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7 jobs found for Ahmedabad in Ahmedabad\

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  • Urgently looking for EXECUTIVE- PPMC for Injectable Mfg. Plant Near Ahmedabad (Guj). BSC/SC/B Pharma with 3 + yrs of Experience of Planning the batches for manufacturing and packing on day to day basis to meet the Marketing priorities. EXECUTIVE- PPMC for Injectable Mfg. Plant Near Ahmedabad (Guj). BSC/SC/B Pharma with 3 + yrs of Experience of Planning the batches for manufacturing and packing on day to day ...

  • Antifungal and others rest on the pillars of innovation and a passion for excellence. The company's modern sophisticated manufacturing facilities are located in Naroda, Ahmedabad, Gujarat The total built-up manufacturing facility measures 2864.8 sq. Mts. Which is a part of the well maintained

  • Guru99 Consultants is looking for Research Associate (Analyst) for its client - A leader in Clinical Research. You will be working in Bioanalytical Department and located in Ahmedabad Job Responsibilities Bioanalytical method development, method validation and project sample analysis Sample

  • Job Description: - Coordinate with Committee members, Investigators & CROs, Regulatory authorities regarding Ethics Committee (EC) activities as required - Manage day to day activities of the EC secretariat viz. Email communications, Calendar management, Documentation management (receiving, sending, stamping, scanning & filing), EC document preparation including but not limited to EC notifications, approvals, submissions ...

  • The selected intern(s) will work on following during the internship: -Conduct extensive desk research on Pharma products as per the requirement of the ongoing project -Prepare a database of the information collected and work on presentation of the same -Remain up to date with new launches & strategic moves of medium and large scale Pharma companies -Verify state drug licenses for a company’s products as ...

  • JOB DESCRIPTION 1 Protocol, Informed Consent From (ICF), case report form (CRF) Preparation: Coordinate with clinical research personal for of Protocol. Coordinate with clinical research personal for preparation of ICF and CRF 2 Ethics submission : Coordinate with the investigator for submitting the study related documents (clinical updated) to independent Ethics Committee. 3 Subject Recruitment/ Screening ...

  • 1) Preparation of Study documents: Coordinate with the Project Manager (PM), Principal Investigator (PI) and/or Clinical Investigator (CI), Bioanalytical team, and Statistician, for protocol preparation Prepare Informed Consent Documents (ICD) in English and coordinate for translation into Local language(s) and it’s back translation into English, if applicable. Preparation of the CRFs and other working documents ...

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