Experienced Specialist QA

• Job title Experienced Specialist QA
• Function Quality
• Sub function Quality Assurance
• Category Experienced Analyst, Quality Assurance (P5)
• Location Sassenheim / Netherlands
• Date posted Sep 03 2026
• Requisition number R-096890
• Work pattern Hybrid Work

Description

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

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Job Description:

We are searching for the best talent for an Experienced Specialist, QA.

Purpose

We are looking for an Experienced Specialist, QA to join our Advanced Therapies (AT) Quality Assurance team in Leiden/Sassenheim, The Netherlands.

Are you interested in helping ensure the delivery of advanced therapies by strengthening GMP compliance, quality oversight, and inspection readiness in a highly regulated manufacturing environment?

In this role, you will provide Quality Assurance support for commercial and clinical manufacturing activities at the Advanced Therapies manufacturing site. Acting as a key quality partner for production facilities and Quality Control laboratories, you will provide oversight for the manufacture of drug substances and starting materials while helping ensure compliance with GMP requirements, company standards, and regulatory expectations.

Working closely with Operations, Quality Control, Warehouse, Manufacturing Asset Management (MAM), Manufacturing Science & Technology (MSAT), and other business partners, you will provide independent review and pragmatic quality guidance to support compliant decision-making, continuous improvement, and reliable product supply.

We look forward to hearing from you!

You will be responsible for

In this role, you will provide Quality Assurance oversight for Advanced Therapies manufacturing operations and help ensure products, processes, equipment, and systems operate in accordance with GMP requirements and regulatory expectations.

You will assess investigations, participate in risk management activities, provide quality guidance on manufacturing and support processes, and help maintain a state of inspection readiness across the site. The role includes partnering closely with cross-functional teams to support compliant operations, identify potential risks, and contribute to the continuous strengthening of quality systems and manufacturing processes.

You will also support key GMP activities including qualifications, validations, technology transfers, analytical transfers, aseptic processing, Annex 1 adherence, facility and equipment projects, and change management programs.

Key responsibilities include:

• Providing oversight for Advanced Therapies production activities at the site
• Providing quality guidance for GMP processes including Change Control, Document Control, GMP Training, and inspection readiness
• Providing quality guidance for facility, utility, and equipment design activities, including new facility projects
• Supporting technology transfers, analytical transfers, qualification programs, and validation activities
• Supporting aseptic processing operations and Annex 1 compliance requirements
• Reviewing and assessing Quality Investigations and monitoring the quality of root cause investigations
• Assessing non-conformances for potential impact on product quality or compliance status and supporting product disposition decisions
• Reviewing and approving appropriate Corrective and Preventive Actions (CAPAs)
• Escalating significant quality, compliance, or GMP issues and supporting local and global escalation activities where patient supply may be impacted
• Participating in hazard assessments and Quality Risk Management activities
• Coordinating, reviewing, and delivering GMP training activities related to investigations, qualifications, and non-conformance management
• Supporting quality culture initiatives across manufacturing and laboratory operations, including GEMBA activities
• Reviewing and approving document changes and change controls
• Leading or participating in local and global quality and capacity projects
• Enhancing process monitoring and quality monitoring approaches
• Acting as a Quality SME during inspection preparation activities and supporting FDA, EMA, and other regulatory inspections
• Supporting Annual Product Reviews (APR), inspection readiness reports, and related compliance activities
• Partnering with site colleagues to ensure changes to manufacturing processes, equipment, facilities, and systems are implemented in a controlled and compliant manner
• Participating in a rotating 24/7 on-call schedule as the QA representative for quality-related issues

As an Experienced Specialist, QA, you will also represent Quality in Advanced Therapies projects, support identification and mitigation of compliance risks, review and approve study protocols and reports, and participate in Quality Risk Management and root cause investigation sessions.

Qualifications / Requirements

We are looking for someone who combines strong quality expertise, sound judgment, and the ability to work effectively across a complex and highly regulated environment.

Education

• Bachelor’s degree or higher in Biochemistry, Biology, Pharmaceutical Sciences, or another relevant scientific field

Experience

• Minimum 6 years of experience in a GMP-regulated environment with a Bachelor's degree, or 4 years of experience with a Master's degree
• Experience within Quality Assurance, Quality Control, manufacturing operations, or related pharmaceutical or biotechnology environments
• Experience with methodologies such as Process Excellence, Co-Think, Kepner-Tregoe, or similar approaches is preferred
• Proven knowledge of the biotechnology and/or pharmaceutical industry

Technical Knowledge

• Strong understanding of global regulatory requirements, including cGMP, ICH, FDA, and EMA expectations
• Knowledge of Quality Systems including change control, deviation management, CAPA, validation, and risk management
• Understanding of manufacturing processes, laboratory operations, facilities, utilities, and technical automation systems
• Experience supporting investigations, troubleshooting activities, and development of compliant solutions to quality issues

Skills

• Ability to work independently and make risk-based decisions in a complex environment
• Strong analytical, problem-solving, and decision-making skills
• Ability to balance business needs, regulatory requirements, quality expectations, and patient impact
• Strong collaboration, influencing, and negotiation skills
• Ability to engage partners and navigate differing viewpoints effectively
• Strong communication skills, both written and verbal
• Fluent in English
• Demonstrates an understanding of AI concepts and frameworks, including awareness of responsible and ethical AI practices, and uses effective prompting techniques to support efficiency and productivity

What we offer

We offer a collaborative environment where learning, innovation, and professional development are encouraged. This role provides opportunities to contribute to Advanced Therapies manufacturing, collaborate across multiple functions, and support products that can make a meaningful difference for patients.

Additional role information

• Location: Leiden/Sassenheim, The Netherlands
• Participation in a rotating 24/7 on-call schedule is required
• Close collaboration with Operations, QC, Warehouse, MAM, MSAT, and Quality functions is expected
• Support for regulatory inspections and audits may be required as part of normal responsibilities

Our commitment to inclusion

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation is powered by bringing together people with different backgrounds, experiences, and perspectives.

We are proud to be an equal opportunity employer and welcome applications from qualified candidates of all backgrounds.

If you require a reasonable accommodation during the application, interview, or onboarding process, support is available. Please let us know how we can help.

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The anticipated base pay range for this position is:

Benefits:

In addition to base pay, we offer the following benefits*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.

*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.