Senior Formulation Scientist

SupportFinity™; New York (NY); On-site; USD 85,000 - 125,000; Full time

Benefits offered by this job

Medical insurance

Vision insurance

Dental insurance

401(k)

Job summary

SupportFinity™ is seeking a Senior Formulation Scientist to contribute to innovative pharmaceutical product development. You will design formulations, improve processes, and oversee projects from concept to commercialization.

Your role includes operating formulation equipment and collaborating with cross-functional teams. The ideal candidate has significant formulation experience, ideally with both pharmaceutical and nutraceutical products.

This position offers a competitive salary, comprehensive benefits, and opportunities for professional growth.

Qualifications

• Minimum of 5 years of formulation experience in pharmaceutical or nutraceutical development.
• Hands-on experience with formulation equipment is required.
• Knowledge of FDA and EU regulatory requirements.

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.

Skills

cGMP knowledge

Project management skills

Effective communication

Troubleshooting skills

Detail-oriented

Education

MS degree

Ph.D. preferred

Tools

Formulation equipment

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
• Work Hours: Monday – Friday, 9:00 AM – 5:00 PM
• 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

Benefits

• Medical insurance
• Vision insurance
• Dental insurance
• 401(k)