1. Prepare and maintain sketches and AutoCAD drawings, work progress schedules and Daily progress report. 2. Verify the contractor work quality, prepare JMR, check contractor bills, track inventory, make and prepare contractual terms and condition for vendor.3. Research potential vendors, compare and evaluate offers from suppliers and make purchase requisition.4. Taking tool box, initiate the work permit, approvals and ensure EHS compliance at work place. 5. Ensure compliance to all statutory requirements, following and documenting the Project Change Control as per the agreed procedures and adherence with building maintenance SOP.

Basic SectionBAND-OGrade-O01-OfficerDesignation- OfficerSkills Skill - QUALITY ASSURANCE Education Specialization - GRADUATION Minimum Qualification -BACHELOR OF PHARMACY (B.PHARM)Job Description 1.To Initiation , review and conduct Calibration of IPQA Instruments.2.To review all usage logs of Manufacturing and Packing Area.3.To review and follow up for Annual Maintenance Activity of IPQA Instruments.4.To fill and review IPQA instruments log books.5.To review and provide Line Clearance for Manufacturing Equipment's / Packing Equipment's.6.To review Batch Manufacturing Records / Batch Packing records.7.To participate Training programs of various cross linked SOPs and effectively ensure its implementation.

Job Description : Hands-on experience in -Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports operations and calibration of the instruments like HPLC, GC etc. Preferred candidate -Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV.OrganisationalEntity Zuventus Healthcare Ltd.Vertical ZHL Sikkim FactoryDepartment Quality ControlContinent AsiaCountry IndiaZone EastLocation TypeS01-ZHL Factory

Basic SectionBAND-OGrade-O01-OfficerDesignation-OfficerDepartmentQuality ControlSkills Skill QUALITY CONTROL HPLCGMP Education Specialization GRADUATION Minimum Qualification BACHELOR OF SCIENCEJob Description1.Preparation and standardize of volumetric solutions and maintaining its record.2.Preparation of standard solutions and reagents and maintaining its record.3.Water Analysis and data punching in SAP.4.Analysis of Raw Material and Miscellaneous samples as per GTPs/ SOPs/ Spec & MOAs.5.Raw materials Control sample management.6.To put results in SAP of analyzed and Reviewed RM Materials.7.To Record & Maintain temperature record of entire QC lab on daily basis. (except Microbiological and PM testing QC).8.To Check & Refill Eye washer equipment on daily basis and Record data of the same.

Hands-on experience in -Perform the Analytical Method Validation by HPLC/GCPreparation and review of AMV Protocol and ReportsOperations and calibration of the instruments like HPLC, GC etc.Preferred candidate -Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV