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Associate Director, Lab Operations-Pharma (GMP)

Pace Analytical Services

  • Oakdale, Minnesota
  • 30 days ago

    Highlights

    The position oversees key operational functions including equipment lifecycle management, facilities, supply chain and vendor coordination, sample management, stability program oversight, EH&S compliance, training/onboarding and the administrative support staff. The Associate Director of Laboratory Operations leads day to day cGMP lab operations, ensuring teams are staffed, trained, and aligned to meet quality and timeline expectations.

    Numbers & Facts

    LocationOakdale, Minnesota
    IndustryOther/Not Classified
    Company Size2,500 to 4,999 employees
    Year Founded1978
    Websitehttps://www.pacelabs.com/

    Description

    Shift:

    Monday through Friday, 8:00 AM - 5:00 PM

    Are you ready to work making the world a safer, healthier place? Join our mission to continuously move science forward; to innovate and advance all aspects of our business to improve the health and safety of our communities and lives.

    Associate Director, Laboratory Operations (GMP) – Oakdale, MN

    Compensation: $115,000 - $130,000 per year 

    The salary for this position reflects a variety of factors. Compensation will be determined based on the candidate’s geographic location, relevant experience, education, skills, and alignment with internal equity. Market conditions, budgetary considerations, and organizational compensation guidelines may also influence the final offer.

    Position Summary
    The Associate Director of Laboratory Operations leads day to day cGMP lab operations, ensuring teams are staffed, trained, and aligned to meet quality and timeline expectations. This role drives performance through clear communication, coaching, and accountability while fostering a collaborative, high trust culture.


    The position oversees key operational functions including equipment lifecycle management, facilities, supply chain and vendor coordination, sample management, stability program oversight, EH&S compliance, training/onboarding and the administrative support staff. The Associate Director also supports budgeting, cost control, and process optimization to ensure operational continuity, compliance, and scalable growth.

    Key Responsibilities
    •    Lead, develop, and coach staff; ensure clear expectations, strong communication, and effective team coordination.
    •    Oversee equipment lifecycle management, including calibration, preventive maintenance, and asset tracking.
    •    Maintain site facilities through environmental controls, space management, and building infrastructure. 
    •    Manage supply chain operations: inventory, procurement, vendor relationships, and service coordination.
    •    Oversee sample management and stability program operations, including sample chain of custody, scheduling, and compliance with protocols.
    •    Ensure EH&S compliance, hazardous waste management, and routine safety checks.
    •    Manage onboarding, training, and competency programs for laboratory personnel.
    •    Manage the administrative staff 
    •    Support financial oversight, including CAPEX/OPEX budgeting and process improvement initiatives.


    Qualifications
    •    Bachelor’s degree in Chemistry, Biochemistry, Biology/Microbiology, Pharmaceutical Sciences, Chemical Engineering, or related field; MS and/or Lean/Six Sigma preferred.
    •    7+ years in a GMP pharmaceutical/biopharmaceutical lab environment.
    •    5+ years of leadership experience in laboratory operations; CRO/CDMO experience preferred.

    Competencies
    •    Strong knowledge of equipment management, sample management, stability programs, inventory control, facilities, EH&S requirements, and training systems.
    •    Experience with budgeting, operational planning, and continuous improvement.
    •    Ability to make sound operational decisions, ensure compliance, and drive team performance.

    Why Join
    •    Lead operations in a GMP regulated pharmaceutical testing environment.
    •    High impact role supporting drug development and commercialization.
    •    Collaborative culture with opportunities for growth and advancement.

    Find Your Place at Pace - We need you - your curiosity, your talents, and your drive - to help us advance this important work.

    Benefits
    When you join Pace®, you commit to work that makes a positive impact on our communities and our world. We commit to supporting you with benefits and perks that make a positive impact on your life. Full-time roles are eligible for our comprehensive benefits program which includes competitive salaries, medical, dental vision, 401K retirement savings plan (100% vested immediately in the employer match), life, disability and voluntary benefits, paid time off for holiday, sick and vacation days, HSA, wellness program, flexible spending accounts, tuition reimbursement, Employee Assistance program, parental leave, optional legal coverage and ID theft.

    Equal Opportunity Employer

    Pace® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, creed, color, religion, genetics, protected veteran status, national origin, sex, age, disability, marital status, sexual orientation, gender identity or expression, citizenship, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

    About Company

    Three divisions. Two countries. 1800 employees. Twenty-eight environmental labs. Two Life Sciences labs. Twenty-four service centers. Hundreds of certifications. 38 years of industry experience. Financial stability. Dynamic thought leadership and strategic management planning with one shared vision: work together to protect our environment and improve our health.

    Pace began on a much smaller scale in 1978, serving Minneapolis and the surrounding areas with founder and CEO Steve Vanderboom at the helm. A commitment to safety and high ethical standards, respect for both clients and employees, and a drive for excellence inspired us as we expanded - and these values are at the core of everything we do today. Still under Vanderboom's directorship, we are proud to be industry leaders, offering an unparalleled range of services delivered by the most experienced scientific professionals. No matter the scope of work or special requirements, we have the people, knowledge and technology to tackle them. Partnering with us, clients are guaranteed to experience the Pace Analytical difference.

    Pace Analytical Services, LLC. provides analytical services including environmental testing and sampling. Laboratories utilize EPA, ASTM Standard Methods, NIOSH and other accepted test procedures and methods in accordance with both federal and state regulations. Pace also provides specialty analytical support for air toxics, aquatic toxicity, bioassay, biota, dioxin/furans, low-level mercury, radiochemistry, vapor intrusion, environmental forensics, industrial hygiene, etc.

    Pace Analytical Life Sciences provides analytical testing services to the pharmaceutical/medical device industries. Services include chemical and microbiology, method development/validation, physical testing, raw material testing, stability testing and storage, and product release testing. Pace operates two FDA-registered, DEA-registered (Class I - V), cGMP-compliant facilities: one located in Oakdale, MN and the other located in San German, PR. The Oakdale, MN facility is ISO/IEC 17025:2005 accredited.

    Pace Analytical Lab Ops Division provides professional scientific staffing - to accommodate full outsourcing or augmentation of staff at a client's on-site location - to various industries as well as research and development organizations. The ISO 9001:2008 certified Lab Ops Division also provides instrumentation sales, repair and qualification services, product and materials testing support and regulatory compliance services.

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