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

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  • Indepth knowledge of QMS standards (ISO,TS) and implementation of same. to Quality Planning for New Product Development.Thorough understanding of APQP, FMEA. Control Plan.Must have completed certification course of Lead Auditor in QMS ...

  • 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

  • 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 ...

  • 1. Position : Manager - QC Location : Dehradun Qualification : MSC / BSC. Age : upto 35 years CTC : 5.00L to 12.00L Job Details : 6-20 years experience in QC department . Responsible for documentation. Exposure into International Audit will be added advantage. 2) QC Chemist 1 -5 Years experience as chemist CTC :2.00L to 4.00L

  • Designation: GM- Corporate QA & RA Formulate Quality policies, procedures to ensure compliance for cGMP,cGLP in mfg, testing, release and distribution practices across the company. Review and approve OOS,change controls and monitor the system. Review and approve protocols for equipment qualification, process qualification, stability etc for finished products. Training of people for cGMP,cGLP, cGRP at plant ...

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