About this opportunity
#LI-OnsiteLocation: Baarle-Nassau, NetherlandsRelocation Support: This role is based in Baarle-Nassau, Netherlands. Novartis is unable to offer relocation support: please only apply if accessible.In this role, you make an impact every day by ensuring our products are safe, reliable, and of exceptional quality. As a QC Analyst, you stand at the forefront of precision and quality: your work not only supports our production processes, but ultimately contributes to improving the lives of patients worldwide. You will do this within a fast growing company operating in a highly dynamic and innovative radiopharmaceutical industry. In an environment where accuracy and responsibility are essential, you will have the opportunity to apply your analytical strengths, laboratory expertise, and quality mindset to their fullest.
Key ResponsibilitiesPerform and document analytical testing on finished products, materials, and stability samples in accordance with GxP standards.Manage, store, and track samples to ensure traceability and accuracy.Conduct, interpret, and report microbiological monitoring within cleanrooms at the Baarle-Nassau site.Report technical complaints, deviations, or special situations within 24 hours of receipt.Maintain an orderly, safe, and compliant QC laboratory environment.Apply and follow safety, radiation, and laboratory regulations to prevent risks.Contribute to continuous quality improvement through proactive identification and solution-oriented actions.Essential RequirementsBachelor’s degree in chemistry, biochemistry, microbiology, or a comparable life-science field.Fluent in EnglishStrong knowledge of good laboratory practices and current Good Manufacturing Practices.Excellent analytical skills and strong attention to detail in documentation and laboratory processes.Openness to working with new technologies and a continuous improvement mindset.Clear, open, and effective communication with internal and external stakeholders.work in weekend shiftsDesirable RequirementsDutch language skills in addition to fluent English.Ability to act quickly and prioritize with a strong sense of urgency.Commitment to Diversity and Inclusion:
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1075 comparable Quality roles across 129 biopharma companies.
Salary context
197 of 1075 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1075 comparable roles
+ 48 more countries
Seniority mix
475 of 1075 peers have a known seniority level
Therapeutic area mix
2 of 1075 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.