Sponsorship verdict
Sponsorship possible
One solid signal, not two. Worth applying, and worth asking about sponsorship early.
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✓
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.
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The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
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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.
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✓
Confirmed live todayWhen a source last listed this job as open.
Details and sources
- Employer is on a government sponsor record
- 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. Source: LCA disclosure data (US Department of Labor (OFLC)).
- No salary bar for this route
- H-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.
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).
A verdict summarises public evidence. It is not legal advice and never a guarantee: the employer and the immigration authority decide. Sign in to factor in where you can already work.
About the role
Salary Range:
44.000,00 € - 81.800,00 €
Job Description Summary
#LI-Hybrid
Location: Huningue, France
Relocation Support: This role is based in Huningue, France. Novartis is unable to offer relocation support: please only apply if accessible.
Bring your biotech and data expertise to the heart of biopharmaceutical manufacturing. As a Biotech Engineer/PAT Specialist, you will take a leading technical role in developing and implementing Process Analytical Technologies (PAT) for real-time analytics and process control. You will apply your experience in biotech processes,Multivariate Data Analysis (MVDA) and statistical process control to turn complex process data into practical solutions for manufacturing. Working with automation engineers, process experts and scientists, you will help implement data-driven tools that strengthen decision-making and improve manufacturing efficiency.
Job Description
Key Responsibilities
• Implement high-throughput approaches for real-time bioprocess monitoring and optimization, leveraging automation, online analytics and advanced data analysis.
• Lead technology development and continuous improvement initiatives supporting process intensification.
• Develop and deploy spectroscopy-based Process Analytical Technology methods, including Raman and dielectric spectroscopies.
• Support the implementation of innovative technologies that advance manufacturing processes and operational performance.
• Interpret spectral data and establish secure data management and analysis procedures aligned with Good Manufacturing Practice requirements.
• Apply multivariate data analysis methods for model development, validation and ongoing maintenance.
• Partner with Production, , Engineering and Automation teams to integrate new technologies in commercial manufacturing processes
• Analyze and communicate complex datasets through clear technical reports and presentations to support informed decision-making.
Essential Requirements
• University degree in Biotechnology, Chemical Engineering or a related scientific field.
• 2–5 years of experience in the biopharmaceutical industry, with practical experience in biotechnology processes.
• Strong knowledge of advanced statistical methods and Multivariate Data Analysis, applied within a biotechnology environment.
• Proven experience with cell culture and/or purification processes, including process scale-up and scale-down.
• Experience working with complex process and spectral datasets, including developing, validating and interpreting data models.
• Good understanding of the pharmaceutical regulatory environment, including Good Manufacturing Practices, Quality Assurance, Quality Control and International Council for Harmonisation guidelines.
• Fluent English, with strong communication, problem-solving and cross-functional collaboration skills.
Desirable Requirements
• Experience with Raman spectroscopy or other spectroscopy-based Process Analytical Technology methods.
• Experience with online biomass monitoring or related real-time bioprocess analytical technologies.
• Previous experience with technology integration in GMP environments is a plus.
We offer you a temporary contract, for the period of covering maternity leave.
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: € 44,000 to € 81,800
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
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