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 115,000 colleagues serve people in more than 160 countries.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
- Career development with an international company where you can grow the career you dream of
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- An excellent retirement savings plan with high employer contribution
- Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree
- A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune
- A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists
The Opportunity
This Regulatory Affairs Specialist I will work on-site out of our Pleasanton, CA location in the Heart Failure Division. As an individual contributor in the function of a Regulatory Affairs Specialist, you will provide support to the Regulatory Affairs department. With limited supervision you will execute tasks and partner across business functions. As an individual contributor, the Regulatory Affairs Specialist will support product registration and regulatory activities.
What You'll Work On
- As a professional in the Regulatory Affairs Sub-Function, possesses developing skills in product registration submission, change order management, progress reports.
- Interacts with regulatory affairs team members and other cross functional team members for regulatory submissions, product licensing and relevant documentation.
- Supports the product release process by creating GTS licenses or reviewing and approving requests for product release.
- Serves as regulatory liaison throughout product lifecycle.
Ensures timely approval of medical devices and continued approval of marketed products.
- May interface with regulatory agencies.
- Conducts reviews of product and manufacturing changes for compliance with applicable regulations.
- Creates, reviews and approves engineering change orders.
- Reviews protocols and reports to support regulatory submissions.
- Supports all business segment initiatives as identified by divisional management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
- Complies with U.S. Food and Drug Administration (FDA) and international regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
- Maintains positive and cooperative communication and collaboration with all levels of employees
Required Qualifications
- Bachelor's Degree or an equivalent combination of education and work experience
- 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. Ability to leverage, manage and/or engage others to accomplish projects.
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
- Strong organizational and follow-up skills, as well as attention to detail and focus towards improving quality.
- Multitasks, prioritizes and meets deadlines in timely manner.
Preferred Qualifications
- Bachelor's Degree in a Science/Technical discipline (engineering, life sciences, mathematics).
- Master's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields.
- Experience working in a broader enterprise/cross-division business unit model.
- Experience working in the Medical Device industry.
- Regulatory Affairs Professionals Society Certification is a plus.
Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is $73,900.00 - $116,000.00. In specific locations, the pay range may vary from the range posted.