Associate Director, Manufacturing Science & Technology

Associate Director, Manufacturing Science & Technology

Location: Philadelphia area preferred/Remote

About Veradermics

Founded in 2019, Veradermics, Incorporated (NYSE: MANE) is a well-funded, publicly listed company that offers the opportunity to work in a performance-driven, highly dynamic environment. At Veradermics, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.

Veradermics is a dermatologist-founded, late clinical-stage biopharmaceutical company focused on developing innovative therapeutics for common aesthetic and dermatological conditions.

Veradermics lead product candidate, VDPHL01, is as an oral, non-hormonal treatment for men and women with pattern hair loss (PHL). We are currently conducting three Phase 3 clinical trials as we work to deliver potentially transformative solutions and aspire to redefine the standard of care in dermatology. Learn more here.

At Veradermics, we combine scientific rigor with a vision for impactful innovation to make a lasting difference in the lives of patients.

Why Work at Veradermics

• You Can Be Part of a Meaningful Mission: Veradermics aims to become a leader in medical dermatology by bringing pharmaceutical innovation to the treatment of common skin conditions to improve the lives of patients.
• Veradermics is Growing: Veradermics is a dynamic and growing company; we are advancing our VDPHL01 Phase 3 clinical trials and preparing for commercialization. PHL affects approximately 80 million people in the U.S. alone.
• The Veradermics Culture: We are an innovative, collaborative, hard-working and performance-driven company that values the contributions of our employees and keeps our focus on patients
• We have been featured in Forbes, Allure, Marie Claire, Bazaar, Dermatology Times, the Slate, The New York Post, The Hartford Courant, The Kansas City Star, and other multi-media platforms.

Position Overview

The Associate Director, Manufacturing Science and Technology will play a critical role in supporting the successful transfer, scale-up, validation, and ongoing performance of drug product manufacturing processes. This individual will serve as a technical expert who ensures robust, compliant, and efficient manufacturing throughout the product lifecycle, partnering closely with contract manufacturing organizations and internal cross-functional teams.

Key Responsibilities

• Develop and maintain technical and business relationships with respective CMOs.
• Participate in the technology transfer of processes and analytical methods between contract manufacturing organizations for a pre-commercial drug product.
• Evaluate scale-up, equipment capabilities, and process parameters, and design manufacturing research studies to demonstrate equivalent performance.
• Evaluate the impact of raw material changes and design manufacturing research studies to demonstrate equivalent performance.
• Provide product expertise to CMOs during manufacturing campaigns, including assistance with troubleshooting.
• Develop and maintain process documentation, including batch records, control strategies, and technical protocols.
• Support process validation activities (PPQ), continued process verification (CPV), and lifecycle management.
• Provide on-the-floor technical support during manufacturing campaigns and resolve process-related challenges.
• Perform risk assessments, such as FMEA, for manufacturing processes, equipment, raw materials, and suppliers.
• Conduct root cause analysis, support deviations, and implement CAPAs.
• Analyze process data using statistical tools, including DOE, SPC, and multivariate analysis.
• Contribute to regulatory filings, including IND, NDA, and BLA submissions, and support regulatory inspections.
• Collaborate closely with R&D, Quality, Operations, Engineering, and Supply Chain partners.

CandidateProfile|WhoYouAre

• MS or PhD in Chemical Engineering, Pharmaceutical Sciences, Chemistry, Biochemical Engineering, or related field; BS with relevant industry experience will be considered.
• 5-15+ years of experience in pharmaceutical manufacturing, MS&T, or process development.
• Strong understanding of cGMP, process validation principles, and ICH guidelines, including Q8-Q11.
• Experience with statistical software, such as JMP or Minitab, and data-driven decision-making.
• Solid knowledge of unit operations relevant to Veradermics' product modalities, including OSD, blending, compression, and packaging.
• Experience with domestic and global tech transfers and commercial manufacturing support.
• Familiarity with QbD principles, PAT tools, or advanced process modeling.
• Demonstrated ability to lead cross-functional technical projects.
• Strong communication, documentation, and problem-solving skills.

CompanyCulture

Veradermics is a small, tight-knit, high-performing team that works with urgency, positivity, and a deep sense of ownership. We set an exceptionally high bar for ourselves and seek someone who is energized by playing an integral role in a fast-moving organization at a pivotal moment in our trajectory—bringing curiosity, clarity, and a drive to get things done at the highest level.

We value strong organization, thoughtful collaboration, and genuine investment in team success. Honest, direct communication is central to how we work and grow together. Accomplishing our collective goals will be fun but also complex.

Location and Travel:

• Location: Philadelphia area preferred/Remote
• Travel: 30%

Salary and Benefits

Veradermics provides a comprehensive compensation package that includes a base salary, annual performance bonus eligibility, and access to the employee stock option plan.

Robust benefits package, including health coverage, retirement benefit matching, dependent care FSA, and unlimited paid time off.

EqualOpportunityEmployer

Veradermics is an equal opportunity employer. All employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, or age.