Director / Senior Director, CMC Drug Product jobs in United States
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Crescent Biopharma · 1 day ago

Director / Senior Director, CMC Drug Product

Crescent Biopharma is focused on building a leading oncology company with innovative therapies for cancer patients. The role involves overseeing formulation development, drug product development, and manufacturing for biologics and ADCs, while providing technical leadership and ensuring alignment with regulatory goals.

BiotechnologyHealth CareMedical Device

Responsibilities

Lead formulation, DP development, and manufacturing strategy for biologics and ADCs
Direct DP efforts from early phase development through process characterization, validation and commercial launch
Provide technical guidance across liquid, lyophilized, and high-concentration DP formats
Oversee CDMO DP manufacturing operations and function as the primary point of contact
Monitor development, MSAT, and manufacturing timelines ensuring alignment with program objectives
Serve as a key subject matter expert contact for both internal teams and external partners
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
Champion a collaborative, diverse, and inclusive team environment

Qualification

Formulation developmentDrug product developmentCDMO oversightGMP complianceBiologics experienceADCs experienceRegulatory submissionsLeadership skillsCommunication skillsProblem-solving

Required

Ph.D., M.S., or B.S. in Biochemistry, Chemistry, Bioengineering, Biotechnology, Chemical Engineering, or related field
At least 8 years' experience in formulation development, DP development, and external CDMO manufacturing
Demonstrated leadership in manufacturing development, including hands-on experience and person-in-plant exposure
Expertise in developing liquid, lyophilized, and high-concentration drug product formulations
Comprehensive understanding of 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

Preferred

Experience working with ADCs is highly preferred

Benefits

100% employer-paid benefits package.
Flexible PTO.
Two, one-week company-wide shutdowns each year.
Medical, dental, vision, life insurance, short- and long-term disability.
401(k)
Unlimited PTO
10 days per calendar year
Holiday pay, including two Company shut downs
16 weeks within one year of the birth/adoption/foster care of a child
FMLA
Military Leave

Company

Crescent Biopharma

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Crescent Biopharma is a biotechnology firm focused on developing novel precision-engineered medicines.

Funding

Current Stage
Public Company
Total Funding
$585M
Key Investors
Fairmount Funds Management
2025-12-04Post Ipo Equity· $185M
2025-06-16Post Ipo Equity· $200M
2025-06-16IPO
Company data provided by crunchbase