Regulatory Affairs Opportunity at Abbott, USA | Apply Now For Medical Device Regulatory Affairs Development (RAD) Program & Earn Upto $116,000
A rare regulatory affairs opportunity to join Abbott’s Medical Device Regulatory Affairs Development (RAD) Program is now available in multiple locations across the United States. This Regulatory Affairs opportunity is ideal for recent graduates with a background in life sciences or engineering, looking to make a significant impact in the healthcare sector.
- Title: Medical Device Regulatory Affairs Development (RAD) Program
- Location: Alameda, Pleasanton, Santa Clara, CA; Minneapolis, MN; Plano, TX
- Job Category: Regulatory Affairs
About The Company
Abbott is a global healthcare leader that helps people live more fully at all stages of life. The organization’s portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines. Abbott’s 122,000 colleagues serve people in more than 160 countries, making a difference in the lives of many.
Job Description
This regulatory affairs opportunity involves performing three 1-year rotations that include specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for regulatory registration, ensuring products and procedures comply with regulatory agency specifications. The role supports necessary regulatory activities required for product market entry and may involve logistics management of global product release during certain rotational periods.
Regulatory Affairs Opportunity – Key Responsibilities
- Assists in the preparation of regulatory applications to achieve departmental and organizational objectives.
- Creates, reviews, and approves engineering changes.
- Acts as a regulatory representative responsible for review and analysis of applicable regulatory guidelines.
- Reviews and evaluates communications to ensure they adhere to applicable regulatory standards.
- Maintains current domestic and international medical device regulations.
- Supports the product release process by creating GTS licenses or reviewing requests for product release.
- May interface directly with FDA and other regulatory agencies.
- Complies with FDA regulations and company policies, maintaining positive communication with all levels of employees.
Eligibility Criteria Required For Regulatory Affairs Opportunity
- Ability to work in a highly matrixed and geographically diverse business environment.
- Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
- Strong verbal and written communication skills.
- Ability to multitask, prioritize, and meet deadlines.
- Strong organizational and follow-up skills.
- Ability to maintain regular attendance.
- Willingness to move to various US locations based on rotational assignment.
Required Skills
- BA or BS degree in life sciences or engineering.
- Some experience with the medical device industry.
- Experience working in a broader enterprise/cross-division business unit model.
Salary: $73,900.00 – $116,000.00 (varies by location)
Abbott offers a unique regulatory affairs opportunity for aspiring professionals in the healthcare sector to join their Medical Device Regulatory Affairs Development (RAD) Program. Qualified candidates are encouraged to apply before the deadline to take the first step toward a rewarding career in regulatory affairs.
