مدیر کنترل کیفیت

افق تولید دارو پارس تهران

منتشر شده 2 سال پیش

Job Description

Work closely with all departments including the commercial and logistics departments to help understand customer requirements and plan the timely testing and release of product batches and assist with the review of all QC analytical data and ensure that the right first Time KPIs are achieved. Role description: ● Install a KPI system. ● Manage and schedule routine and annual maintenance, troubleshooting, and all analytical equipment and analytical practices and procedures in order to uphold continuous improvement. ● Manage Analyst work schedules and ensure that planned work is effectively communicated and adhered to. ● Manage Analyst timesheets, holidays and coordinate all laboratory events and manage laboratory audits and findings. ● Manage analyst training curriculum and maintain and update all laboratory and analytical documentation. ● Manage and maintain all laboratory software. ● Troubleshoot all QC analytical methods, equipment, and calibrations. ● Support continuous improvement in the laboratory and identify gaps in the current QC processes and plan improvement/ implementation with the QC manager. ● Act as primary contact for laboratory-related queries and liaise extensively with internal and external customers. ● Ensure all testing and associated activities are performed in accordance with GMP and strict industry compliance standards. ● Manage the QC laboratory waste program and ensure that all QC-generated waste is properly segregated and disposed of. ● Manage all laboratory OOS, OOT, deviations, and change controls and liaise with QA, etc.

Requirements

● Familiar with sampling standards. ● Familiar with product and process auditing. ● Familiar with quality tools. ● Familiarity with statistical quality control. ● Familiarity with relevant software. ● At least five years of relevant work experience. ● Top PR.

Employment Type

  • Full Time

Seniority

Details

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