Manager Quality Control

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.

Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

People Leader

All Job Posting Locations:

Geel, Antwerp, Belgium

Job Description:

Please note that a preferred candidate has been identified for this position. However, we welcome applications from qualified individuals and will consider all candidates in accordance with our recruitment process.

Within Johnson & Johnson (J&J) Innovative Medicine Supply Chain, we are recruiting a Quality Control (QC) NPI Manager (M/F/X) as member of our Quality team overseeing Synthetics Active Pharmaceutical Ingredients (API) and Drug Product (DP) Intermediates based in Geel, Belgium.

J&J Innovative Medicine Supply Chain Geel serves as Centre of Excellence for the development and manufacturing of Synthetics API and DP used in treatments that improve the health and lifestyle of people worldwide. The Supply Chain Quality (SCQ) team supports the Geel site in its mission as Launch & Grow site and is responsible for the quality oversight and final release of Synthetics API and DP guaranteeing reliable supplies in compliance with applicable regulations.

As QC NPI Manager, reporting to the Head QC Geel, you lead the Quality Control New Product Introduction (QC NPI) organization at the Geel site. You are responsible for a team of NPI analysts and analytical integrators supporting the transfer, optimization and co-validation of analytical methods for new products, while partnering closely with R&D and commercial Supply Chain to enable the successful commercialization of Synthetics APIs and Drug Product Intermediates.

In this role, you provide both people leadership and scientific leadership, guiding the team towards business objectives, fostering individual development, and continuously strengthening the capabilities and performance of the QC NPI organization. You act as a catalyst for innovation, collaboration and scientific excellence, ensuring the successful introduction of innovative medicines at the Geel site.

Job Description:

The QC NPI Lead, reporting to the Head QC Geel, acts as a people leader.

Key responsibilities include:

• Lead a team of analytical experts (NPI analysts and analytical integrators) by supporting, coaching and developing team members in reaching quality, business and personal objectives.

• Define and implement analytical strategies, laboratory standards and processes to support successful new product introductions.

• Champion analytical innovation in collaboration with R&D, influencing them to meet our operational requirements for best-in-class methods and technologies.

• Partner with Quality, Supply Chain and R&D to support NPI governance, risk-based decision-making and operational readiness.

• Represent QC in NPI reviews, scientific forums and stage-gate meetings, providing technical expertise and leadership.

• Establish partnership and engagement with QC Operations (IPC and release labs) to ensure alignment of planning, workflows, instrument utilization and material supply by clear and proactive communication.

• Ensure effective resource planning and the availability of materials, instruments and new technologies to meet business priorities.

• Ensure compliant execution of QC NPI activities, including GMP documentation, quality records, data integrity and regulatory requirements.

• Provide analytical expertise for investigations, root-cause analysis and CAPA development.

• Promote Environmental, Health, Safety and Sustainability (EHSS) excellence and ensure compliance with company standards.

• Remain current in knowledge and skills towards analytical technologies and industry trends.

• Ensure inspection readiness and act as spokesperson during audits and inspections.

Job Qualifications:

• Master's degree in Chemistry, Pharmaceutical Sciences, Engineering, or a related scientific field (PhD preferred).

• Minimum 6 years of experience in the pharmaceutical or biopharmaceutical industry within Quality, Manufacturing, Development, or a related function.

• Proven people leader with experience coaching and developing teams in R&D or Quality.

• In-depth knowledge of analytical techniques, laboratory operations, and GMP-regulated environments.

• Demonstrated ability to drive scientific innovation and translate complex concepts into practical business solutions.

• Strong stakeholder management, communication, and influencing skills across functions and organizational levels.

• Solid understanding of cGMP, ICH guidelines, risk management, and regulatory compliance.

• Strong analytical and problem-solving skills, with the ability to make sound risk-based decisions in a fast-paced environment.

• Ability to manage multiple priorities, work independently, and collaborate effectively with diverse stakeholders.

• Fluent in Dutch and English.

Our offer

An exciting position in an international and dynamic environment with continuous learning and growth opportunities. An attractive remuneration package with additional benefit packages (for example hospital insurance, and other health care incentives). An inclusive team environment where diversity, and different opinions are respected and valued, and the importance of a good work-life balance is recognized.

Diversity, Equity and Inclusion

Johnson & Johnson is an equal opportunity employer, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

#SCQuality

 

 

Required Skills:

 

 

Preferred Skills:

Benchmarking, Compliance Management, Developing Others, Human-Computer Relationships, Inclusive Leadership, Leadership, Operational Excellence, Performance Measurement, Product Testing, Quality Control (QC), Quality Control Testing, Quality Management Systems (QMS), Quality Standards, Quality Validation, Standard Operating Procedure (SOP), Tactical Planning, Team Management

  

 

The anticipated base pay range for this position is:

€79 800,00 - €137 770,00

 

 

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.