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Group Leader / Supervisor, Extractable & Leachable (E&L)

Pace Analytical Services

  • Morrisville, North Carolina
  • 8 days ago

    Highlights

    The successful candidate will build a high-performing team that consistently delivers quality results, meets client expectations, maintains regulatory compliance, and supports the continued growth of the E&L business within a dynamic analytical development environment. This role is responsible for overseeing daily laboratory operations, managing and developing scientific staff, ensuring high-quality technical deliverables, and supporting client projects from initiation through completion.

    Numbers & Facts

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

    Description

    Shift:

    M-F 8:00am-4:30pm

    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.

    Group Leader / Supervisor, Extractable & Leachable (E&L)

    Analytical Development | GMP CRO Environment

    Location: On-site
    Schedule: Full-Time M- F Dayshift

    Position Summary

    We are seeking an experienced Group Leader/Supervisor to lead our Extractables & Leachables (E&L) team within a fast-paced, GMP-regulated Contract Research Organization (CRO). This role is responsible for overseeing daily laboratory operations, managing and developing scientific staff, ensuring high-quality technical deliverables, and supporting client projects from initiation through completion. The successful candidate will combine strong technical expertise with effective leadership to drive operational excellence, regulatory compliance, and customer satisfaction.

    Key Responsibilities

    • Lead, coach, and develop a team of scientists and analysts performing E&L studies.
    • Manage project timelines, laboratory resources, and workload prioritization to meet client commitments.
    • Serve as a technical and operational resource for E&L projects and client interactions.
    • Review and approve protocols, reports, data packages, investigations, and laboratory documentation.
    • Ensure compliance with GMP regulations, company quality systems, and data integrity requirements.
    • Partner with Quality Assurance and cross-functional teams to maintain inspection readiness.
    • Drive continuous improvement initiatives to enhance laboratory efficiency, quality, and productivity.
    • Support business growth through technical expertise, client engagement, and team development.

    Qualifications

    • Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline; advanced degree preferred.
    • Minimum 5 years of experience in a pharmaceutical, biopharmaceutical, CRO, or GMP-regulated analytical laboratory.
    • Previous leadership or supervisory experience preferred.
    • Strong organizational, communication, problem-solving, and people leadership skills.
    • Ability to manage multiple priorities in a fast-paced, client-focused environment.

    Preferred Technical Skills

    • Experience with Extractables & Leachables (E&L) study design, execution, and data interpretation.
    • Proficiency with LC-MS and GC-MS, analytical platforms.
    • Knowledge of GMP regulations, data integrity principles, and pharmaceutical analytical development.
    • Experience with analytical method development, validation, and troubleshooting.
    • Familiarity with USP, PQRI, and applicable E&L regulatory guidance.
    • Ability to review complex technical data, mentor scientists, and support client-facing projects.

    What Success Looks Like

    The successful candidate will build a high-performing team that consistently delivers quality results, meets client expectations, maintains regulatory compliance, and supports the continued growth of the E&L business within a dynamic analytical development environment.

    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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