Pharmaceutical R&D Jobs at Azurity Pharmaceuticals | Pharma Candidates Eligible
Looking for the latest Pharmaceutical R&D Jobs? Azurity Pharmaceuticals Careers brings an exciting opportunity for an Analytical Scientist to join its innovative R&D Analytical team. This position is ideal for Pharmacy and Science graduates with experience in analytical R&D or QC who are looking to build a rewarding career in pharmaceutical product development, analytical method development, stability studies, and formulation analysis with a leading specialty pharmaceutical company.
- Position: Analytical Scientist
- Location: Telangana
About the Company
Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline.
Job Description
The analytical team at R&D is playing an important role in the product development of various dosage forms. The analytical team involves different workflows like analytical method development, stability studies, method verifications at CMO/CTL, and post-filling activities.
This role is with Azurity R&D as an Analytical Scientist, which requires working in the product development team’s analytical method development, Formulation sample analysis, method verification, Compendial method evaluation, Stability sample analysis, and instrument calibrations.
Key Responsibilities
- Follow Good documentation practices.
- Execution of analytical ATR, documentation, and sharing of test results with the concerned formulation team.
- Ensuring all documents and data are adequate, accurate, and complete during the execution and documentation.
- Execution of Formulation developmental samples analysis as per ATR, recording of online documentation, and completion of the analysis on time.
- Adhere to current GLP procedure, data integrity, and meet SOP compliance requirements.
- Development of Analytical methods using different analytical techniques, method verification of compendial methods, and verification of Drug substance test methods.
- Follow the safety procedure in the laboratory.
- Should have exposure in preparing the STP, MDR, and MOA for the allocated products.
Qualifications
- Graduate / Postgraduate in Pharmacy or Science.
- A minimum of 2 years of experience in pharmaceutical analytical R&D or QC comes under this category.
- Well-versed with analytical instruments handling, technical skills, and understanding of Analytical importance in Pharmaceutical Research and Development. Understanding Good Laboratory Practices and Good Document Practices.
- Should have exposure to electronic eLN/DMS systems.
- Proficient in written and spoken English.
