D.Pharm Council Registration Certificate will be required under the National Urban Health Mission

Candidate having experience in network pharmacology, cell culture protocols, molecular biology protocols, animal handling, surgery in experimental animals, will be given preference. Experience or basic knowledge in in vitro cell culture and fundamental knowledge of molecular pharmacology will be preferred.

PhD with 3 years experience in Biological Science, Biotechnology, Biochemistry, Bioengineering, Pharmaceutical Technology or any branch of Life Sciences Relevant to essential criteria. 

Post Graduate degree in Biotechnology Life Science subject with two year experience from recognized university. Post Graduate degree in Bio informatics subjects with two year experience from recognized university.

Hands-on experience in a professional pharmaceutical environment. Exposure to innovative practices, research methodologies, and industry standards. Opportunity to collaborate with skilled professionals and enhance your career prospects.

Have good exposure in Plant Maintenance & Instrumentation related work in sterile facility. Have good exposure in Sterile IPQA & Sterile Qualification Related activity.

Must be from Parenteral background & exposure to Aseptic vial, Bottle filling process is desirable. To be aware and responsible for achieving quality objective and fulfilling the requirements of applicable quality procedures. Sound technical knowledge of Aseptic area & Controlled area related activities.

As per the batch manufacturing procedures and packing protocols, samples such as in-process samples, finished product samples, stability samples, control samples, cleaning samples, and other samples should be collected and submitted

Having Injectable Experience of Analysis of raw material. In-process, Finish products, Stability testing, Process validation. Hands on Experience of HPLC, GC, LBPC, Osmometer, KF Auto titrator and UV - Visible spectrometer, LIMS,QMS,Participate in Lab incident , OOS, OOT, Analysis of deviation.

Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. Conducting signal detection and risk assessment activities to identify potential safety issues.

Conduct preliminary review of laboratory results relative to established protocol-specific reference range guidelines, using relevant clinical laboratory experience and compares current results with prior laboratory values to evaluate or note clinically significant increases, decreases and contacts the investigator site for pertinent additional clinical contact for distribution to project team

Novo Nordisk is now discontinuing its Human Mixtard penfill by the year's end. However Mixtard in India will continue to be available in vials. Along with it, other forms of insulin including human insulin from Novo Nordisk will continue to be available in vials & devices for patients across India.

Aclaris Therapeutics, Inc, a clinical-stage biopharmaceutical company focused on developing novel product candidates for immuno-inflammatory diseases, today announced that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for a Phase 1a/1b clinical trial of ATI-052, a potential best-in-class bispecific anti-TSLP/IL-4R monoclonal antibody.

Antibodies are best known for their ability to latch onto and neutralize bacteria, viruses and other pathogens. But these immune proteins can do more than that: They also activate other components of the immune system, which then go to work to clear an infection. A new study from Scripps Research explores the factors that influence how effectively antibodies engage specific immune cells.

This workshop is designed to empower faculty members, researchers, and postgraduate students with practical knowledge and skills for the ethical and effective use of Artificial Intelligence in academia and research. It offers comprehensive, hands-on training in utilizing advanced Al tools for literature review, research writing, manuscript development, data analysis, presentation, and responsible publishing practices.

Diploma in Pharmacy from an Institute recognised by Govt and Bachelor in Pharmacy from an Institute recognised by Govt. Candidate must be registered with State Pharmacy Council, Pharmacy Council of India.

Qualification Norms as per the Pharmacy Council of India & The Tamil Nadu Dr. MGR Medical University, Chennai

Compounders, Pharmacists having Diploma in Homeopathic, Ayurveda, Unani from recognized Institutions 2 years or more work post-qualification experience in a relevant field from government or government-recognized institutions.