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Regulatory Affairs Program Manager Jobs (NOW HIRING)

Regulatory Affairs Manager Provo, Utah In-office About the Company Unicity was founded with a bold ... and programs that promote metabolic health and improve quality of life. Our person-to-person ...

Regulatory Affairs

Fort Lauderdale, FL · On-site

$19 - $20/hr

If you are passionate about regulatory affairs and looking for an opportunity to grow within a ... Excellent organizational and time management skills. * Strong attention to detail and ability to ...

The Regulatory Affairs Manager plays a critical role in ensuring that pharmaceutical and biotechnology products comply with all applicable regulatory requirements throughout their development and ...

Regulatory Affairs Manager Provo, Utah · In-office About the Company Unicity was founded with a ... and programs that promote metabolic health and improve quality of life. Our person-to-person ...

The Regulatory Affairs Manager is responsible for monitoring, interpreting, and influencing ... Provide regulatory insight and support related to rulemaking, energy efficiency programs, incentive ...

Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited to mentoring, coaching, performance reviews, developmental plans, succession planning.

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Regulatory Affairs Program Manager information

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How much do regulatory affairs program manager jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for regulatory affairs program manager 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 as a Regulatory Affairs Program Manager, and why are they important?

To thrive as a Regulatory Affairs Program Manager, you need expertise in regulatory guidelines, project management, and a relevant science or healthcare degree. Familiarity with regulatory submission systems, document management tools, and certifications such as RAC (Regulatory Affairs Certification) are highly beneficial. Strong attention to detail, strategic communication, and collaborative problem-solving are crucial soft skills in this role. These competencies ensure efficient navigation of complex regulatory requirements, timely submissions, and successful product approvals.

What is the difference between Regulatory Affairs Program Manager vs Regulatory Affairs Specialist?

AspectRegulatory Affairs Program ManagerRegulatory Affairs Specialist
CredentialsTypically requires a bachelor’s degree in life sciences, regulatory affairs certification (RAC) preferredUsually holds a bachelor’s degree in life sciences or related field; RAC certification is a plus
Work EnvironmentManages multiple projects, oversees teams, and collaborates with cross-functional departmentsFocuses on preparing and submitting regulatory documents, supporting project teams
Employer & Industry UsageUsed in pharmaceutical, biotech, and medical device companies for leadership rolesCommonly employed in similar industries for entry- to mid-level regulatory roles

The Regulatory Affairs Program Manager oversees regulatory strategies and manages teams, while the Regulatory Affairs Specialist handles document preparation and submission. Both roles require relevant credentials and are vital in ensuring compliance within regulated industries.

What are some typical challenges faced by Regulatory Affairs Program Managers when coordinating cross-functional teams?

Regulatory Affairs Program Managers often encounter challenges in aligning the objectives and timelines of different departments such as clinical, quality, and R&D. Balancing varying priorities, managing tight submission deadlines, and ensuring consistent communication between teams are common hurdles. Successful Program Managers proactively foster collaboration, clarify regulatory requirements, and facilitate regular updates to keep projects on track. Being able to anticipate and resolve conflicts, while adapting to evolving regulations, is key to driving effective program execution.

What does a Regulatory Affairs Program Manager do?

A Regulatory Affairs Program Manager oversees and coordinates regulatory activities to ensure that a company's products comply with all applicable laws and regulations. They manage submission processes for product approvals, communicate with regulatory agencies, and develop strategies to maintain compliance throughout the product lifecycle. Additionally, they collaborate with cross-functional teams such as research and development, quality assurance, and manufacturing to align regulatory requirements with business objectives. Their role is crucial in minimizing regulatory risks and accelerating the time to market for new products.
More about Regulatory Affairs Program Manager jobs
What cities are hiring for Regulatory Affairs Program Manager jobs? Cities with the most Regulatory Affairs Program Manager job openings:
What states have the most Regulatory Affairs Program Manager jobs? States with the most job openings for Regulatory Affairs Program Manager jobs include:

Regulatory Affairs Manager

Unicity

Provo, UT

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Job description

Regulatory Affairs Manager Provo, Utah In-office

About the Company

Unicity was founded with a bold mission to make healthy living a reality in an on-the-go world. For over 30 years, we have been dedicated to developing innovative, science-based products and programs that promote metabolic health and improve quality of life. Our person-to-person business model gives a personal touch to our growth, and we are looking for dedicated individuals to help us continue Making Life Better.

In addition to competitive pay we can offer:

  • Heath, Dental, Vision, Life and other benefits that begin within a month
  • Paid Parental Leave
  • Generous vacation allowance in addition to company paid holidays
  • 401(k) with company match
  • Substantial company product allowance
  • Reimbursement for internet, cell phone and gym/wellness activities

Unicity sells nutritional and personal care products in more than 40 countries. The regulatory path into each of those markets is different, and our regulatory team is how we navigate it. We're hiring a manager to lead that team.

The role

You'll lead Unicity's regulatory affairs team, overseeing product registrations across more than 40 international markets. Day to day, that means:

  • Managing a team of regulatory specialists: setting priorities, reviewing work, developing their skills, and holding performance accountable
  • Carrying your own caseload of registrations and renewals alongside the team's work
  • Acting as the primary regulatory partner to our international markets, providing documentation and technical guidance, while working in close coordination with R&D, operations, legal, and marketing
  • Taking direct ownership of registrations in markets without local regulatory staff, including consultant management and government interaction
  • Developing regulatory strategy for new product launches and market expansions
  • Serving as the escalation point for complex regulatory questions from markets and internal teams
  • Tracking launch pipelines and being accountable to executives on targets and timelines

Who we want

  • Effective Communicator: Prioritizes high-bandwidth communication; you recognize when a quick call is more effective than a long email thread to keep projects moving.

  • Global Mindset: Comfortable collaborating across international time zones and adapting to the needs of our global markets.

  • Empowering Leader: Believes in decentralized decision-making by encouraging specialists to engage directly with R&D, operations, and market partners.

  • Anticipatory Service: Operates with a proactive mindset, identifying needs and delivering solutions before they become urgent requests.

  • Decisive Under Ambiguity: Exercises strong judgment when data is limited, knowing how to balance thoroughness with the need for timely action.

  • Operational Efficiency: Proven ability to streamline workflows, reduce bottlenecks, and replace outdated manual processes with more efficient systems.

Requirements

  • B.S. in a technical field, or equivalent regulatory affairs experience
  • Regulatory affairs experience, including some management or supervisory work
  • Strong project management and prioritization
  • Experience collaborating across R&D, legal, marketing, and supply chain

Favorable

  • Hands-on experience with agentic AI.
  • Working knowledge of international regulatory requirements for foods, dietary supplements, and personal care products
  • Language skills relevant to our markets