Strategic Leader, GMP Lab Operations

Pace® Labs; Oakdale (MN); On-site; USD 115,000 - 130,000; Full time

Benefits offered by this job

Competitive benefits

401K with employer match

Paid time off

Parental leave

Job summary

Pace Labs in Oakdale, MN is seeking an Associate Director of Laboratory Operations (GMP) to provide strategic leadership in a cGMP pharmaceutical testing environment, ensuring compliant, efficient operations and readiness for audits.

You will oversee equipment lifecycle management, stability and sample programs, supply chain and procurement, site training, and facility infrastructure while driving KPI-based performance, continuous improvement, and staff development.

Qualifications

• Bachelor’s degree in Chemistry/Biochemistry/Biology, Pharmaceutical Sciences, Chemical Engineering or related field (MS preferred)
• 8+ years in a GMP pharmaceutical/biopharmaceutical lab environment
• 5+ years of leadership in laboratory operations, CRO/CDMO experience preferred

Responsibilities

• Oversee equipment lifecycle management, including CAPEX/OPEX planning and asset tracking
• Oversee sample management and stability program operations, ensuring chain of custody and protocol compliance
• Manage supply chain operations, including inventory, procurement, vendor relationships, and service contracts
• Lead onboarding, site-wide training, and competency programs for laboratory personnel
• Maintain site facilities through environmental controls, space management, and building infrastructure
• Drive operational excellence through KPI monitoring, capacity planning, and continuous improvement initiatives
• Lead, develop, and coach laboratory operations staff with accountability and collaboration

Skills

Leadership

GMP knowledge

Process optimization

Strategic planning

Education

Bachelor’s degree in Chemistry/Biochemistry/Biology

MS and Lean/Six Sigma preferred

Job description

Pace Labs in Oakdale, MN is seeking an Associate Director of Laboratory Operations (GMP) to provide strategic leadership in a cGMP pharmaceutical testing environment, ensuring compliant, efficient operations and readiness for audits.

You will oversee equipment lifecycle management, stability and sample programs, supply chain and procurement, site training, and facility infrastructure while driving KPI-based performance, continuous improvement, and staff development.