ARAGEN IS A TRUSTED R&D AND MANUFACTURING PARTNER TO THE GLOBAL LIFE SCIENCES INDUSTRY. FROM CONCEPT TO COMMERCIAL, WE TRANSFORM YOUR IDEAS INTO SOLUTIONS FOR BETTER HEALTH.
Whether large pharma or biotech, an agrochemical or animal health company, we provide you global resources and proven capabilities at every stage of the biopharma lifecycle, in small and large molecules. Our ability to offer end-to-end solutions or support standalone programs is underpinned by an innovation mindset, enabling technologies, and a partnership approach to every engagement.
Hiring Aragen Life Sciences – HYD
Role : Senior Research Associate
Scope –
This role is responsible to work as analyst and perform method development and analysis of formulation samples.
Responsibilities –
· To perform analysis of all dosage forms formulation samples for different type of tests.
· To perform analytical method development, method validation, method transfer for different analytical methods.
· To perform stability study analysis of formulation samples.
· To perform calibration of laboratory Instruments.
· To receive and to prepare working standards and to maintain tracking & monitoring, of reference standards and impurity standards.
· To do the data compilation of stability batches and formulation batches and to prepare COAs and reports.
· To prepare specifications, standard testing procedures, standard operating procedures and instructions for sampling.
· To ensure effective implementation of GLP activities in the ARD lab.
· To verify maintenance of facility and instruments of the ARD.
· To co-ordinate in investigations related to OOS results, incidents, deviations and customer complaints.
· To review analytical data and project reports.
· To update & to review Instrument usage logs.
· To perform daily calibrations and to update calibration schedules.
· To maintain tracking of chemicals, reagent and solvent consumption for timely indent.
· To maintain HPLC columns and GC columns and tracking the inventory of the same.
· To maintain all analytical instruments in good working conditions
Educational Qualification:
M. Pharm (Pharmaceutical analysis and quality assurance)/ MSc (Analytical/Organic Chemistry) with 3-6 yrs of relevant experience
Basic knowledge of MS Office and exposure in CRO industry
Interested candidates with desired qualifications, please mail your CV at [email protected]
