DRA

  • PharmaTutor
    12 June 2011

    Post for a Regulatory Medical Writing - Safety Lead in Novartis

    A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

  • 9 June 2011
    Requirement of Regulatory Affairs Manager in Brawn Laboratories Limited

    BRAWN, with its inception barely 21 years back(1988) has today evolved into a fully integrated, healthcare group, marking its presence in India and dotting various major markets across the globe. With its claim of quality and certified with ISO 9001:2000, 13485, WHO : cGMP, BRAWN is proud to possess product registration with major health and govt. institutions throughout India and in many other countries worldwide.

  • 7 June 2011
    Career as Regulatory Executive/ Officer in Ultratech India Limited

    Ultratech India Limited is a FDA, GMP & ISO certified manufacturer that caters to worldwide pharma markets for products across the pharmaceutical value chain ranging from a wide range of Pharmaceutical Formulations in various dosage forms ( Tablets, Capsules, Syrups, Injections, Nasal Sprays, Metered Dose Inhalers) to Active Pharmaceutical Ingredients and upto advanced drug intermediates.

  • 6 June 2011
    Post for a Senior Regulatory Affairs Manager @ Venus Remedies

    Venus start each day by focussing on Innovation & Creativity. We make sure that best healthcare is provided to our patients worldwide.
    From a humble beginning in 1991, now we are engaged & engrossed in discovering, developing and delivering innovative pharmaceuticals that help patients to alleviate sufferings.

  • 31 May 2011
    Requirement of Senior Executive - Regulatory Affairs in Naari

    NAARI aspires to be a world leader in the area of female healthcare, providing medical solutions from puberty to menopause. Our aim is to be the world’s first 100% integrated generic female health pharmaceutical company. This implies complete involvement in every step of production, going from plant extract to final dosage forms. By giving our stake holders cutting edge expertise, we set the standard for female health products, globally.

  • 31 May 2011
    Job as a Documentation / Medical Writing - R&D at Flamingo Pharmaceuticals

    Flamingo Pharmaceuticals Ltd. is a quality driven pharmaceutical company with an experience of over two decades in global markets, exporting to 52 countries and having Rs.200 crores+ turnover. Flamingo has WHO-GMP/UK MHRA certified 100% EOU unit.

  • 30 May 2011
    Work as a DRA Executive at Genpharma

    GenPharma is a GMP approved pharmaceutical company having its state of art manufacturing Units in Pune and have global presense in Pharmaceutical Formulations.

    Post: DRA Executive

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  • 24 May 2011
    Applications are Invited in Sree Chitra Tirunal Institute for Medical Sciences and Technology for the Post of Fellowship

    Sree Chitra Tirunal Institute for Medical Sciences & Technology (SCTIMST), Thiruvananthapuram is an Institute of National Importance  established by an Act  of the Indian Parliament  and  under the 2 administrative control of the Department of Science and Technology, Government of India.

  • 23 May 2011
    Openings for Regulatory Affairs Manager @ Chemilines Healthcare India (P) Ltd. - 2 Openings

    Well established and continually expanding, Chemilines are recognised as one of the UK's leading pharmaceutical importers and distributors of sourced branded medicines, generics and perfumes in the UK. In Southern Ireland, Chemilines is a major distributor of branded fragrances and over the counter products.

  • 10 May 2011
    Job in Troikaa Pharma as Officer RA - corporate affairs

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