About the Company
The company founded in the year 2001, from then it is supporting the major innovative companies in development of drug moieties. The company has over 2500 skilled employees with the state of art facility labs and highly qualified scientists. the company has 55 acres of land, and have 5 labs in India. the company has 1.2 million sft chemistry and biological labs. it was acquired Aragen Bio science, Inc. in the year 2014, enabling its clients to deal both with the small and larger pharma molecules.
With the sophisticated labs the firm providing a hand to develop high quality and cost effective drugs for the top innovator companies. The company working in the areas but not limited to integrated drug discovery, analytical, formulation developments.
The firm established its operations across the globe in the locations of USA and Netherlands, locally Bangalore, Hyderabad. GVK Bio has the certifications like FDA,EDQM,MHRA,PDMA,WHO-GMP. which certifies that company has a quality in their operations.
About the Job
Experience: 3-6 yrs experience in relevant area mentioned above.
Education: M. Pharmacy in Pharmaceutical Analysis
Responsibilities –
Design, screening, and characterization of pharmaceutical salt, co-crystals and polymorph for product development.
Conduct pre-formulation research on new chemical entity (NCE) including compound profiling, physicochemical property, and solid-state characterization.
Set-up and maintain solid state and formulation equipment/instrument including XRPD, DSC, TGA, DVS, PSD, etc.
Execute solid form process development, and scale-up for preclinical formulation development.
Execution of planned short-term stability studies.
To help in trouble shooting and problems solving within the projects for successful development and delivery of the project.
Managing NCEs and raw materials for the projects.
Interaction and effective coordination with cross functional teams and clients for successful completion of projects.
Ensuring appropriate documentation for projects as per standard operating procedures and policies.
Managing laboratory notebooks for all concerned projects.
Compilation and interpretations of results and reports writing.
Preparation and review of SOP (Standard operating procedures).
Compliance and adhering to the quality systems of the company, ICH, pharmacopoeia guidelines and respective regulatory authority.
Support in preparation of project proposal.
Identification of vendors and sourcing of raw material.
Compliance to EHS policies and systems.
Interested candidates with relevant qualification and experience, please share your CV at [email protected]