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Company Jobs

  • Abbott looking for Pharmaceutical Scientist

    Post Graduation in Pharmacy or Pharmaceutical Science; Providing technical support to Abbott manufacturing facilities and Third-Party Manufacturers in the region. Collaboration with Manufacturing, Supply Chain, Commercial, Quality Assurance and Regulatory Affairs is critical to the success of this role.
  • Require Senior Regulatory Associate at Indegene
    Candidate will be responsible for preparing and managing regulatory dossiers, coordinating with regulatory authorities for EU and ASEAN markets and providing guidance on regulatory requirements to internal teams.
  • Hiring Executive for ADL Department at Torrent Pharma - M.Pharm, MSc Apply

    Torrent Pharma has a broad portfolio, comprising BGx medicines, which keeps us ahead in bringing quality medicines for patients all over the globe. Our Team of 700+ Scientists dedicate their lives for finding solutions for patients, who suffer from different ailments at varying levels of severity. Our Cutting-edge research and development enables us to continuously enhance our portfolio, explore new therapeutic areas and contribute to better life care for everyone.

  • Walk In Interviews for OSD Production & Packing at Zydus Lifesciences
    B.Sc, B.Pharma, B.Tech CVC Bottle line with 3 to 7 years of experience in handling of Primary Packing activities. Perform packing line clearance, supervise operation for Bottle packing line.
  • Vacancy for Ph.D, Pharm.D, M.Pharm as Medical Scientific Liaison at Novartis
    Acts with credibility and clarity of purpose to build and maintain effective and collaborative relationships, working knowledge of the Healthcare System and research procedures as well as the guidelines relevant to the pharmaceutical industry.
  • Work as Reg CMC Associate at Pfizer
    Bachelor or Master degree Biotechnology, Pharmacy, Science or Ph. D Biotechnology, Biological Sciences or equivalent. Minimum 3-5 Years of experience in Pharmaceutical Industry with major experience in Regulatory Sciences group handling new submissions and, or LCM submission to global health authorities especially USFDA, EMA and other EU authorities.
  • Vacancy for M.Pharm, B.Pharm, M.Sc in Purchase, Analytical Development at Bioplus Life Sciences

    For over 75 years, Bioplus has served the pharmaceutical industry with high quality products, service, and technology. While continuing to build our global partnerships in Contract Manufacturing and EU / ANZ pharma generic pharmaceuticals, we are increasingly focused on utilizing our advanced skill set in Biotechnology. Today we are a late-stage clinical phase company with 2 programs for large global unmet needs both of which are Clinical phase 3 ready.

  • Natco Pharma Limited Walk in Drive for M.Pharm, B.Pharm, MSc in Production, QC & Microbiology
    Gl QC documents review, QMS and trainings, GLP and Standards Management Packing materials sampling and testing, LIMS masters preparations & Review.
  • Job for B.Pharm, M.Pharm in Regulatory Affairs at Amneal Pharmaceuticals

    Amneal Pharmaceuticals, Inc. is a global pharmaceutical company. Our team of 7,500+ colleagues helps make healthy possible through the development, manufacturing, and distribution of a diverse portfolio of 270+ high-quality medicines.

    Looking for candidates with relevant experience in Regulatory Affairs

    Post : Sr. Manager / Manager - Strategic International Expansion – RA

  • Require Clinical Research Associate at Novo Nordisk
    The CRA is as such responsible for recruitment at site level. The CRA thereby delivers results that have a direct impact on the successful completion of the clinical programme.
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