Regulatory affairs

Vacancy for Regulatory Affair Executive at Oracity Life Sciences

Oracity Life Sciences was focusing on solid oral dosage forms (Tablets / capsules) with immediate as well as modified release technology. We will be catering Granules for immediate release, modified release tablets, different range of pellets formulation ready to encapsulate, MUPS ready to compress along with finished dose formulation of tablets and capsules. We have designed the facility / systems to meet all regulatory standards (like WHO, MHRA, USFDA etc…) and will be catering to domestic, ROW and highly regulated market.

Post : Regulatory Affair Executive - 03 posts

Walk in interview in Production, Quality Assurance, Quality Control, Regulatory Affair at Biogen pharmaceutical

Biogen pharmaceutical co’s services continue to care from prevention and cure. Biogen pharmaceutical co is devoted to the Innovation, manufacture, co-market and export of Pharmaceuticals and hospital products for Human. Biogen pharmaceutical co will ensures its presence in Indian markets for its products and services to companies with marketing alliance. Biogen pharmaceutical co today, has a strong reputation in marketing to the healthcare solutions.

11th Annual Clinical Trials Summit 2020 at Mumbai

The 11th Annual Clinical Trials Summit 2020 to be held in Mumbai, India during 28th May 2020. The global Contract Research Organization (CRO) market size was estimated at US$ 34.5 billion in 2018 and is projected to reach US$ 55.3 billion by 2024, growing at a CAGR of 8.2% during 2019 to 2024. Indian clinical trials market size is expected to reach US$ 3.15 billion by 2025. It is projected to register a CAGR of 8.7% over the forecast period.Increasing cost of drug development is expected to drive the growth. Drug maker and sponsor companies are under pressure to replace the revenue loss caused by generics, increasing patent expiry, number of partnerships to identify biologics, and growing R&D costs, which has made drug development more expensive and complex. In addition, growing pressure on market players to follow stringent timelines has increased the demand for outsourcing of research activities.This Conference brings together Researchers, Doctors, Principle Investigators, Clinical research sites, CROs, CMOs, Investors, and senior executives from Biopharma, Medical devices and Pharmaceutical industries around the globe to discuss, reflect on and develop their ideas.

Associate Director require at Abbott

Abbott India Limited is a subsidiary of Abbott Laboratories, USA, a global, iversified 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 : Associate Director - Global Preclinical Development, EPD

Work as Associate Domestic Regulatory Affairs at Himalaya Drug Company

Every year, 300 million Himalaya products enter the homes of consumers around the world. With a range of over 300 healthcare and personal care products including brands like Liv.52, Cystone, and Bonnisan, we touch the lives of millions of customers worldwide, giving them products that help them lead healthier, enriched lives. Himalaya’s story began way back in 1930. A curious young man riding through the forests of Burma saw restless elephants being fed the root of a plant, Rauwolfia serpentina, which helped pacify them.

Post : Associate Domestic Regulatory Affairs

Require Executive Regulatory Affairs & Packaging at Johnson & Johnson

Johnson & Johnson was founded more than 120 years ago on a revolutionary idea: Doctors and nurses should use sterile sutures, dressings and bandages to treat peoples’ wounds.  Johnson & Johnson is ranked by Fortune Magazine as the 3rd most Admired Pharmaceutical Company in the world with an outstanding product range as well as an extensive research base with a number of life saving original research molecules.

Post : Executive Regulatory Affairs & Packaging

Opportunity for M.Pharm, M.Sc as Regulatory Affairs Associate at Teva Pharmaceuticals

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

Post : Regulatory Affairs Associate I

Job for M.Pharm, B.Pharm as Regulatory Affairs Associate at Teva Pharmaceuticals

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.

Post : Regulatory Affairs Associate I

Work as Deputy / Assistant Manager in Regulatory Affairs at Panacea Biotec

Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.

Post : Deputy / Assistant Manager – Regulatory Affairs

Work as Associate Regulatory Affairs Specialist at Medtronic

This is a question we’ve asked ourselves over and over. It’s how we at Medtronic have made hearts beat stronger and longer. It’s how we’ve pushed the limits of what technology can do in and for the body. It’s how we will continue to alleviate pain, restore health and extend life. Rising costs, an aging population, and the burden of chronic disease impact us all. And no single entity in the healthcare system can solve these challenges alone.

Post : Associate Regulatory affairs specialist

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