Mgr 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:

Job Sub Function:

• On time delivery of release and stability sample testing results of the AVA/myco team
• Ensuring tasks are performed in a manner consistent with the safety policies, quality systems and cGMP requirements.
• Setting goals and objectives for the department and define Key Performance Indicators that are indicative for excellent performance.
• Ensuring that data is generated, trended, and maintained according to current regulatory requirements, including data integrity.
• Lead Supervisors and specialists and provide operational and strategic guidance.
• Contributes to global strategies related to QC laboratories which align with compliance and business objects as well as the overall J&J vision.
• Act as a Servant Leader to coach and develop team members, driving business performance by successful talent development.
• Manage departmental budget, project budgets and resources; prepares staffing plans. Align roles and responsibilities of department to meet business needs.
• Collaborate with Quality Assurance, Stability Owners, Development, Manufacturing, Technical Operations, Engineering and Maintenance and other local and global stakeholders to support business needs.
• Responsible for timely completion of laboratory investigation of OOS/ invalid assays, CAPAs and change controls
• Acting as change agent and build and maintain team capabilities to meet current and future needs.
• Achieving innovation and excellence in business processes.
• Sponsoring projects at site/department/quality level.
• Lead internal and Health Authority audits inspections and related investigations.

We would love to hear from YOU, if you have the following essential requirements:

• Masters / PhD or equivalent degree required in virology, microbiology, life sciences, biotechnology or equivalent.
• 5 - 10 years of experience in:
  • Expertise in viral and microbiological method development and validation,
  • Leading a med (> 20) sized specialized group (5-10 direct reports),
  • Quality Control in pharmaceutical industry with marketed products.
• Profound knowledge of pharmaceutical regulations/cGMP principles (FDA, EU, etc.) in general, and viral and microbiological topics specifically
• Organizational planning and problem-solving experience.
• Strong leadership & development qualities.
• Experience with principles of Process Excellence
• Good presentation skill
• Personal and social skills: informed decision making, digitalization and digitization, analytical thinking, strong quality awareness and flexible.
• Prior experience with Next Gen Sequencing and rapid microbiology testing methods is preferred.

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.

Janssen Biologics B.V . is one of the Janssen Pharmaceutical Companies of Johnson & Johnson that has been for more than 25 years a leader in the field of biomedicines. We continue to seek innovative ways to treat cancer, infectious diseases, cardiovascular and metabolic diseases, and immune-mediated inflammatory disorders, such as rheumatoid arthritis and psoriasis. Janssen Biologics in Leiden is manufacturing key Biotherapeutic products, like Remicade, Stelara, and Simponi, and is also launching new products.    

The QC laboratories department in Leiden is part of the supply chain (JSC) organization and is responsible for testing of raw materials, release and stability of Active Pharmaceutical Ingredients and Drug products manufactured at Leiden, other internal J&J sites and at external third parties. Leiden JSC QC is uniquely positioned as the worldwide HUB for Stability and for AVA and Mycoplasma testing. The AVA/Mycoplasma department consists of approximately 25 people. 

You'll be part of the QC Management team working on successes for today and the future. You will lead with credo principles at hand ensuring diversity and inclusion, shaping, simplifying, and innovating the testing methods in close collaboration with Analytical Development (AD) colleagues. Your team will be onboarding several New Product Introduction (NPI’s) and pioneering automated testing solutions.

Janssen Biologics is currently recruiting a Manager AVA/Mycoplasma Quality Control within our Quality department. The successful candidate needs to have a background in release of products that are on the market, people and team management skills, viral and bacterial knowledge, and a profound knowledge of pharmaceutical GMP principles. You will be reporting to the QC Director Biotherapeutics.