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Formulation Development Cmc Jobs in Princeton, NJ

Abzena Inc.

Project Manager

Bristol, PA · On-site

Broad knowledge of all aspects of CMC including process development, regulatory and quality requirements, analytical development, formulation and drug product technologies. * 3+ years experience in a ...

WuXi Biologics

Associate Project Manager

Cranbury, NJ · On-site

$49K - $96K/yr

Serve as interface between WuXi Biologics and clients in Biologics CMC development program ... chemistry, formulation, DS/DP manufacturing, regulatory, quality, engineering qualification ...

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Formulation Development Cmc information

See Princeton, NJ salary details

$31

$53

$100

How much do formulation development cmc jobs pay per hour?

As of Aug 17, 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 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?

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 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.

What are popular job titles related to Formulation Development Cmc jobs in Princeton, NJ?

For Formulation Development Cmc jobs in Princeton, NJ, the most frequently searched job titles are:

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 August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 19% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $110,958 per year, or $53.3 per hour.

Project Manager

Abzena Inc.

Bristol, PA • On-site

Full-time

Posted 6 days ago

Job description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.
Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.
We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.
We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.
The Program Manager is responsible for managing integrated development and Chemistry, Bioconjugation Development and manufacturing programs of key clients while ensuring alignment with Abzena's functions, goals, and values. The Program Manager II manages the planning, scheduling, and budgeting of CMC-related product/process development activities, including new product development, analytical methods development/validation, process improvements, and product characterization. In addition to managing key programs and their client relationships, the Program Manager II will also support in the development of the PM organization through coaching and guidance.
Responsibilities
  • Create project plans to meet client needs.
  • Track, adjust and report milestone deliverables to clients, as well as internally to the Director of Project Management, Site Leadership, and Executive Leadership.
  • Communicate all changes, plans, and goals to partnering departments and functions.
  • Assist with risk and mitigation planning.
  • Create kick-off meetings and Joint Team Meeting (JTM) content, agenda, and minutes.
  • Document agreements and any changes to the statement of work.
  • Complete ERP system activities, invoicing, cost control, revenue recognition, material tracking and procurement and assist with forecasting and change management activities.
  • Provide support with project budgets, including but not limited to: review cost/price analysis', pressure test and align assumptions in the forecast, ensuring transparency and communication of the approved plan and funding status of activities.
  • Assist with development of others in the PM organization by providing coaching and guidance; may support OJT.
  • Identify and support PM improvement initiatives.
  • Provide support for the transfer of services between sites.
  • Maintain positive personnel and client relationships and communication.
  • Operate to the highest ethical and moral standards and participate effectively as a team player in all aspects of Abzena's business and adhere to quality standards set by regulations and Abzena policies, procedures, and mission.
  • Other related duties as assigned.

Qualifications
  • MS in Life Science, Engineering or related field.
  • 4+ years project management experience, leading multiple complex projects/programs
  • 2+ years in CDMO
  • Experience in small molecules or antibody drug conjugates preferred
  • Broad knowledge of all aspects of CMC including process development, regulatory and quality requirements, analytical development, formulation and drug product technologies.
  • 3+ years experience in a client facing position.
  • Experienced with Microsoft Project
  • Quick learner, independent and accountable for their work/projects, and can quickly adapt to changes
  • Ability to work on site all 5 days
  • Ability to work with clients overseas in different time zones

FLSA: Exempt
Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.

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