QC Scientist III

Work Schedule

First Shift (Days)

Environmental Conditions

Laboratory Setting

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 6%

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.

DESCRIPTION:
Join our collaborative team at Thermo Fisher Scientific, where you'll contribute to our mission of making the world healthier, cleaner, and safer. As a QC Scientist III, you'll perform diverse microbiological testing to ensure the safety and efficacy of pharmaceutical products. You will perform chemical, physical, and microbiological analysis to support manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments. Our collaborative environment provides opportunities for continuous learning and career advancement as you help deliver vital therapies to patients.

In addition to testing, you’ll perform data review, troubleshoot technical issues, and provide oversight to junior staff. Key responsibilities include executing and reviewing tests for product release, stability, and in-process samples; authoring and reviewing technical documentation; driving and or participating in quality records investigations; and interfacing with clients and regulatory authorities as needed. Your work will directly impact patient safety and product quality while advancing scientific innovation.

REQUIREMENTS:
• Advanced Degree plus 2 years of experience, or Bachelor's Degree plus 5 years of experience in GMP pharmaceutical/biopharmaceutical quality control
• Preferred Fields of Study: Biology, Microbiology, or related scientific field
• Expertise in Compendial Microbiological testing such as Sterility, Bacterial Endotoxin Testing, Bioburden Testing and Subvisible Particulate Matter testing.

PREFERRED

• Knowledge of Pharmaceutical Regulatory Guidance (FDA and EMA)

• Proficiency in data analysis and laboratory information management systems (LIMS)
• Good technical writing and documentation skills
• Strong organizational abilities
• Excellent interpersonal and communication skills
• Ability to work independently and work with cross-functional teams
• Experience with quality investigations and CAPAs
• Proficiency with Microsoft Office
• Ability to wear PPE and work in laboratory environments
• May require weekend/flexible scheduling based on business needs
• Physical requirements include standing, lifting up to 25 lbs, and manual dexterity
• Strong attention to detail and problem-solving skills
• Experience mentoring team members