QC Supervisor, Incoming Materials Lab

Work Schedule

First Shift (Days)

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.

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

Greenville, NC

• 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.

Lead a Quality Control team while ensuring compliance with cGMP standards and regulatory requirements. As an Incoming Materials Lab QC Supervisor, you will provide technical leadership and oversight for laboratory operations supporting pharmaceutical manufacturing.

Support operational excellence through mentoring staff, optimizing workflows, and implementing continuous improvement initiatives while maintaining high quality standards.

• Advanced Degree plus 3 years of experience, OR
• Bachelor’s Degree plus 5 years of experience in pharmaceutical/biotech quality control
• Preferred Fields:
  Chemistry, Biology, Biochemistry, Microbiology or related scientific field

• 2+ years in a leadership role
• Experience managing laboratory operations (scheduling, planning, improvements)
• Experience with LIMS, Prolink, and SAP desired
• Experience supporting regulatory audits and inspections
• Ability to manage multiple priorities while maintaining quality
• Flexibility to adjust schedules to support manufacturing operations
• Certifications in quality systems or regulatory compliance (preferred)

• Strong knowledge of cGMP, FDA regulations, ICH guidelines, USP, EP, JP compendia
• Analytical testing methods and instrumentation experience
• Technical writing (SOPs, investigations, regulatory documentation)
• Leadership and team development
• Project management and organizational skills
• Strong communication and interpersonal skills
• Problem-solving and investigation leadership
• Data integrity and documentation knowledge
  
  Risk assessment and root cause analysis
• Microsoft Office proficiency