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Director Formulation Development Jobs in Livingston, NJ

Nuvation Bio, Inc.

Director, Drug Product

NY · On-site +1

$215K - $235K/yr

What you'll be doing The Director of Drug Product is responsible for development of new molecular ... The primary focus is on Phase 1 and Phase 2 formulation and process development. This role also ...

Nuvation Bio, Inc.

Director, Drug Product

NY · Remote

$215K - $235K/yr

What you'll be doing The Director of Drug Product is responsible for development of new molecular ... The primary focus is on Phase 1 and Phase 2 formulation and process development. This role also ...

New

IMCD Group

Associate Scientist

Allendale, NJ · On-site

Our customers benefit from direct access to a largeportfolio of high-quality products, avoiding the ... Supports formulation development projects for oral solid, liquid, topical, and nutraceutical ...

IMCD Group

Associate Scientist

Allendale, NJ · On-site

Our customers benefit from direct access to a largeportfolio of high-quality products, avoiding the ... Supports formulation development projects for oral solid, liquid, topical, and nutraceutical ...

System One

R&D Food Scientist

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Experience with clean-label formulation and ingredient replacement strategies. * Experience working ...

System One

R&D Food Scientist

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Experience with clean-label formulation and ingredient replacement strategies. * Experience working ...

System One

R&D Food Scientist

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Experience with clean-label formulation and ingredient replacement strategies. * Experience working ...

System One

R&D Food Scientist

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Experience with clean-label formulation and ingredient replacement strategies. * Experience working ...

System One

R&D Food Scientist

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Experience with clean-label formulation and ingredient replacement strategies. * Experience working ...

Nuts.com

Director of R&D, Product Innovation

Cranford, NJ · On-site

$190K - $200K/yr

As the Director of R&D, Product Innovation, you will build and lead Nuts.com's in-house recipe ... Working knowledge of food safety, quality, and regulatory considerations in formulation development

Nuts.com

Director of R&D, Product Innovation

Cranford, NJ · On-site

$190K - $200K/yr

As the Director of R&D, Product Innovation, you will build and lead Nuts.com's in-house recipe ... Working knowledge of food safety, quality, and regulatory considerations in formulation development

Nuts.com

Director of R&D, Product Innovation

Cranford, NJ · On-site

$190K - $200K/yr

As the Director of R&D, Product Innovation, you will build and lead Nuts.com's in-house recipe ... Working knowledge of food safety, quality, and regulatory considerations in formulation development

System One

Food Scientist - Dough Rheology

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Formulation Development * New Product Development (NPD) * Product Innovation * Dough & process ...

System One

Food Scientist - Dough Rheology

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Formulation Development * New Product Development (NPD) * Product Innovation * Dough & process ...

System One

Food Scientist - Dough Rheology

Paterson, NJ · On-site

$110K - $125K/yr

Direct Hire Compensation : $110,000-$125,000 Shift: 8:30am-5pm (some flexibility) Position Overview ... Formulation Development * New Product Development (NPD) * Product Innovation * Dough & process ...

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Director Formulation Development information

See Livingston, NJ salary details

$97K

$208.7K

$313.4K

How much do director formulation development jobs pay per year?

As of Sep 12, 2026, the average yearly pay for director formulation development in Livingston, NJ is $208,655.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,500.00 and $271,400.00 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 Livingston, NJ are hiring for Director Formulation Development jobs?

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

Director Formulation Development jobs near you
Infographic showing various Director Formulation Development job openings in Livingston, NJ as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 18% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $208,655 per year, or $100.3 per hour.

Director, Drug Product

NY • On-site, Remote

Nuvation Bio, Inc.
Pharmaceutical and Medicine Manufacturing • 51 - 200 employees
Learn more about Nuvation Bio, Inc.external

$215K - $235K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 4 days ago

Job description

Job Description
Who we are...
Nuvation Bio is a biopharmaceutical company tackling some of the greatest unmet needs in oncology by developing differentiated and novel therapeutic candidates. Our vision is to significantly change the practice of oncology by developing medicines that provide truly meaningful improvements in quality of life and survival for people with cancer.
What you'll be doing
The Director of Drug Product is responsible for development of new molecular entities across the company portfolio from discovery through all clinical phases to product registration and commercialization, as applicable. The primary focus is on Phase 1 and Phase 2 formulation and process development. This role also serves as the liaison to bridge the findings from preclinical/discovery studies to viable clinical and commercial drug product candidates.
You will be responsible for...
  • Responsible for all drug product activities from preclinical development through all clinical phases to product regulatory filing, commercialization, and life cycle management if required. The activities involve active third-party vendor management under aggressive business timelines to achieve project deliverables.
  • Act as a liaison to translate preclinical PK, pharmacological/toxicological drug candidate findings into appropriate clinical drug dosage forms for first in human studies and beyond. Formulations may include but are not limited to capsule, tablet, injectable, etc.
  • Identification, selection, and management of contract development research and manufacturing organizations (CRMOs) for formulation screening, formulation development/optimization, process development, scale-up, and validation.
  • Oversight of GMP manufacture of drug product in support of clinical programs.
  • Delivery of robust, scalable, and cost-effective manufacturing routes and drug product formulations that meet or exceed the target clinical product profile
  • Projection of drug substance and drug product needs for preclinical and clinical programs, and associated budgets
  • Communicate, coordinate, and establish collaborative working relationships with internal Pre-Clinical, Clinical, Analytical, CMC, Quality (GCP/GxP), Regulatory, Project Management and consultants, as well as with external CROs/CMOs counterparts. Develop and manage relationships with cross functional representatives, strategic alliance partners, vendors and collaborators.
  • Develop policies, SOPs, and systems to aid workflow within CMC/Quality.
  • Author and review internal Nuvation Bio technical reports and presentations.
  • Author and review CMC DP module sections of all regulatory submissions (Briefing Documents, Meeting Packages, INDs, IMPDs, NDAs, etc).
  • Manage critical activities involving drug product GMP batch record review, along with supporting documentation.
  • Lead pre-formulation and drug product formulation activities, including excipient compatibility, dosage form selection, etc.
  • Support contractor sites with active telecon meeting updates, remote and on-site involvement pertaining to OOS/OOT, investigations/deviations, and other pertinent documentation.
  • Support CMC activities associated with the company's programs. Work closely with colleagues and external CRMO collaborators to rapidly advance programs to key decision points, in preparation of regulatory submission, approval and post-approval commitments.
  • Provide critical, detailed review of external CRMO documents including supporting excipient information, drug product paperwork, equipment information, developmental reports, etc. Involves significant involvement with external sites on a routine basis.
  • Support CMC development strategies to ensure that project development timelines are in place and aligned with the project's overall company objectives. Involves key proactive participation in external partner meetings (technical and as well business related) and may involve site visits (travel).
What Knowledge & Experience you'll bring to us...
  • MS/PhD in Pharmaceutical Sciences, Chemical Engineering or closely related field preferred.
  • 8+ years of related experience within a pharmaceutical or biotechnology related field.
  • A commiserate combination of education and experience may be considered.
  • This position requires an individual with progressive, broad experience covering preclinical through later phase development. Background in contract pharma is preferred.
  • Comprehensive knowledge and experience in CMC functions, including drug substance, drug product, analytical, quality, and regulatory.
  • Understanding of GMP practices, principles, and regulatory guidelines.
  • Strong background in traditional and complex dosage forms.
  • Ability to understand program details across multiple functions and programs, and to develop stage-appropriate strategy for drug product development.
  • Demonstrated ability to lead and manage internal development, and manufacturing operations and influence external partners.
  • Proven track record and ability to proactively manage multiple clients/vendors, including appropriate prioritization of activities and tasks.
  • Demonstrated ability to bring focus and structure to problems in order to manage execution of deliverables in a timely manner.
  • Strong problem-solving skills to address a broad range of topics and to be ahead of the program in terms of planning and execution.
  • Excellent working knowledge of cGMP regulations required, including compendial (USP, EP, JP) and guidance documents.
  • Strong team player with strong interpersonal skills and exceptional leadership ability with a proven ability of building and maintaining a core culture and team environment.
  • Broad experience in the pharmaceutical industry with knowledge of drug discovery and clinical development through product registration and commercial readiness.
  • Excellent verbal and written communication skills with ability to deliver highly-effective reports and presentations which demonstrate audience specific technical expertise.
  • Office environment with domestic travel required (depends). Virtual/remote office (working from home).
  • Demonstrated alignment with Nuvation Bio's values and culture.
  • Oversight of Nuvation Bio activities at multiple vendors, including telecommunication and on-site visits, if necessary

  • Communication & Interpersonal Skills:
    • Excellent communication and interpersonal skills.
    • Leadership skills for internal and external activities
    • Must be able to write clearly and summarize information effectively.
    • Must be able to present complex information to various audiences.

  • Significant Contacts:
    • Internal employees, including executive team members.
    • Contract Research and Manufacturing Organizations (CRMOs), site team members, and consultants.
Behavioral skills to be successful...
  • Problem-Solver - As an action-oriented self-starter, you're eager to apply your expertise in diagnosing inefficiencies, determining root causes, and recommending solutions to complex challenges.
  • Personable - You establish and nurture highly effective relationships with colleagues and key stakeholders that support and advance project goals and objectives.
  • Credible - Thorough understanding of clinical methodologies and providing sound analytical support, you quickly establish credibility as a reliable resource.
  • Emotional intelligence, curiosity, and a knack to figure out a way to build something better
  • Communication - Effectively listens, conveys, and receives ideas. Maintains a consistent flow of information. A strong presenter and effective communicator with the ability to influence stakeholders.
  • Accountability - Acts with a clear sense of ownership - whether the task is in their role description. Holds yourself and others accountable to execute all tasks at hand through seen and unforeseen circumstances with high quality and integrity.
  • Adaptability - Can manage in an environment of ambiguity. Embraces the change of a new system, process, technology, or idea in the organization. You could reassess priorities, alter goals and take risks.
What we have for you!
  • Competitive Base Salary, Bonus, and Equity Plans
  • Unlimited Vacation and 10 Sick Days Annually
  • Excellent Medical, Dental, and Vision Coverage
  • 401K with Company Matching
  • and much more!

The base pay offered will take into account internal equity and also may vary depending on the candidate's job-related knowledge, skills, experience, and location among other factors. Our full-time regular positions also include an annual performance-based bonus and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, depending on the level and position offered.
Disclaimer
Nuvation Bio, Inc. is an equal opportunity employer, and, in accordance with applicable federal, state, and/or local law, all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by the law.
This job description reflects the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Nothing restricts management's right to assign or reassign duties and responsibilities to this job at any time.
Note to all external Recruiters & Staffing Agencies
All of our open positions are managed by our Talent Acquisition department. Any resumes submitted through the website or directly by recruiters or staffing agencies in advance of an executed agreement with Nuvation Bio, Inc., will be considered unsolicited and the company will not be responsible for any related fees. Resumes sent directly to employees or hiring managers will also not be accepted as referrals.

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