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Director, Oral Drug Product Development
Biibhr
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About this role
About the Role
Biogen is seeking a Director, Oral Drug Product Development to provide scientific and strategic leadership for the development of small molecule oral drug products . This role leads s cie nt ifi c and en gin eering e ff orts supp orting formulation and process development across early- and late-stage programs . This t e chnical lead wil l d rive enabling technologies for typ ically low so lubil ity and lo w perm eabil ity compounds, clinical manufacturing readiness, technology transfer, and commercialization . The Director serves as a senior drug product leader and mentor on cross-functional CMC and asset teams, influencing development strategy, manufacturing readiness, and regulatory submissions. This role will also be responsible for managing external partnerships and advancing new technologies and workflows that strengthen Biogen’s oral drug product development capabilities.
What You’ll Do
• Lead formulation design, process development, manufacturability assessment, scale-up, technology transfer, and clinical manufacturing of small molecule oral dosage forms across all stages of development .
• Develop enabling formulation approaches for challenging compounds, including poorly soluble, poorly permeable, unstable, or complex molecules su ch as orally delivered pe pti des .
• Serve as the senior drug product representative on cross-functional CMC and asset teams, driving alignment across regulatory, quality, manufacturing, analytical, clinical pharmacology, DMPK, and external partner functions.
• Influence portfolio decisions through assessment of developability, manufacturability, biopharmaceutical performance, technical risk, and investment priorities.
• Champion technology transfer, clinical manufacturing readiness, and scale-up activities at internal and external manufacturing sites. Provide strategic oversight and establish manufacturing strategies.
• Mentor and develop scientists and engineers supporting oral drug product development.
• Oversee completion of drug product sections for regulatory submissions and related technical documentation.
• Identify and implement new formulation technologies, predictive tools, digital workflows, and best practices that improve development efficiency and portfolio execution.
Who You Are
You are an innovative scientific leader with a passion for advancing drug development processes through rigorous science and data-driven decision-making. You excel at transforming experimental findings into development strategies, using deep technical expertise and sound scientific judgment to solve complex drug product challenges. Your expertise drives you to develop cutting-edge solutions ensuring manufacturability, scalability, and readiness for commercialization. You thrive in collaborative environments, influencing strategic decisions, and fostering alignment across diverse functions. Your mentoring skills inspire teams to achieve excellence, while your forward-thinking approach maximizes Biogen's capabilities in oral drug product development.
Required Skills:
• PhD in Pharmaceutical Sciences, Chemical Engineering, Chemistry , or a related scientific discipline with a minimum of 1 2 years’ experience in oral drug product development.
• Demonstrated track record leading formulation and process development for oral solid dosage forms from early development through clinical manufacturing and/or late-stage development.
• Experience with scale-up, technology transfer, clinical manufacturing , and external manufacturing organizations.
• Strong knowledge of CMC development, regulatory expectations, technical documentation, and phase-appropriate development strategies.
• Proven ability to lead across functions, influence program strategy, manage technical risk, and communicate effectively with diverse stakeholders.
• Experience mentoring, developing , or leading scientists and engineers.
Preferred Skills:
• Deep e xpertise in enabling technologies such as amorphous solid dispersions, spray drying, hot-melt extrusion, lipid-based formulations, modified release, or particle engineering.
• Experience with late-stage development, commercial readiness, process characterization, or process validation.
• Experience supporting at least one NDA/MAA or commercial product and regulatory agency interaction experience .
• Strong understanding and hands on experience with oral solid dose manufacturing unit operations and manufacturability considerations.
• Experience implementing new technologies , digital tools, knowledge platforms, or best practices across multiple programs.
• Demonstrated success managing external CDMO/CMO relationships and technology transfer activities.
Job Level: Management Additional Information
The base compensation range for this role is: $188,000.00-$259,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being ; including, but not limited to: • Medical, Dental, Vision, & Life insurances • Fitness & Wellness programs including a fitness reimbursement • Short- and Long-Term Disability insurance • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31) • Up to 12 c
Salary insight
The midpoint of this range ($224k) is about 39% above the median disclosed salary for Boston roles listed on ForgeApply ($161k across 1,687 jobs).
Based on live postings with disclosed pay on ForgeApply; refreshed daily. Not an estimate of this employer's offer.
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