Regulatory Strategy Sr. Associate (m/f/d) - Medical Devices - German & English speaking — Alcon
NewCHF 79'000 - 120'000
Alcon · Schaffhausen (SH)
- Location
- Schaffhausen
- Contract
- full-time
- Posted
- Yesterday
SalaryCHF 79'000 - 120'000
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
