Regulatory affairs

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

Gracure Pharmaceutical Ltd. is a Delhi based pharmaceutical company, established in 1992 by Mr. A.S Bhargava with the vision of making world class affordable medicines. Gracure is a research driven forward looking pharmaceutical company with expertise in development of various finished dosage. Gracure R&D and EU-GMP approved Manufacturing Unit is located in Bhiwadi, Rajasthan.

Executive - Regulatory Affairs (ROW Market)
Qualification : M.Pharma
Experience : 3-6 Years

Exemed is a regulatory-compliant, customer-centric, and global leading pharmaceutical company in India.  It was established in 2009 as part of a venture initiated by Mr. Pranav Patel. It is supported by two manufacturing facilities involved in the manufacturing of Drug-intermediates and specialty chemicals. Our state-of-the-art US FDA, EDQM, EU GMP certified facility is located in Luna and Vapi and headquartered in Vadodara, Gujarat.

Hetero Drugs is an Indian pharmaceutical company and the world’s largest producer of anti-retroviral drugs. Hetero’s business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics. Globally renowned, vertically integrated pharmaceutical player engaged in Research and Development (R&D), manufacturing, and marketing of high-quality chemical and biologic medicines across diverse therapeutic areas.

Hiring for Formulation Regulatory Affairs

Rusoma Laboratories Private Limited, is committed to producing high quality, lifesaving & effective pharmaceutical products that patients & consumers can depend on. To meet this commitment we dedicate ourselves to the creation of a safe & quality-focused production environment As the pioneers in Large Volume Parenteral (LVP) production, we ensure that all our procedures & processes are enforced with consumer safety at the centre & in compliance with the applicable rules, regulations & standards.

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.

MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has nine API and five finished dosage facilities established across Hyderabad, USA and Myanmar. Innovation and speed form the crux of our business strategy.

AUROBINDO PHARMA LTD is a growing Indian multinational pharmaceutical manufacturing firm with turnover of over USD 2.8 Billion revenues for 2018-19, with presence in more than 34 countries fronted presence with products exported to 155 nations.

Department : Regulatory Affairs (Oral Solids) - CMC 

Experience : 04 to 10 Years

Roche has established Global Analytics and Technology Center of Excellence (GATE) at Chennai to drive analytics and technology driven solutions by partnering with Roche affiliates across the globe.  As an Analyst / Sr Analyst, you will work closely with stakeholders in the business teams across Roches global affiliates and deliver high quality analytics solutions to real-world business problems.