Senior Formulation Scientist - Pharmaceuticals/Nutraceuticals
Listed on 2026-01-12
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Pharmaceutical
Pharmaceutical Manufacturing, Pharmaceutical Science/ Research
Senior Formulation Scientist - Pharmaceuticals/Nutraceuticals
Join Contract Pharmacal Corp as a Senior Formulation Scientist. 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 and focuses on drug formulation or nutraceutical formulation.
Location:
Hauppauge, NY
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
- Diverse formulation experience – nutraceuticals, OTC, and prescription oral solid dosage forms.
- Hands‑on innovation – operate formulation equipment such as 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.
- 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.
- 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.
- 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; ability to collaborate with R&D, production, and regulatory teams.
- Detail‑oriented, organized, and proactive with a strong problem‑solving mindset.
- 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.
At CPC, we have set the standard in pharmaceutical development and contract manufacturing since 1971. We pride ourselves on quality, 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.
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