Formulation Scientist, R&D; Solid Dose Drugs
CONTRACT PHARMACAL CORP
Summary
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 description
The Sr. Scientist Formulation is primarily responsible for formulation product development and leading the process development activities from concept through commercialization.
Responsibilities
- Development of solid dosage nutraceutical, OTC or prescription products e.g. Tablet (Immediate Release, Controlled release, Effervescent) and Capsule with a working knowledge of tableting, two-piece encapsulation, granulation, fluid bed drying, and tablet coating
- Manage multiple development projects and develop formulations in a timely manner
- Assist in execution of Sampling Protocols, Process Validation Protocols, Stability Protocols and reports for OTC/ANDA products as per cGMP guidelines
- Write and review challenge study protocols, master manufacturing records, product development reports and technical transfer reports
- Performing project management by coordinating the activities and keeping strong communication amongst multiple disciplines for all technical transfer projects
- Provide support to production in process improvement and troubleshooting
- Manage, coach, mentor and motivate junior scientists, operators, and technicians for exceptional performance
- Other responsibilities as assigned by senior management
Education and Experience
- BS or MS degree in Pharmaceutical Sciences or related field is required
- Experience in Pharmaceutical R&D formulation is required
- Experience with formulation equipment such as blender, fluid bed dryer, high shear granulator, tablet press and other such equipment is preferred
- Outstanding oral, written and computer skills is required
- Desire to work in a fast-paced manufacturing facility with unlimited career growth potential
Skills, Knowledge, and Abilities
- Excellent oral and written communications skills, working knowledge of MS Office
- Knowledge of CGMPs related to US FDA Manufacturing environments
- Ability to prioritize and multitask
- Motivated, detailed, organized
- Knowledge of cGMP, computer software including word processing, Excel, and PowerPoint
Supervisory Responsibilities
Limited
Requirements
- BS or MS degree in Pharmaceutical Sciences or related field
- Experience in Pharmaceutical R&D formulation
- Experience with formulation equipment such as blender, fluid bed dryer, high shear granulator, tablet press
- Outstanding oral, written and computer skills
- Excellent oral and written communications skills
- Working knowledge of MS Office
- Knowledge of CGMPs related to US FDA Manufacturing environments
- Ability to prioritize and multitask
- Motivated, detailed, organized
- Knowledge of cGMP, Excel, and PowerPoint
Company overview
Contract Pharmacal Corp (CPC) is a leading contract development and manufacturing organization (CDMO) specializing in pharmaceutical products, over-the-counter drugs, and dietary supplements. Founded in 1971 and headquartered in Hauppauge, New York, the company has established itself as one of the oldest and largest leaders in the nutraceutical and pharmaceutical industries. With nearly one million square feet of manufacturing facilities and over 1,250 highly skilled professionals, CPC operates as an employee-owned company focused on quality and innovation. The organization boasts an impressive annual capacity of 25 billion solid doses and has developed over 5,000 unique formulas since its inception, averaging approximately 100 new products per year. CPC serves major pharmaceutical companies, marketing firms, retailers, and wholesalers globally, with more than 60 international partners trusting them as their CDMO partner. Their comprehensive services span from early-stage product innovation and development to commercial manufacturing, packaging, and analytical testing, helping clients navigate complex regulatory landscapes and bring products to market efficiently.