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3.0 - 7.0 years
0 Lacs
hyderabad, telangana
On-site
Azurity Pharmaceuticals is a specialty pharmaceutical company dedicated to providing innovative products for underserved patients. With a focus on unique, accessible, and high-quality medications, Azurity continuously expands its commercial product portfolio and late-stage pipeline through integrated capabilities and a vast partner network. The company's patient-centric products cover various markets including cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan, benefiting millions of patients globally. As an inclusive workplace and Equal Opportunity Employer, Azurity attributes its success to a talented and dedicated team committed to improving patients" lives with a strong emphasis on science and quality. We are looking for individuals who are highly motivated, possess integrity, dedication, and a creative spirit to excel in our organization. **Job Responsibilities:** - Design, supervise, and conduct formulation development, process optimization, scale-up, and manufacturing of products. - Prepare and review essential documents including batch records, SOPs, stability protocols, specifications, and reports. - Analyze test results, identify variances, and recommend solutions to achieve project goals. - Schedule experiments, prioritize assignments, and meet project objectives and deadlines. - Maintain laboratory equipment and adhere to company safety standards. - Conduct laboratory experiments, prepare detailed reports with conclusions, and recommendations. - Develop and follow laboratory procedures to meet project objectives efficiently. - Identify and manage potential risks within complex projects promptly. - Maintain accurate documentation of experimental methods and results as per good documentation practices. - Serve as the primary scientific contact for external collaborators. - Manage inventories of supplies and raw materials. - Ensure completion of all required training on time. **Qualifications And Education Requirements:** - M. Pharm or Ph.D. in Pharmacy with a minimum of 3 to 6 years of industrial experience in pharmaceutical development and product scale-up. - Expertise in oral dosage forms, particularly in Modified Release, Extended Release, Targeted Release, Immediate Release solid/suspensions/solutions. - Experience in Global Product Development across markets like US, EU, China, and ROW. - Experience in developing branded and differentiated products, preferably in the 505(b)(2) category. - Familiarity with working with CROs/CDMOs is preferred. - Proficiency in Microsoft Office applications. By applying for this role, you confirm your ability to fulfill the job responsibilities outlined in the job description without any restrictions. If you have any concerns or disabilities that may affect your performance, please inform HR in advance.,
Posted 3 days ago
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