Auxilla Pharmaceuticals and Research LLP
At Auxilla, a 70-member team works across formulation development, analytical development, quality assurance, regulatory affairs, business development, project management, engineering and administration on products for regulated markets.
If you want to work on complex sterile and non-sterile dosage forms in a focused, delivery-driven environment, we would like to hear from you.
Injectable, ophthalmic, liquid oral, liposomal and microsphere-based formulations.
Method development and validation, stability studies, characterization and impurity profiling.
Quality assurance, documentation, regulatory affairs and business development.
Sterility, endotoxin, microbial limit testing and environmental monitoring.
Planning and coordinating development projects to time-bound delivery.
Keeping our facility and our people running smoothly.
We are growing our formulation, analytical, quality and microbiology teams at our R&D site in Sanand, Ahmedabad.
Develop sterile injectable and lyophilized formulations, run pre-formulation studies and prepare development reports for regulated markets.
Lead HPLC method development and validation, impurity profiling and stability studies, and review analytical data for submissions.
Manage SOPs and protocols, review validation documentation and handle deviations and CAPA across development projects.
Perform sterility, bacterial endotoxin and microbial limit testing, and support environmental and cleanroom monitoring.
Don’t see a role that fits? Send a general application and our HR team will keep your profile for future openings.
Fill in your details and our HR team will receive your application by email. Please also email your CV to hr@auxillapharma.com.