Veterans at Abbott
Abbott Senior Regulatory Affairs Specialist in Pleasanton, California
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. Our 103,000 colleagues serve people in more than 160 countries.
We are recruiting for a Senior Regulatory Affairs Specialist to join our team in the Pleasanton, CA location. In this role, you be responsible for coordinating, planning, preparation, assembly, and review of regulatory submissions to the FDA and other worldwide regulatory agencies.
Develops domestic and/or international strategies for regulatory approval of company products
Coordinates, compiles and submits U.S, and/ or International regulatory submissions, including filing and/or creation of PMAs, IDEs, Premarket Notifications, Supplements, Change Notifications, and other country-specific product registrations
Prepares robust regulatory applications to achieve departmental and organizational objectives
Represents RA on cross-functional product development and manufacturing support teams. Guide teams to provide content for US and/or International submissions, participates in design reviews as needed
Acts as liaison between the Company and the various appropriate regulatory agencies, ensuring that communications on both sides are germane, specific and convey all necessary detail
Maintains ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are current, up-to-date and are entered into regulatory submission data base and file systems. Ensures that information of such regulations and requirements, especially those that are new or modified, are distributed to appropriate personnel
Reviews device labeling and marketing materials for compliance with FDA submissions and applicable regulations
Supports the product release process by creating GTS licenses or reviewing and approving requests for product release
Interfaces directly with U.S. Food and Drug Administration (FDA) and other regulatory agencies.
Conducts reviews of product and manufacturing changes for compliance with applicable regulations. Reviews protocols and reports to support regulatory submissions. Creates, reviews and approves engineering change orders
Communicates with and maintain productive, constructive relationships with external customers as required – US FDA, Health Canada, regulatory representatives, and notified-bodies
Support Department and Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Complies with FDA and international regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors
Provides mentoring and leadership to Regulatory Specialist I and II team members.
Performs other related duties and responsibilities, on occasion, as assigned
Bachelor’s Degree in life sciences or engineering, or other technical discipline
5+ years of technical experience, including at least 4 years of regulatory experience in a medical device industry
Experience with, PMA supplements, 510(k) applications and US device regulations and/or experience with EU and other international medical device regulations and submissions
Must be familiar with relevant US/international regulatory requirements for medical devices including Quality Systems standards and clinical investigations
Proficient with MS Office Suite (Word, Excel, PowerPoint, Outlook)
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
MBA in life sciences or engineering discipline
Experience working in a broader enterprise/cross-division business unit model
Ability to work in a highly matrixed and geographically diverse business environment
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call 224-667-4913 or email firstname.lastname@example.org