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. 

Pharmacist to work in the Self Financing scheme on Establishment of Retail Pharmacy outlet for the Supply of Veterinary Health Care Products and Supplements in Madras Veterinary College Hospital, Chennai functioning at Directorate of Clinics, Madras Veterinary College Campus, Chennai

M.Sc. in Chemistry or equivalent degree minimum of 55% marks or equivalent grade with specialization in Organic Chemistry.  Working experience in Industry or chemical research laboratory; Experience in Electro organic Chemistry and Natural Product Synthesis

AstraZeneca is committed to contributing to our broader society, and encourages an environment for talents from a broad diversity of backgrounds, providing equal opportunities for learning and growth. With this in mind, Project iDEA was created to connect students from diverse cultures, perspectives and ethnicities to the pharmaceutical industry.

Intas is expanding and evolving its Biopharmaceutical capabilities. We invite ambitious professionals to be a part of its future growth story.

 IPQA Mfg. & Packing, Shop floor activities, Review of equipment audit trails, BMR, BPR review, line clearance. Process Validation, equipment, Utility qualification.

Handling HPLC. Compilation of Raw Data for Review. Sampling and Release of Raw material and Packaging Mate. Analysis & preparation of water Trends.

0-2 years Knowledge of GMP, FFS, Semi solid manufacturing process, BMR -BPR preparation, knowledge of ALCOA, Audit readiness, EHS adherence in manufacturing