VVF INDIA Job Vacancy For MSc B.Pharma M.Pharma
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| VVF INDIA Job Vacancy For MSc B.Pharma M.Pharma |
Designation: Manager-Quality Control
Education: M. Sc / B. Pharma / M. Pharma
Experience:08 -12 years
Location:Daman & Diu.
Salary: 12,00,000 – 15,00,000 P.A.
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Job Description:
Technical Skills & Knowledge
Handel instrument such as HPLC, GC, UV, Conductivity
Analysis of FG, RM, PM, Chemical,
Handel SAP
Key Responsibilities
To drive Quality Policy and encourage continual
Improvement in quality system at site to meet regulatory and customer requirements
To Ensure GLP, GxP and CSV compliance and audit trail review in laboratory instruments/equipment
To review and investigate by finding out root cause for OOS/ OOT/ Incident / Laboratory errors impacting Quality analytical results and closure within time as per frequency of SOP
To plan, supervise and review analytical testing and releasing of RM/PM/BULK/FG on time as per urgency
To establish Quality Measurement System and keep the top management informed
To ensure instrumental, chemical and microbiology test report raw data review and approval on time Monitoring of In QLI/ AQL
Approval of Standard Operating Procedure and Specifications, Standard Test Method, Method of analysis and other quality documents
To review Annual product quality review Review and approval of Quality Assurance / Quality control documents and records
To ensure timely calibration, review and approval of instrument/equipment calibration as per SOP
To ensure process validation of each and every new product
Approval and Execution of Validation Master Plan
To review and ensure periodic Trend Analysis of Purified Water and Environment monitoring
To ensure periodic Training Program on GMP and GLP
To ensure the Job Description and Training Matrix of all Quality personnel is prepared as per current Job profile and each individual performing the particular task is trained
Monitoring of Environmental Controls
Ensure Validation of Mfg. / Filling Equipments by swab and rinse water
To ensure investigation has been performed for any failure and CAPA
Responsible for the approval of stability study protocol , stability study as per protocol, stability charging , stability sample retrieval and analysis, stability report review , evaluation of stability data and handling of stability chamber
To Review and approval of Site Master File
To ensure that every instrument/equipment used in Quality is calibrated as per frequency of the SOP, review of the calibration records and related communication with the vendor/third party
To communicate and justify to management the resource requirement to implement the quality management system to meet regulatory and customer requirements
To strive for the continual improvement in Quality by conducting internal audits and review
To prepare and execute the technical agreement between contract giver (VVF) and contract acceptor (Party) is signed and agreed by both
Ensuring proper and systematic functioning of Quality System to meet regulatory and customer requirements Ensure review of Batch Mfg. Records prior to release
To give training to Quality personnel of SOPs and related to OOS, OOT, Laboratory error, Deviation to avoid reoccurrence
To monitor and ensure that the Quality productivity is as per organization requirement
To timely short out any type troubleshooting on instrument /equipment and other occurring in Quality
To monitor , supervise and handle the team knowing their competency for the best productivity and least error in Quality
To take and complete any other responsibility as given by reporting Head and above management on time to time as per requirement
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