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Manager, Quality Control

Thermo Fisher Scientific

Thermo Fisher Scientific

Quality Assurance
High Point, NC, USA
Posted on Oct 16, 2025

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office

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 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 Information:

High Point, NC

Click here for site video: High Point Softgels

Essential Duties and Responsibilities

  • Ensures that the QC laboratory is well-equipped with the necessary personnel to conduct timely testing of non-commercial and pre-commercial samples, encompassing both process and cleaning validations.
  • Provide mentorship and technical support to staff in troubleshooting instrumentation, root cause analysis, and implementing Corrective/Preventative Actions (CAPAs).
  • Collaborate with internal and external customers to support site and company initiatives.
  • Uphold and implement safety regulations and company policies.
  • Conduct regular 1-on-1 mentoring sessions and annual performance evaluations for team members.
  • Represent Quality Control during audits and regulatory inspections.

Qualifications

  • BS degree with 8 years of laboratory experience preferably within a cGMP, pharmaceutical laboratory environment, including 2-3 years of supervisory experience. ​
  • Meet applicable DEA security clearance requirements.
  • Skilled in the interpretation of guidelines and employing rational or scientific reasoning.
  • Proficiency in operating basic and complex laboratory equipment and software such as Empower, Chromeleon, MS Word, and Excel.