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

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  • Position type: Full-time Salary period: Monthly Dear candidate we have accepted qualification 10th 12th Ba Bsc Bca Bcom BBa Ma Msc Mcom Mba ITI Diploma all trade B-tech BE all trade Fresher Experience candidate LG Electronic Company Dear candidate we have available post 1:- helper 2:- Supervisor 3:- manager 4:- Production 5:- Quality 6:- Maintenance 7:- Dispatch 8:- Store incharge Computer basice knowledge press ...

  • 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

  • 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 ...

  • Will be heading QA for Oral Solid Dosage manufacturing / USFDA approved site. Qualification (equipments and area), Process validation, Cleaning validation, Technology transfer, Vendor development and audits, Internal audit, Change management, Deviation, Incident, OOS, Market complaint, Returned goods, CAPA, preparation of system SOPs, review of APQR, SOP/ MPCR/Protocol/ Report, batch release, training and others area ...

  • Qualification Required : B.Sc - Microbiology Experience required : 1 to 4years Location : Haridwar Vacancies : 1 Salary Range: 15k to 25kper month ...

  • Qualification Required : B.Sc - Microbiology Experience required : 1 to 4years Location : Haridwar Vacancies : 1 Salary Range: 15k to 25kper month ...

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