Jobs / United States / Novartis Pharmaceuticals Corporation
Quality Control Officer
Novartis Pharmaceuticals Corporation · 🇺🇸 Baarle Nassau
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 75 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 31 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
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Sponsor Radar — Novartis Pharmaceuticals Corporation
The US Department of Labor certified 75 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 31 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Novartis Pharmaceuticals Corporation →
About the role
Salary Range: €44,100.00 - €81,900.00 Job Description Summary #LI-Onsite 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. The QC Officer contributes to the quality control processes of the medicinal products of Novartis RLT according to the Standard Operating Procedures, Work Instructions, Specifications and Methods of Analysis as laid down in the quality system. The QC Officer has a deep knowledge in the analytical processes and systems in a strong GMP environment and acts as Subject Matter Expert. The QC Officer contributes to writing of investigations (deviations, Out-of-Specifications, etc), quality risk/impact assessments and qualification documentation, and execution of investigational/qualification activities for laboratory systems and processes, including laboratory equipment, computerized systems and analytical methods. Job Description Deadline for applications: 18th of September 2026. Major Accountabilities: • The accurate execution of the quality control as defined in the specification of the respective medicinal product, intermediate or raw material. • Awareness for any uncommon or unexpected incident, condition or detail during these controls and immediate notification of such deviation to the Qualified Person. • Execution of the routine quality control testing conform analytical procedures and methods. • Sampling, review and documentation of environmental monitoring according to the environmental control program effective on site. Reviewing the data and perform trend analysis. • Manage and maintains the progress on document generation, qualification execution, document review and approval. Escalate the issue/delay to management team. • Collaboration with AS&T in project management, validation, revalidation and/or technology transfer related to analytical equipment.Coordinate and manage deviation and out-of-specification/out-of-expectation (OOX) investigations to be initiated, assessed, and closed out in timely manner • Responsible for all other activities related to qualification activities but not limited to change control, tag out, PM/Calibration program, equipment configuration, SOP generation. • Communicate needs and opportunities for improvement of devices / software / methods conform GMP requirements and needs of customer. • Ensuring the QC Laboratory is maintained in an orderly and clean state. • Adherence to radiation and conventional regulations, and preventing oneself to a state that could expose her/him or colleagues to any hazardous situation. Obligatory Requirements: • 1+ years of experience as radiopharmaceutical QC laboratory or company equivalent in a strongly regulated environment. • Excellent knowledge of good laboratory practices and cGMP. • Analytical mind-set and eye for detail. • Open to new technologies and continuous improvement behaviour. • Open and clear collaboration and communication with third parties. • Shows the appropriate sense of urgency around given tasks. • Fluent English, written and spoken. Benefits & Rewards At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. Expected Annual Base Salary Range for role: €44,100 to €81,900. The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We