ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology,
Thorough knowledge of EU, MENA and ASEAN markets country requirements, regulatory affairs procedures for initial submission, licensing, post-approval submission management
Candidate with major in Life Science in Forensic Science obtained from any other educational institution in India deemed to be or recognized as a University as declared by or under a Central or State Act or declared under Section 3 of the University Grants Commission Act, 1956. OR Forensic Pharmacy OR Forensic Nanotechnology OR Botany OR Zoology OR Bio-Chemistry OR Micro-Biology OR Life Science OR Bio-Science OR Bio-Technology or should possess a post-graduate degree in Genetics
Possess A degree in Pharmacy or a diploma in Pharmacy of a recognized university or an equivalent educational qualification and must have registered his her name with the Gujarat pharmacy council. Provided that preference shall be given to a candidate having experience in dispensing the medicine in hospitals or dispensaries.
Candidate should have done Bachelor of Pharmacist, Diploma Pharmacist from a recognized College, University. Candidate should have registration of Pharmacist Council of Gujarat.
Master Degree or PG Diploma in Life Sciences or Biomedical Sciences or Pharmacy or Public Health or Clinical Research.
at least 4 years of demonstrated experience in clinical trial monitoring or clinical site management experience.
Doctoral Degree in Science from a recognised university or equivalent in stem cell biology, developmental biology, pharmacology, and or maternal or child health.
Having exposure related Environment Monitoring in formulation, water analysis, various Microbiological test like sterility, BET, MLT etc. Having exposure related to regulatory plant and basic know of GLP GMP. Ready to work in rotational shift.
Dr. Akram Ahmad, founder of Academically Global, has been recognized as one of the recipients of the prestigious BW HealthcareWorld 40 Under 40 Awards 2024. The awards ceremony took place on August 31, 2024, at The Imperial Hotel, Janpath, New Delhi. This accolade celebrates the dynamic young leaders shaping the future of healthcare in India.
Bachelor Degree in Pharmacy B.Pharm from a recognized university or equivalent and Registered as Pharmacist under the pharmacy Act 1948 The selected candidate has to be registered in Delhi Pharmacy Council within six months of joining.
Must have at least 02 years experience in hospital/clinics. In case B.Pharm candidate is not available then D.Pharm candidates with minimum 02 years experience will be considered. Must have computer knowledge.
Applications are invited from eligible candidates for the following posts on contractual and contractual basis as shown in the table below recruitment process for Nandurbar districts under National Health Mission.
PG Professional degree in Life Sciences, Pharmacology, Chemical Sciences or equivalent, M.Tech, M.Pharma or equivalent with two 2 years of post-qualification experience in the field of bioanalytical chemistry with emphasis on drug metabolism and pharmacokinetic DMPK studies.
The candidate must have a M.S, M.Pharm, degree in Medicinal chemistry, Natural Products, Pharmaceutical Analysis from a PCI, AICTE, UGC, NAAC recognized, accredited University, Central Autonomous Institutes with 60% marks or above.
M.D Pharmacology M.V.Sc. Pharmacology M.Pharma, M.Sc. Medicinal Plants with specialization in Pharmacology from a recognized University Institution. Post Graduate degree in the Chemistry from a recognized University, Institution.
After a journey of growth spanning 27 years as Cadila Healthcare Ltd. and the Zydus Group, we have evolved and transformed ourselves in response to the changing times.
Production QMS Quality Management System Handling of QMS activities like Deviation, Incident, Investigation, CCP, Protocol Preparation, Risk Assessment etc.
Responsible for Execution of Placebo, Scale up & Trial batches. Review Validation protocol, Report, responsible for validation batches manufacturing. Preparation of scale up and trial batch summary to support the commercialization of products.