QC Supervisor, Incoming Materials Lab

Thermo Fisher ScientificGreenville, NC
Onsite

About The Position

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. 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.

Requirements

  • Advanced Degree plus 3 years of experience, OR Bachelor's Degree plus 5 years of experience in pharmaceutical/biotech quality control
  • 2+ years in a leadership role
  • Experience managing laboratory operations (scheduling, planning, improvements)
  • Ability to manage multiple priorities while maintaining quality
  • Flexibility to adjust schedules to support manufacturing operations
  • Strong knowledge of cGMP, FDA regulations, ICH guidelines, USP, EP, JP compendia
  • Analytical testing methods and instrumentation experience
  • Microsoft Office proficiency

Nice To Haves

  • Chemistry, Biology, Biochemistry, Microbiology or related scientific field
  • Experience with LIMS, Prolink, and SAP desired
  • Certifications in quality systems or regulatory compliance (preferred)

Responsibilities

  • Lead a Quality Control team while ensuring compliance with cGMP standards and regulatory requirements.
  • 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.
  • Manage laboratory operations (scheduling, planning, improvements).
  • Support regulatory audits and inspections.
  • Manage multiple priorities while maintaining quality.
  • Adjust schedules to support manufacturing operations.
  • Technical writing (SOPs, investigations, regulatory documentation).
  • Leadership and team development.
  • Project management and organizational skills.
  • Problem-solving and investigation leadership.
  • Risk assessment and root cause analysis.

Benefits

  • 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
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