Expertise of Finish goods testing. Stability, RM Analytical Method Validation, Dissolution, HPLC, PMQC and knowledge of handle other sophisticated instruments like GC, XRD, ICPMS, LCMS.
For paper studies, ensures all CRFs and DCFs received are returned for filing in the Document Control Room per the Data Tracking Guidelines for the assigned projects.
Master in Life Sciences, pharmaceutical sciences, animal sciences, biotechnology, microbiology, MVSc with NET, GATE or other national level examination conducted by Central Government departments like DBT, DST or equivalent
M.Sc. Medical Sciences, Pharm.D, BDS, MPH. Prior experience in field work or project management in medical research or experience in Pulmonary function testing
Advanced degree in life sciences, healthcare or clinically relevant degree is required. Masters, PharmD, M.Pharma, PhD, MBBS, BDS, MD strongly preferable. Fluent English
Responsible for process validation and cleaning validations and respective documentation. Responsible for Equipment and utilities qualification and periodic validation.
Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.
Post : Team Lead Medical Communications (Scientific Engagements)
Liaise with key partners, including Pfizer Country Organizations, Clinical Development, License Partners, and other stakeholders regarding safety data collection and data reconciliation.
Masters degree in Pharmacy or Pharmaceutical Chemistry or Pharmacology or Chemistry or Biochemistry or Bacteriology or Medicine or Microbiology or Biotechnology; in the Regional Drugs Testing Laboratory, Guwahati, CDSCO, DGHS, Ministry of Health and Family Welfare.
ECHS Unites application to engage the following vacancies Medical. Para Medical & Non Medical Staff on contractual basis in 02 x Polyclinic. Devlali and Dhule for a period of one year renewable for additional period of one year/ till attaining the maximum age subject to performance of candidates/ other conditions according to the criteria as mentioned against each post :
M.S (Pharm)/ M. Pharm/ M.Sc in Pharmacy/ Biomedical Engineering, Biotechnology; The project involves development of synthetic tracheal tubes, evaluation of in vitro cytotoxicity and in vivo biocompatibility in animal model.
M.Sc. In Biochemistry/ Pharmacology/ Biotechnology/ Life Scienccs or equivalent with two years of research experience or M.Tech. Study of selected Ayurvedic herbs for their anti-angiogenic potential and toxicity profile in zebrafish embryo model for cancer management.
Development and Evaluation of the Effectiveness of Improved Take-home Foods in Combination with Behaviour Change Intervention to Improve Nutritional Status. in Children in Selected Districts of Six States of India, A Cluster Randomized Controlled Trial
PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries.
Post : Senior Regulatory Affairs Associate (Labelling)
M.Pharm/B.Pharm/M.Sc/B.Sc; IPQA/APQR/Validation and Qualification; Handling Change Control/ CAPA/ Deviation/ Investigation and Audit Management; Issuance and Retrieval of GMP Document
Centaur Pharmaceutical is the largest specialty of drug manufacturing Organization. We provide high quality affordable medicines trusted by healthcare professionals like USFDA and MHRA. We are one of the rapidly growing Pharmaceutical Company in India. To keep pace with our growth plan, we required young and energetic professionals for our Pune site, having experience in Formulation / Oral solid dosage.
Ph. D, MD, MS, MDS or equivalent degree or having 3 years of research, teaching and design and development experience after MVSc, M.Pharm, ME, M.Tech with at least one research paper in Science Citation Indexed journal.
Passed Madhyamik, Secondary from a recognised Board and Diploma, Certificate course in Ayurvedic Pharmacy, Homeopathic Pharmacy conducted by the Paschim Banga Ayurved Parishad, Council of Homeopathic Medicine, West Bengal.