Mumbai

The Central Government Health Scheme (CGHS) is a welfare scheme introduced by Govt.of India under Ministry of Health and Family welfare initially in Delhi on 1st July 1954. Over time, it has grown all over the country both in coverage and scope. Now there are 25 CGHS units in different cities to provide comprehensive Medical care facilities to the Central Government employees (serving & pensioners), their family members, and other entitled categories for a token contribution.

Colgate-Palmolive is a leading global consumer products company, tightly focused on Oral Care, Personal Care, Home Care and Pet Nutrition. Colgate sells its products in over 200 countries and territories around the world under such internationally recognized brand names as Colgate, Palmolive, Speed Stick, Lady Speed Stick, Softsoap, Irish Spring, Protex, Sorriso, Kolynos, elmex, Tom’s of Maine, Sanex, Ajax, Axion, Fabuloso, Soupline and Suavitel, as well as Hill’s Science Diet, Hill’s Prescription Diet and Hill’s Ideal Balance.

Post : Global Regulatory Affairs Associate

Homi Bhabha Centre for Science Education (TIFR), Mumbai hereby invites applicants for Walk-in-Interview for one position of Project Scientific Assistant- B (Junior Science Olympiad) in HBCSE.

Post : Scientific Assistant

HelpAge India is a leading charity in India working with and for disadvantaged elderly for more than 3 decades. It was set up in 1978 and is registered under the Societies' Registration Act of 1860. Traditionally the focus was to improve the quality of life of destitute elders primarily in the rural areas through its welfare projects by providing free rations, free medicines and consultations and conduct free cataract surgeries.

Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!  Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team.

Cactus Medical offers medical writing services to multinational pharma, clinical research organizations, and researchers worldwide. We work with clinicians and researchers to help them communicate their science to the world. We are currently looking to add to our team of medical writers, researchers and healthcare professionals who want to explore the field of medical writing, be part of a world-class delivery team, and work in an exciting, fast-paced global environment.

Post : Project Manager, Pharma – Only Night Shifts

Abbott India Limited is a subsidiary of Abbott Laboratories, USA, a global, diversified health care company devoted to the discovery, development, manufacture and marketing of pharmaceutical, diagnostic, nutritional and hospital products. The company now employs approximately 70,000 people and markets its products in 130 countries worldwide.

Post: National Sales Manager

Cactus Communications—a company dedicated to the pursuit of good English. We provide editing, educational, transcription, and training services to individual and institutional clients worldwide. All our businesses are linked together by one common factor—great written English. Since our establishment in April 2002, we have carved a niche for ourselves as a company providing language solutions of the highest quality.

Post : Quality Control Specialist

The incumbent will be responsible to support analytical research and development activities for NCE (new chemical entity), LCM (life cycle management) and NEB (new established brand) projects. The person hired into this position will work in close collaboration with other functional line colleagues (chemistry, formulation, API scale up etc) to best support product and process development in line with project plan. Candidate will be responsible for supporting multiple projects and the interfacing with various customers and partner groups across the organization such as global development team, regulatory, quality, manufacturing and clinical organizations as well as coordinate the analytical activities outsourced to vendors. The candidate will be responsible for authoring various documentations such as specifications, test procedures, method validation plans, protocols, reports, stability data, SOPs, CMC technical sections for regulatory submission etc.

Post : Principal Scientist - Analytical Research and Development (ARD) (JR28022017)