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QC Manager, Lab Support

External
Biogen logoBiogen · Research Triangle Park, NC
Full-timeOn-siteToday
ComplianceExcelLeadership
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Responsibilities

  • Lead and develop the QC Lab Support team, overseeing hiring, training, performance, and daily operations
  • Manage core lab support activities including sample management, stability pulls, equipment cleaning, autoclave/glass wash operations, and lab supply coordination
  • Ensure equipment readiness, calibration, lifecycle management, and support OOT investigations
  • Maintain GMP compliance, audit readiness, and data integrity across all lab support processes
  • Drive deviation investigations, CAPAs, and continuous improvement initiatives
  • Optimize and standardize lab support processes, including procedures and training programs
  • Partner cross-functionally with QC and manufacturing to align support with testing and production needs
  • Manage resources, staffing, and budget to ensure efficient, cost-effective operations

Requirements

  • You are a strategic, results-driven leader with strong expertise in GMP quality control operations. You bring a passion for developing teams, driving continuous improvement, and ensuring high-quality, inspection-ready laboratory environments.
  • Required skills
  • Bachelor's degree in Biological Sciences or related field
  • Minimum 5 years of QC experience managing samples and stability pulls in a GMP-regulated biologics or pharmaceutical environment
  • At minimum 2 years of supervisory or team leadership experience
  • Experience with autoclave and glasswasher operations
  • Experience supporting equipment/instrument lifecycle management and OOT investigations
  • Experience supporting regulatory inspections and maintaining audit readiness
  • Proficiency with systems such as LIMS, Smart QC, Excel, and PowerPoint
  • Preferred skills
  • Prior experience leading sample management or lab support teams
  • Project management experience
  • Job Level: Management
  • Additional Information
  • The base compensation range for this role is: $111,000.00-$149,000.00
  • Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
  • Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
  • In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being ; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation
  • Why Biogen?
  • All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, nati

Benefits

Dental insuranceVision insurance401(k)Paid time offEquity / stock optionsPerformance bonusParental leave

Additional Information

About this role We are seeking an experienced and motivated QC Manager, Lab Support to lead the lab support function within our biologics drug substance manufacturing facility. This role is critical to ensuring seamless QC laboratory operations, overseeing sample management, stability programs, and core lab support activities that enable compliant, inspection-ready performance. As a key leader, you will drive operational excellence, support both clinical and commercial manufacturing, and ensure alignment across QC and manufacturing teams. This is an onsite role (Monday-Friday) with occasional off-shift and weekend support as needed.


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