Holidays

·         Retirement Savings Plan

·         Tuition Reimbursement

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