Inhalation Scientist, Formulation R&D
Amneal Pharmaceuticals
September 02, 2026
Remote friendly (Piscataway, NJ)
United States
Clinical Research and Development
Scientist II will support and contribute toward the development of drug products intended for regulatory registration, including development of product and process and creation of documents for ANDA submission. Leads developmental activities at the bench level and maintains cGMP compliance.
Essential Functions:
- Assist in development of oral solid formulations, topical (cream, gel), oral liquid, or other dosage forms under guidance of project leaders; perform experiments and report results.
- Conduct literature searches and relevant pre-formulation activities to characterize the brand product; perform stability studies during development.
- Write and review technical documentation (reports, protocols, and other documents) for ANDA submission.
- Maintain accurate records and documents; stay up to date with cGMP and maintain compliance.
- Operate formulation, manufacturing, and filling equipment for metered-dose inhaler and dry powder inhaler drug products; operate lab equipment (e.g., density measurement equipment, balances, pH meters, and other instruments) for characterization and evaluation.
Additional Responsibilities:
- Other duties as assigned.
Qualifications:
- Education: Bachelors (BA/BS) in Pharmacy or related scientific field (Required); Master (MS/MA) in Pharmacy or related scientific field (Preferred).
- Experience: 3+ years (Bachelorβs) in Pharmaceutical; 1+ year (Masterβs) in Pharmaceutical.
Specialized Knowledge:
- Ability to operate formulation, manufacturing, and filling equipment for metered-dose inhaler and dry powder inhaler drug products.
Compensation/Benefits:
- Salary range: $80,000β$95,000 per year; short-term incentive opportunity (bonus or performance-based award) within first 12 months.
Essential Functions:
- Assist in development of oral solid formulations, topical (cream, gel), oral liquid, or other dosage forms under guidance of project leaders; perform experiments and report results.
- Conduct literature searches and relevant pre-formulation activities to characterize the brand product; perform stability studies during development.
- Write and review technical documentation (reports, protocols, and other documents) for ANDA submission.
- Maintain accurate records and documents; stay up to date with cGMP and maintain compliance.
- Operate formulation, manufacturing, and filling equipment for metered-dose inhaler and dry powder inhaler drug products; operate lab equipment (e.g., density measurement equipment, balances, pH meters, and other instruments) for characterization and evaluation.
Additional Responsibilities:
- Other duties as assigned.
Qualifications:
- Education: Bachelors (BA/BS) in Pharmacy or related scientific field (Required); Master (MS/MA) in Pharmacy or related scientific field (Preferred).
- Experience: 3+ years (Bachelorβs) in Pharmaceutical; 1+ year (Masterβs) in Pharmaceutical.
Specialized Knowledge:
- Ability to operate formulation, manufacturing, and filling equipment for metered-dose inhaler and dry powder inhaler drug products.
Compensation/Benefits:
- Salary range: $80,000β$95,000 per year; short-term incentive opportunity (bonus or performance-based award) within first 12 months.