Senior Regulatory Affairs Specialist – Lingo

Regulatory Jobs; Alameda (CA); On-site; USD 90,000 - 180,000; Full time

Benefits offered by this job

HIP PPO health coverage

Excellent retirement savings plan with

Tuition reimbursement

FreeU education benefit

Recognition as a great place to work

Job summary

Abbott's Lingo team in Alameda, CA seeks a Senior Regulatory Affairs Specialist to support product development and regulatory activities for US commercialization of Class II software medical devices.

You will provide regulatory input to design and development teams, review labeling and promotional materials for compliance, prepare robust regulatory submissions, and help maintain post-market regulatory requirements across the product lifecycle.

Qualifications

• Bachelor's degree in a technical discipline.
• Minimum 2 years regulatory experience.
• Advanced degree preferred.
• 4–6 years in regulated industry preferred.
• Experience with 510(k)/PMA submissions or class I/II software devices.
• Strong cross-functional collaboration and problem solving.

Responsibilities

• Represent Regulatory Affairs on cross-functional project teams.
• Assess documentation for medical device submissions.
• Review labeling and promotional materials for compliance.
• Lead SOP development for ads and promotions.
• Prepare regulatory submissions to regulatory authorities.
• Support post-market regulatory requirements.
• Provide regulatory input to design and development teams.

Skills

Regulatory knowledge

Communication skills

Cross-functional collaboration

Education

Bachelor's degree

Advanced degree in Engineering/Sciences

Job description

JOB DESCRIPTION:

About Abbott

Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.

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. 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 on-site opportunity at Lingo in Alameda, CA.

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
• Review and analyze labeling, advertising and promotional materials while working with Marketing teams to provide regulatory strategy and compliance input.
• Assist with promotional content development and review for compliance before distribution.
• Lead Regulatory Affairs Ad & Promo SOP development and review.
• 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.
• 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.

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

$90,000.00 – $180,000.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:

Regulatory Operations

DIVISION:

LNGO Lingo

LOCATION:

United States > Alameda : 2601 Harbor Bay Parkway

WORK SHIFT:

Standard

TRAVEL:

Yes, 5 % of the Time

MEDICAL SURVEILLANCE:

No

SIGNIFICANT WORK ACTIVITIES:

Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf