QC Officer

Summary

\#LI\-Onsite (80% on site, 20% work from home, based on the agreement)

Temporary contract with possibility to extend to permanent

Weekend work in teams applicable

Location: Baarle Nassau, Netherlands

Relocation Support: This role is based in Baarle Nassau, Netherlands. Novartis is unable to offer relocation support: please only apply if accessible.

If you care about doing work that genuinely protects patients, this is the role where your precision really matters. As a Quality Control Officer at Novartis, you’ll be at the heart of the quality control laboratory \- running analytical testing, spotting anything unusual early, and supporting clear, high\-quality investigations when results fall outside specifications. You’ll also help with qualification work for laboratory equipment and computerized systems, contribute to strong documentation, and keep laboratory processes reliable, compliant, and continuously improving \- so every release meets the standards patients depend on.

About the Role

Key Responsibilities

• Perform routine quality control testing of raw materials, intermediates, and finished products following approved analytical methods.


• Identify, document, and escalate deviations or unexpected results promptly to protect product quality and compliance.


• Conduct sampling, documentation, and trend analysis for environmental monitoring in line with site programs.


• Lead and contribute to investigations, including deviations and out\-of\-specification results, ensuring timely and robust closure.


• Support qualification and re\-qualification of laboratory equipment, analytical methods, and computerized systems.


• Maintain accurate, complete, and compliant laboratory documentation within a highly regulated environment.

Essential Requirements

• Bachelor’s degree in chemistry, biochemistry, microbiology, or a comparable life science field.


• At least 1 year of experience (preferred more) in a pharmaceutical quality control laboratory in a highly regulated environment.


• Strong knowledge of good laboratory practices and current good manufacturing practice expectations.


• Proven ability to document and support investigations, including deviations and out\-of\-specification results, with strong attention to detail.


• Fluent English, with a collaborative and proactive mindset focused on continuous improvement and timely delivery.


• Analytical mind\-set and eye for detail

Desirable Requirements

• English


• Dutch language skills are an advantage.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.

Read our handbook (PDF 30 MB)

Division
Operations
Business Unit
Quality
Location
Netherlands
Site
Baarle Nassau
Company / Legal Entity
NL42 (FCRS \= NL042\) IDB Holland BV
Functional Area
Quality
Job Type
Full time
Employment Type
Temporary (Fixed Term)
Shift Work
No

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