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Regulatory affairs

  • Walk in interview for M.Pharm, M.Sc, B.Pharm in Regulatory Affairs – API Division at MSN Laboratories Pvt. Ltd

    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.

  • Walk in interview for M.Sc, B.Pharm in Regulatory Affairs, Production at SMS Pharmaceuticals Ltd

    SMS Pharmaceuticals Ltd. is a global player in API manufacturing having a strong research and manufacturing team supported by state of the art facilities. What started off as a single facility single product manufacturing company in 1990 grew to be a multi-location group having product list spreading across an array of therapeutic segments. SMS was given the export house status in the year 1997-98. SMS is currently a listed company having ever appreciating international and domestic customer base.

  • Zydus Cadila looking for Regulatory Affairs - Vaccines & Diagnostics Manager

    Zydus Cadila, a leading Indian Pharmaceutical company is a fully integrated, global healthcare provider. With in-depth domain expertise in the field of healthcare, it has strong capabilities across the spectrum of the pharmaceutical value chain.

    Post : Regulatory Affairs - Vaccines & Diagnostics Manager

  • Work as Regulatory Affairs Executive at Piramal Healthcare Limited

    Piramal Healthcare Limited A major force in the pharmaceuticals and healthcare segment, Piramal Healthcare Limited, incorporating Healthcare Solutions and Pharma Solutions, has an unequivocal vision to become the most admired pharmaceutical company, with leadership in market share and profits.

    Post : Executive Regulatory Affairs

  • Teva Pharmaceutical looking for Regulatory Affairs Associate | B.Pharm, M.Pharm, M.Sc apply

    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.

  • Job Openings for M.Pharm, M.Sc at Accuprec Research Labs

    Accuprec Research Labs Pvt Ltd. is FDCA approved, NABL accredited and ISO 9001:2015 certified CRO. Head Quarter of the CRO is located at Ahmedabad and branch offices at Canada and USA. Accuprec provides all type of Pharmaceutical testing solutions to its domestic and MNC clients.

    Post: Manager (MB), Research Assistant (RA)

  • Opportunity for M.Pharm, M.Sc, B.Pharm in Regulatory Affairs at Lambda Therapeutic Research Limited

    Lambda Therapeutic Research Limited is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad - India, with facilities and operations in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA), Fargo (USA) and Canada (Toronto), with a collective workforce of more than 1500 employees.

    Post : Officer/ Executive/ Sr. Executive

  • Walk in for QC, Production, Regulatory Affairs at SMS Pharmaceuticals

    SMS Pharmaceuticals Ltd. is a global player in API manufacturing having a strong research and manufacturing team supported by state of the art facilities. What started off as a single facility – single product manufacturing company in 1990 grew to be a multi-location group having product list spreading across an array of therapeutic segments. SMS was given the export house status in the year 1997-98. SMS is currently a listed company having ever appreciating international and domestic customer base.

  • Opportunity for M.Pharm, M.Sc in Regulatory Affairs at Zydus Cadila

    Zydus Cadila, a leading Indian Pharmaceutical company is a fully integrated, global healthcare provider. With in-depth domain expertise in the field of healthcare, it has strong capabilities across the spectrum of the pharmaceutical value chain.

    Post : Assistant Manager / Deputy Manager - Regulatory Affairs (API)

    The incumbent should have M.Sc / M.Pharm with 8 to 10 years of relevant experience in API Regulatory Affairs.

  • Walk in interview for B.Pharm, M.Sc in Production, Regulatory Affairs at SMS Pharmaceuticals Ltd

    SMS Pharmaceuticals Ltd. is a global player in API manufacturing having a strong research and manufacturing team supported by state of the art facilities. What started off as a single facility – single product manufacturing company in 1990 grew to be a multi-location group having product list spreading across an array of therapeutic segments. SMS was given the export house status in the year 1997-98. SMS is currently a listed company having ever appreciating international and domestic customer base.

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