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Regulatory Director Jobs (NOW HIRING)

Director, Regulatory Affairs

Hatfield, PA

$151.50K - $200K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Frisco, TX

$140.60K - $185.60K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Redwood City, CA

$183.70K - $242.40K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Birmingham, AL

$140.60K - $185.60K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Union City, GA

$145K - $191.40K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Pierre, SD

$149.50K - $197.30K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Redmond, WA

$168K - $221.70K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Fort Smith, AR

$128.10K - $169.20K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Rockville, MD

$152.90K - $201.80K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Norfolk, VA

$145.10K - $191.60K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

The Director, Regulatory Compliance will build upon NRG's existing trade compliance program continuing the development and implementation of a first-class program. NRG's trading operation is ...

Position Summary The Director, Regulatory Affairs will support the development and execution of domestic and international regulatory strategy for Codera. This position involves planning, preparing ...

Director, Regulatory Affairs

Sarasota, FL · On-site

$144.60K - $190.80K/yr

The Director of Regulatory Affairs provides strategic leadership and oversight for all food safety regulatory compliance and policy matters within the company. This role ensures that all products ...

Director, Regulatory Affairs

Williamsport, PA

$136K - $179.50K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Boston, MA

$163K - $215.10K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

New Orleans, LA

$138.30K - $182.60K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Boise, ID

$142.80K - $188.50K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Billings, MT

$147.60K - $194.90K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

Director, Regulatory Affairs

Bradenton, FL

$136K - $179.50K/yr

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This ...

New

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Showing results 1-20

Regulatory Director information

See salary details

$91K

$176.2K

$248.5K

How much do regulatory director jobs pay per year?

As of May 28, 2026, the average yearly pay for regulatory director in the United States is $176,150.00, according to ZipRecruiter salary data. Most workers in this role earn between $150,000.00 and $198,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Regulatory Director, and why are they important?

To thrive as a Regulatory Director, you need deep expertise in regulatory affairs, compliance frameworks, and industry-specific regulations, typically supported by an advanced degree in law, science, or a related field. Familiarity with regulatory submission systems, document management tools, and certifications such as RAC (Regulatory Affairs Certification) are highly valued. Strong leadership, strategic thinking, and effective communication enable you to navigate complex regulations and lead cross-functional teams. These skills ensure timely product approvals, mitigate compliance risks, and support organizational growth in highly regulated industries.

How does a Regulatory Director typically collaborate with cross-functional teams to ensure compliance across the organization?

A Regulatory Director works closely with departments such as legal, quality assurance, research and development, and marketing to interpret and apply relevant regulations throughout the product lifecycle. They lead or participate in cross-functional meetings to provide regulatory guidance, address compliance risks, and help teams prepare for audits or submissions. This collaboration ensures that all departments are aligned with regulatory standards, minimizing risks and supporting smooth market access. Effective communication and negotiation skills are essential, as the Regulatory Director often acts as a bridge between technical teams and regulatory agencies.

What is a Regulatory Director?

A Regulatory Director is a senior professional responsible for overseeing and managing a company's compliance with regulations and laws relevant to its industry. They develop regulatory strategies, ensure products and processes meet legal standards, and often interact with government agencies. Their role is critical in industries like pharmaceuticals, finance, and healthcare, where regulations are complex and constantly evolving. Regulatory Directors also guide teams, provide regulatory advice during product development, and help minimize business risks associated with non-compliance.

What is the difference between Regulatory Director vs Regulatory Manager?

AspectRegulatory DirectorRegulatory Manager
ResponsibilitiesOversees regulatory strategies, compliance policies, and interacts with senior leadershipManages daily regulatory activities, ensures compliance, and implements policies
Required CredentialsTypically requires advanced degrees and extensive regulatory experienceRequires relevant certifications and several years of experience
Work EnvironmentStrategic, leadership-focused, often in corporate or global settingsOperational, team-oriented, often in specific departments or regions

The Regulatory Director focuses on strategic oversight and high-level compliance initiatives, while the Regulatory Manager handles daily regulatory operations and team management. Both roles require regulatory knowledge, but the director position involves broader leadership responsibilities.

More about Regulatory Director jobs
What cities are hiring for Regulatory Director jobs? Cities with the most Regulatory Director job openings:
What are the most commonly searched types of Regulatory jobs? The most popular types of Regulatory jobs are:
What states have the most Regulatory Director jobs? States with the most job openings for Regulatory Director jobs include:
Infographic showing various Regulatory Director job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 84% Full Time, 14% Part Time, and 1% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $176,150 per year, or $84.7 per hour.
Director, Regulatory Affairs

Director, Regulatory Affairs

Bausch + Lomb

Hatfield, PA

$151.50K - $200K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday


Bausch & Lomb rating

8.4

Company rating: 8.4 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

47th of 511 rated manufacturers


Job description

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the worldfrom the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.

Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

The Director, Regulatory Affairs leads global regulatory strategy, reporting, compliance, labeling, and regulatory intelligence to support product development, approval, and market expansion. This role provides regulatory leadership for ophthalmology drug and combination product programs from early development through registration and global launch, using a U.S.-led approach aligned with key exU.S. regions.The Director partners crossfunctionally with Clinical, Nonclinical, CMC, Quality, Safety, and Regulatory Operations to develop global regulatory strategies, lead health authority interactions, ensure highquality submissions, and manage regulatory risk across the product lifecycle. Responsibilities include preparation for and leadership of health authority meetings (e.g., preIND, endofphase, preNDA/BLA).The Director, Regulatory Affairs typically includes people and/or matrix leadership of regulatory teams and external vendors.

Responsibilities:

  • Define and execute global regulatory strategies for ophthalmology drug and combination product programs, aligned with development, CMC, and commercial objectives.
  • Provide guidance and direction regarding regulatory strategy to department.
  • Interpret Regulatory Authority policies and guidance and correctly apply them as appropriate in product development and labeling regulatory activities.
  • Drive innovative strategies to enable successful regulatory submissions and improve the probability of approval.
  • Point of contact with Health Authorities and ability to manage the relationship with Health Authorities as assigned.
  • Develop and mentor team of individual contributors/subject matter experts.
  • Provide input to regulatory budget process.

Qualifications:

  • Bachelors degree required; advanced degree (Masters, PhD, PharmD) preferred
  • 10-15+ years in Regulatory Affairs or relevant experience in a regulated environment
  • Global portfolio management and strategy experience and strong familiarity with registration requirements in exU.S. regions.
  • RAPS certification desired

Specific Skills:

  • Deep understanding of regulatory authority policies, processes, and information systems, with the ability to apply them to product development, labeling, and pre and postmarket submissions.
  • Strong scientific and analytical skills to critically evaluate data, technical arguments, and risk, serving as a regulatory subject matter expert internally and externally.
  • Strategic mindset with strong business acumen to anticipate regulatory changes, make riskbased recommendations, and drive successful approvals while minimizing business impact.
  • Proven leadership and people management abilities, including coaching and mentoring, influencing crossfunctional teams, and providing strategic direction beyond direct reporting lines.
  • Excellent communication, organizational, and writing skills, with strong attention to detail and document accuracy.
  • Demonstrated ability to manage multiple priorities, coordinate resources, meet tight deadlines, and work independently in a fastchanging environment.
  • Strong interpersonal and influencing skills to engage internal and external stakeholders, including key opinion leaders, advisory boards, and advocacy groups.
  • Commitment to teamwork, continuous learning, process improvement, operational excellence, and performance metrics.

We offer competitive salary & excellent benefits including:

  • Medical, Dental, Eye Health, Disability and Life Insurance begins on your hire date
  • 401K Plan with company match and ongoing company contribution
  • Paid time off vacation (3 weeks - prorated upon hire), floating holidays and sick time
  • Employee Stock Purchase Plan with company match
  • Employee Incentive Bonus
  • Tuition Reimbursement (select degrees)
  • Ongoing performance feedback and annual compensation review

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

For U.S. locations that require disclosure of compensation, the starting pay for this role is between $165,000.00 and $220,000.00. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors.

U.S. based employees may be eligible for short-term and/or long-term incentives. They may also be eligible to participate in medical, dental, vision insurance, disability and life insurance, a 401(k) plan and company match, a tuition reimbursement program (select degrees), company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive sick time, floating holidays and paid vacation.

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.

To learn more please read Bausch + Lomb's Job Offer Fraud Statement (https://performancemanager.successfactors.eu/doc/custom/BauschLomb/Bausch_job_posting_statement.docx) .

Our Benefit Programs:Employee Benefits: Bausch + Lomb (https://www.bausch.com/careers/benefits/)

Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.


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About Bausch & Lomb

Sourced by ZipRecruiter

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world--from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better. Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers across the full spectrum of their eye health needs throughout their lives. Our iconic brand is built on the deep trust and loyalty of our customers established over our nearly 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 12,500 employees and a presence in approximately 100 countries, extending our reach to billions of potential customers across the globe. We have long been associated with many of the most significant advances in eye health, and we believe we are well positioned to continue leading the advancement of eye health in the future.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Bridgewater, NJ, US

Year founded

1853