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.

If Intrested kindly share us your updated profile, Mail Id:

trupti.chandarana@vvfltd.com

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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