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Director Formulation Development Jobs in Princeton Junction, NJ

System One

Hair Care Formulation Scientist

Cranbury, NJ · On-site

$70/hr

Direct Hire Compensation: $70-80k Contractor Work Model: Onsite - onsite Hours: 8:30 AM- 4:30 PM M ... Partner with cross-functional teams (Product Development, Regulatory, Quality, Manufacturing) to ...

System One

Hair Care Formulation Scientist

Cranbury, NJ · On-site

$70/hr

Direct Hire Compensation: $70-80k Contractor Work Model: Onsite - onsite Hours: 8:30 AM- 4:30 PM M ... Partner with cross-functional teams (Product Development, Regulatory, Quality, Manufacturing) to ...

System One

Hair Care Formulation Scientist

Cranbury, NJ · On-site

$70/hr

Direct Hire Compensation: $70-80k Contractor Work Model: Onsite - onsite Hours: 8:30 AM- 4:30 PM M ... Partner with cross-functional teams (Product Development, Regulatory, Quality, Manufacturing) to ...

System One

Hair Care Formulation Scientist

Cranbury, NJ · On-site

$70/hr

Direct Hire Compensation: $70-80k Contractor Work Model: Onsite - onsite Hours: 8:30 AM- 4:30 PM M ... Partner with cross-functional teams (Product Development, Regulatory, Quality, Manufacturing) to ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

System One

R&D Skin Care Manager

Cranbury, NJ · On-site

$92K - $120K/yr

Direct Hire Compensation: $92,000 - $120,000 Contractor Work Model: Onsite - onsite Hours: 8:30 AM ... Manage bench-level formulation development, mentoring scientists and technicians in new chassis ...

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All JobsFormulation Development JobsDirector Formulation Development JobsDirector Formulation Development Jobs in Princeton Junction, NJ

Director Formulation Development information

See Princeton Junction, NJ salary details

$93.7K

$201.5K

$302.7K

How much do director formulation development jobs pay per year?

As of Sep 10, 2026, the average yearly pay for director formulation development in Princeton Junction, NJ is $201,503.00, according to ZipRecruiter salary data. Most workers in this role earn between $99,000.00 and $262,100.00 per year, depending on experience, location, and employer.

What is a Director Formulation Development?

A Director of Formulation Development leads the design and optimization of pharmaceutical formulations, ensuring they meet quality, regulatory, and performance standards. They oversee research, guide teams in developing new drug delivery systems, and collaborate with regulatory and manufacturing teams. This role requires expertise in chemistry, pharmaceutics, and process development to ensure successful product commercialization. Additionally, they manage project timelines, budgets, and technical challenges to drive innovation in drug formulation.

What does a Director Formulation Development do?

As a Director Formulation Development, you will oversee the design and optimization of drug formulations, lead a multidisciplinary team of scientists, and ensure that projects meet quality, budget, and timeline expectations. Your daily activities often include strategic planning, reviewing progress reports, troubleshooting formulation challenges, and collaborating with regulatory, manufacturing, and quality assurance departments. You may also interact with upper management to report on key milestones and contribute to long-term product development strategies. This role offers opportunities to influence project pipelines and play a central part in bringing new therapies to market.

What are the key skills and qualifications needed to thrive as a Director Formulation Development?

A Director Formulation Development typically requires an advanced degree in pharmaceutical sciences, chemistry, or a related field, along with significant experience in drug formulation and team management. Familiarity with industry-standard formulation software, regulatory compliance systems, and relevant certifications such as PMP or Six Sigma are highly valued. Excellent leadership, communication, and strategic planning skills help set high performers apart in this role. These skills and qualities are critical for driving innovative product development, ensuring regulatory compliance, and effectively leading cross-functional teams.

What cities near Princeton Junction, NJ are hiring for Director Formulation Development jobs?

Cities near Princeton Junction, NJ with the most Director Formulation Development job openings:

Director Formulation Development jobs near you

Director, Formulation Development

Princeton, NJ • Hybrid

Acadia Pharmaceuticals Inc.
See more jobs at Acadia Pharmaceuticals Inc.external

Full-time

Re-posted 25 days ago

Job description

Please note that this position can be based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average.Position Summary

The Director, Formulation Development leads formulation, primary packaging, and manufacturing process development across Acadia's portfolio of drug candidates from early development through commercialization. This role provides technical leadership for externalized drug product development across oral solid, liquid, and injectable dosage forms, with a primary focus on oral solid dosage forms. The position is responsible for managing Contract Service Providers (CSPs), resolving complex technical issues, and advancing manufacturing process technologies that support clinical supply, process validation, and lifecycle management. This role plays a key part in reducing development risk, improving execution, and accelerating program progression.

Primary Responsibilities
  • Design and develop pharmaceutical formulations and manufacturing processes to support clinical development, registration, and product launch
  • Evaluate and qualify Contract Service Providers (CSPs) to support development, scale-up, and commercialization, and manage related supplier agreements as needed
  • Lead and oversee the development and scale-up of clinical formulations and finished dosage forms at CSPs, serving as on-site technical support when required
  • Plan and direct scientific and technical activities, including data interpretation, evaluation of results, development of conclusions, and preparation of technical reports and presentations
  • Partner with clinical supply management to define supply requirements and align CSP manufacturing schedules to ensure uninterrupted availability of clinical trial materials
  • Conduct risk assessments of manufacturing processes and products at key development milestones and drive resolution of findings with relevant CSPs
  • Author and review technical reports and development documentation to support regulatory submissions, including review of MBRs, BPRs, and CSP-generated reports
  • Collaborate with analytical, manufacturing, quality, and regulatory teams to develop plans and protocols for drug product development and lifecycle management
  • Ensure compliance with cGMP and applicable GxP requirements, and support CSP readiness for health authority and pre-approval inspections
  • Perform other responsibilities as assigned
Education, Experience, and Skills
  • Advanced degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or a related field required; an equivalent combination of education and relevant industry experience may be considered. Minimum of 10 years of progressively responsible experience in formulation and manufacturing process development, including leadership responsibilities. Proven success in formulation and dosage form development, with experience authoring technical reports and CMC sections for regulatory submissions.
  • Deep understanding of dosage form formulation, primary packaging, manufacturing process development, scale-up, optimization, and validation
  • Demonstrated success in oral solid dosage form development of new chemical entities
  • Strong knowledge of cGMP requirements and experience supporting regulatory filings, including NDAs or other marketing authorization applications
  • Proven ability to manage external development and manufacturing partners, including CROs, CMOs, and CSPs
  • Strong written and verbal communication skills, with the ability to translate complex technical information for cross-functional audiences
  • Demonstrated leadership, influence, and resource alignment across functions to achieve development and organizational goals
  • Flexibility to travel domestically and internationally
Physical Requirements

While performing the duties of this job, the employee is regularly required to stand, walk, sit, use hands to handle or feel objects, reach with hands and arms, climb or balance, stoop, kneel, crouch, and see, speak, or hear in a standard office environment and independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. Ability to travel domestically and internationally is required.

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