Non-conformance Specialist (QC Microbiology)
Leiden - Netherlands
Job Summary
At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at .
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:
QualityJob Sub Function:
Quality ControlJob Category:
Business Enablement/SupportAll Job Posting Locations:
Leiden South Holland NetherlandsJob Description:
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
Join us in developing treatments finding cures and pioneering the path from lab to life while championing patients every step of the way.
Learn more at are searching for the best talent for Non-conformance Specialist (QC Microbiology) to be based in Leiden.
Join our QC Microbiology team to lead investigations that protect product quality and patient safety. Youll manage non-conformance records drive corrective actions and help keep our labs inspection-ready while working closely with QC QA and manufacturing teams. English is required and Dutch is a plus!
As a non-conformance Specialist (QC Microbiology) you will:
- Lead thorough investigations of non-conformances in microbiology testing and related processes to protect product quality and safety.
- Define coordinate and implement corrections CAPAs ACTs and effectiveness checks to close issues and prevent recurrence.
- Use structured root-cause methods (e.g. Fishbone 5 Whys KT) and interviews to identify causes and recommend robust corrective actions.
- Assess product impact and advise on disposition and regulatory/compliance implications.
- Maintain clear timely documentation; contribute to trending and reporting for audits inspections and management review.
- Partner with QC QA manufacturing and other teams to resolve quality issues update procedures and support continuous improvement.
Qualifications/Requirements:
- Bachelors or Masters degree in Chemistry Biology Pharmaceutical Sciences or related field; microbiology background is a strong advantage.
- 3 years (MSc) to 5 years (BSc) experience in QC QA or related roles in the pharmaceutical industry with non-conformance/investigation exposure.
- Solid understanding of GMP and relevant guidelines (FDA EMA ICH) and quality procedures.
- Practical experience with quality management and lab systems (COMET or similar); LabVantage eLIMS is a plus.
- Strong analytical root-cause and organizational skills with attention to detail and the ability to manage multiple priorities.
- Clear written and verbal English; Dutch is a plus; collaborative communicator who works well independently and in cross-functional teams.
Heres what you can expect:
Application review:Well carefully review your CV to see how your skills and experience align with the role.
Getting to know you:If theres a good match youll be invited to a short call with one of our recruitment team to understand more about you and answer any questions that you might have.
Staying informed:We know waiting can be hard and processes can evolve; our recruitment team will keep you updated and make sure you know what to expect at each step.
Final steps:For successful candidates you will need to complete country-specific checks before starting your new role. We will help guide you through these.
Finally at the end of the process well invite you to share feedback in a short survey your input helps us continue improving the experience for future candidates. Thank you for considering a career with Johnson & Johnson. Were excited to learn more about you and wish you the best of luck in the process! #RPOEMEA #LIHybrid
Required Skills:
Preferred Skills:
Administrative Support Communication Compliance Management Controls Compliance Execution Focus ISO 9001 Persistence and Tenacity Problem Solving Quality Control (QC) Quality Control Testing Quality Standards Quality Systems Documentation Quality Validation Report Writing Standard Operating Procedure (SOP) Teamwork Technologically SavvyThe anticipated base pay range for this position is:
44700.00 - 70840.00Benefits:
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 locations 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.
Required Experience:
IC
About Company
About Johnson & Johnson A t Johnson & Johnson, we believe good health is the foundation of vibrant lives, thriving communities and forward progress. That’s why for more than 130 years, we have aimed to keep people well at every age and every stage of life. Today, as the world’s larges ... View more