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Regulatory Affair Strategy Associate Jobs (NOW HIRING)

Vrtx

Regulatory Strategy Associate Director

Boston, MA · Hybrid

$168K - $252K/yr

The Regulatory Strategy Associate Director will be responsible for overseeing the development of ... This role requires advanced understanding of regulatory affairs frameworks in the US, Europe, or ...

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Regulatory Affair Strategy Associate information

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How much do regulatory affair strategy associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for regulatory affair strategy associate in the United States is $32.21, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $38.22 per hour, depending on experience, location, and employer.

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For Regulatory Affair Strategy Associate jobs, the most frequently searched job titles are:

Regulatory Affairs Strategy Associate

Lake Forest, CA • On-site

Astrix Inc
Recruiting and Staffing Services • 1 - 5K employees
Learn more about Astrix Incexternal

Contractor

Medical, Dental, Retirement, PTO

Re-posted 23 days ago

Job description

Pay Rate Low: 50 | Pay Rate High: 58
Exciting development Regulatory Affairs Strategy Associate opportunity to work for a global leader dedicated to helping people see brilliantly. The largest device company in the world - with complementary businesses in Surgical and Vision Care
Regulatory Affairs Strategy Associate
Location: Lake Forest, CA (Onsite)
Pay: 50.00-58.00
Benefits: Medical, Dental, Holiday, PTO 401K matching
Contract: 8 month contract with extension potential
Play a key role in bringing innovative ophthalmic products to market. We're looking for an experienced Regulatory Affairs professional to lead regulatory strategy and support product registrations for medical devices and pharmaceutical products.
  • Develop and execute regulatory strategies for new and existing ophthalmic products.
  • Manage product submissions, renewals, and regulatory approvals.
  • Partner with manufacturing sites, regulatory agencies, and global teams to ensure compliance.
  • Support medical device and pharmaceutical product portfolios.
  • Maintain compliance with GxP regulations, SOPs, and quality standards.
  • Bachelor's degree (or equivalent experience).
  • 7+ years of Regulatory Affairs experience.
  • Experience with medical devices and/or pharmaceuticals.
  • Strong knowledge of regulatory submissions and global compliance.
  • Excellent communication skills and attention to detail.
  • Work on industry-leading eye care products.
  • Collaborative, innovative team environment.
  • Opportunity to make a global impact in healthcare.

This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
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