Analytical Scientist / Scientist

About Azurity Pharmaceuticals

Azurity Pharmaceuticals is a privately owned specialty pharmaceutical company committed to creating innovative medicines for patients whose needs are often not fully met. The company is known for delivering accessible, high-quality products through its integrated capabilities and wide partner network. Its portfolio and late-stage pipeline cover cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan therapy areas, and its medicines have helped millions of patients. Azurity also states that it is an inclusive workplace and an equal opportunity employer.

Team Overview

The R&D analytical group supports product development across multiple dosage forms. Its work includes analytical method development, stability testing, method verification at CMO/CTL sites, and activities after filling. This position sits within the R&D analytical function and contributes to product development through method development, sample testing, compendial method evaluation, stability analysis, and instrument calibration.

Role Overview

The Analytical Scientist / Scientist will support pharmaceutical R&D testing and documentation activities, with a focus on analytical method execution and development, formulation sample analysis, and compliance with laboratory quality systems. The role also involves preparing and maintaining technical documents for assigned products.

Key Responsibilities

• Maintain good documentation practices in all work performed.
• Carry out analytical ATR tasks, complete documentation accurately, and share results with the relevant formulation team.
• Check that all records and data are complete, correct, and fit for purpose during execution and documentation.
• Perform analysis of formulation development samples according to the ATR, update online records, and complete testing within the required timeline.
• Work in line with current GLP requirements, data integrity expectations, and SOP compliance.
• Develop analytical methods using appropriate techniques and carry out verification of compendial methods as well as drug substance test methods.
• Follow laboratory safety procedures at all times.
• Prepare STP, MDR, and MOA documents for assigned products.

Qualifications and Experience

• A graduate or postgraduate degree in Pharmacy or Science.
• At least 2 years of experience in pharmaceutical analytical R&D or QC.
• Strong hands-on knowledge of analytical instruments, with a good understanding of the role of analytics in pharmaceutical research and development.
• Working knowledge of GLP and good documentation practices.
• Experience with electronic eLN/DMS systems.
• Good written and spoken English communication skills.

Important Declaration

By applying, you confirm that you are mentally and physically fit to perform all responsibilities described for the role without restrictions. If you have any concern, including even a minor disability that could affect job performance, you are expected to inform HR in advance.

Additional Information

This position is based in Mareedpally, Telangana, India and is a full-time onsite role.