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ARMRA Colostrum

Job Title: Manager of Regulatory Affairs Job Type: Full-Time (Remote) ARMRA Schedule: Monday-Friday, 9 am - 6 pm EST About ARMRA: ARMRA was born from a near-fatal health crisis that forced its ...

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Calibr

Director of Regulatory Affairs

San Diego, CA · On-site

$159.30K - $210.20K/yr

Director of Regulatory Affairs POSITION SUMMARY: Calibr-Skaggs is seeking an experienced and ... IND & Submission Management: * Lead preparation and submission of U.S. INDs and support global ...

Blue Origin, LLC

Director of Regulatory Affairs

Arlington, VA · On-site

$172.60K - $227.80K/yr

... of experts in Washington DC, you will lead Blue Origin's Regulatory Affairs function, engaging ... managing federal and state agency interactions, and providing strategic direction to external ...

Blue Origin

Director of Regulatory Affairs

Arlington, VA · On-site

$172.60K - $227.80K/yr

... of experts in Washington DC, you will lead Blue Origin's Regulatory Affairs function, engaging ... managing federal and state agency interactions, and providing strategic direction to external ...

Philips

Regulatory Affairs Program Manager

Plymouth, MN

$127.50K - $178.50K/yr

Leads and supports validation of Regulatory Affairs IT platforms, performing the roles of tester ... Management, Continuous Improvement or equivalent. * Preferred experience: One or more years of ...

AstraZeneca

Regulatory Affairs Director

Gaithersburg, MD · On-site

$162.10K - $213.90K/yr

Regulatory Affairs Director Oncology R&D Gaithersburg, MD Hybrid Work- on average 3 days a week ... management of the assigned cell and gene therapy (CGT) product(s). You'll serve as the global ...

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

As of May 28, 2026, the average hourly pay for manager of regulatory affairs 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 Manager of Regulatory Affairs, and why are they important?

To thrive as a Manager of Regulatory Affairs, you need a solid understanding of regulatory guidelines, compliance processes, and industry standards, typically supported by a relevant science degree and experience in regulatory affairs. Familiarity with regulatory submission systems, document management tools, and certifications such as RAC (Regulatory Affairs Certification) are highly valued. Strong leadership, attention to detail, and effective communication skills help navigate complex regulations and lead cross-functional teams. These skills are crucial for ensuring products meet legal requirements and reach the market efficiently while minimizing compliance risks.

What are some common challenges faced by a Manager of Regulatory Affairs when working with cross-functional teams?

A Manager of Regulatory Affairs often faces challenges in aligning regulatory requirements with the objectives of departments like R&D, marketing, and manufacturing. Balancing compliance while supporting innovation and business timelines requires strong communication and negotiation skills. Additionally, interpreting evolving regulatory guidelines and ensuring all stakeholders are informed can be complex, especially in global operations. Successful managers build strong relationships across teams and proactively address potential compliance issues early in the development process.

What does a Manager of Regulatory Affairs do?

A Manager of Regulatory Affairs oversees the process of ensuring that a company complies with all regulations and laws relevant to its business. This professional leads the preparation and submission of documents and applications to regulatory agencies, manages communication with regulatory bodies, and monitors changes in regulations that could affect the company’s products or processes. They also develop strategies to obtain and maintain product approvals, and often collaborate with other departments like research, development, and quality assurance. Their work is crucial for companies in industries such as pharmaceuticals, biotechnology, medical devices, and food to ensure products are safe, effective, and legally marketed.
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Infographic showing various Manager Of Regulatory Affairs job openings in the United States as of May 2026, with employment types broken down into 18% As Needed, 8% Full Time, 68% Part Time, 2% Temporary, and 4% Contract. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $118,493 per year, or $57 per hour.

Manager of Regulatory Affairs

ARMRA Colostrum

Remote

Full-time

Posted yesterday

Job description

Job Title: Manager of Regulatory Affairs
Job Type: Full-Time (Remote)
ARMRA Schedule: Monday-Friday, 9 am - 6 pm EST
About ARMRA: ARMRA was born from a near-fatal health crisis that forced its Founder & CEO, Dr. Sarah Rahal, to uncover what modern life has stolen. As a pediatric neurologist, she turned to exhaustive research and ancient wisdom to find a solution-not just for herself, but for the growing health crisis affecting us all. Your body isn't broken-it's brilliantly designed for strength, resilience, and vitality. But the modern world scrambles the signal, disconnecting you from the intelligence encoded within. ARMRA ColostrumTM is nature's original blueprint with 400+ bioactive nutrients that restore what modern life strips away. It works at the cellular level to remind your body of its original code and reawaken its innate intelligence-so you can reclaim your birthright to thrive.
Who We Are
  • Builders, not passengers - We take ownership, thrive on momentum, and embrace challenges.
  • Resilient and resourceful - We find a way forward, even when the answer isn't obvious.
  • Mission-driven - We believe in what we're building and are passionate about making an impact.
  • Direct and constructive - Feedback is a gift, and we embrace it in order to grow.
  • ONE ARMRA - We succeed together, as one team.
Who We Are Not
  • Performative - We don't play games, manipulate optics, or curate an image for external approval.
  • Entitled - We don't expect rewards without contribution.
  • Clock punchers - We don't attract those looking for just a "job"; we seek individuals who want to build careers, take ownership, and find joy in their work every day.
  • Divisive - We talk about problems and projects, not people. There's no "your team" or "my team" - there's only ARMRA's team.
The Role: We're seeking a Manager of Regulatory Affairs to support ARMRA's compliance efforts across product lines, marketing, and operations. This role requires strong knowledge of dietary supplement regulations, attention to detail, and the ability to collaborate effectively with cross-functional teams.
Reporting to the Sr. Manager of Regulatory Affairs, you'll work closely with Marketing, Product Development, Quality Assurance, and Science teams to ensure accuracy, transparency, and compliance across all communications and product offerings. This is a hands-on role for someone passionate about regulatory excellence and eager to contribute to ARMRA's mission-driven growth.
Responsibilities:
Regulatory Compliance
  • Stay current on FDA, FTC, and dietary supplement regulations relevant to ARMRA. Flag regulatory developments and potential impacts.
  • Review and support approval of marketing materials, influencer content, and digital platforms to ensure claims are substantiated, truthful, and compliant.
  • Assist with product labeling requirements, including supplement facts panels and allergen declarations, ensuring adherence to FDA compliance (21 CFR 101).
Documentation & Support
  • Maintain regulatory documentation, including SOPs, substantiation dossier and claims source-of-truth file.
  • Assist in the development of internal employee training and external education.
  • Support the Sr. Manager with regulatory submissions, inquiries, and audits as needed.
Quality Systems & Product Development
  • Assist in maintaining cGMP-compliant systems (21 CFR 111).
Cross-Functional Collaboration
  • Partner with Marketing, Science, & Growth teams to provide regulatory input and ensure alignment on claims and messaging.
  • Act as a resource for compliance questions and escalate complex issues to the Sr. Manager of Regulatory Affairs.
Qualifications & Skills:
  • Bachelor's degree in Food Science, Chemistry, Biology, or related field required.
  • 3-5 years of experience in regulatory affairs within the dietary supplement, cosmetics, personal care, or pharmaceutical industry.
  • Strong understanding of FDA regulations (21 CFR 111 and 101) and FTC guidelines.
  • Experience reviewing marketing claims or product labels for dietary supplements or CPG.
  • Quick learner who can internalize compliance frameworks and apply them consistently across a high volume of content reviews.
  • Comfortable working independently in a fast-paced, remote environment..
  • Excellent written and verbal communication skills with strong attention to detail.
  • Analytical thinker capable of interpreting and applying regulatory requirements.
  • Proven ability to manage multiple projects and deadlines in a fast-paced environment.
  • Highly collaborative, with strong interpersonal skills to partner across teams.

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