Director, CMC External Manufacturing

praxisprecisionmedicines; United States; Remote; USD 210,000 - 320,000; Full time

Job summary

Praxis Precision Medicines seeks a Directors External Manufacturing (CMC) to lead outsourced manufacturing across CDMOs for API and drug product. The role ensures compliant, on‑time clinical supply and commercial readiness, while driving supplier performance and cost efficiency.

You will partner with Process Chemistry, Formulation, Analytical, Quality, and Regulatory teams, shaping development strategies and aligning them with clinical timelines and regulatory expectations.

Qualifications

• 15+ years of CMC or manufacturing experience in biopharma.
• ≥8 years managing external manufacturing relationships (CDMOs).
• 10+ years of small molecule experience.
• Strong understanding of GMP, GDP, and ICH guidelines in a commercial setting.
• Experience overseeing drug substance and drug product manufacturing at clinical/commercial scale.

Responsibilities

• Lead strategy, selection, and management of CDMOs for drug substance and drug product.
• Serve as primary interface between Praxis and external manufacturing partners.
• Oversee technology transfer, process scale‑up, validation, and clinical supply readiness.
• Establish and maintain Quality and Technical Agreements with partners.
• Manage end‑to‑end supply chain including procurement, production planning, logistics and inventory.

Skills

Strategic leadership

Vendor management

Contract negotiation

Program management

Education

Advanced degree in Chemistry/ Chemical Engineering/ Pharmaceutical Sciences

Job description

Location:

This position may be performed remotely, but requires the flexibility and willingness to travel as needed.

The Opportunity

The Director, External Manufacturing (CMC) will lead and manage outsourced manufacturing operations supporting Praxis's clinical and future commercial programs. This role will oversee Contract Development and Manufacturing Organizations (CDMOs) responsible for drug substance (API) and drug product manufacturing, ensuring high-quality, compliant , and timely supply of clinical materials. The ideal candidate is a strategic, hands‑on CMC leader experienced in managing external partnerships and driving operational excellence in a dynamic biotech environment.

Primary Responsibilities

External Manufacturing Oversight

• Lead the strategy, selection, and management of CDMOs for both drug substance and drug product manufacturing.
• Serve as the primary operational interface between Praxis and external manufacturing partners.
• Oversee technology transfer, process scale‑up, validation, and clinical supply readiness.
• Establish and maintain robust Quality and Technical Agreements with manufacturing partners.
• Manage and optimize the end‑to‑end supply chain process, including raw materials procurement, production planning, logistics, inventory management, and distribution.
• Lead supplier qualification, monitoring, and performance evaluations, addressing risks and identifying opportunities for improvement.
• Negotiate contracts and pricing agreements with suppliers and CMOs to achieve cost‑effective outcomes while maintaining supply security.

CMC Operations and Program Support

• Collaborate closely with Process Chemistry, Formulation, Analytical, Quality, and Regulatory teams to ensure seamless execution of CMC deliverables.
• Support CMC development strategies aligned with clinical timelines, regulatory expectations, and company objectives.
• Manage manufacturing planning, scheduling, and inventory to ensure uninterrupted clinical supply.

Governance, Compliance, and Continuous Improvement

• Ensure all outsourced manufacturing is performed under appropriate GMP and regulatory standards.
• Implement key performance indicators (KPIs) and governance mechanisms to monitor and improve CDMO performance.
• Proactively identify and mitigate technical and operational risks across the external supply network.
• Drive operational excellence and process improvements to enhance efficiency and compliance.

Qualifications and Key Success Factors

• Advanced degree preferred in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related field; bachelor's degree with extensive relevant experience considered.
• 15+ years of progressive CMC or manufacturing experience within the biopharmaceutical industry, including ≥8 years managing external manufacturing relationships.
• 10+ years of small molecule experience.
• Proven experience in managing global CMC supply chains for commercial products in a regulated environment. Includes strong understanding of GMP, GDP, and ICH guidelines and their application in a commercial setting.
• Demonstrated experience overseeing both drug substance and drug product manufacturing at clinical and/or commercial scale.
• Excellent negotiation and vendor management abilities including experience working with CMOs and managing third‑party relationships.
• Proven ability to manage complex projects and external relationships with technical and business acumen.
• Ability to navigate complex regulatory and compliance requirements.

The physical and mental requirements of our roles include but are not limited to regular use of a computer, devices or other office equipment, clear communication, and occasional movement. You'll need comfort with screen work, basic hand coordination, and focus. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.

Compensation & Benefits

At Praxis, we believe that taking care of our people (and their people) is important, so we provide a world class benefits package to help you thrive. This includes 99% of the premium paid for medical, dental and vision plans. We also provide company-paid life insurance, AD&D, disability benefits, and voluntary plans to personalize your coverage. Thinking about the future? We match dollar-for-dollar up to 6% on eligible 401(k) contributions and sweeten the deal with long‑term stock incentives and ESPP. We provide a discretionary quarterly bonus, an extremely flexible wellness benefit, generous PTO, paid holidays and company-wide shutdowns. Not to mention, you'll also be joining a phenomenal crew of colleagues who are smart, engaged and inspiring. We aim high, collaborate hard, and produce results. Let’s achieve the impossible together!

To round out our world-class total rewards package, we provide annualized base salary in the range listed below. This range reflects the base salary the Company reasonably expects to pay for the position at the time of posting. Placement with