Basel Region | 100% | 6-month temporary assignment
Your Responsibilities
* Manage regulatory activities in pharmaceutical and IVDR products
* Ensure compliance of technical documentation and regulatory standards
* Prepare and submit regulatory filings and product registrations
* Act as a key contact for regulatory authorities and external partners
* Monitor and interpret regulatory changes and translate them into internal requirements
* Provide strategic advice on regulatory and quality matters
* Support product development and lifecycle projects
* Contribute to the development and improvement of quality systems, SOPs and processes
Your Profile
* Degree in Life Sciences, Pharmacy, Chemistry, or a related field
* Experience in Regulatory Affairs (Pharma, MedTech, or Diagnostics)
* Knowledge of IVDR, GMP, and international regulatory frameworks
* Experience with regulatory submissions and authority interactions
* Strong analytical and problem-solving skills
* Team-oriented with excellent communication skills
* Fluent in English (German is a plus)
What to Expect
* Opportunity to work in a highly regulated, international environment
* Exposure to impactful cross-functional projects
* Collaborative and dynamic team setting
* Possibility to contribute to strategic regulatory initiatives
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