April 2025

Project titled Advance Center for Clinical Evaluation of Diagnostics of National Importance. Three years Graduate in Biochemistry, Biotechnology, Life Science from recognized university plus Three-year experience Or PG in relevant subject, field from recognized university, Institute

ITM SLS Baroda University, Vadodara is at the forefront of radical and student serving educational innovations. It has been crafted to serve as a hub where all the stakeholders can collaborate in optimizing teaching-learning processes to create a quality outcome for the society in general.

PhD in Microbiology, Biotechnology. The candidate must have at least one first author research publication in SCI-indexed Journals. Experience in microbiology testing and assay development. Isolation of microbes from human samples DNA, RNA, plasmid isolation, real-time PCR, etc. evidenced by PhD thesis.

Excellent written and oral communication skills. Dynamics of personality in handling multiple tasks simultaneously. Hard working, research inclination, sincerity, and commitment toward a research career.

B.Pharm, M.Pharm, M.Sc, B.E. with 2 to 10 Years of relevant experience of IPQA, Qualification, QMS, Sterility Assurance, QA IT related activities in Injectable Manufacturing Plant.

Keep a daily log to document all activities completed each day. Perform duties in compliance with Company’s policies and procedures, including but not limited to those related to HIPAA and compliance.

CORONA Remedies Pvt. Ltd. Our journey started in 2004, with a commitment to creating a better quality of health for all by being at the forefront of research, manufacturing and marketing of high quality products.

The candidate must possess a thorough understanding of relevant disease biology, the clinical landscape, emerging technologies, and the competitive environment. The candidate should demonstrate exceptional laboratory technical skills in cell and molecular biology, and, or in vivo pharmacology and proficient at devising strategic solutions to identify and resolve potential challenges.

Audit Response writing skill, Audit handling skill. Current Guideline assessment and compliance. Gap Assessment to overall Regulatory Compliance. Proficient in risk assessment, cleaning procedure optimization. Adept at collaborating with cross-functional teams to maintain robust cleaning validation programs.