Senior Director, Head of Quality Control, T1D Mfg Ops

Job Description

Vertex is seeking a Senior Director Head of Quality Control to lead QC strategy and external laboratory oversight for our Type 1 Diabetes Cell Therapy external manufacturing network. This leader will be responsible for building and scaling a robust QC partnership model supporting complex stem cell-derived therapies across CDMOs external testing laboratories and commercial/clinical supply operations.

This role is focused on QC network oversight including outsourced testing governance method transfer into external laboratories QC scheduling and budgets sample management strategy assay readiness analytical performance monitoring and QC compliance across the external network.

What Youll Do

• Lead Quality Control strategy and external QC oversight for stem cell therapy manufacturing and testing partners
• Oversee outsourced release in-process raw material stability microbiology and environmental monitoring-related testing activities as applicable
• Ensure timely compliant and reliable execution of critical assays supporting product quality and lot release across external laboratories
• Lead method transfer assay implementation lab readiness and performance governance for CDMOs and contract test labs
• Oversee QC investigations assay performance trends data review expectations and testing-related escalation management across the network
• Partner closely with QA Manufacturing MSAT Analytical Development Supply Chain and Regulatory teams to ensure continuity of supply and analytical readiness

What Were Looking For

• Deep experience in QC for cell therapy or other advanced therapy products including outsourced testing or CDMO oversight
• Strong knowledge of GMP laboratory operations method transfer assay lifecycle management and lab investigations in an external network model
• Experience overseeing cell-based molecular microbiological and/or potency-related methods across internal and external labs
• Strong people leadership and cross-functional collaboration skills
• Advanced degree in a relevant scientific discipline; significant industry leadership experience required

Minimum Qualifications

• Advanced degree in Biology Cell Biology Molecular Biology Biochemistry Analytical Chemistry Bioengineering Pharmaceutical Sciences or a related field.
• Typically 15 years of relevant industry experience in biotechnology biopharmaceutical stem cell therapy cell therapy or other advanced therapy environments.
• 8 years of progressive people leadership experience including leadership of managers and cross-functional teams.
• Demonstrated success leading GMP Quality Control organizations in a regulated environment.
• Deep knowledge of QC operations supporting complex biologic cell therapy or stem cell-derived products.
• Strong experience with method transfer method qualification/validation assay lifecycle management and laboratory investigations.
• Strong understanding of cGMP data integrity regulatory expectations and inspection readiness for QC laboratories.
• Proven ability to influence across Manufacturing Quality Assurance Analytical Development Regulatory and technical operations functions.

Preferred Qualifications

• PhD in a relevant scientific discipline.
• Experience building or scaling QC organizations for late-stage clinical or commercial manufacturing.
• Experience with phase-appropriate assay qualification and validation strategies for advanced therapy products.
• Experience with external testing laboratories CDMOs or distributed manufacturing/testing networks.
• Familiarity with LIMS electronic laboratory systems digital data review tools and QC laboratory automation.
• Experience supporting regulatory submissions responses to health authority questions and inspection management.

Leadership Profile

The ideal candidate will bring:

• strong scientific and operational depth in QC for advanced therapies
• the ability to build and scale high-performing laboratory organizations
• sound judgment in balancing compliance speed and scientific rigor
• strong leadership in highly regulated and rapidly evolving environments
• the ability to create clarity at functional interfaces especially across QC QA Analytical Development Manufacturing and MSAT
• a track record of developing talent and strengthening organizational capability
• a strong commitment to quality compliance and patient impact

At Vertex we embrace continuous learning and encourage employees to stay informed on advances in AI technology automation and industry trends. We seek talent who bring an external perspective demonstrate curiosity and sound judgment and thoughtfully adopt new capabilities that improve decision-making drive innovation increase efficiency and help deliver better outcomes for patients.

Pay Range:

Disclosure Statement:

Flex Designation:

Flex Eligibility Status:

In this Hybrid-Eligible role you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertexs Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Hybrid

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry ethnicity disability veteran status genetic information sexual orientation marital status or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager or contact Talent Acquisition at