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Regulatory Affairs Manager Jobs (NOW HIRING)

Regulatory Affairs Manager

Dallas, TX · On-site

$85 - $142/hr

We are seeking a Regulatory Affairs Manager. We are seeking a Regulatory Affairs Manager. This is a remote, work-from-home position, preferably based in the Dallas-Fort Worth Metroplex, Texas. Other ...

Regulatory Affairs Manager

Concord, NC · On-site +1

$85K - $141K/yr

We are seeking a Regulatory Affairs Manager. We are seeking a Regulatory Affairs Manager. This is a remote, work-from-home position, preferably based in the Dallas-Fort Worth Metroplex, Texas. Other ...

Provide Regulatory Affairs support during internal and external audits * Responsible for communicating business related issues or opportunities to next management level * Responsible for following ...

Regulatory Affairs Manager

Los Angeles, CA · On-site +1

$85K - $141K/yr

We are seeking a Regulatory Affairs Manager. We are seeking a Regulatory Affairs Manager. This is a remote, work-from-home position, preferably based in the Dallas-Fort Worth Metroplex, Texas. Other ...

The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic products, including FDA 510(k), CLIA categorization/waiver activities, and other applicable regulatory ...

New

The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic products, including FDA 510(k), CLIA categorization/waiver activities, and other applicable regulatory ...

The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic products, including FDA 510(k), CLIA categorization/waiver activities, and other applicable regulatory ...

The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic products, including FDA 510(k), CLIA categorization/waiver activities, and other applicable regulatory ...

New

$120 - $180/hr

Provides Regulatory Affairs support during internal and external audits. * Communicates business related issues or opportunities to next management level. * Follows all Company guidelines related to ...

Symmetrio is recruiting for our client for a Regulatory Affairs Manager to lead U.S. regulatory strategy and submissions for innovative healthcare software products. This role will focus on FDA 510(k ...

Showing results 21-40

Regulatory Affairs Manager information

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$28

$56

$86

How much do regulatory affairs manager jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for regulatory affairs 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 does a regulatory affairs manager do?

A Regulatory Affairs Manager oversees the process of ensuring that a company’s products comply with all regulations and laws applicable to their industry, such as pharmaceuticals, medical devices, or food. They coordinate the preparation and submission of regulatory documents to government agencies and serve as a liaison between the company and regulatory authorities. Their role includes monitoring changes in regulations, developing strategies for approval, and ensuring ongoing compliance throughout the product lifecycle.

What does a regulatory affairs manager do?

As a regulatory affairs manager, your responsibilities entail ensuring that your employer observes all relevant laws and regulations. You can find employment in various sectors, including pharmaceutical, healthcare, and manufacturing industries. Your duties include compiling all necessary paperwork, evidence, and documentation to report to regulatory authorities. In addition to the management of paperwork and legal requirements, you help companies make operational and strategic decisions based on the regulations they are obligated to follow. You sometimes perform or coordinate audits to ensure compliance, and, in a large company, you oversee a staff of compliance specialists who handle various regulatory affairs tasks.

What are some common challenges faced by regulatory affairs managers when working with cross-functional teams?

Regulatory Affairs Managers often encounter challenges in aligning regulatory requirements with the goals of other departments, such as R&D, marketing, and manufacturing. Navigating differing priorities and timelines can be complex, especially when ensuring compliance without delaying product development. Effective communication and negotiation skills are essential to bridge gaps between teams, clarify regulatory expectations, and facilitate smooth collaboration. By proactively engaging stakeholders and providing regulatory guidance early in projects, Regulatory Affairs Managers can help teams work together more efficiently and avoid costly compliance issues.

What are the key skills and qualifications needed to thrive as a regulatory affairs manager, and why are they important?

To thrive as a Regulatory Affairs Manager, you need a comprehensive understanding of regulatory guidelines, scientific or technical expertise, and typically a degree in life sciences or a related field. Experience with submission management systems, regulatory databases, and knowledge of global regulatory frameworks (such as FDA, EMA, or ICH) are highly valuable. Strong attention to detail, communication skills, and the ability to manage cross-functional teams distinguish top performers in this role. These competencies are crucial for ensuring product compliance, minimizing approval risks, and facilitating smooth market entry.

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

AspectRegulatory Affairs ManagerRegulatory Affairs Specialist
CredentialsBachelor's degree, often advanced certifications (e.g., RAC)Bachelor's degree, entry-level certifications
Work EnvironmentOversees teams, strategic planning, cross-department collaborationExecutes regulatory submissions, document preparation, detailed compliance tasks
Industry UsageUsed in pharmaceutical, biotech, medical device companies for leadership rolesCommonly found in similar industries, focusing on technical regulatory tasks
Search & Comparison IntentUnderstanding managerial responsibilities and scopeFocus on specific regulatory tasks and compliance details

The Regulatory Affairs Manager typically holds a leadership role, overseeing regulatory strategies and teams, while the Regulatory Affairs Specialist handles detailed compliance work and documentation. Both roles require relevant certifications and are essential in regulated industries like pharma and medical devices.

What cities are hiring for Regulatory Affairs Manager jobs?

Cities with the most Regulatory Affairs Manager job openings:

What are the most commonly searched types of Regulatory Affairs jobs?

The most popular types of Regulatory Affairs jobs are:

Who are the top companies hiring for Regulatory Affairs Manager jobs?

The top employers for Regulatory Affairs Manager jobs are:

What states have the most Regulatory Affairs Manager jobs?

States with the most job openings for Regulatory Affairs Manager jobs include:

Infographic showing various Regulatory Affairs Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $118,493 per year, or $57 per hour.

Regulatory Affairs Manager

RXinsider LTD.

Dallas, TX • On-site

$85 - $142/hr

Other

Posted 17 days ago


Job description

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve – we care.

What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.

We are seeking a Regulatory Affairs Manager. We are seeking a Regulatory Affairs Manager. This is a remote, work-from-home position, preferably based in the Dallas–Fort Worth Metroplex, Texas. Other locations considered are: Arkansas, Illinois, Kansas, Louisiana, Mississippi, Missouri, Oklahoma.

This role’s primary responsibility is to support the regional Director of Regulatory Affairs (DRA) by conducting customer due diligence assessments focused on McKesson’s U.S. Pharmaceutical Distribution accounts and in accordance with McKesson’s Controlled Substances Monitoring Program (CSMP). This will require interaction and partnership with internal teams, report writing and data analysis, and interaction with DRAs to evaluate findings from the aforementioned activities.

Key Responsibilities
  • Conduct customer site visits as necessary to support CSMP processes.
  • Perform customer due diligence reviews that include assessments of prospective customers and ongoing assessments of current customers.
  • Review and analyze data to support due diligence efforts and identify/validate controlled substance trends and sourcing profiles.
  • Prepare written reports to document reviews and statistical analysis.
  • Engage with account managers and customers, as well as internal team personnel as needed to support the CSMP process.
  • Drive CSMP process awareness and communication with Sales and individual Account Managers.
  • Seek opportunities to improve CSMP operational excellence through people, processes, or technology.
Minimum Requirement

Degree or equivalent and typically requires 4+ years of relevant experience.

Education

Four‑year degree in a related field or equivalent experience

Critical Skills
  • 4+ years of experience managing regulatory compliance in the pharmaceutical supply chain, with a focus on controlled substance compliance (Pharmacy, DEA experience, or law enforcement background preferred).
  • Strong ability to learn quickly and adapt in fast‑paced environments.
  • Proven collaboration skills across cross‑functional teams.
  • In‑depth knowledge of retail pharmacy operations, controlled substance compliance, and diversion control programs.
  • Expertise in making data‑driven, strategic decisions based on thorough analysis.
  • Excellent relationship‑building and people engagement skills.
  • Working knowledge of Federal and State regulations related to controlled substance compliance.
  • Proficiency in MS Office (Word, PowerPoint, Excel).
Additional Skills
  • Excellent communication, collaboration, and influencing skills at all levels of the organization.
  • Proficient interviewing and technical writing skills, attention to detail.
  • Strong Analytical Skills.
  • Experience with Tableau, SAP, and Salesforce.
  • Results Orientation and Energy.
  • Building Relationships.
  • Mature Confidence and Integrity.
  • Assertiveness and Influence.
Physical Requirements
  • Traditional office requirements. A large percentage of time performing computer‑based work is required.
  • 10% travel for client visits.

This role is a hybrid position if you live near DFW. The selected candidate is expected to work on‑site at our Las Colinas office a minimum of two (2) days per week, with the remaining days worked remotely. Specific in‑office days may be designated based on team needs and business priorities.

Work Authorization

Must be authorized to work in the U.S. Sponsorship is not available for this position

We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long‑term incentive opportunities may be offered.

Our Base Pay Range for this position

$85,100 - $141,800

McKesson is an Equal Opportunity Employer

McKesson provides equal employment opportunities to applicants and employees, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other legally protected category. For additional information on McKesson’s full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.

McKesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to (United States) Disability_Accommodation@McKesson.com or (Canada) Accessibility@mckesson.ca. Resumes or CVs submitted to this email box will not be accepted.

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