Senior Regulatory Affairs Specialist Ion

Primary Function of Position

The Sr. Regulatory Affairs serve as the primary regulatory representative on product and project teams assisting with product lifecycle management activities. Responsibilities include developing regulatory plans reviewing design input/output documentation identification of applicable standards and guidance documents performing regulatory assessments to establish the impact of design/process changes preparing regulatory submissions maintaining regulatory filings and licenses and interacting with regulatory agencies

Essential Job Duties

• Serve as the global regulatory liaison and primary point of contact for product and project teams.
• Provide regulatory guidance to product teams develop regulatory plans and review and approve product design control documentation.
• Establish regulatory pathways and formulate regulatory strategies for the U.S. and Canadian markets. Assess regulatory impact on design materials labeling packaging manufacturing processes and facility changes. Influence and steer global regulatory strategies.
• Author and run regulatory documentation and submissions including U.S. FDA 510(k) premarket notifications internal Letters to File presubmissions and Health Canada registrations and amendments with minimal supervision.
• Coordinate with technical experts to provide additional data/information requested by regulatory agencies and prepare responses to facilitate regulatory approvals.
• Provide riskbased guidance and regulatory input to projects and issues ensuring crossfunctional alignment and resolution.
• Partner with international counterparts to assist with global regulatory submissions approvals and implementation rollouts.

Qualifications :

Required Skills and Experience

• Minimum 8 years of regulatory affairs experience working in a medical device company (can be in combination with a regulatory affairs master degree; e.g. Masters in Regulatory Science)
• Indepth knowledge of US Medical Device regulations and EU MDR. Canada experience is a plus but not required.
• Regulatory working knowledge of product lifecycle management design controls risk management verification and validation and product labeling requirement
• Ability to work in a fastpaced environment and handle multiple projects simultaneously
• Exceptional verbal and written communication skills proven ability to translate technical documentation into effective internal documentation and regulatory submissions
• Team player who seeks to help and learn from colleagues seeing the department success as their own
• Excellent relational and negotiation/influencing skills while maintaining a high level of professionalism
• Proactively seeks to develop and become wellversed within the regulatory landscape.

Required Education and Training

• Minimum B.S. or higher in Biomedical Engineering Electrical Engineering Mechanical Engineering or Pharmacy preferred. Nontechnical degrees with equivalent complex medical device experience are acceptable.

Preferred Skills and Experience

• RAPS Regulatory Affairs Certification (RAC) is a plus.

Additional Information :

Due to the nature of our business and the role please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID19. Details can vary by role.

Intuitive is an Equal Employment Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees and prohibit discrimination and harassment of any type without regard to race sex pregnancy sexual orientation gender identity national origin color age religion protected veteran or disability status genetic information or any other status protected under federal state or local applicable laws.

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

We provide marketcompetitive compensation packages inclusive of base pay incentives benefits and equity. It would not be typical for someone to be hired at the top end of range for the role as actual pay will be determined based on several factors including experience skills and qualifications. The target salary ranges are listed.

Due to the nature of our business and the role please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID19.  Details can vary by role.

Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees and prohibit discrimination and harassment of any type without regard to race sex pregnancy sexual orientation gender identity national origin color age religion protected veteran or disability status genetic information or any other status protected under federal state or local applicable laws.

Mandatory Notices

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

Preference will be given to qualified candidates who do not reside or plan to reside in Alabama Arkansas Delaware Florida Indiana Iowa Louisiana Maryland Mississippi Missouri Oklahoma Pennsylvania South Carolina or Tennessee.

We provide marketcompetitive compensation packages inclusive of base pay incentives benefits and equity. It would not be typical for someone to be hired at the top end of range for the role as actual pay will be determined based on several factors including experience skills and qualifications. The target salary ranges are listed.

Remote Work :

No

Employment Type :

Fulltime