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Exciting Regulatory Affairs Job Alert: Join Abbott USA

Regulatory Affairs Specialist Role at Abbott USA

Looking for a career in regulatory affairs? Abbott is hiring a Regulatory Affairs Specialist II in Pleasanton, CA. Contribute to lifesaving heart failure solutions while advancing your career in a global healthcare leader.

Job Details:

  • Job Title: Regulatory Affairs Specialist II – Heart Failure
  • Location: Pleasanton, California, USA (On-site)
  • Category: Regulatory Affairs
  • Experience Required: Minimum 2 years in a regulated industry
  • Employment Type: Full-time
  • Industry: Medical Devices / Healthcare
  • Preferred Qualification: Science, engineering, or medical-related degree

About Abbott:

Abbott is a global healthcare leader helping people live fully at all stages of life. Their portfolio includes diagnostics, medical devices, nutritionals, and branded generics. With 114,000 employees across 160+ countries, Abbott is committed to innovation, diversity, and career growth. Explore more regulatory affairs job offers.

Educational Requirements:

  • Bachelor’s degree in science, medical technology, or related fields
  • Master’s degree preferred (not mandatory)
  • Relevant regulatory affairs certification is a plus

Key Responsibilities of Regulatory Affairs Specialist Role:

  • Prepare FDA and international regulatory submissions to ensure compliance
  • Review and approve engineering changes and documentation
  • Analyze regulatory guidelines and conduct project assessments
  • Maintain updated domestic and international regulatory requirements
  • Interface with FDA and other regulatory agencies when needed
  • Support product release processes, including GTS licenses
  • Ensure compliance with company policies, Quality Management Systems (QMS), and Environmental Management Systems (EMS)

Skills Required for Regulatory Affairs Specialist Role:

  • Strong verbal and written communication skills for technical documentation
  • Ability to work with cross-functional teams and diverse cultures
  • Attention to detail with analytical and critical thinking skills
  • Excellent organization, multitasking, and project management abilities
  • Knowledge of regulatory and business ethics

Benefits of the Regulatory Affairs Specialist Role:

  • Career growth and development in a global company
  • Health Investment Plan (HIP) PPO medical coverage
  • Excellent retirement savings with high employer contribution
  • Tuition reimbursement, student debt programs, and FreeU education benefits
  • Recognition as a great place to work with inclusive and diverse culture

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