Job TitleRegulatory Affairs Specialist Job Description Your role: Develop global regulatory strategies for software medical devices ensuring ongoing compliance throughout the product lifecycle. Prepare and manage regulatory submissions and approvals in the US, Europe, and Canada.
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical,