Director/Senior Director, Drug Product

United States·WalthamFull-timesenior

OtherDirector

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Overview

Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program,

Technical Tools

OtherDirector

Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X.

We are seeking an accomplished CMC professional to oversee drug product development, technology transfer, and external manufacturing for our pipeline of biologics and antibody drug conjugates. Within the Technical Operations Team, you will help build CMC strategy and deliver technical leadership across all stages of drug product development from IND-enabling activities through late-stage process validation and commercialization. In this role, you will bring extensive subject matter expertise along with a proven track record of effective program management and external CDMO oversight.

Lead DP development, technology transfer, and manufacturing operations for biologics and ADCs
Direct DP efforts and contribute to strategy for early phase development, tech transfer, process characterization, validation, and commercial launch
Provide technical subject matter guidance across liquid, lyophilized, and high-concentration DP formats
Oversee CDMO GMP DP manufacturing and MSAT operations functioning as the primary point of contact
Monitor development and manufacturing timelines ensuring alignment with program objectives
Serve as a key DP subject matter expert contact for both internal teams and external partners
Contribute to formulation development efforts working with CMC and Analytical Sciences teams
Partner with Quality Assurance to investigate manufacturing deviations
Prepare and review CMC sections for regulatory submissions (IND/IMPD/BLA)
Coordinate CMC activities with Quality, Regulatory, and Clinical functions to ensure alignment with development and regulatory goals
Promote continuous improvement and uphold GMP, data integrity, and compliance standards
Support budgeting, vendor selection, and contract management of CDMO partners
Embrace a collaborative, diverse, and inclusive team environment

Ph.D., M.S., or B.S. in Biochemistry, Chemistry, Bioengineering, Biotechnology, Chemical Engineering, or related field
At least 12 years of experience in DP development, MSAT, and external CDMO DP manufacturing
Demonstrated track record in DP manufacturing development, including hands-on technical skill, external CDMO management, and person-in-plant exposure
Deep knowledge of liquid, lyophilized, and high-concentration drug product development
Expertise in managing external CDMO teams from early phase development through late phase process characterization and validation
Thorough understanding of the interdependencies at the interface of DP with DS, AS, QC, supply chain, and QA
Prior experience working with ADCs is highly preferred
Comprehensive familiarity with GMP, ICH guidelines, and regulatory requirements for biologics and ADCs
A track record of innovation, problem-solving, and ability to deliver high-quality work supporting Company objectives
Outstanding communication and leadership skills, capable of influencing across organizational levels
Ability to excel in fast-paced environments and manage multiple priorities

Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environment.

Competitive compensation, including base salary, performance bonus, and equity.

100% employer-paid benefits package.

Flexible PTO.

Two, one-week company-wide shutdowns each year.

A commitment to your professional development, with access to resources, mentorship, and growth opportunities.

The salary range for this position is $250,000 to $285,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography.

Additional Description for Pay Transparency:

The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography. Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. Subject to the terms of their respective policies and date of hire, Employees are eligible for the following time off benefits: Vacation – Unlimited PTO; Sick time – 10 days per calendar year; Holiday pay, including two Company shut downs; Parental Leave – 16 weeks within one year of the birth/adoption/foster care of a child; FMLA; Military Leave. Additional information can be found - https://www.crescentbiopharma.com/careers/#benefits

Please note:

Crescent Biopharma is an Equal Opportunity Employer. We are committed to fostering a diverse, inclusive, and equitable workplace where all individuals are valued and respected. Employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, sexual orientation, national origin, disability, veteran status, or any other protected status.

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