Senior Director, Global Market Access Lead Jobs Everywhere
(Found 173 Jobs)
Pulmonx Corporation
Pulmonx is looking for an experienced Director/Sr. Director* of Regulatory Affairs to join our dynamic Regulatory Affairs team! * Will consider Sr. Director level depending upon experience. Workplace...
Aug 25, 2024
San Jose, CA
CSL
The Associate Director of US Payer Marketing will lead US value, access, and reimbursement strategy for the launch of CSL Behring’s pipeline assets. The role will serve as a critical partner and work...
Apr 3, 2025
King of Prussia, CSL Behring, PA
CSL
As the Director of HIZENTRA, you will be responsible for the development and execution of marketing strategies to achieve business objectives and goals. You will work with internal and external partne...
Apr 1, 2025
King of Prussia, CSL Behring, PA
CSL
The OpportunityThe Director of Strategic Pricing – NA executes critical pricing capabilities, including strategy development for the complete product lifecycle, price management, governance, analytics...
Jan 10, 2025
Summit, NJ
E.L.F. BEAUTY
About the Companye.l.f. Beauty, Inc. stands with every eye, lip, face and paw. Our deep commitment to clean, cruelty free beauty at an incredible value has fueled the success of our flagship brand e.l...
May 31, 2025
Los Angeles, CA
Director/Sr. Director Regulatory Affairs
San Jose, CA
Aug 25, 2024

Pulmonx is looking for an experienced Director/Sr. Director* of Regulatory Affairs to join our dynamic Regulatory Affairs team!

* Will consider Sr. Director level depending upon experience.

Workplace type: Hybrid with 3-4 days/week onsite in Redwood City

Not sure who Pulmonx is and how our Zephyr valves help people to breathe better? Check out some of the videos on our YouTube Channel: https://www.youtube.com/@zephyr-by-pulmonx

Responsibilities and Capabilities:

  • Create, lead and manage 510(k), PMA, and IDE submissions in US and submissions in OUS, ensuring timely completion and compliance with applicable regulations.
  • Provide strategic regulatory guidance to cross-functional teams (e.g., R&D, clinical, operations, legal, marketing) to ensure regulatory requirements are met throughout the product life cycle.
  • Act as the main point of contact for regulatory authorities, managing all communication, including pre-submissions, Q-subs, and meetings with regulatory bodies.
  • Ensure timely preparation and submission of post-market reports, supplements, and required regulatory filings to maintain compliance.
  • Evaluate and provide guidance on product claims, labeling, advertising, and promotion to ensure compliance with FDA and global regulations.
  • Collaborate with clinical teams on regulatory submissions and trial designs, ensuring compliance with regulatory requirements for clinical trials.
  • Evaluate preclinical, clinical, and manufacturing changes, determining regulatory impact and submission requirements.
  • Provide regulatory intelligence, keeping teams updated on changes to global standards and regulations. Assess and communicate changes which impact our products
  • Prepare cross-functional teams for interactions with regulatory authorities, including advisory committees and panel meetings.
  • Develop and implement regulatory policies and processes to streamline submission processes and improve compliance oversight.
  • Manage relationships with external regulatory consultants, vendors, and notified bodies to facilitate submission processes and certifications.
  • Present regulatory risks, strategies, and potential product impacts to senior leadership, providing insight into business and regulatory decision-making.
  • Train and mentor internal teams on regulatory compliance, keeping leadership updated on any regulatory changes affecting product development or market access.

Requirements:

  • Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, or a related field (Advanced degree preferred).
  • RAC Certification
  • Minimum of 12 years of regulatory affairs experience in the medical device industry, with demonstrated success in managing 510(k), PMA, and IDE submissions.
  • Proven ability to present complex regulatory strategies and risks to senior leadership and executive teams.
  • Strong understanding of FDA, EU MDR, and global medical device regulations, with experience in regulatory strategy development.
  • Experience managing post market activities for commercialized products.
  • Demonstrated strength in regulatory submissions activities. PMA experience is strongly desired.
  • Knowledge of international regulatory requirements is strongly desired.
  • Strong project management skills and experience.
  • Excellent communication and leadership skills, with the ability to lead cross-functional teams.

Requirements:

When joining Pulmonx, you are part of an organization that attracts and hires the best talent on the planet! You will be working with a great team of dedicated, friendly and collaborative individuals, developing novel and game changing product(s). We are dedicated to the development and growth of our colleagues.

Compensation: $200,000 - $240,000/year annual bonus for Director level. Competitive market salary for Sr. Director level depending upon experience.

Please note that an application and resume must be completed and submitted for consideration for this opportunity.

Pulmonx Corporation is an Equal Opportunity Employer and embraces diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any characteristic protected by applicable law.

#LI-post

PDN-9c4a1fce-fa27-44f8-af29-4a8c66f6fc7c
©2025 TalentAlly.
Powered by TalentAlly.
Apply for this job
Director/Sr. Director Regulatory Affairs
Pulmonx Corporation
San Jose, CA
Aug 25, 2024
Your Information
First Name *
Last Name *
Email Address *
Zip Code *
Password *
Confirm Password *
Create your Profile from your Resume
By clicking the Apply button, you agree to the terms of use and privacy policy and consent to receive emails from us about job opportunities, career resources, and other relevant updates. You can unsubscribe at any time.
Continue to Apply

Pulmonx Corporation would like you to finish the application on their website.

Supercharge Your Resume with AI

Boost your resume with AI-driven enhancements. The tool analyzes and refines your content, highlighting your strengths and tailoring it for maximum impact. Get personalized suggestions and apply improvements instantly to stand out in the job market.