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16 jobs found for Quality / Testing / Process Control in Uttarakhand

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  • Responsible for all test conducted on HPLC, UV and Dissolution apparatus. Maintain equipment in an orderly manner Ensure column and other spares are maintained in requisite quantity for uninterrupted working Preparing reagents, samples, solutions as might be required for testing. Prioritizing test in order of request. KRAs Timely completion of Stability Studies and due tests ...

  • 1) To ensure sampling, chemical analysis and approval/rejection of semifinished or finished products. 2)To ensure internal calibrations of lab instruments. 3)Preparation of QC test reports for domestic as well as exported finished goods. B.Sc/M.Sc (Chemistry) with 1-3 Years experience in FMCG/Pharma/Cosmetics or ayurvedic manufacturing industry

  • Must have experience in small volume parentals in quality assurance department ...

  • #Analysis of Finished product, Stability samples and Raw Material #Sound knowledge of Operation and Calibration of HPLC, GC, Dissolution & UV #Calibration of HPLC, GC #Preparation of working standard #Preparation of Method Verification Protocols #Experience In Formulation Plant #Operating HPLC #Qualification: B.Pharma, M.Pharm, B.Sc , M.Sc #Experience: 2 to 5 years #Position: - Jr. officer / Officer / Executive - Quality Control ...

  • To Follow the Standard specification for testing To Carry out routine analysis of raw material in process finished product as the specification To prepare the testing report To carry out process validation ,revalidation activities

  • Qualification Required : Diploma / Degree Mechanical Experience required : 4 - 5 years. Location : Haridwar. Vacancies : 1

  • 1. Preparation & review of SMF, VMP, SOPs & protocols, documents to DRA 2. check ware house of RM & PM, Training to juniors on documentation 3. bottle packing activity. Verify the Stereo management. Check and Verify the Finish good store activity ...

  • (From Injectable/Parental Co.) 1. To receive the BMRs & BPRs from production department. 2. perform the IPQA & dispensing activity. 3. check and verify the material status i.e. quarantine, sampled & approved 4. review the all off line BMRs & BPR

  • > Performing Analysis as per GLP., Calendar Preparation > Operation of Manual HPLC for Stability Analysis, Calibration of UV Spectrophotometer > Maintenance of Temperature Monitoring Records of Stability Chambers > Working Standard Preparation

  • To Follow the Standard specification for testing To Carry out routine analysis of raw material in process finished product as the specification To prepare the testing report To carry out process validation ,revalidation activities

  • To Follow the Standard specification for testing To Carry out routine analysis of raw material in process finished product as the specification To prepare the testing report To carry out process validation ,revalidation activities

  • To Follow the Standard specification for testing To Carry out routine analysis of raw material in process finished product as the specification To prepare the testing report To carry out process validation ,revalidation activities

  • B.Tech / Diploma in Engineering, having 10 years plusrelevant Experience of Quality functions in lighting company manufacturing, bulbs tube light CFL LED

  • Monitoring & ensuring implementation of current GMP & GLP norms in Manufacturing Unit of parenteral and solid oral dosage forms. Conducting internal audit as per USFDA, MHRA, TGA, MCC & WHO-GMP requirement Facing different regulatory audits (USFDA, MCC, WHO & MHRA) Preparing & implementing Quality Management System (QMS) Training, framing the documentation for all the departments (sops / protocols, and various other cGMP ...

  • Monitoring & ensuring implementation of current GMP & GLP norms in Manufacturing Unit of parenteral and solid oral dosage forms. Conducting internal audit as per USFDA, MHRA, TGA, MCC & WHO-GMP requirement Facing different regulatory audits (USFDA, MCC, WHO & MHRA) Preparing & implementing Quality Management System (QMS) Training, framing the documentation for all the departments (sops / protocols, and various other cGMP ...

  • Educational Qualification : B. Tech. Location : Any where in india. Salary Range: 50 Lac to 60 Lac per annum. Experience : 10 - 12 Yrs

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