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Clinical courses

 

Clinical courses

  • Exemed Pharmaceuticals Hiring RA Officer / Sr Officer / Executive

    Exemed is a regulatory-compliant, customer-centric, and global leading pharmaceutical company in India.  It was established in 2009 as part of a venture initiated by Mr. Pranav Patel. It is supported by two manufacturing facilities involved in the manufacturing of Drug-intermediates and specialty chemicals. Our state-of-the-art US FDA, EDQM, EU GMP certified facility is located in Luna and Vapi and headquartered in Vadodara, Gujarat.

  • Work as Regulatory Affairs Dossier at Rusoma Laboratories

    Rusoma Laboratories Private Limited, is committed to producing high quality, lifesaving & effective pharmaceutical products that patients & consumers can depend on. To meet this commitment we dedicate ourselves to the creation of a safe & quality-focused production environment As the pioneers in Large Volume Parenteral (LVP) production, we ensure that all our procedures & processes are enforced with consumer safety at the centre & in compliance with the applicable rules, regulations & standards.

  • PHARMA IMPURITY CONCLAVE 2023

    A fresh dawn emerges, revealing another intriguing program, but the familiar and persistent challenge remains steadfast.

    PHARMA IMPURITY CONCLAVE 2023
    September 7th - 8th

  • Teva Pharmaceuticals Hiring Regulatory Affairs Associate - M.Pharm, B.Pharm, MSc 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.

  • Aurobindo Pharma Hiring candidates for Regulatory Affairs Department

    AUROBINDO PHARMA LTD is a growing Indian multinational pharmaceutical manufacturing firm with turnover of over USD 2.8 Billion revenues for 2018-19, with presence in more than 34 countries fronted presence with products exported to 155 nations.

    Department : Regulatory Affairs (Oral Solids) - CMC 

    Experience : 04 to 10 Years

  • Job for M.Pharm in Regulatory Affairs at Roche

    Roche has established Global Analytics and Technology Center of Excellence (GATE) at Chennai to drive analytics and technology driven solutions by partnering with Roche affiliates across the globe.  As an Analyst / Sr Analyst, you will work closely with stakeholders in the business teams across Roches global affiliates and deliver high quality analytics solutions to real-world business problems. 

  • GSK looking for Regulatory Specialist

    GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. 

  • AstraZeneca looking for CMC Regulatory Affairs Associate Director

    AstraZeneca contributes meaningfully to the UK beyond the provision of our medicines and the benefits they provide to the health of the nation. We commissioned a report in 2009 to measure our significant investment to the UK economy, which includes investment in jobs and wealth creation. Oxera, an independent economic consultancy provided the analysis for this report.

  • Regulatory Affairs Lead Associate Require at Genpact Limited

    Genpact Limited, a global leader in business process and technology management services, leverages the power of smarter processes, smarter analytics and smarter technology to help its clients drive intelligence across the enterprise. Genpact’s Smart Enterprise Processes (SEP) framework, its unique science of process combined with deep domain expertise in multiple industry verticals, leads to superior business outcomes.

    Post : Lead Associate - Regulatory Affairs-LIF012815

  • Syneos Health looking for Regulatory Consultant | M.Pharm, B.Pharm, M.Sc Apply

    Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their objectives.

    Post : Regulatory Consultant

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