Sr Manager Quality Control

Johnson & Johnson • Malvern, PA

2d • Hybrid

About The Position

The Senior Manager, Quality Control (QC) is a strategic, multi-site people leader accountable for the compliant, reliable, and efficient operation of QC testing laboratories supporting biotherapeutic and advanced therapy programs at Malvern and Spring House. This position is a member of the Site Quality Leadership Team and reports directly to the Site Quality Head. The role provides end-to-end oversight of laboratory operations supporting clinical and commercial products, including testing strategy, method lifecycle, data review, investigations, capacity, resources, and inspection readiness. The Senior Manager leads an organization of 80+ full-time employees and contractors across both sites. This leader establishes an integrated operating model, develops leaders and technical talent, ensures timely delivery of high-quality test results, and partners with Manufacturing, Quality Assurance, Analytical Development, Technical Operations, Supply Chain, Regulatory, and external laboratories to protect product quality, patient safety, and supply continuity. The incumbent is expected to serve as a competent delegate for the Site Quality Head, as assigned.

Requirements

• Bachelor’s degree in biology, biochemistry, microbiology, chemistry, biotechnology, engineering, or a related scientific discipline required; advanced degree preferred.
• Minimum of 10 years of relevant, progressive experience in the pharmaceutical, biotechnology, or biopharmaceutical industry, with substantial experience in GMP Quality Control laboratories.
• Minimum of five years of direct people-management experience, with demonstrated success leading large, complex organizations through multiple layers of leadership; experience with organizations comparable to 80+ employees and contractors strongly preferred.
• Strong experience supporting biologics or biotherapeutics; direct experience with advanced therapies, particularly cell and gene therapy testing, is strongly preferred.
• Broad knowledge of analytical and microbiological laboratory operations, analytical method lifecycle activities, laboratory investigations, data review, statistical trending, electronic laboratory systems, sample management, and equipment lifecycle management.
• Strong working knowledge of applicable FDA, EMA, ICH, pharmacopeial, and global cGMP expectations for biologics and advanced therapy products.
• Proven success managing multi-site operations, operating and capital budgets, laboratory capacity, competing priorities, organizational change, and complex cross-functional initiatives.
• Excellent judgment, communication, influence, problem-solving, and stakeholder-management skills, with the ability to make timely, risk-based decisions in a complex regulated environment.

Nice To Haves

• Advanced degree preferred.
• Experience with organizations comparable to 80+ employees and contractors strongly preferred.
• Direct experience with advanced therapies, particularly cell and gene therapy testing, is strongly preferred.

Responsibilities

• Lead, develop, and retain a multi-site QC organization of 80+ full-time employees and contractors, including managers, supervisors, analysts, and support roles.
• Set the QC vision, organization design, operating model, goals, performance expectations, succession plans, and workforce strategy for Malvern and Spring House.
• Exercise leadership authority for talent acquisition, performance management, development, recognition, compensation recommendations, promotions, employee relations, organizational design, and appropriate corrective actions in partnership with Human Resources.
• Build a culture of quality, safety, accountability, inclusion, technical excellence, collaboration, and continuous improvement.
• Provide integrated oversight of QC testing laboratories supporting biotherapeutics and advanced therapies, including cell and gene therapy programs, across Malvern and Spring House.
• Ensure accurate and timely sampling, testing, review, approval, and reporting for raw and incoming materials, in-process samples, drug substance, drug product, release, stability, environmental and utility monitoring, validation studies, reagents, media, and buffers, as applicable.
• Oversee sample management, reference standards, critical reagents, laboratory inventory, and the qualification, calibration, maintenance, and lifecycle management of QC equipment.
• Oversee the lifecycle of diverse analytical platforms and assays, including identity, purity, potency, safety, microbiological, molecular, cell-based, and compendial methods, with appropriate controls for complex and time-sensitive advanced therapy products.
• Ensure effective execution of method development support, qualification, validation, transfer, and verification activities, together with QC support for Process Performance Qualification, Continued Process Verification, and product comparability.
• Maintain laboratory compliance with applicable cGMP requirements, global quality standards, approved procedures, data integrity principles, and health, safety, and environmental expectations.
• Ensure robust governance and timely closure of nonconformance investigations, invalid assays, out-of-specification and out-of-trend results, laboratory investigations, CAPAs, change controls, method transfers, qualifications, and validations.
• Maintain validated, reliable, and inspection-ready computerized laboratory systems, including eLIMS, Empower, and other systems used for sample, instrument, method, and data management.
• Provide accurate QC data and trend analyses for annual product reviews, quarterly management reviews, Continued Process Verification, investigations, regulatory submissions, and product quality complaint assessments.
• Establish and monitor leading and lagging metrics for testing delivery, right-first-time performance, backlog, cycle time, capacity, compliance, and reliability; lead recovery and risk-mitigation plans when performance is off target.
• Define and execute the multi-site QC strategy, including laboratory capacity, headcount and contractor planning, scheduling, asset and facility needs, digital laboratory systems, automation, operating budgets, and strategic capital projects.
• Partner with Manufacturing, Quality Assurance, Analytical Development, Technical Operations, Supply Chain, Regulatory, Procurement, and external testing laboratories to support technology transfers, product introductions, supplier material qualification, reduced-testing programs, comparability, investigations, release, and supply continuity.
• Make timely, risk-based decisions within delegated authority for staffing, laboratory priorities, resource allocation, budgets, external testing, quality events, and operational recovery; escalate significant quality, compliance, safety, or supply risks appropriately.
• Serve as the senior QC representative during health authority inspections, internal audits, governance forums, and escalations; maintain sustained inspection readiness and ensure commitments are completed effectively and on time.
• Model visible, inclusive, and accountable leadership across Malvern and Spring House.
• Ensure patient safety, product quality, compliance, and employee safety remain central to all decisions.
• Set clear priorities, remove barriers, and hold leaders and teams accountable for sustainable results.
• Develop successors, strengthen technical capability, and provide timely coaching and performance feedback.
• Champion science- and risk-based improvement, digital enablement, standardization, and collaboration while upholding J&J Credo values and respect for people.

Benefits

• Inclusive work environment where each person is considered as an individual.
• Respect for the diversity and dignity of employees and recognition of their merit.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager