LEAD THE SCIENCE. DRIVE THE STRATEGY. SHAPE THE FUTURE.

As Vice President (VP), Chemistry, Manufacturing, and Control (CMC), you’ll be at the forefront of developing and advancing drugs, biologics, and medical devices. You’ll guide everything from formulation and scale-up to regulatory submissions and Health Authority interactions, making you the trusted expert who helps bring breakthrough therapies to patients faster. It’s your chance to influence global development, mentor top talent, and make a lasting impact on the industry.

ABOUT YOU

Are you a seasoned CMC expert who blends scientific depth with strategic vision? Are you confident in leading regulatory interactions and solving complex challenges? If you thrive on collaboration and take pride in guiding therapies from development to patients, you will thrive here.

To be successful we are looking for the following traits and behaviors:

• Advanced scientific and regulatory knowledge of drug, biologic, or device development
• Critical thinking and analytical skills, financial acumen, influencing and leading teams, risk assessment, problem solving skills, decision making, strong written and verbal communication skills in English
• Requires a B.S., R.Ph., M.S., Ph.D., or equivalent degree, in a scientific area, and equivalent combination of relevant experience in drug, biologic, or device development
• 15 years’ post-degree of directly relevant experience in drug, biologic, or device development desirable

ABOUT THE ROLE

As VP, CMC, you’ll not only lead critical interactions with global Health Authorities and shape submission strategies, but also mentor teams, provide technical leadership, and serve as a trusted advisor across multiple projects. This is your opportunity to combine scientific expertise, regulatory insight, and leadership to directly accelerate life-changing therapies. This is an exciting contractor position rather than a permanent role.

YOUR MAIN RESPONSIBILITIES WILL INCLUDE BUT NOT LIMITED TO:

• Lead Regulatory Writing & Strategy: Write, review, and guide CMC documents and submissions with accuracy and insight.
• Shape Product Development: Influence strategies and plans from early development through post-approval.
• Engage with Health Authorities: Lead meetings, prepare briefing packages, and serve as the expert voice in regulatory interactions.
• Provide Scientific Leadership: Share expertise in CMC, compliance, and audits while mentoring teams and supporting client success.
• Drive Collaboration & Solutions: Partner with clients and cross-functional teams to solve challenges and deliver innovative outcomes.