Analyst Quality Control

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 MedTech

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for Analyst Quality Control to be based in Nijmegen!

This role drives the accuracy and reliability of our products by performing QC testing, maintaining the QC laboratory, and ensuring compliance with regulatory standards. You’ll be part of the Quality Control team, collaborating with manufacturing, compliance, and cross-functional colleagues to deliver high-quality results and continuous improvement. This is an on-site role with evening shift flexibility.

As an Analyst Quality Control, you will:

• Perform routine and non-routine QC tests to evaluate the quality of raw materials, intermediate products, and finished goods.
• Follow established procedures for sample collection, preparation, and analysis to ensure accurate results.
• Record and report test results accurately, ensuring compliance with regulatory requirements.
• Maintain the QC laboratory in a clean and organized state and ensure availability of necessary supplies and equipment.
• Perform incoming inspection of chemicals and materials upon order and delivery to the QC laboratory.
• Calibrate and maintain laboratory instruments to ensure accurate and reliable test results; troubleshoot issues as needed.

Qualifications/Requirements:

• Hold a diploma from a university or technical college in medicine, science or engineering (e.g., Biology, Microbiology, Chemistry, Biochemistry, Material sciences or comparable technical background) with a minimum of 1 year of laboratory experience.
• Proficient in laboratory software and computer applications; able to work both independently and collaboratively.
• Familiarity with regulatory requirements and quality assurance principles; fluent written and spoken English.
• Proficiency in Word, Excel, PowerPoint, and Outlook.

The anticipated base pay range for this position is 38,300 to 61.410 on an annual basis and includes 8% holiday allowance.

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 #LI_Onsite

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