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Formulation Development Cmc Jobs in Princeton, NJ

System One

Product Engineer

Franklin Township, NJ · On-site

$28 - $36/hr

Support development of both traditional battery materials and new active materials intended for ... Slurry formulation (aqueous and NMP-based), dispersion, deagglomeration * Coating (tape casting ...

System One

Product Engineer

Franklin Township, NJ · On-site

$28 - $36/hr

Support development of both traditional battery materials and new active materials intended for ... Slurry formulation (aqueous and NMP-based), dispersion, deagglomeration * Coating (tape casting ...

All JobsFormulation Development Cmc JobsFormulation Development Cmc Jobs in Princeton, NJ

Formulation Development Cmc information

See Princeton, NJ salary details

$31

$53

$100

How much do formulation development cmc jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for formulation development cmc in Princeton, NJ is $53.35, according to ZipRecruiter salary data. Most workers in this role earn between $36.30 and $85.43 per hour, depending on experience, location, and employer.

What is the role of CMC in drug development?

In formulation development, CMC (Chemistry, Manufacturing, and Controls) ensures the quality, safety, and efficacy of a drug by establishing manufacturing processes, quality standards, and regulatory documentation. Formulation scientists and CMC teams collaborate to develop stable, scalable drug products that meet regulatory requirements throughout development and commercialization.

What is the salary of formulation R&D?

The salary for a Formulation Development CMC professional typically ranges from $70,000 to $130,000 annually, depending on experience, education, and location. Entry-level roles may start lower, while senior positions with specialized skills or certifications can earn higher salaries. Compensation often includes benefits such as health insurance and bonuses.

What is the highest paying job in pharmaceuticals?

In pharmaceuticals, senior roles such as Vice President of Research and Development or Chief Scientific Officer typically have the highest salaries, often exceeding several hundred thousand dollars annually. These positions require extensive experience, advanced degrees, and leadership skills, and they oversee drug development, regulatory strategies, and company innovation.

What is the difference between Formulation Development Cmc vs Formulation Scientist?

AspectFormulation Development CmcFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fields; industry certificationsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields
Work EnvironmentPharmaceutical or biotech R&D labs, manufacturing settingsResearch labs, development facilities, pharmaceutical companies
Industry UsageRegulatory submissions, product development, manufacturing supportFormulation research, experimental design, product optimization

Formulation Development Cmc focuses on developing formulations suitable for regulatory approval and manufacturing, often involving documentation and compliance. Formulation Scientists primarily conduct research and experiments to create and optimize formulations. While both roles require similar educational backgrounds and work in related environments, Cmc roles emphasize regulatory and manufacturing aspects, whereas Scientists focus on experimental research and innovation.

Is formulation part of CMC?

In formulation development roles within CMC (Chemistry, Manufacturing, and Controls), formulation is a core component, involving the design and optimization of drug formulations to ensure stability, efficacy, and manufacturability. These professionals work with analytical tools, quality standards, and regulatory requirements to develop suitable formulations for clinical and commercial products.

What is Formulation Development CMC?

Formulation Development CMC (Chemistry, Manufacturing, and Controls) refers to the process of designing and optimizing the composition of a drug product, ensuring it is safe, effective, and stable for patient use. This role involves selecting appropriate excipients, developing the manufacturing process, and generating the data required to support regulatory submissions. CMC professionals collaborate with research, quality, and regulatory teams to ensure that the drug product meets all necessary standards throughout its lifecycle.

What are the key skills and qualifications needed to thrive as a Formulation Development CMC specialist, and why are they important?

To thrive as a Formulation Development CMC specialist, you need expertise in pharmaceutical sciences, chemistry, and regulatory guidelines, often supported by an advanced degree in a relevant field. Familiarity with analytical techniques, formulation equipment, and regulatory submission systems like eCTD is crucial. Strong problem-solving skills, attention to detail, and effective collaboration are essential soft skills in this role. These competencies ensure the successful development, optimization, and regulatory approval of safe and effective pharmaceutical products.

What are some typical challenges faced by professionals in Formulation Development CMC, and how are they addressed?

Professionals in Formulation Development CMC often encounter challenges such as ensuring formulation stability, meeting regulatory requirements, and scaling up from laboratory to manufacturing. Addressing these challenges requires close collaboration with analytical, regulatory, and manufacturing teams, as well as staying current with evolving guidelines. Effective project management, rigorous experimental design, and proactive risk assessment are key strategies to successfully navigate these complexities and ensure timely progress of drug development projects.
What job categories do people searching Formulation Development Cmc jobs in Princeton, NJ look for? The top searched job categories for Formulation Development Cmc jobs in Princeton, NJ are:
What cities near Princeton, NJ are hiring for Formulation Development Cmc jobs? Cities near Princeton, NJ with the most Formulation Development Cmc job openings:
Formulation Development Cmc jobs near you
Infographic showing various Formulation Development Cmc job openings in Princeton, NJ as of July 2026, with employment types broken down into 2% Locum Tenens, 24% Internship, 58% Full Time, 11% Part Time, 3% Contract, and 2% Summer. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $110,958 per year, or $53.3 per hour.
Director, Formulation Development

Director, Formulation Development

Acadia Pharmaceuticals Inc.

Princeton, NJ • Hybrid

Other

Posted 10 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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