Abbott Senior Specialist Regulatory Affairs in Santa Clara, California

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve.

This Senior Regulatory Affairs Specialist position supports Abbott Vascular's Endovascular product portfolio . This role is focused on leading and supporting major projects; specifically, new product submissions, re-registrations, maintenance etc. for our class III products. We are ideally looking for someone with significant PMA submissions experience; medical device experience is a must have.

Primary Job Function:

As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment. The individual may execute tasks and play a consultative role by partnering across business functions. The individual may assist in identifying data needed, obtaining these data and ensuring that they are effectively presented for the registration of products worldwide. The individual may prepare and submit documentation needed for registration worldwide or may oversee such preparation.

Core Job Responsibilities:

Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Core job responsibilities for this function may include:

Strategic Planning:

· Assist in SOP development and review

· Provide regulatory input to product lifecycle planning

· Continue to revisit and compare regulatory outcomes with initial product concepts to make recommendations on future actions

· Assist in the development of regional regulatory strategy and update strategy based upon regulatory changes

· Understand, investigate and evaluate regulatory history/background of class, disease/ therapeutic/diagnostic context in order to assess regulatory implications for approval

· Determine trade issues to anticipate regulatory obstacles

· Determine and communicate submission and approval requirements

· Participate in risk-benefit analysis for regulatory compliance

Premarket:

· Assess the acceptability of quality, preclinical and clinical documentation for submission filing

· Compile, prepare, review and submit regulatory submission to authorities

· Monitor impact of changing regulations on submission strategies

· Monitor applications under regulatory review

· Monitor and submit applicable reports to regulatory authorities

· Evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies

· Negotiate and interact with regulatory authorities during the development and review process to ensure submission approval

Postmarket:

· Maintain annual licenses, registrations, listings and patent information

· Assist compliance with product postmarketing approval requirements

· Review and approve advertising and promotional items to ensure regulatory compliance

· Assess external communications relative to regulations

· Review regulatory aspects of contracts

· Assist with label development and review for compliance before release

· Submit and review change controls to determine the level of change and consequent submission requirements

· Analyze the input of cumulative product changes to current product submissions

· Contribute to the development and functioning of the crisis/ issue management program

· Ensure product safety issues and product-associated events are reported to regulatory agencies

· Provide regulatory input for product recalls and recall communications

Minimum Education/Qualifications:

Bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields is preferred. 3-4 years’ experience in a regulated industry (e.g., medical products, nutritionals). 2-3 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Note: Higher education may compensate for years of experience.

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 corpjat@abbott.com