QC Scientist I

Thermo Fisher Scientific • Lenexa, KS

1d • Onsite

About The Position

Join Thermo Fisher Scientific as a QC Scientist I to contribute to global health by ensuring the safety and efficacy of pharmaceutical products through quality control testing. This role involves performing chemical, physical, and microbiological analyses to support manufacturing operations, strictly adhering to Good Manufacturing Practices (GMP). The scientist will utilize advanced analytical instruments to conduct testing on raw materials, in-process samples, finished products, and stability samples. The position offers a collaborative environment with opportunities for continuous learning and career growth, aiming to deliver vital therapies to patients and help make the world healthier, cleaner, and safer.

Requirements

• Bachelor's degree required
• 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

Nice To Haves

• Preferred Fields of Study: Chemistry, Biology, Biochemistry or related scientific field
• Experience in pharmaceutical/regulated environment

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

Benefits

• Resources needed to achieve individual career goals
• Opportunities for continuous learning and career growth
• Reasonable accommodation for individuals with disabilities to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees