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Switzerland Recruitment Manager (Pharma & Med Device)
Are you a Regulatory Affairs professional ready for your next exciting move? We are looking for a Regulatory Affairs Specialist to join our team and support key regulatory activities for international markets. This is a fantastic opportunity to contribute to product lifecycle management, new registrations, labeling compliance, and strategic regulatory planning.
Key Responsibilities:
1. Lead regulatory submissions for product maintenance, international registrations, and licenses with minimal supervision.
2. Ensure compliance with all relevant federal, state, and local regulations.
3. Prepare and submit responses to Health Authority queries.
4. Develop regulatory outlines, summaries, reports, and slides for internal stakeholders.
5. Provide independent regulatory guidance to cross-functional teams during product development and launch phases.
6. Review and validate labeling for regulatory compliance.
7. Support audits by providing regulatory documentation and guidance.
8. Help develop best practices for Regulatory Affairs processes and workflows.
What We’re Looking For:
1. Bachelor’s degree or equivalent in a scientific field (required).
2. 2–4 years of experience in Regulatory Affairs or a closely related field.
3. Strong written and verbal communication skills.
4. Highly organized and able to manage multiple priorities.
5. Detail-oriented with a strong sense of accountability.
6. Ability to apply risk-benefit analysis in decision-making.
Ready to step into your next career challenge? Apply now or reach out directly if you’re interested in learning more!
Additional Details
* Seniority level: Associate
* Employment type: Contract
* Job function: Other
* Industries: Medical Equipment Manufacturing
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Regulatory Affairs Specialist - 6482 ADA
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