QC Microbiology Scientist I

Work Schedule 10 hr shift/days

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

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.

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.

REQUIREMENTS:
• Bachelor's degree required plus 1 year of work experience.
• 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

Compensation and Benefits

The hourly pay range estimated for this position based in Massachusetts is $25.60–$38.39.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs

• Employee assistance and family support programs, including commuter benefits and tuition reimbursement

• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: