Total 274 Jobs
PharmaEdge 2-5 years experience
PharmaEdge Date posted: 18 Dec 2014Job Description Ensure the documentation is maintained in line with the QMS, timely changes in QMS. Providing micro level information by MIS reports to Management.Continuous training for self and department so as to make highly motivated and ...
KRM Global 7-13 years experience
Minimum 6 8 years of experience in relevant sectorQualification: Graduate Engineer in Mechanical/Chemical/Plastic/Printing Must have hands on experience in implementing ISO 9001
Omam Consultants 10-20 years experience
Omam Consultants Date posted: 05 Dec 2014Quality Assurance: To ensure the supply of working standards & related impurities as per customer requirements. Carry out internal audits To organize proper investigation from the section where the deviation has occurred in batch ...
Theon Pharmaceuticals Limited 10-15 years experience
M.Pharma/B.Pharma with minimum 10 years of experience in a formulation unit. Exposure of International Regulatory Audits like MHRA, MCC, TGA & WHO is must
Theon Pharmaceuticals Limited 15-22 years experience
M.Pharma/B.Pharma with minimum 15 years of experience in a formulation unit. Exposure of International Regulatory Audits like MHRA, MCC, TGA & WHO is must
Hr Services 1-4 years experience
Looking for QC Officer/ Sr.Officer / Exec. Qualification Required MSc Chemistry/Bio Chemistry Expertise Analysis of Finished Goods/ Raw Materials/ Stability section. Knowledge of HPLC is a must. Company Reputed
Sharp Point HR Consulting 8-18 years experience
My client is a Plastic Polymer Manufacturing company , requires Quality Manager for HP Location
Kapasa Jobs 1-2 years experience
To manage Plant QC ( Basically work on QA rather than QC). Emphasise on corrective analysis, data collection and remedial action on shop floor. Put into operation Quality tools with knowledge of paper and packaging industry . Process correction to deliver Quality and NPDs in ...
Nootan Pharmaceuticals , Barotiwala, Baddi 3-8 years experience
Responsible for overall Regulatory affair & Supportive QA activities. Should be well versed with Dossier(ACTD, CTD, ECTD & country Specific) preparation, submission, query solving & product registration in various countries