Quality Control Analyst

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 https://www.jnj.com

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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 https://www.jnj.com/innovative-medicine

We are searching for the best talent for Quality Control Analyst to be based in Leiden, Netherlands!

This exciting role is pivotal in our Quality Control department for Advanced Therapies, where you will contribute to groundbreaking advancements in healthcare. Join a dedicated team at JnJ Biologics B.V., part of Johnson & Johnson Innovative Medicine, committed to developing and promoting advanced therapies that combat and prevent diseases.

We offer flexible working hours, opportunities to work on exciting projects, and a dynamic environment that fosters personal and professional development. With an excellent record in employee continuous professional development, your contributions will directly impact our mission!

This is a full-time position with a focus on supporting production activities while conducting quality control release and stability testing. Proficiency in English is essential to communicate optimally across our team!

You will be responsible for:

• Carrying out complex testing activities on schedule, maintaining a strong record of first-time accuracy.
• Reviewing and approving results from colleagues to ensure quality standards.
• Training team members and continuously improving your own skill set.
• Collaborating actively with QA and Analytical Development to support team initiatives and project goals.
• Complete and document new method introduction activities, including gap assessments and method qualifications.

Qualifications/Requirements:

• A Bachelor's or Master’s degree or equivalent experience in Life Sciences, Molecular Biology , or a related field.
• Proven experience with techniques such as ELISA, cell culturing, binding assays, cell-based bioassays, qPCR, and dPCR is a must.
• Strong analytical thinking and technical problem-solving capabilities.
• Familiarity with GMP documentation and experience with systems like Truvault, eLIMS, and Summit is a plus.
• Full proficiency in English Required.

If you’re ready to make a meaningful impact in our Quality Control department and grow in a supportive environment, we’d love to hear from you! This is a fantastic opportunity to be part of a motivated team where your contributions are valued. Apply today and join us in making a difference! #RPOAMS