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  • 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.

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

  • Quality Assurance Associate require at Dr. Reddys Laboratories | 04 vacancies
    Quality Assurance Associate require at Dr. Reddys Laboratories | 04 vacancies

    Dr. Reddys Laboratories is an emerging global pharmaceutical company with proven research capabilities. The company is vertically integrated with a presence across the pharmaceutical value chain. It produces finished dosage forms, active pharmaceutical ingredients and biotechnology products and markets them globally, with focus on India, US, Europe and Russia. The Company conducts research in the areas of cancer, diabetes, cardiovascular, inflammation and bacterial infection.

  • Vacancy for B.Pharm, M.Sc in Production, Packing at Lupin Pharmaceuticals
    Vacancy for B.Pharm, M.Sc in Production, Packing at Lupin Pharmaceuticals

    Lupin Pharmaceuticals, Inc. is the U.S. wholly owned subsidiary of Lupin Limited, which is among the top six pharmaceutical companies in India. Through our sales and marketing headquarters in Baltimore, MD, Lupin Pharmaceuticals, Inc.

    Post : Production (Oral contraceptive & High Potent Drug) & Packing (Oral contraceptive & High Potent Drug)

  • Walk in interview for M.Pharm, M.Sc, B.Pharm in QC, Production at Torrent Pharma
    Walk in interview for M.Pharm, M.Sc, B.Pharm in QC, Production at Torrent Pharma

    Torrent Pharma, the flagship Company of Torrent Group, with a turnover of Rs. 8005 Cr is one of the leading Pharma companies in the Country. We are the pioneers in initiating the concept of niche marketing in India and today is ranked amongst the leaders in therapeutic segment of cardiovascular (CV), central nervous system (CNS), gastro-intestinal (GI) and women healthcare (WHC). The Company also has significant presence in diabetology, pain management, gynaecology, oncology and anti-infective segments.

  • Openings for MPharm or MSc at NARIP - Ministry of Ayush
    Openings for MPharm or MSc at NARIP - Ministry of Ayush

    National Ayurveda Research Institute for Panchakarma, Cheruthuruthy was started on 21st June, 1971 and has over the years grown tremendously in terms of infrastructural facilitates and the number of patients who are being treated, both in OPD and IPD. The Institute has a Pharmacy which not only meets the requirements of the Institute but also provides medicines to other Institutes/ Units. The Quality Control laboratory of the Institute ensures that the medicines proposed in the Pharmacy are as per prescribed standards.

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

  • Walk in for Pharma Quality Assurance, Quality Control, Production, Packing for Zydus Cadila Ahmedabad plant
    Walk in for Pharma Quality Assurance, Quality Control, Production, Packing for Zydus Cadila Ahmedabad plant

    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.
    Zydus Cadila is recruiting for Greenfield, formulation manufacturing plant located at Ahmedabad.

    Post: Asst. Manager/Dy. Manager - QA, QC, Technical Assistant and Deputy Manager / Associate Manager / Manager Shift Incharge - Production, Technical Assistant - Packing

  • Maithri Drugs Pvt Ltd walk in Interview for QA Department | M.Pharm, MSc, B.Pharm apply
    Maithri Drugs Pvt Ltd walk in Interview for QA Department | M.Pharm, MSc, B.Pharm apply

    MSN Group is one of the fastest growing manufacturers of Active Pharmaceutical Ingredients (APIs) and Finished dosages in India. Established in the year 2003, MSN Group comprises of 330 API manufacturing plants (including one for Oncology), three finished dosage facility ( including one for Oncology)and a dedicated R&D Center . Our plants are ISO 9001-2000 certified, WHO: GMP, EU:GMP and USFDA approved.

    QA Department

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

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