Skip to main content

Specialist QC Raw Materials

Apply now
Share
Download (1)
  • Job title Specialist QC Raw Materials
  • Function Quality
  • Sub function Quality Control
  • Category Analyst, Quality Control (P4 – E24)
  • Location Leiden / Netherlands
  • Date posted
  • Requisition number R-079924
  • 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.

Job Function:

Quality

Job Sub Function:

Quality Control

Job Category:

Professional

All Job Posting Locations:

Leiden, Netherlands

Job Description:

Job Description:

Janssen Biologics is currently looking for a 1 year ad interim QC-Raw Material (RM) Specialist 2 LCM within our Quality Control department. The successful candidate needs to understand the QC testing environment and has relevant educational background. The candidate is responsible for supporting timely execution of QC RM projects, including but not limited to: lifecycle management of analytical methods, vendor driven-, compendial-, and internal changes.

The Leiden Quality Control department is a Business Unit within the Leiden Janssen Biologics site, a biotherapeutics and advanced therapies manufacturing site that is part of the Janssen Supply Chain. The Leiden QC department is responsible for raw material, in-process and release testing for products manufactured at the site.

The Leiden QC-RM Team has a unique global responsibility and exposure by being the RM Global SMEs for large molecule Biotherapeutics and Advanced Therapies products within QC laboratories and by partnering with multiple sites and teams both internally and externally to perform RM testing for multiple sites.


You will be responsible for:

  • Supporting QC-RM (project) activities in relation to lifecycle management of analytical methods, (compendial) raw material testing, and/or technology transfers.
  • Initiation and owning change controls for internal projects and make sure actions and the change itself are closed in a timely manner.
  • Assessing changes regarding supplier change notifications.
  • Lead deviation and non-conformance investigations related to QC Raw Materials and ensure timely closure.
  • Participates in/or lead meetings with various local/global/internal/external stakeholders.
  • Creates, reviews, and approves related documentation.

Qualifications/Requirements:

  • Bachelor’s degree (or equivalent) in a relevant discipline, with 3–5 years of experience in a GMP-regulated environment.
  • Working knowledge of raw materials testing and QC processes.
  • Experience using systems such as Comet, eLIMS, and SAP. Proven experience with owning change controls is a pre.
  • Strong critical thinking and verbal and written communication skills, including ability to effectively communicate with stakeholders
  • Proactive, pragmatic with excellent analytical and problem-solving skills.
  • Work independently but is also a team player.

At Johnson & Johnson, we want every candidate to feel supported throughout the hiring process. Our goal is to make the experience clear, fair, and respectful of your time.

Here’s what you can expect:

  • Application review: We’ll carefully review your CV to see how your skills and experience align with the role.
  • Getting to know you: If there’s a good match, you’ll 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, we’ll 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. We’re excited to learn more about you and wish you the best of luck in the process! #RPOEMEA

Required Skills:

Preferred Skills:

Analytical Reasoning, Business Behavior, Compliance Management, Continuous Improvement, Controls Compliance, Data Analysis, Execution Focus, ISO 9001, Persistence and Tenacity, Quality Control (QC), Quality Control Testing, Quality Standards, Quality Systems Documentation, Report Writing, Sample Testing, Technologically Savvy

The anticipated base pay range for this position is:

€44.700,00 - €70.840,00

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.

Specialist QC Raw Materials

Apply now
Share

Not ready for a new role right now?

No worries. Join our talent community. We’ll reach out when we post new jobs that match your interests and skills so you can apply when the time is right.

Man reading on phone