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Regulatory Affairs Strategy Jobs (NOW HIRING)

Alcon

Director, Regulatory Affairs Strategy

Lake Forest, CA · On-site

$159K - $210K/yr

As a Director, Regulatory Affairs Strategy (Management Path) supporting Alcon's Quality & Regulatory Affairs organization, this onsite role based at our Lake Forest, California main campus is ...

Alcon

Director, Regulatory Affairs Strategy

Lake Forest, CA · On-site

$159K - $210K/yr

The Director, Regulatory Affairs Strategy (Management Path) is primarily responsible for directing product registration activities, providing strategic regulatory guidance, and leading negotiations ...

Travere

Director, Regulatory Affairs Strategy

San Diego, CA · On-site +1

$159K - $210K/yr

The Director, Regulatory Affairs Strategy is responsible for developing and executing global regulatory strategies for Phase 2 and Phase 3 development programs to support successful clinical ...

AstraZeneca

Regulatory Affairs Strategy Director

Boston, MA · On-site

$186K - $279K/yr

Are you passionate about science and experienced within regulatory affairs and drug development? Do you possess strategic and operational leadership skills? Then, join us at Cardiovascular, Renal or ...

AstraZeneca

Regulatory Affairs Strategy Director

Boston, MA · On-site

$186K - $279K/yr

Are you passionate about science and experienced within regulatory affairs and drug development? Do you possess strategic and operational leadership skills? Then, join us at Cardiovascular, Renal or ...

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Regulatory Affairs Strategy information

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$28

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$86

How much do regulatory affairs strategy jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for regulatory affairs strategy in the United States is $56.97, according to ZipRecruiter salary data. Most workers in this role earn between $42.07 and $66.59 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Regulatory Affairs Strategy, and why are they important?

To thrive in Regulatory Affairs Strategy, you need a deep understanding of regulatory guidelines, scientific backgrounds (often with a degree in life sciences or pharmacy), and experience in regulatory submissions and compliance. Familiarity with regulatory databases, submission management systems, and certifications such as RAC (Regulatory Affairs Certification) are highly valued. Strong analytical thinking, attention to detail, and effective communication skills help professionals anticipate regulatory changes and collaborate across departments. These skills ensure that products meet global regulatory requirements efficiently, reducing approval risks and supporting successful market entry.

What is the difference between Regulatory Affairs Strategy vs Regulatory Affairs Specialist?

AspectRegulatory Affairs StrategyRegulatory Affairs Specialist
CredentialsTypically requires a degree in life sciences, regulatory affairs certification preferredSimilar credentials, often with a focus on specific regulations or regions
Work EnvironmentStrategic planning, cross-department collaboration, senior-level projectsOperational tasks, document preparation, regulatory submissions
Employer & IndustryPharmaceutical, biotech, medical device companies, often in a strategic roleSame industries, more focused on compliance and submission processes
Search & Comparison IntentUnderstanding strategic roles in regulatory affairsOperational regulatory tasks and responsibilities

Regulatory Affairs Strategy professionals focus on planning and aligning regulatory pathways with business goals, while Regulatory Affairs Specialists handle the day-to-day compliance and submission tasks. Both roles require similar credentials and work within the same industries, but differ in scope and focus.

What is Regulatory Affairs Strategy?

Regulatory Affairs Strategy refers to the planning and execution of processes to ensure that products—such as pharmaceuticals, medical devices, or food—meet all regulatory requirements for approval and ongoing compliance in different markets. Professionals in this field develop strategies to navigate complex regulations, communicate with regulatory agencies, and help bring products to market efficiently and legally. They play a critical role in minimizing delays, reducing risks, and ensuring that products remain compliant throughout their lifecycle.

How does a Regulatory Affairs Strategy professional typically collaborate with cross-functional teams during product development?

Regulatory Affairs Strategy professionals play a pivotal role in product development by working closely with R&D, clinical, marketing, and legal teams to ensure products meet all necessary regulatory requirements. They provide regulatory guidance during early development stages, help interpret changing regulations, and facilitate communication between internal teams and regulatory agencies. This collaboration ensures that regulatory considerations are integrated into project timelines and strategies, reducing risks of delays or non-compliance. Effective cross-functional teamwork is essential for timely submissions and successful product launches.
More about Regulatory Affairs Strategy jobs
What cities are hiring for Regulatory Affairs Strategy jobs? Cities with the most Regulatory Affairs Strategy job openings:
What job categories do people searching Regulatory Affairs Strategy jobs look for? The top searched job categories for Regulatory Affairs Strategy jobs are:
Regulatory Affairs Strategy jobs near you
Infographic showing various Regulatory Affairs Strategy job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 80% Physical, 3% Hybrid, and 17% Remote job distribution, with an average salary of $118,493 per year, or $57 per hour.
Regulatory Affairs Strategy Associate

Regulatory Affairs Strategy Associate

Astrix Inc

Lake Forest, CA • On-site

Contractor

Medical, Dental, Retirement, PTO

Posted 6 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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