Top 8 Director/director of formulation development cmc Jobs in Bronx Ny

Sr. Director/Director of Formulation Development CMC
EPM Scientific —New York, NY
- $200,000 - $260,000 a year
- 11+ years
- Continuous improvement
- Doctor of Philosophy
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Sr. Director/Director, CMC Lead
EPM Scientific —New York, NY
- $200,000 - $250,000 a year
- Remote
- 11+ years
- Doctor of Philosophy
- Senior level
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Director, CMC – Biologics & ADC
Pathos AI —New York, NY
- $210,000 - $250,000 a year
- Hybrid work
- Bachelor of Science
- Office
- 8 years
5d
Director, CMC – Biologics & ADC
Pathos —New York, NY
- $210,000 - $250,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Office
- 8 years
Quick Apply
5d
Senior Manager Clinical Drug Supply & Logistics
Regeneron —Armonk, NY
- $134,400 - $219,200 a year
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Health insurance
- Dental insurance
Director, CMC – Small Molecule Chemistry
Pathos AI —New York, NY
- $210,000 - $250,000 a year
- Hybrid work
- Bachelor of Science
- Office
- 8 years
5d
Director, CMC – Small Molecule Chemistry
Pathos —New York, NY
- $210,000 - $250,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Office
- 8 years
Quick Apply
5d
Associate Manager, Regulatory Affairs
Exeltis & Xiromed —Florham Park, NJ
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Writing skills
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5d

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Sr. Director/Director of Formulation Development CMC
EPM Scientific —New York, NY
Provide strategic and technical leadership across preformulation, formulation development, process development, scale-up, technology transfer, and GMP…
$200,000 - $260,000 a year
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Sr. Director/Director of Formulation Development CMC

EPM Scientific -
New York, NY

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Job Details

$200,000 - $260,000 a year

Qualifications

FDA submissions
Biotechnology
Developing new product formulations
Clinical development
Team leadership
Investigational new drug (IND) applications
Chemical scale-up projects
Pharmaceutical company experience
Vendor relationship management
Chemistry, manufacturing & controls
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Chemical new product development projects
Senior leadership
Pharmaceutical manufacturing facility experience

Full Job Description

Senior Director/Director, Formulation Development (Small Molecules)

New York City, NY

Position Summary:

We are with a leading Clinical Stage Biopharma who are seeking a Senior Director/Director of Formulation Development to lead all drug product development activities across a portfolio of small molecule programs. This individual will be responsible for developing and executing formulation strategies from preclinical development through commercialization, ensuring robust, scalable, and patient-centric drug products.

The successful candidate will serve as the formulation subject matter expert within the CMC organization and provide strategic leadership across preformulation, formulation development, process development, technology transfer, manufacturing, regulatory submissions, and lifecycle management activities. This role requires extensive collaboration with Process Chemistry, Analytical Development, Regulatory Affairs, Quality, Supply Chain, and external manufacturing partners.

Responsibilities:

Formulation Strategy & Leadership

Lead formulation and drug product development strategies supporting small molecule programs from IND-enabling studies through registration and commercialization.
Define phase-appropriate formulation approaches that balance clinical needs, manufacturability, regulatory expectations, and commercial considerations.
Guide dosage form selection and product presentation strategies to support program objectives and future lifecycle opportunities.
Develop integrated development plans, budgets, timelines, and risk mitigation strategies for drug product activities.

Drug Product Development & Manufacturing

Provide strategic and technical leadership across preformulation, formulation development, process development, scale-up, technology transfer, and GMP manufacturing.
Oversee development of oral solid dosage forms, including tablets, capsules, immediate-release, modified-release, and enabling formulations.
Drive formulation approaches for challenging compounds with solubility, bioavailability, stability, or manufacturability limitations.
Establish and maintain robust control strategies, specifications, and critical quality attributes aligned with regulatory expectations.
Support process validation, registration batches, and commercial launch readiness activities.

External Partner & CDMO Management

Lead selection, oversight, and governance of CDMOs, CROs, and external development partners.
Serve as the primary technical interface for outsourced drug product development and manufacturing activities.
Ensure external partners meet established quality, timeline, cost, and supply objectives.
Drive issue resolution, technical investigations, and risk mitigation strategies across partner networks.

Regulatory & Technical Support

Author, review, and approve CMC sections related to drug product development for INDs, IMPDs, CTAs, NDAs, and global regulatory submissions.
Support interactions with regulatory agencies and contribute to responses for health authority questions.
Ensure compliance with FDA, EMA, ICH, and other applicable global regulatory requirements.
Provide technical leadership during inspections, audits, and due diligence activities.

Cross-Functional Collaboration

Partner closely with Process Chemistry, Analytical Development, Regulatory Affairs, Quality Assurance, Supply Chain, Clinical Operations, and Commercial teams.
Serve as the formulation representative on cross-functional development teams and governance committees.
Communicate program progress, key risks, and development recommendations to senior leadership.
Support integrated CMC planning and execution across multiple development programs.

Organizational Leadership

Mentor and develop formulation scientists within the organization.
Foster a culture of scientific excellence, innovation, collaboration, and accountability.
Contribute to broader CMC organization strategy, capability development, and continuous improvement initiatives.
Support resource planning, budget forecasting, and portfolio prioritization activities.

Education, Experience & Qualifications:

Ph.D. or M.S. in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related scientific discipline.
12+ years (Director) or 15+ years (Senior Director) of experience within the pharmaceutical or biotechnology industry.
Significant experience leading formulation and drug product development for small molecule programs.
Demonstrated experience advancing compounds from preclinical or Phase I development through late-stage clinical development and commercialization.
Deep understanding of oral solid dosage formulation development, pharmaceutical manufacturing, scale-up, and commercialization.
Strong knowledge of biopharmaceutics principles, dissolution, bioavailability enhancement technologies, and product performance characterization.
Experience managing external CDMOs and development partners within an outsourced operating model.
Proven track record supporting successful IND, NDA, and global regulatory submissions.

Quick Apply

Refine Your Search

director/director of formulation development cmc jobs in bronx ny

Sr. Director/Director of Formulation Development CMC

Sr. Director/Director, CMC Lead

Director, CMC – Biologics & ADC

Director, CMC – Biologics & ADC

Senior Manager Clinical Drug Supply & Logistics

Director, CMC – Small Molecule Chemistry

Director, CMC – Small Molecule Chemistry

Associate Manager, Regulatory Affairs

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