Jobs in the Netherlands, in English.

Mgr Quality Control

Remote, Leiden·Full-time·Added 8 days ago

Still open when we checked on 8 Oct

Overview

Job details

  • €68,600 a year

    Gross, as stated in the ad.

  • Full-time

    Per the ad.

  • Fully remote

    Per the ad.

Skills

Requirements

Nice to have

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

Education & certifications

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.

Pay & benefits

What you'll get

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.

The role

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.

What you'll do

Quality

Quality Control

  • 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.

Job Category

People Leader

All Job Posting Locations

Leiden, South Holland, Netherlands

The anticipated base pay range for this position is

€68 600,00 - €119 600,00

Hiring process

2 steps3 interviews
  1. Apply

  2. Digital interview

    Video call · 30–60 min

    Either pre-recorded answers to sent questions (about 10 minutes, you can re-record twice) or a live video interview of 30 minutes to an hour.

  3. Interviews with the team

    With hiring manager, sometimes other team members · 1–2 sessions

    Questions about your academic and work experience, with time for your own questions.

  4. Offer

  • Reviewing applications for popular roles can take several weeks.
  • Interviewers are trained in fair hiring and ask behavioural, competency-based questions.

About Johnson & Johnson

Industry
Pharma
Founded
1886
Employees
100,000+
Headquarters
New Brunswick, USA
Website
jnj.com

In their own words

About the company & team

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.

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