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Bausch + Lomb

Director, Regulatory Affairs

OR · On-site +1

$140K - $185K/yr

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

McKesson

Sr. Director, Regulatory Affairs

Richmond, VA · Hybrid

$148K - $195K/yr

The Sr. Director of Regulatory Affairs leads the development and execution of regulatory strategies ... Regulatory Intelligence & Sensing * Create programs to monitor the evolving regulatory landscape ...

Icon plc

Director, Regulatory Affairs

Blue Bell, PA

$143K - $189K/yr

Director, Regulatory Affairs ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

Takeda

Director, Regulatory Site CMC

Boston, MA

$163K - $215K/yr

The Director Regulatory Site CMC ensures efficient and compliant management of regulatory change ... intelligence as well as regulations and guidelines. * Able to deal with issues of critical ...

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Director Regulatory Intelligence information

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$91K

$176.2K

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How much do director regulatory intelligence jobs pay per year?

As of Jun 11, 2026, the average yearly pay for director regulatory intelligence 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 Director of Regulatory Intelligence, and why are they important?

To thrive as a Director of Regulatory Intelligence, you need deep expertise in regulatory affairs, strategic analysis, and industry guidelines, often backed by an advanced degree in life sciences or law. Familiarity with regulatory databases, global compliance platforms, and relevant certifications like RAC is highly beneficial. Exceptional communication, leadership, and critical thinking skills set successful candidates apart by enabling effective cross-functional collaboration and proactive risk management. These skills ensure that organizations stay ahead of regulatory changes, maintain compliance, and achieve business objectives in dynamic markets.

What is the difference between Director Regulatory Intelligence vs Regulatory Affairs Manager?

AspectDirector Regulatory IntelligenceRegulatory Affairs Manager
Required CredentialsBachelor's or Master’s in Life Sciences, Regulatory Affairs Certification (RAC)Bachelor's or Master’s in Life Sciences, Regulatory Affairs Certification (RAC)
Work EnvironmentStrategic, cross-functional teams, senior managementOperational, project management, compliance-focused
Employer & Industry UsagePharmaceutical, biotech, healthcare companiesPharmaceutical, biotech, healthcare companies
Search & Comparison IntentUnderstanding strategic regulatory rolesManaging regulatory submissions and compliance

The main difference is that the Director Regulatory Intelligence focuses on analyzing and interpreting regulatory trends to inform strategic decisions, while the Regulatory Affairs Manager handles day-to-day regulatory submissions and compliance activities. Both roles require similar credentials and are common in the pharmaceutical and biotech industries, but they differ in scope and strategic versus operational focus.

How does a Director of Regulatory Intelligence typically collaborate with cross-functional teams within an organization?

A Director of Regulatory Intelligence regularly partners with departments such as clinical, legal, quality, and R&D to interpret and communicate evolving regulatory requirements. This collaboration ensures that all functions are aligned with current global regulations and that strategic decisions are informed by the latest intelligence. Effective teamwork is critical for anticipating regulatory changes, guiding product development, and maintaining compliance across markets. Strong communication and relationship-building skills are essential, as the role often involves leading cross-functional meetings and providing actionable insights to senior leadership.

What does a Director of Regulatory Intelligence do?

A Director of Regulatory Intelligence is responsible for monitoring, analyzing, and interpreting regulatory trends, policies, and changes that could impact their organization, particularly in highly regulated industries like pharmaceuticals or medical devices. They lead teams to gather intelligence on global regulations, assess the potential impact on business strategies, and advise leadership on compliance and risk management. This role often involves liaising with regulatory agencies, developing strategies to address regulatory challenges, and ensuring the company's products and operations remain compliant with current and emerging regulations.
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Director Regulatory Intelligence jobs near you
Infographic showing various Director Regulatory Intelligence job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% 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

OR • On-site, Remote

$140K - $185K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Bausch & Lomb rating

8.4

Company rating: 8.4 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

46th of 518 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 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 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 ex-U.S. regions. The Director partners cross-functionally with Clinical, Nonclinical, CMC, Quality, Safety, and Regulatory Operations to develop global regulatory strategies, lead health authority interactions, ensure high-quality submissions, and manage regulatory risk across the product lifecycle. Responsibilities include preparation for and leadership of health authority meetings (e.g., pre-IND, end-of-phase, pre-NDA/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 ex-U.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 post-market 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 risk-based recommendations, and drive successful approvals while minimizing business impact.
  • Proven leadership and people management abilities, including coaching and mentoring, influencing cross-functional 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 fast-changing 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.
Our Benefit Programs: Employee Benefits: Bausch + Lomb
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

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