- 102
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Active Jobs Found
(Last Updated: May 15, 2024)
- 2+ years
- Not Disclosed
- Hyderabad, India
- Post Date: Mar 15, 2024
- End Date: May 15, 2024
- 2+ years
- Not Disclosed
- Hyderabad, India
- Post Date: Mar 15, 2024
- End Date: May 15, 2024
Qualification & Experience B.sc / M.sc Nuclear Medicine 2 to 5 years of experience Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years of Experience"
- Operations
- Inspection
- Management
- 5+ years
- Not Disclosed
- Hyderabad, India
- Post Date: Feb 16, 2024
- End Date: May 16, 2024
- 5+ years
- Not Disclosed
- Hyderabad, India
- Post Date: Feb 16, 2024
- End Date: May 16, 2024
Responsibilities Lead internal and external cross-functional groups to focus efforts on specific knowledge domains and high-impact topics related to complex generics and complex excipients. Determine deliverables, requirements, and timelines for the development of Complex Generics and complex excipient standards and solutions. Execute against the standards and solutions roadmap through tight integration of activities within USP and with external stakeholders, including but not limited to industry, academia, and regulators. Advocate for Complex Generics development to support the generic pharmaceutical industry and use of USP standards and solutions across the broader scientific and regulatory communities. Maintain awareness of the current trends and issues in the industry by attending scientific seminars, conferences, industry consortia meetings, and other fora. Represent USP science and standards at industry conferences and symposia as well as through written articles. Lead internal and external Complex Generics and Complex Excipient capability-building activities, including training, education, and knowledge-sharing across the organization. Assist in the activities of the USP Expert Committees and Expert Panels, as needed. Communicate and collaborate with USP laboratories regarding projects related to validation studies, method development, and reference standards. Perform other related duties as required. Qualification & Experience Ph.D. degree in Organic, Analytical, Pharmaceutical/Formulation, or a related field and a minimum of 7-10 years, or M.Sc./M. Pharm with a minimum of 11-13 years of relevant experience with USP-NF test and standards required. Minimum of 5 years of experience with Complex generic formulation development and analytical testing (Injectables, ophthalmic, topical, or transdermal, Inhalation, and other complex formulations) working in the pharmaceutical industry. Specific expertise dealing with complex excipients including polymeric excipients
- pharma
- mpharm
- Operations
- Inspection
- Management