7 Pharmaceutical Qc Jobs in Hyderabad
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Analytical Chemist UMED PHARMA LAB PRIVATE LIMITED - Hyderabad, IN written and verbal. Having experience on Empower software is required. Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&D or a contract pharmaceutical analytical More than 30 days ago
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Technical Associate, Reference Standard Lab Hyderabad, India US Pharmacopeia - Hyderabad/ Secunderabad (Andhra Pradesh) and participating in compendial methods for reference materials (USP, FCC, NF, etc.). - Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&D, or a contract pharmaceutical 10 days ago
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Scientist IV, Reference Standards Laboratory Hyderabad, India US Pharmacopeia - Hyderabad/ Secunderabad (Andhra Pradesh) manufacturing QC laboratory or Analytical R&D, or a contract pharmaceutical analytical laboratory testing organization is a plus. Awareness of ISO/IEC 17025 is desirable. Supervisory Responsibilities None Note 10 days ago
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Scientist II, RSL US Pharmacopeia - Hyderabad,Other Telangana in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&D, or a contract pharmaceutical analytical laboratory testing organization is a plus. Awareness of ISO/IEC 17025 is desirable 28 days ago
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Analytical Chemist Umed Pharma Lab - Hyderabad / Secunderabad, Telangana, India written and verbal. Having Experience On Empower Software Is Required. Prior experience in a high-volume pharmaceutical manufacturing QC laboratory or Analytical R&D or a contract pharmaceutical analytical Not Mentioned 8 days ago
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Require_Male_B.Pharma_QA/QC@hyd candidates SQUIRCLE IT CONSULTING SERVICES PRIVATE LIMITED - Hyderabad / Secunderabad, Telangana, India EXPERIENCE: 0 to 3 years experience in Quality Control activities in Pharmaceutical Oral Solid Dosage / Pellets Manufacturing Company. JOB LOCATION: Karkapatla NO. OF VACANCY IN QC DEPT. : 04 Not Mentioned 8 days ago
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Regulatory Coordinator Novartis - Hyderabad / Secunderabad, Telangana, India reports and QC of NDA annual reports from previous versions (US). Where appropriate, perform QC of approved label versus previous versions with adequate management oversight Role Requirements Minimum of 3 Not Mentioned More than 30 days ago
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