Principal Scientific Manager
2 weeks ago
Key Responsibilities:
Candidate must be a good mentor and motivator.
Develop robust formulations and processes for immediate release and modified release tablet and capsule dosage forms.
Evaluate patents and develop non-infringement strategies. Capable of developing Paragraph IV products.
Scale-up and optimization of manufacturing process; execution of pre-exhibit and exhibit batches; scale up and technology transfer from R&D to production to meet timelines.
Plan and contribute to project-related scientific/technical activities (e.g., interpret results, critical assessment of data, draw relevant conclusions, and write reports).
Interaction with API manufacturers, CROs and CMOs as needed.
Work proactively with other cross-functional groups to execute change controls associated with Manufacturing and Packaging master records, SOPs and protocols.
Create and review SOPs, as well as review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GMP requirement.
Coordinate with RA for filing ANDAs and addressing deficiencies; provide relevant documents to Regulatory Affairs in a timely manner for ANDA filings and Supplements filing.
Required Educational Qualification & Relevant Experience:
Masters with a minimum of 15 years or a Ph.
D.
degree in Pharmacy with a minimum 5 years of relevant experience in oral solids product development in generic pharmaceutical industry.
Generic R&D experience and successful track record of AND submissions is a must. Experience with modified release dosage forms is a plus. Candidates must be self motivated with excellent written and verbal communication skills. Good interpersonal and project management skills are critical for this position.Functions:
Responsible for development of oral solid dosage forms of Non-DEA and DEA substances, Literature Search, Pre-Formulation, Formulation Design, and Development of stable, Bioequivalent and Manufacturable Generic Solid Oral Formulations.
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