Global Leader, Injectable Aesthetics Regulatory Strategy

Galderma Laboratories; Newport Beach (CA); On-site; USD 260,000 - 365,000; Full time

Benefits offered by this job

Competitive benefits

Annual incentive opportunities

401(k) plan with employer match

Job summary

Galderma Laboratories in the United States seeks a Global Head of Injectable Aesthetics Regulatory Strategy to lead the Regulatory Affairs Injectable Aesthetics team and shape regulatory strategies for neurotoxins, fillers and devices. The role drives timely approvals and ongoing compliance across product lifecycles.

You will guide submissions, manage agency interactions, and work with Global R&D and commercial teams to support product development and market launches.

Qualifications

• Bachelor's degree from a four-year university is required.
• Advanced degree preferred.
• Minimum of twenty (20) years of experience in Pharmaceutical Regulatory Affairs is required.
• Minimum of ten (10) to fifteen (15) years of experience in reviewing clinical and nonclinical data for advertising and promotion.
• Extensive knowledge of regulations for prescription drugs and medical devices.

Responsibilities

• Lead the development and execution of regulatory strategies for injectable aesthetics to ensure timely approvals.
• Oversee and input to submissions supporting clinical research and marketing applications.
• Act as global subject matter expert guiding local and international partners.
• Manage regulatory requirements for acquisitions and new product development.
• Drive innovation and optimize cross-functional collaboration and communications.

Skills

Regulatory strategy

Leadership

Cross-functional collaboration

Regulatory guidance

Regulatory agency liaison

Education

Bachelor's degree

Advanced degree preferred

Job description

Galderma Laboratories in the United States seeks a Global Head of Injectable Aesthetics Regulatory Strategy to lead the Regulatory Affairs Injectable Aesthetics team and shape regulatory strategies for neurotoxins, fillers and devices. The role drives timely approvals and ongoing compliance across product lifecycles.

You will guide submissions, manage agency interactions, and work with Global R&D and commercial teams to support product development and market launches.