Regulatory affairs

The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products. The JAMP Pharma Group has also made a major investment in biosimilars which is one of the fastest growing markets in the pharmaceutical industry.

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 & TGA approved Manufacturing Unit is located in Bhiwadi, Rajasthan.

HIRING FOR REGULATORY AFFAIRS (CANADA, AUSTRALIA AND UK)

Post : Executive / Sr. Executive

Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company’s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries.

Post : Principal Specialist, Regulatory Affairs (Hybrid)

At Lilly, we make a difference for people the world over by discovering, developing and delivering the breakthrough medicines that help them live longer, healthier more active lives. What’s more, you can also count on us and our people to be incredibly civic-minded, supporting our communities through philanthropy, volunteerism and a creative and innovative can-do spirit.

Post : Associate/Sr. Associate - Regulatory Affairs - Clinical RA

Endo India Par Formulations is a pharmaceutical company that develops, manufacturers and markets safe, innovative and cost effective pharmaceuticals that help improve patient quality of life. At Endo our investment in state-of-the-art equipment and facilities, commitment to ethical standards, and growing portfolio of products makes us a company where you can enjoy a productive career with long-term potential.

Post : Regulatory Affairs Associate (Mumbai)

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

Apotex Inc. is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 8,000 people worldwide in manufacturing, R&D, and commercial operations.  Apotex Inc. exports to more than 100 countries and territories and operates in more than 45 countries, with a significant presence in Canada, the US, Mexico, and India.

Apotex Inc. is a proudly Canadian, global pharmaceutical company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 8,000 people worldwide in manufacturing, R&D, and commercial operations.  Apotex Inc. exports to more than 100 countries and territories and operates in more than 45 countries, with a significant presence in Canada, the US, Mexico, and India.

FDC is a people-oriented organization, dedicated to innovate, manufacture and market high-quality healthcare products that enhance the quality of human life all over the globe, and in turn, increase shareholders value.

Post : Executive / Senior Executive

Regulatory Affairs (US/EU) - Executive/ Senior Executive
No of post : 01
Experience : 4 to 8 years
Job Description : Preparation of New Applications, Query responses, Post approval changes for EU & US market