QC - Executive

Benefits Provided:

1 Free Air-Conditioned Transportation to the Factory
2 Paid Leave3 Tea/Coffee & Canteen Facility4 Accident Insurance5 Provision for Bonus & Gratuity6 Training programs for professional advancement7 Progressive work environment conducive to personal and professional growth

Job Title - QC Executive

Role & Responsibility:

1.To follow and ensure Good Laboratory Practices.
2.To perform the work according to work allotment.3.To follow good documentation practices while making entries in Documents and records.4.Make sure that materials are appropriately tested and results are reported.5.To perform the Initiation and review of any change related to the department.6.Make sure that deviations and Out of Specification Investigation are investigated and solved it with CAPA.7.To perform the Preparation and review of all SOPs related to department, Specification and test procedures.8.Preparation and execution of validation protocol for method validation and Analyst validation.9.SOP Review, revision and Harmonization.10.To perform the new products analysis method, review and arrange for necessary Corrections in test procedures.11.To perform the Analytical method, transfer activity and report protocol review.12.Arranging AMC of Instrument and servicing.13.To perform the Instrument spare procurement and maintenance.14.To Review of periodic calibration of Instruments.15.Reference Standard procurement and management.16.Monitoring the activity of working standard preparation and managements.17.In- house training of Analysis and training of corporate training modules.18.Review Analyst Qualification/ certification.19.Departmental correspondence, Internal and external Audit compliance action.20.Co-ordination with maintenance Dept. for QC Dept. utilities and its Maintenance.21.To Review Qualification of Laboratory Instruments Equipment.22.Handling Change control, OOS, OOT, Incident and deviation & CAPA.23.Monitoring stability sample analysis, Microbiology Lab record review.24.To check pharmaceutical addendum & supplement to make necessary amendment in the specification, whenever change in the Pharmacopoeia is observed.25.Co-ordination for SCM related activity with IT and QA.26.Storage of Laboratory data & records.27.Instrument Data back up, and software users rights.28.Arranging for outside testing and calibrations and its report Review.29.To ensure the Approval and Rejection of Raw Material, Packing Material & Intermediates products.30.Review of analytical results/data of in-process. Intermediate, water analysis finished API and issue COA for each batch of API.31.Trouble shooting of the QC Instruments32.If any additional responsibility assigned by senior.33.To ensure all QC staff do the performance under GLP34.Any additional job responsibilities as assigned by HOD.

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