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  • Work as Clinical Trial Project Manager at Lilly

    Clinical Trial Project Manager Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trials with quality, on time, and within scope and budget. Leverage scientific and regulatory knowledge to prepare and/or provide technical consultation for clinical and regulatory documents, prepare for meetings with regulatory agencies
  • Dr. Reddy's Laboratories Hiring Clinical Research Associate
    Seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other groups. Master degree in pharmacy/ life science/Biology/Biotechnology/ Biochemistry/Diploma in Clinical Research
  • Work as Global Clinical Publishing Associate at Novartis
    Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system.
  • Abbott looking for Regulatory Affairs Manager
    Provide technical inputs on review of CMC data for Central CDSCO and State dossiers related to new products under development Liaison with other departments such as l&D, Quality, Supply chain, Project Management, etc to deliver high quality dossiers, in accordance with business priorities
  • Job for Women in Pharma Rx Sales at Dr. Reddy's Laboratories
    You will be executing the Product Management Teams marketing strategy, analysing market trends, consulting with doctors on new product potential, and relaying feedback to the Product Management Team. Additionally, responsibilities include identifying key opinion leaders, monitoring product availability, and implementing brand strategies to facilitate a successful product launch.
  • Interview for M.Pharm, B.Pharm, MSc Freshers for AR&D, Synthesis R&D at Biophore
    Biophore, an established pharmaceutical company, is engaged in the development and manufacturing of niche pharmaceutical products for the generic industry.
  • Walk In Drive at Indore for M.Pharm, B.Pharm, MSc in QC & ARD at Hetero Drugs
    B.Sc/M.Sc/ B. Pharm/ M.Pharm with relevant experience. HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC/ GLP; Hetero Drugs is an Indian pharmaceutical company and the worlds largest producer of anti-retroviral drugs. Heteros business includes APIs, generics, biosimilars, custom pharmaceutical services, and branded generics.
  • Walk In Drive for M.Pharm, B.Pharm, MSc in Production, QA, QC at Sudeep Nutrition
    B.Sc / M.Sc / B.Pharma / M.Pharma; Review HPLC methods, chromatograms, and system suitability. Ensure HPLC sequences comply with methods. Prepare and review IQ, OQ, and PQ for new instruments. Conduct pre-investigations for OOS, OOC, OOT, and lab incidents. To perform line clearance, FG Sample withdrawal, Online GMP Monitoring, To Support of Product and Process Validation
  • Interview for D.Pharm, B.Pharm Freshers for Production & Packing at Natco Pharma
    Diploma/D. Pharmacy/B. Pharmacy; Operating Granulation, Compression, Coating, Capsule Filling, Blister & Bottle Packing Equipment. Supervising Granulation & Packing Lines. Experience in Autoclave, Filling, Vial Washing, Packing Areas
  • Walk In Drive for QA Analyst, Shift In Charge, Operator at Zydus Life Science - Only experience M.Pharm, B.Pharm, D.Pharm Apply
    M.Sc, M.Tech, B.Pharm having 2 to 6 years of experience of Biotech and Chemical Analysis e.g., Electrophoresis, Bioassay, HPLC & GC.
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