A

Abbott

Makes heart devices, glucose sensors and lab tests

Regulatory Affairs Manager – APAC - Diabetes Care

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeAlameda, CA, USA$114k - $228k

About the Job

Requirements

  • A bachelor's degree or an equivalent combination of education and experience is required.
  • Four to five years of experience in a regulated industry, such as medical products or nutritionals, is required.
  • Strong verbal and written communication skills, including the ability to communicate and present effectively at multiple organizational levels, are required.

Responsibilities

  • Manage a team of regulatory specialists.
  • Develop and advance organizational policies and procedures for regulatory affairs and compliance to establish a compliant culture.
  • Represent Regulatory Affairs on cross-functional project teams and provide strategic input and technical guidance on regulatory requirements in the APAC region for Diabetes Care projects.
  • Use technical regulatory skills to propose strategies for complex issues.
  • Work closely with in-country regulatory representatives to compile, prepare, and review medical device or in vitro diagnostic submissions to regulatory agencies in the APAC region.
  • Provide strategic input and technical guidance on regulatory authority queries.
  • Evaluate proposed design and manufacturing changes for regulatory impact and implement required regulatory actions.
  • Anticipate regulatory and related obstacles and emerging issues throughout the product lifecycle.
  • Oversee processes for maintaining annual licenses, registrations, listings, and patent information.
  • Ensure compliance with product post-marketing approval requirements.
  • Review product labeling and promotional materials for compliance with relevant regulatory requirements.
  • Provide regulatory support for internal and external audits.

Desired Qualifications

  • Two to five years of regulatory experience; candidates with experience in quality assurance, research and development/support, scientific affairs, operations, or a related area may also be considered.
  • A bachelor's degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, or pharmacology), math, engineering, or a medical field.
  • A master's degree in a technical area or an MBA; a PhD in a technical area or law.
  • Five or more years of experience in regulatory affairs.
  • Supervisory experience.
  • Scientific writing experience.
  • Working knowledge of ISO and EN standards, as well as country-specific standards in the APAC region.
  • Strong working knowledge of APAC regulatory requirements.
  • Certification such as RAC from the Regulatory Affairs Professionals Society.

About the Company

Abbott

Makes heart devices, glucose sensors and lab tests

Abbott makes medical devices, diagnostic tests, nutrition products and branded generic drugs for hospitals, laboratories, pharmacies and patients. Its best-known product is the FreeStyle Libre, a coin-sized sensor worn on the upper arm that tracks blood sugar around the clock without routine finger pricks. Its other lines run from heart valves, pacemakers and brain stimulators to lab analyzers, rapid tests and mail-in colon cancer screening kits, and Abbott earns money by selling these products to health systems, labs, retailers and consumers. The company was founded in 1888 by Chicago physician Wallace Abbott and is based in Abbott Park, Illinois.

Company size
10,001+
Company stage
IPO
Headquarters
Abbott Park, IL
Founded
1888

Recently Posted Jobs

Explore more opportunities at Abbott

See more jobs