Senior Formulation Scientist

Contract Pharmacal Corp

Hauppauge (NY)

On-site

USD 85,000 - 125,000

Full time

14 days+
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Benefits offered by this job

Competitive benefits
Opportunities for career growth
Collaborative work environment

Job summary

A pharmaceutical development company in Hauppauge is seeking a Senior Formulation Scientist to join its dynamic R&D team. You will design and develop formulations for oral solid dosage forms, manage multiple projects, and write protocols. The role requires an MS or Ph.D. with at least 5 years of relevant experience. The company fosters a collaborative culture and provides competitive benefits. This position offers the opportunity to work with cutting-edge technologies and engage in diverse product development activities.

Qualifications

  • 5+ years of formulation experience in pharmaceutical and/or nutraceutical product development.
  • Hands-on experience with formulation equipment.
  • MS required, Ph.D. preferred.

Responsibilities

  • Design and develop formulations for oral solid dosage forms.
  • Manage multiple formulation projects and deliver results on time.
  • Write protocols and product development reports.
  • Provide process improvement support.

Skills

Knowledge of cGMPs, US FDA, and EU/EMEA regulatory requirements
Strong project management skills
Effective oral and written communication
Detail-oriented and organized
Ability to troubleshoot formulation issues
Willingness to learn new technologies

Education

MS required; Ph.D. preferred
Minimum 5 years of formulation experience

Tools

Blenders
Fluid bed dryers
High shear granulators
Tablet presses

Job description

We are seeking a Senior Formulation Scientist to join our dynamic R&D team, where you’ll play a key role in developing innovative pharmaceutical and nutraceutical products. In this hands-on role, you’ll design formulations, support process improvements, and contribute directly to product development from concept to commercialization. This position offers exposure to oral solid dosage forms. Candidates may specialize in drug formulation or nutraceutical formulation, with the opportunity to grow into broader product development responsibilities.

Job Type: Full-Time

Works Hours: Monday – Friday, 9:00AM – 5:00PM

Pay Range: $85,000 - $125,000 per year, depending on experience

Start Date: ASAP

What makes this role exciting

  • Diverse formulation experience – work on nutraceuticals, OTC, and prescription oral solid dosage forms
  • Hands-on innovation – operate formulation equipment like blenders, high shear granulators, fluid bed dryers, and tablet presses
  • End-to-end impact – take ideas from early development through regulatory submission and commercialization
  • Collaborative environment – partner with R&D, production, and regulatory teams, contributing to problem-solving and process improvements

Why Join CPC?

At CPC, you’ll be part of a team that has set the standard in pharmaceutical development and contract manufacturing since 1971, helping bring high-quality OTC, dietary supplement, and prescription products to market faster and safer than ever. We pride ourselves on quality as a core value, innovative problem-solving, and a collaborative culture where everyone plays a role in advancing formulation and manufacturing excellence. CPC offers an inclusive, respectful workplace with opportunities to grow your skills and career while working with cutting-edge technologies and serving leading global brands. With a commitment to employee success, competitive benefits, and a culture built on teamwork and integrity, CPC is a place where your contributions truly make an impact

Responsibilities

  • Design and develop formulations for oral solid dosage forms across nutraceutical, OTC, and prescription products
  • Manage multiple formulation projects and deliver results on time
  • Write protocols, Master Manufacturing Records (MMRs), and product development reports
  • Provide process improvement support and troubleshoot production issues
  • Stay current with emerging trends in drug delivery technology and regulatory policies

Education & Experience

  • MS required; Ph.D. preferred
  • Minimum 5 years of formulation experience in pharmaceutical and/or nutraceutical product development
  • Hands-on experience with formulation equipment such as blenders, fluid bed dryers, high shear granulators, and tablet presses

Skills, Knowledge & Abilities

  • Knowledge of cGMPs, US FDA, and EU/EMEA regulatory requirements
  • Familiarity with Quality System standards, ICH guidelines, USP, and EP requirements
  • Experience preparing protocols, Master Manufacturing Records (MMRs), and product development reports
  • Ability to troubleshoot formulation or process issues and recommend practical solutions
  • Strong project management skills, able to prioritize and manage multiple development projects
  • Effective oral and written communication; able to collaborate with R&D, production, and regulatory teams
  • Detail-oriented, organized, and proactive with a strong problem-solving mindeset
  • Willingness to learn new technologies and adapt to evolving project needs
  • Experience with regulatory submissions preferred for pharmaceutical candidates
  • Exposure to multi-product development is preferred but not required
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