#Candidate should have exposure of training activities of regulatory units #Exposure of QMS, in-process, validation and analytical review are essential #Pleasant Personality and influential communication skills #Should handle USFDA & MHRA Audit #Should have exposure in Formulation Plant #Qualification: B. Sc / B. Pharma/ M. Sc / M Pharma #Experience: 2+ Years
#To establish system as per requirements of cGMP/ Statutory/ Regulatory #To prepare and review standard operating procedures #To review the stability reports ensuring the retest / expiry dates of the API'S and Intermediates #Handling of CCP's, TCC
of continual improvements - Demonstrated competence in executing a wide gamut of functions viz. analytical method development, purification process development, fermentation process development, validation, quality system documentation and co-ordination. - Expertise in driving process improvement initiatives
#Exposure of QMS, in-process, validation and analytical review are essential #Review of Analytical data generated in quality control lab during analysis #Reporting to department head of deviations and abnormality observed during analytical revie #Initiation, Evaluation and review of change control, CAPA, Deviation and any other investigation. Review of all types of qualification and requalification protocol ...
- Exposure of all quality assurance & control activities in Fastner division. - Resp for achieving QA / QC / QMS / PPM targets in Receiving, In-Process & final Quality Assurance. - Resp for Internal Quality Audits or Customer Handling or discuss & resolve all quality issues - Plan & conduct
1.Should manage the portfolio for Gold Loan/financial business within its territory. 2.Leading a team of Branch Managers to ensure business growth. 3.Identifying & taking initiatives for launching new branches across the assigned territory. 4.Should be able to generate revenue and ensure overall