Regulatory Strategy Sr. Associate (m/f/d) - Medical Devices - German & English speaking — Alcon
- Location
- Schaffhausen
- Contract
- full-time
- Posted
- 22 days ago
Role overview
At Alcon, we are driven by the meaningful work we do to help people see brilliantly.
We innovate boldly, champion progress, and act with speed as the global leader in eye care.
Here, you’ll be recognized for your commitment and contributions and see your career like never before.
- At Alcon, we are driven by the meaningful work we do to help people see brilliantly.
- We innovate boldly, champion progress, and act with speed as the global leader in eye care.
Company and context
- Strong organizational and time‑management abilities to support multiple tasks, submissions, and deadlines in a structured environment
- Commitment to quality, including adherence to GxP, SOPs, accurate documentation practices, and continuous learning through required trainings HOW YOU CAN THRIVE AT ALCON:
- Play a key role in the entire product lifecycle, from innovation to market success
- Collaborate with a dedicated, high-performing team in a dynamic, supportive workplace
- Join a global leader in medical technology, where your work contributes to life-changing advancements in eye care Alcon Careers
- See your impact" under https://alcon.com/about-us/careers LI-DNI
- ATTENTION: Current Alcon Employee/Contingent Worker
- If you are currently an active employee/contin
Additional details
- You’ll contribute to regulatory submissions, ensure compliant promotional materials, assist with lifecycle updates, and collaborate across teams to keep products aligned with regulatory standards, playing a key part in bringing safe, high‑quality solutions to patients worldwide. In this role, a typical day will include:
- Maintain strict compliance with GxP and quality systems by following SOPs, keeping thorough documentation, completing required training, and contributing to audits, inspections, and ongoing process improvements. WHAT YOU’LL BRING TO ALCON:
- Commitment to quality, including adherence to GxP, SOPs, accurate documentation practices, and continuous learning through required trainings HOW YOU CAN THRIVE AT ALCON:
- Join a global leader in medical technology, where your work contributes to life-changing advancements in eye care
- See your impact" under https://alcon.com/about-us/careers
Notes and original content
- You’ll contribute to regulatory submissions, ensure compliant promotional materials, assist with lifecycle updates, and collaborate across teams to keep products aligned with regulatory standards, playing a key part in bringing safe, high‑quality solutions to patients worldwide.
- In this role, a typical day will include:
- Maintain strict compliance with GxP and quality systems by following SOPs, keeping thorough documentation, completing required training, and contributing to audits, inspections, and ongoing process improvements.
- WHAT YOU’LL BRING TO ALCON:
- Commitment to quality, including adherence to GxP, SOPs, accurate documentation practices, and continuous learning through required trainings
- HOW YOU CAN THRIVE AT ALCON:
- Alcon Careers
Questions about this listing
What salary does Alcon offer for this role?
Alcon lists CHF 79'000 - 120'000 gross per year for this position in Schaffhausen. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Alcon offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Alcon during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Schaffhausen?
EU/EFTA residents living in the border zone of the country adjoining Canton Schaffhausen can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Schaffhausen's cantonal migration office or with HR during the application.
How do I apply for this position at Alcon?
Use the "Apply now" button on this page — it links directly to Alcon's original listing at alcon.wd5.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
