Job Description

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 114,000 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. ABOUT LINGO Meet Lingo, a new biosensing technology that provides users a window into their body. Lingo tracks key biomarkers - such as glucose, ketones, and lactate - to help people make better decisions about their health and nutrition. Biowearable technology will digitize, decentralize and democratize healthcare, enabling consumers to take control of their own health. THE OPPORTUNITY Personalized healthcare is the future. Working on Lingo, you will help build a next-generation technology that enables individuals to make decisions about how to improve energy, lose weight or enhance athletic performance. The Lingo team embodies a start-up culture and mindset with the backing of Abbott, a company with a rich history of healthcare innovation. Join us and grow your career as you help Abbott shape the future of healthcare. As an individual contributor, the Senior Regulatory Affairs Specialist will support product development and regulatory activities to commercialize products in the US on-site at our Alameda, CA location. In this role, you will provide regulatory input on design and development activities to cross-functional teams, including software development and systems engineering members, and ensure availability of documentation to support submission activities to meet program objectives and timelines. This is an exciting opportunity at Lingo. What You'll Work On · Represent Regulatory Affairs on cross functional project teams and provide strategic input and technical guidance on product lifecycle planning and regulatory requirements for Class II software medical devices · Assess the acceptability of documentation for medical device submissions and effectively communicate regulatory guidance · Prepares robust regulatory applications/submissions to regulatory authorities. · Assist in SOP development and review in support of "next-gen" product offerings. · Evaluate proposed design, labeling, and distribution changes for regulatory impact and implement any required regulatory action · Utilize technical regulatory skills to propose strategies on complex issues · Ensure compliance with product post marketing requirements · Review product labeling to ensure compliance with relevant regulatory requirements. · Review and approve advertisement and promotional material pertaining to the cleared product · Individual may provide limited work direction and guidance to peers and/or skilled non-exempt levels of employees. · Establishes and cultivates an extensive network of support to facilitate completion of assignments. · Influences middle management on technical or business solutions. Required Qualifications · Bachelor's Degree; preferably in a technical discipline such as biology, chemistry, microbiology, immunology, medical technology, etc. · Minimum 2 yrs. regulatory experience and or 2 years relevant industrial experience typically with a quality; product-development/support; scientific affairs function. Preferred Qualifications · Advanced degree in Engineering, Sciences, or related discipline · Previous experience with 510(k)/PMA submissions or class I / II exempt software devices · Experience with software medical devices · 4-6 years' experience in a regulated industry. Regulatory area is preferred but may consider quality assurance, software or systems research and development, or related area. · Ability to work effectively on cross-functional teams. · Must be able to juggle multiple and competing priorities · Ability to identify and solve problems and work independently with little oversight. · Strong written, verbal, presentation, and organizational skills. · Working knowledge of FDA QSR. · Has a sound knowledge of a variety of alternatives and their impact on the business. The base pay for this position is $86,700.00 - $173,300.00. In specific locations, the pay range may vary from the range posted. 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

Job Tags

Similar Jobs