Regulatory Affairs Specialist

• Ways of Working:
  Set Schedule - This job will be onsite weekly, the percentage of onsite work will be defined by the leader.
• Employee Type:
  Employee
• Min. Salary Region 1: 151700 USD
• Global Job Level (HCM):
  Professional 4 (11)
• Min. Salary Region 2: 128900 USD

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive
. As a global leader in robotic-assisted surgery and minimally invasive care
, our technologies—like the da Vinci surgical system and Ion
—have transformed how care is delivered for millions of patients worldwide.

We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.

The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful—because every improvement we make has the potential to change a life.

If you’re ready to contribute to something bigger than yourself and help transform the future of healthcare
, you’ll find your purpose here.

Primary Function of Position

The Senior Regulatory Affairs Specialist serves as the primary point of contact for regulatory strategy and execution of projects involving complex electromechanical, software controlled robotic systems, instruments and accessories, SaMD and advanced imaging systems. The Senior RA Specialist works across the organization and liaises with global regulatory counterparts on a wide range of products including capital equipment, instruments and accessories (single use or re-usable), and software, focusing on supporting ongoing changes and continuous improvement to these products.

• Support product engineering and manufacturing teams on regulatory issues, including review of design input, risk management and test documentation
• Evaluate changes to products including changes to design, material, labeling, packaging, manufacturing process, and facility
• Assess the impact of the product/process changes and determine regulatory pathway for US markets
• Present regulatory strategy and status in internal group settings
• Gather information from international counterparts for ROW regarding the impact of changes and work with international counterparts to coordinate global regulatory submissions/approvals
• Prepare internal documentation, and prepare and submit regulatory filings including non-filing justifications (NFJ) and 510(k) s Provide oversight of third party agency testing (UL, EMC, biocompatibility, sterilization) as required Perform other duties as required

Required Skills and Experience

• Minimum of 8 years experience working in a medical device company performing regulatory submissions and technical documentation (can be in combination with a Masters in Regulatory Science or Master of Engineering, Biomedical Engineering) Experience working with cross-functional teams including engineering, manufacturing, quality, marketing, clinical, labeling, packaging, etc.
• Working understanding of FDA regulations
• Ability to work with cross functional project teams and understand complex products
• Ability to work in a fast-paced environment and handle multiple projects simultaneously
• Strong verbal and written communication skills, proven ability to translate technical documentation into effective internal documentation, and regulatory submissions
• Ability to review and provide critical feedback on design documentation
• Strong interpersonal and project management skills

Required Education and Training

• Minimum B.S. or higher in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, or Pharmacy preferred.

Working Conditions

• Must wear personal protective equipment as defined/required by job assignments.
• Must be able to lift/carry 50lbs
• May be exposed to radiation or electromagnetic fields, lasers, noise > 80dB TWA, allergens/biohazards/chemicals (cautery smoke)
• Subject to and expected to comply with all applicable Intuitive policies and procedures

Preferred…