Multi-centric Syndromic Surveillance of Acute Febrile Illness. Indian Council of Medical Research require M.Sc. in Microbiology / Biotechnology with a experience in molecular diagnostics, public health programmes and surveillance systems.

B.Pharmacy from a recognized university. Registered with Pharmacy council. AIIMS Bathinda for Bharat Health Initiative for Sahyog, Hita and Maitri, BHISHM Cube.

Performing routine analysis of raw materials, intermediates, and finished products using sophisticated instruments like HPLC, GC, and UV to ensure strict quality standards. WALK IN FOR FRESHERS at Ipca Laboratories

IPQA Officer / Executive with strong exposure to OSD manufacturing operations including Granulation, Compression, Coating.

Candidate for direct recruitment to the service must possess a diploma in Pharmacy from a recognized institution and must also be registered with the State Pharmacy Council.

Two years Diploma in Pharmacy (D-Pharma) (Allopathic) recognized by the Government of state pharmacy Council and registered as "A" category Pharmacist under West state Pharmacy Council.

MSc Biotechnology / Biochemistry with First Class OR Integrated M.Sc Biotechnology / Biochemistry with First Class.

Emcure is fast-growing Indian pharmaceutical company engaged in developing, manufacturing, and marketing a broad range of pharmaceutical products globally

Officer of State Government of India/State statutory/Autonomous Bodies/Universities holding analogous post on regular basis. Or Officers from the post of Senior Pharmacist with three years of regular service in Level-06 or equivalent or above.

Bachelor / Master degree in Pharmacy. The project aims to estimate impact of medical adherence app and manual pill organiser on medication adherence and clinical outcomes in geriatric patients on multiple medications.

Responsible for one or several of the following: processing of Individual Case Safety Reports (ICSRs) from various sources, Literature search and review, signal detection and management, tracking regulatory information

Post Graduate in Science (M.Sc.) in any discipline (preferably Clinical Research/Life Sciences) with Degree/Diploma in Clinical Research (mandatory if not M.Sc. in Clinical Research).

M.Pharm / M.S.Pharm / M.Tech with specialization in Pharmaceutics, Biotechnology, Medical Devices, Nanomedicine or equivalent. GPAT, GATE, NET will be preferred.

Looking for enthusiastic fresher candidates for production activities in the Manufacturing Department, who are eager to start and grow their career in the pharmaceutical industry.

Adequate understanding on respective authority guidance and filing of new product and post approval changes. Review of documents related to product registration and dossier submission leading to faster approval

Contribute to preparation and delivery of regulatory submissions from a global and regional perspective. Preparation and review of Marketing Authorization Applications & Variations for filing in US, EU, Japan, Canada Switzerland, Australia.

D.Pharm plus two Years experience in relevant subject/field. Managing Ocular Surface Disorders, Randomized Trials on Dry Eye Disease and Meibomian Gland Dysfunction

The regulator has announced that companies will now receive the No Objection Certificate, NOC more quickly, helping to streamline regulatory procedures and reduce approval timelines.

M.Pharm in Pharmaceutics / Pharmacology or any other equivalent Degree. Previous research/industry experience in exosome formulation and development, animal handling skills.

M.Sc / M.Tech in Biotechnology / Biochemistry / Molecular Biology / Life Sciences / Pharmaceutical Biotechnology or allied disciplines.