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Regulatory affairs

 

Clinical courses

 

Clinical courses

  • Job for Pharmacovigilance Associate at Accenture

    Accenture is a global management consulting, technology services and outsourcing company, with approximately 275,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the world’s most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments.

  • Job for Professor, Associate Professor, Assistant Professor at Chandigarh College of Pharmacy

    Chandigarh Group of Colleges, Landran has become a synonym to excellence. Situated on the National Highway 205A, Chandigarh Group of Colleges bespeaks A-class educational facilities. CGC, Landran has come a long way in the field of education. In the year 2001, it got incepted with a hope to bridge the gap between inquisitive minds and education.  Initially, Engineering was the flagship program at CGC, Landran and with time, more & more programs got added to the curriculum. Currently, the college offers 40+ programs under eight domains namely Engineering, Biotechnology, Computer Application, Management, Education, Pharmacy, and Hotel Management.

    Post : Professor/ Associate Professor/ Assistant Professor

  • Vacancy for B.Pharm, M.Pharm as Regulatory Affairs Associate at PAREXEL

    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 : Regulatory Affairs Associate

  • Require Research Scientist at Jubilant Pharma Limited | M.Pharm

    Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients.

    Post : Research Scientist - DRA (Formulations)

  • Require Regulatory Affairs Specialist at Medtronic

    Together, They can change healthcare worldwide. At Medtronic, They push the limits of what technology can do to help alleviate pain, restore health and extend life.  We challenge ourselves and each other to make tomorrow better than yesterday.  It is what makes this an exciting and rewarding place to be.

    Post : Regulatory Affairs Specialist

  • Work as Senior Manager in Regulatory Affairs at Pfizer

    Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

    Post : Sr Manager, Regulatory Affairs

  • Walk in interview in Production, Quality Control, Regulatory Affairs at Shilpa Medicare Limited

    Shilpa Medicare Limited (SML) started its operations as API manufacturer way back in 1987 at Raichur, Karnataka- India. The commercial production in the SML was started in November 1989. Today Shilpa Medicare Limited is a global brand in manufacturing and supplying of affordable API and Formulation globally in different regulated markets.

  • Vacancy for Regulatory Affairs Associate Analyst at Novo Nordisk

    Novo Nordisk is a global healthcare company with 89 years of innovation and leadership in diabetes care. The company also has leading positions within Haemophilia care, growth hormone therapy and hormone replacement therapy. Headquartered in Denmark, Novo Nordisk employs approximately 33,300 employees in 75 countries, and markets its products in more than 190 countries Novo Nordisk’s B shares are listed on NASDAQ OMX Copenhagen (Novo-B).

    Post : Regulatory Affairs Associate Analyst

  • Walk in interview for M.Pharm, M.Sc, B.Pharm in Quality Control, Quality Assurance, Regulatory Affairs, Research & Development at Everest Organics Limited

    The company was incorporated on 19.02.1993 to carry on the business of manufacturing of bulk drugs viz. Omeprazole, Ciprofloxacin, Dichloroflurobenzene, Benzimadizole, etc., having its factory at Sadasivpet Medak District Hyderabad. The construction activities have started in the year 1994 and the commercial production of the company has started in 1996. During the Year 1995 the company went into public issue and the shares of the company have been Over-subscribed by 39.632 times. With full swing the company started its production and got a good market share for their products.

  • PAREXEL looking for Senior Regulatory Affairs Associate | B.Pharm, M.Pharm

    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

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