Director QC

EPM Scientific; Lenoir (NC); On-site; USD 150,000 - 210,000; Full time

Job summary

EPM Scientific, a growing pharmaceutical manufacturing organization in North Carolina, seeks a Director of Quality Control to lead QC operations across a GMP-regulated site. You will oversee analytical chemistry, microbiology, environmental monitoring, and stability programs while driving the next phase of site growth.

Ideal candidates will have a Bachelor's degree (advanced degree preferred) and significant QC leadership experience in GMP environments, with strong regulatory and

Qualifications

• Bachelor’s degree required; advanced degree preferred.
• Significant QC leadership experience in pharmaceutical/biotech GMP environments.
• Strong knowledge of analytical testing, microbiology, stability studies, and lab operations.
• Experience supporting FDA inspections and regulatory compliance.
• Proven ability to lead teams and influence cross-functional stakeholders.

Responsibilities

• Lead Quality Control operations in a GMP manufacturing environment.
• Provide leadership across analytical, microbiology, environmental monitoring, and stability functions.
• Partner closely with Quality Assurance, Manufacturing, Regulatory Affairs, and Technical Operations.
• Oversee laboratory compliance, investigations, CAPAs, and continuous improvement initiatives.
• Support regulatory inspections and interactions with health authorities.
• Develop and mentor a high-performing QC team.
• Drive laboratory efficiency, compliance, and operational excellence.

Skills

Quality Control leadership

Analytical testing knowledge

GMP manufacturing

Education

Bachelor's degree

Advanced degree preferred

Job description

A growing pharmaceutical manufacturing organization is seeking a Director of Quality Control to lead QC operations across a GMP-regulated manufacturing site.

This individual will provide leadership for laboratory operations and quality control strategy, overseeing analytical chemistry, microbiology, environmental monitoring, stability programs, and release testing activities while helping drive the next phase of site growth.

Key Responsibilities:

• Lead Quality Control operations in a GMP manufacturing environment
• Provide leadership across analytical, microbiology, environmental monitoring, and stability functions
• Partner closely with Quality Assurance, Manufacturing, Regulatory Affairs, and Technical Operations
• Oversee laboratory compliance, investigations, CAPAs, and continuous improvement initiatives
• Support regulatory inspections and interactions with health authorities
• Develop and mentor a high-performing QC team
• Drive laboratory efficiency, compliance, and operational excellence

Qualifications:

• Bachelor's degree required, advanced degree preferred
• Significant Quality Control leadership experience within pharmaceutical, biotechnology, or related GMP-regulated manufacturing environments
• Strong knowledge of analytical testing, microbiology, stability studies, and laboratory operations
• Experience supporting FDA inspections and regulatory compliance activities
• Proven ability to lead teams and influence cross-functional stakeholders

Why Consider This Opportunity?

• High-impact leadership role
• Visible position with executive-level interaction
• Opportunity to shape the future direction of the Quality Control organization
• Growing manufacturing environment with strong investment and long-term plans