- البحث عن وظائف
- Egypt
وظائف في Egypt
آخر تحديث: منذ يوم واحد
QC authorized person Accountable for Products / Materials analysis revision / disposition.Management, utilization and upgrade of the different Lab resources.
Man power, Equipment and consumables).Act ...أظهر المزيدآخر تحديث: منذ أكثر من 30 يومًا

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عرض العمل هذا غير متوفر في بلدك.
Quality Control Supervisor
AstraZenecaEgyptمنذ أكثر من 30 يومًا
نوع الوظيفة
- وقت كامل
الوصف الوظيفيManagement, utilization and upgrade of the different Lab resources. (Man power, Equipment and consumables). Lead the QC PDCA. Act as the QP for release of Procured and manufactured products within the QC including micro review activities. Support in achieving the analysis lead times. Provide support and training to QC staff. Hold the initial and extended Lab investigation with the QC analyst in case of OOS / OOT Responsible for purchasing, qualification and calibration of new lab equipment (PQ, OQ and IQ) Responsible for periodic equipment calibration and qualification Follow up with agents on preventative maintenance Responsible for following up the preventive and corrective maintenance, cleaning and labelling of all QC lab equipment. Responsible for following up the calibration plan and ensuring that all the calibrations were done before the due dates. Support the QC team members in troubleshooting of minor issues related to equipment and provide the proper training for equipment usage. Preparing the QC consumables (OPEX) budget and budget phasing. Follow up of the available stock every month or quarterly whatever appropriate based on consumption rates. Ordering the required consumables on time to avoid running out of stock. Monthly check to remove any expired consumable. Ensure all the consumable are stored in their relevant recommended storage conditions. Performing chemical and physical analysis of water samples, raw materials, imported and manufactured bulk products according to the approved standard official methods. Performing micro activities as required (microbial analysis of water, EM, microbial analysis of raw materials and manufactured bulk) and after completing needed qualifications. Checking the imported bulk received at the warehouse. Reporting any deviations, OOS / OOT results Documentation, recording and reporting of analytical results according to the predetermined instructions. Reporting and documenting any incidents, out of specifications and out of trend results according to the predetermined procedures. Prepare the SOMs, SOPs, instructions and records in compliance to AstraZeneca’s standard. Managing changes according to the predetermined procedures. Preparation of validation protocols and worksheets Responsible for the proper implementation of 5S in the lab. Properly disposing all contaminants and different hazardous and bio-hazardous materials. Acquiring and following all the consumables MSDS. Adhere to the site’s SHE policies and requirements Own and close audit observations against different areas in the Lab.
Years of experience
- 7-9 years of experience
QC authorized person Accountable for Products / Materials analysis revision / disposition
Management of lab equipment
Instruments
QC stock management
Analysis
Documentation
Audit observation
Date Posted
25-Jun-2024
Closing Date
06-Jul-2024