Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products 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, no prior experience required but previous experience is preferred
• Preferred Fields of Study: Microbiology, Chemistry, Biology, Biochemistry or related scientific field
• Proficiency with microbiological techniques including Sterility Testing, Bacterial Endotoxin Testing, Particulate Matter, membrane filtration, TOC and conductivity
• Experience with 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/pushing for extended periods, lifting up to 50 lbs, and manual dexterity
• Possibility for gowning into controlled areas
• Ability to work various shifts including nights, weekends, and holidays as needed
• Experience in pharmaceutical/regulated environment preferred but not required