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Job Description
QC Scientist I, Micro Thermo Fisher Scientific - 3.4 Greenville, NC Job Details Full-time 15 hours ago Benefits Paid parental leave Paid holidays Health insurance Dental insurance Tuition reimbursement Paid time off Parental leave Vision insurance 401(k) matching Employee discount Benefits from day one Opportunities for advancement Referral program Qualifications Cleanroom protocols Personal protective equipment (PPE) adherence Bachelor's degree Cleanroom Safety equipment Full Job Description Work Schedule Standard (Mon-Fri) Environmental Conditions 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. Excellent Benefits Package Review our company's Total Rewards Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Holidays 401K Company Match up to 5% Tuition Reimbursement - eligible after 90 days! Employee Referral Bonus Employee Discount Program Recognition Program Charitable Gift Matching Company Paid Parental Leave Career Advancement Opportunities Location/Division Specific Information Greenville, NC
RELOCATION ASSISTANCE IS NOT PROVIDED
Must be legally authorized to work in the United States
WITHOUT SPONSORSHIP OF ANY KIND NOW OR IN THE FUTURE.
Must be able to pass a comprehensive background check, which includes a drug screen.
POSITION SUMMARY
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.
Key Responsibilities:
Performs a variety of microbiological and bioanalytical testing; including Sterility Testing Bacterial, Endotoxin Testing, Particulate Matter, membrane filtration, TOC and conductivity to support release of product and making quality decisions. Generates valid data, document testing procedures and results in appropriate notebooks and database according to cGMP Compares laboratory results with specifications for acceptability and determines with QA and Management if repetition or OOS is required. Maintains equipment and laboratory cleanliness and report any issues to supervisor. Conducts tasks in a safe manner. Follows scheduled assigned activities to meet target dates for customer needs. Interacts effectively with teams across departments and functions to increase efficiency, solve problems, generate cost savings and improve quality. Performs all duties in strict compliance with Safety guidelines and procedures, Standard Operating Procedures, Good Manufacturing Practices and Good Laboratory Practices. Maintains the necessary compliance status required by company.
Qualifications:
Bachelor's degree required, no prior experience required
Preferred Fields of Study:
Chemistry, Biology, Biochemistry or related scientific field Experience with microbiological identifications, 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
