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Biotechnology Research

Senior Director, Quality Control

Waltham, MAOnsiteFull TimeDirector$240,000–$330,000 /yrPosted 4 days agoVisa sponsorship available

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Required skills

  • Quality Control
  • cGMP
  • analytical testing
  • microbiology
  • environmental monitoring
  • raw material disposition
  • stability
  • sample management
  • analytical lifecycle
  • laboratory systems

Nice to have

  • Lean Six Sigma
  • Lean Lab
  • Digital Lab
  • multi-program
  • CDMO

Role summary

ElevateBio is seeking a Senior Director, Quality Control to lead all QC operations at their Waltham site. This role is responsible for the safe, compliant, and predictable execution of QC activities, including analytical testing, microbiology, raw material disposition, and stability support. The Senior Director will establish the QC operating strategy, capacity, and resource plan, focusing on laboratory excellence, data integrity, and meeting manufacturing and client commitments. Key responsibilities include leading the QC organization, developing leaders, ensuring reliable seven-day operations, managing quality systems, and partnering with various site functions. A Bachelor's degree in a related scientific discipline and at least 15 years of progressive GMP QC experience with substantial leadership are required.

ElevateBio is a technology-driven company powering the industry forward by helping partners realize the potential of their therapies from design to commercialization. We have integrated a differentiated set of technologies, end-to-end services, and industry-leading manufacturing expertise to develop advanced therapies faster and more efficiently.

The Role

The Senior Director, Quality Control leads all Quality Control operations at ElevateBio’s Waltham site, including QC Analytical Technologies (QCAT), QC Analytics, Testing Core, QC Microbiology, QC Raw Materials, and QC Logistics. The role is accountable for safe, compliant, inspection-ready, and predictable execution across a seven-day operating model, including product release and in-process testing, STAT support to Manufacturing, environmental and microbiological testing, raw material disposition, stability support, sample management, and analytical lifecycle enablement. The Senior Director establishes the QC operating strategy, capacity and resource plan, performance system, and leadership model required to meet manufacturing, client, and business commitments while sustaining laboratory excellence and data integrity.

Here’s What You’ll Do

QC Strategy and Leadership

  • Lead the integrated QC organization, operating model, objectives, decision rights, talent strategy, and capability roadmap.
  • Develop QC management and technical leaders while aligning headcount, seven-day coverage, facilities, equipment, systems, operating expense, and capital with demand.

    • Predictable QC Operations and Laboratory Excellence

  • Own safe, compliant, and predictable execution of product release and in-process testing, environmental and microbiological monitoring, raw material disposition, stability, sample management, and client commitments.
  • Ensure reliable seven-day operations through capacity planning, schedule control, tiered daily management, performance review, and timely escalation and recovery.
  • Partner with Manufacturing to align readiness, prioritization, and rapid execution of STAT in-process samples within required decision windows.
  • Drive laboratory excellence through standard work, right-first-time execution, efficient review and reporting, backlog control, structured problem solving, and continuous improvement.

    • Analytical Technologies and Lifecycle Enablement

  • Provide leadership oversight for QCAT, including client technical interface, technology and method transfer, qualification and validation, method lifecycle management, equipment qualification, controls and critical reagents, and Digital QC.
  • Ensure effective utilization of shared QC Resources, handoffs between QCAT and operational laboratories through clear readiness criteria, accountability, sustainable capacity, and post-implementation monitoring.

    • Quality, Compliance, and Partnership

  • Ensure QC activities meet cGMP, approved procedures, specifications, quality agreements, data-integrity expectations, and regulatory commitments.
  • Provide senior oversight of laboratory events, atypical or out-of-specification results, deviations, investigations, CAPAs, changes, risks, and inspection readiness.
  • Represent QC in client governance, audits, regulatory inspections, release-readiness reviews, and escalations; communicate performance, constraints, risks, and recovery plans clearly.
  • Serve as the senior QC partner to Manufacturing, Quality Assurance, Facilities & Engineering, MSAT, Regulatory Affairs, Supply Chain, Digital, Process and Analytical Development, and site leadership.

    • Requirements

  • Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry, Pharmaceutical Sciences, Engineering, or a related scientific discipline; an advanced degree is preferred.
  • At least 15 years of progressive experience in GMP Quality Control or analytical laboratory operations, including substantial leadership of managers and multi-functional teams.
  • Demonstrated leadership of a broad QC organization supporting complex biopharmaceutical, biologics, cell therapy, gene therapy, or other regulated manufacturing operations.
  • Strong knowledge of GMP laboratory controls, analytical testing, microbiology, environmental monitoring, raw materials, stability, sample management, analytical lifecycle activities, laboratory systems, data integrity, contract laboratory oversight, and quality systems.
  • Demonstrated success improving schedule reliability, turnaround time, right-first-time performance, capacity utilization, investigation management, and inspection readiness.
  • Experience leading seven-day operations and partnering with Manufacturing on time-critical in-process testing and operational decision windows.
  • Experience supporting client audits, regulatory inspections, client governance, and significant quality or delivery escalations.
  • Strong strategic planning, financial stewardship, organizational design, talent development, communication, decision-making, and stakeholder-management capabilities.
  • Lean Six Sigma certification or demonstrated experience applying Lean Six Sigma, Lean Lab, and Digital Lab practices to improve laboratory flow, capacity, data visibility, and operational performance is preferred.
  • Experience in a multi-program or CDMO environment is preferred.

    • Physical and Environment Requirements:

  • Ability to stand, walk, bend and stretch for extended period of time
  • Ability to lift 15-20 lbs
  • Ability to push, pull, bend, kneel, twist and climb step ladders while wearing PPE.
  • Ability to perform routine repetitive motions with use of arms, wrists and hands

    • The budgeted range for this position is $240,000 - $330,000. This range is a good faith estimate of the expected salary range for this position, based on a wide range of factors including qualifications, experience and training, operational and business needs and other considerations permitted by law.

    ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

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