Johnson & Johnson Hiring: Associate Director Quality Control – Pennsylvania

Johnson & Johnson Hiring: Associate Director Quality Control – Pennsylvania

Johnson & Johnson (J&J) is hiring an Associate Director Quality Control for its Innovative Medicine organization in Pennsylvania. This is a senior Quality Control leadership opportunity based primarily in Malvern, Pennsylvania, with Spring House, Pennsylvania as a secondary location.

The Associate Director Quality Control will provide strategic and operational leadership for QC laboratory activities supporting biotherapeutic and advanced therapy programs. The role is responsible for maintaining compliant, reliable and efficient laboratory operations while supporting clinical and commercial products.

Job Details

Job Information	Details
Company	Johnson & Johnson
Job Title	Associate Director, Quality Control
Job Function	Quality
Sub Function	Quality Control
Job Category	People Leader
Location	Malvern / Spring House, Pennsylvania, USA
Work Pattern	Fully Onsite
Department	Quality Control
Reports To	Site Quality Head
Requisition Number	R-100521
Posted Date	October 6, 2026
Expected Closing Date	October 27, 2026

The official J&J listing identifies Malvern as the primary location and Spring House as the secondary location.

About the Role

The Associate Director, Quality Control is a strategic multi-site Quality Control leader responsible for the compliant and efficient operation of QC testing laboratories.

The successful candidate will provide leadership across laboratory operations, testing strategy, analytical method lifecycle activities, data review, investigations, capacity planning, resources and inspection readiness.

The Associate Director Quality Control will also work closely with Quality Assurance, Manufacturing, Analytical Development, Technical Operations, Supply Chain, Regulatory and external laboratory partners.

Key Responsibilities

1. Quality Control Leadership

• Lead QC laboratory operations across the Malvern and Spring House sites.
• Establish an integrated QC operating model across multiple locations.
• Ensure reliable, timely and high-quality laboratory testing.
• Provide strategic direction for QC activities supporting clinical and commercial products.
• Maintain strong focus on product quality, patient safety and supply continuity.

2. People Leadership

• Lead and develop a large multi-site QC organization.
• Support managers, supervisors, analysts and laboratory support personnel.
• Build technical capabilities and leadership talent within the QC organization.
• Establish clear objectives, performance expectations and development plans.
• Promote a culture of quality, compliance, collaboration and continuous improvement.

3. Laboratory Operations

The Associate Director Quality Control will oversee laboratory activities including:

• Routine QC testing.
• Laboratory operations and capacity planning.
• Analytical testing strategy.
• Data review and laboratory investigations.
• Method lifecycle management.
• Laboratory performance and resource management.
• Coordination with internal and external testing laboratories.

4. GMP and Compliance

• Ensure QC laboratories operate in accordance with applicable GMP requirements.
• Maintain laboratory compliance and data integrity.
• Support regulatory and health-authority inspection readiness.
• Ensure appropriate investigation and resolution of laboratory issues.
• Partner with Quality Assurance to maintain a robust quality system.

5. Cross-Functional Collaboration

The Associate Director Quality Control will collaborate with:

• Quality Assurance
• Manufacturing
• Analytical Development
• Technical Operations
• Supply Chain
• Regulatory Affairs
• External laboratories
• Site Quality leadership

This cross-functional leadership is essential to support product quality and continuity of supply.

Candidate Profile

Candidates applying for the Associate Director Quality Control position should bring strong leadership experience in pharmaceutical, biopharmaceutical or related quality-control laboratory environments.

The ideal candidate should demonstrate:

• Strong Quality Control leadership experience.
• Experience managing laboratory organizations and technical teams.
• Knowledge of GMP and pharmaceutical quality requirements.
• Experience with laboratory investigations and data review.
• Understanding of analytical testing and method lifecycle activities.
• Strong inspection and regulatory readiness experience.
• Excellent people-management and communication skills.
• Ability to work effectively across Quality, Manufacturing, Regulatory and Technical Operations functions.

Why This Opportunity Is Important

The Associate Director Quality Control role provides an opportunity to lead a significant QC organization within Johnson & Johnson Innovative Medicine.

The position combines Quality Control leadership, GMP compliance, laboratory operations, people development, technical strategy and inspection readiness in support of innovative therapies.

How to Apply

Interested candidates should review the official Johnson & Johnson job posting and submit their application through the company’s careers portal.

Company: Johnson & Johnson
Position: Associate Director, Quality Control
Location: Malvern / Spring House, Pennsylvania
Requisition: R-100521
Work Pattern: Fully Onsite
Application Deadline: October 27, 2026, subject to extension.

Official Application: Johnson & Johnson Careers – Associate Director, Quality Control

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About Johnson & Johnson

Johnson & Johnson is a global healthcare company operating across Innovative Medicine and MedTech. Its Innovative Medicine organization focuses on developing treatments and advancing healthcare innovation.

For this opportunity, the company is seeking an experienced quality leader capable of supporting high-quality laboratory operations and developing a strong multi-site QC organization.

Frequently Asked Questions

1. What is the job title at Johnson & Johnson?

The position is Associate Director, Quality Control. The Associate Director Quality Control role is part of the Quality function and Quality Control sub-function.

2. Where is the Associate Director Quality Control job located?

The position is based in Malvern, Pennsylvania, with Spring House, Pennsylvania listed as a secondary location.

3. Is the Associate Director Quality Control position onsite?

Yes. Johnson & Johnson lists the work pattern as Fully Onsite.

4. What is the requisition number?

The J&J requisition number is R-100521.

5. What department does the position belong to?

The position belongs to the Quality Control department and reports to the Site Quality Head.

6. What type of leadership is expected?

The Associate Director Quality Control is expected to provide multi-site people leadership, strategic QC direction and operational oversight across laboratory activities.

7. What areas will the Associate Director Quality Control oversee?

The role includes oversight of QC testing strategy, laboratory operations, analytical method lifecycle activities, data review, investigations, capacity, resources and inspection readiness.

8. When was this J&J job posted?

The current listing was posted on October 6, 2026.

9. When is the expected closing date?

The anticipated closing date is October 27, 2026, although Johnson & Johnson states that the posting may be extended.

10. Where can candidates apply?

Candidates can apply through the official Johnson & Johnson Careers website using requisition R-100521.

Important: Job details, availability and closing dates can change. Candidates should verify the current information on the official J&J careers page before applying.