QC Microbiology Scientist I

Thermo Fisher Scientific•Plainville, MA

1d•Onsite

About The Position

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 or equivalent required with at least 1 year of experience preferably within a lab setting.
Proficiency with analytical techniques including HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods preferred.
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
Must be legally authorized to work in the United States now and in the future, without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.

Nice To Haves

Experience in pharmaceutical/regulated environment preferred but not required.

Responsibilities

Perform chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP).
Conduct testing of raw materials, in-process samples, finished products, and stability samples using advanced analytical instruments.

Benefits

Competitive remuneration
Annual incentive plan bonus
Healthcare
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
Short- and long-term disability
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