Regulatory Affairs Director
1 month ago
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines.
As a key member of our team, you will play a critical role in shaping our regulatory strategy and ensuring compliance with global regulations. You will work closely with cross-functional teams to develop and implement regulatory plans, manage submissions, and maintain relationships with regulatory agencies.
Key Responsibilities- Develop and implement regulatory strategies to support business objectives
- Manage the preparation and submission of product approval applications to regulatory agencies
- Provide guidance on regulatory requirements and strategies to product development project teams
- Maintain expert working knowledge of laws, regulations, and industry trends
- Collaborate with senior management to develop and implement regulatory policies and procedures
- Lead and manage a team of regulatory affairs professionals
- Develop and maintain relationships with regulatory agencies and industry stakeholders
- Bachelor's degree in a relevant field (science, math, engineering, or medical field)
- Minimum 10 years of progressive work experience in regulatory affairs or a related discipline
- Experience in a regulated industry (diagnostics, medical products, or related area)
- Minimum 5 years of demonstrated experience at a supervisory/managerial level
- Advanced credential in a relevant discipline/concentration desired
Abbott is an Equal Opportunity Employer, committed to employee diversity. We provide a competitive salary and benefits package, as well as opportunities for professional growth and development.
Join our team and contribute to shaping the future of healthcare.
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