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Director Drug Product Formulation Development Jobs in Ridgefield, CT

Principal Scientist

Darien, CT ยท On-site

$110K - $120K/yr

Independently lead the formulation design, development, optimization, and scale-up of hair care and styling products from ideation through commercialization * Apply advanced technical expertise in ...

CMC Technical Writer

Ridgefield, CT ยท On-site

$54 - $55.70/hr

We are seeking an experienced Analytical Subject Matter Expert (SME) and CMC Technical Writer to support external drug substance (DS) and drug product (DP) development programs within External ...

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Showing results 1-20

Director Drug Product Formulation Development information

See Ridgefield, CT salary details

$72.7K

$163K

$243.5K

How much do director drug product formulation development jobs pay per year?

As of Jun 13, 2026, the average yearly pay for director drug product formulation development in Ridgefield, CT is $163,021.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,000.00 and $184,700.00 per year, depending on experience, location, and employer.

What does a Director of Drug Product Formulation Development do?

A Director of Drug Product Formulation Development leads teams responsible for designing and optimizing pharmaceutical formulations, ensuring that drugs are safe, effective, and manufacturable at scale. This role involves overseeing the development of drug products from early-stage research through to clinical trials and commercial manufacturing. The director collaborates with cross-functional teams, manages regulatory compliance, and ensures that product development aligns with company goals and industry standards.

What are the key skills and qualifications needed to thrive as a Director of Drug Product Formulation Development, and why are they important?

To thrive as a Director of Drug Product Formulation Development, you need an advanced degree in pharmaceutical sciences or a related field, extensive experience in formulation development, and a deep understanding of regulatory requirements. Familiarity with analytical instrumentation, formulation software, and quality management systems, as well as certifications like PMP or Six Sigma, are highly beneficial. Strong leadership, strategic thinking, and cross-functional communication skills set outstanding candidates apart. These competencies ensure the successful development, optimization, and regulatory approval of drug products in a highly competitive and regulated environment.

What are some typical challenges faced by a Director of Drug Product Formulation Development, and how are they addressed within the team?

A Director of Drug Product Formulation Development often encounters challenges such as balancing innovative formulation approaches with regulatory compliance, managing cross-functional timelines, and ensuring scalability from laboratory to commercial manufacturing. Addressing these challenges typically involves close collaboration with analytical, regulatory, and manufacturing teams to align goals and troubleshoot issues early. Open communication, regular project reviews, and fostering a culture of continuous learning help the team adapt quickly to evolving project requirements and industry standards.
Infographic showing various Director Drug Product Formulation Development job openings in Ridgefield, CT as of June 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $163,021 per year, or $78.4 per hour.
Director, CMC Team Lead

Director, CMC Team Lead

Alexion Pharmaceuticals

New Haven, CT โ€ข On-site

Full-time

Posted 4 days ago


Job description

Are you ready to lead the CMC strategy for high-potential therapies and turn scientific promise into first approvals? This is your opportunity to guide an asset across the entire development lifecycle-from Candidate Selection through First Approval-while shaping how we bring life-changing medicines to people with serious, underserved conditions.

As Director, CMC Team Lead, you will run a cross-functional, matrix team that sets the direction for drug substance, drug product, analytical, quality, regulatory, and clinical supply to deliver on critical landmarks! You will craft the CMC Development Plan, drive decisions at pace, and ensure operational execution aligns to strategy, risk, and value. Do you thrive at the intersection of science, operations, and governance, where decisive leadership accelerates patient impact?

Accountabilities:

  • Asset Lifecycle Leadership: Own CMC leadership for a defined asset from Candidate Selection through First Approval, ensuring strategy, execution, and risk management stay aligned to program objectives.
  • CMC Strategy and Planning: Own the development of the integrated CMC Development Plan, setting clear priorities and team goals that enable timely submissions, clinical starts, and approval readiness.
  • Execution and Delivery: Translate strategy into actionable operational plans, define critical paths, and drive delivery across drug substance, drug product, analytical, quality, regulatory CMC, and clinical supply.
  • Dependency and Risk Management: Identify key interdependencies across execution teams, proactively manage risks and issues, and advance according to enterprise governance to protect timelines and quality.
  • Enterprise Representation and Governance: Serve as the sole CMC point of contact to enterprise Global Product/Medicine Teams and internal governance bodies, providing transparent updates and securing decisions.
  • Cross-Functional Decision Making: Facilitate timely, data-driven decisions across all CMC functions, ensuring clarity of responsibilities, deliverables, and success criteria.
  • Collaborator Influence and Communication: Build positive relationships across the organization and with senior leaders; communicate succinctly, align team members, and create momentum behind the plan.
  • Team Leadership and Culture: Prioritize and encourage a diverse, high-performing team; foster accountability, continuous improvement, and a patient-centered approach.

Essential Skills/Experience:

  • Minimum of 8-10 years of experience in the biopharmaceutical industry, with prior experience in a CMC leadership role
  • Demonstrated critical thinking capabilities with forward looking perspective.
  • Strong communication, leadership, and collaboration skills are required.
  • Solid understanding of drug development and clinic supply processes
  • Demonstrated ability to build, coordinate, and lead teams.
  • Strong interpersonal skills; proficient and able to influence others in spoken and written English.
  • The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours.

Desirable Skills/Experience:

  • Prior experience as a liaison with corporate partners preferred.
  • High level of proficiency in MS Office software including Word, Excel, Outlook, Visio, Project, and PowerPoint.
  • Knowledge of MS Project Server a plus

When we put unexpected teams in the same room, we ignite ambitious thinking with the power to encourage life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

Here, you will combine the agility of an entrepreneurial environment with the reach of a global biopharma, working alongside colleagues who value kindness as highly as ambition. We bring diverse expertise together to solve complex problems, stay close to patients' lived experiences, and turn bold science into meaningful outcomes. You will have the autonomy to move fast, the support of experienced leaders, and access to cutting-edge platforms that help you grow while advancing therapies for people who need them most.

Lead the CMC journey that transforms scientific innovation into approval-ready medicines-step forward and shape what comes next with us today!

Date Posted

08-Jun-2026

Closing Date

30-Aug-2026

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.