Coord 3, Regulatory Affairs - Onsite

Job Description

Support US and EU regulatory submissions (exercising judgment to protect proprietary information).

Participate in assessing and collating regulatory impact and developing regulatory strategy.

Collaborate and approve change requests/change notifications.

Participate in providing guidance and feedback to business unit regulatory teams on registration requirements for product and process changes.

Additional Skills

• Coursework, seminars, and/or other formal government and/or trade association training required
• Proven expertise in Microsoft Office Suite including Word, PowerPoint and Excel
• Good written and verbal communication skills and interpersonal relationship skills
• Good problem-solving, organizational, analytical and critical thinking skills
• Solid knowledge and understanding of global regulations relevant to medical devices, Class II and/or Class III devices
• Solid knowledge and understanding of global regulatory requirements for new products or product changes.
• Strict attention to detail
• Ability to interact professionally with all organizational levels
• Ability to manage competing priorities in a fast paced environment
• Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects
• Ability to build productive internal/external working relationships

Requirements

• Bachelor's Degree or equivalent in scientific discipline (e.g., Biology, Microbiology, Chemistry)
• 5-7 years of experience required