Antonious Fares fathi’s Post

Nerhadou International,6th of October, Giza Senior IPC Specialist Job Description Checks and assures the implementation of safety measures in all production areas and the warehouse. Checking the receiving step of all raw/packaging materials in the warehouse and inspecting all containers for cleanness, correct identification, sealing conditions /damaged containers and the consignment quantity. Checks the sampling process of raw/packaging materials and its related documents according the sampling SOP. Inspecting monthly retained samples and checking the destruction process for all retained samples of the raw, packaging materials and finished products which reached its destruction date. Reporting any deviation in all production areas and warehouse to the Head of IPC. Review the production batch record for completion and assure that it is done according GDP rules before transferring it to QA. Checks the internal calibration and external calibration for ipc instruments. Performing periodic ipc tests during the manufacturing processes according to the batch record or ipc sops and recording all ipc activities in the related documents. Withdrawing all needed samples according to the batch record or ipc sops, sending it to the quality control lab for analysis and following up its results. Ensuring the setup of machines, cleanness of production areas and monitoring the temperature, relative humidity and differential pressure in all production areas, dispensing area, sampling area and the retained store. Checking all production activities during dispensing, manufacturing and packaging processes according to the batch record and related sops. Job Requirements B.Sc. of science / pharmacy. More than 5 years in relevant job. Active and organized person. Precise reporting skills. Good observation and communication skills. Computer skills: good in using Microsoft package (word / Excel / PowerPoint). Preferable to be 6th of October residents. Available for day and night shifts. https://lnkd.in/dsbUqm-F #manufacturing #vacancy #pharmaceutical #recruiting #jobvacancy #jobalert #vacancy #qualitycontrol #qualitycontrolanalyst #qualityanalyst #Otsukapharmaceutical #Obourcity #QC #QCanalyst #regulatoryaffairs #pharmaceuticalindustry #pharmaceutical #CTD #cmc #Regulatory #Pharma #pharmacy #science #Hiring #vacancy #pharmaceuticals #pharmacist #pharmaceuticalmanufacturing #hospital_pharmacist #hospitals #qualitycontrol #quality_control #veterinarymedicine #qualitysystems #qualityassurance #quality_control_professional #egypt #sciencejobs #sciencejobs #pharmaceutical #pharmaceuticalindustry #pharmaceuticalmanufacturing #pharma #pharmacy #pharmacists #sciencejobs #biochemistry #agriculture #agriculturelife #fresherjobs #freshers2024 #freshers2023 up, mention and share please follow to see more jobs #antonious_fares

good opportunity

Nerhadou International, 6th of October, Giza, Egypt QC Supervisor Stability & Methodology. Job Description Review, check & follow up on all activities in the QC lab (Chemist lab). Responsible for ensuring that all new hires in QC lab (Chemist lab) are well qualified through the reports of senior analysts. Reviewing & Checking of the protocols & Reports. NODCAR File review & follow up. Follow up on the ministry’s requirements. Review & Follow up on comparative dissolution. Distribution of tasks & duties for seniors. Participate in CTD file preparation. Awareness of references (ICH – FDA – ISO17025) & any reference updates. Reviewing & checking of all packaging materials with approved artwork. Job Requirements Bachelor of Science or Pharmacy Good manners. Work under pressure. Problem solving & Logic thinking. An Organized person. Teamwork. Has ability to improve & is able to learn. Good Communication skills. Basic Quality tools. Quick intuitive – humility. Team leader. Soft Skills (Time Management, Team Building) https://lnkd.in/dgE3R5bp #manufacturing #vacancy #pharmaceutical #recruiting #jobvacancy #jobalert #vacancy #qualitycontrol #qualitycontrolanalyst #qualityanalyst #Otsukapharmaceutical #Obourcity #QC #QCanalyst #regulatoryaffairs #pharmaceuticalindustry #pharmaceutical #CTD #cmc #Regulatory #Pharma #pharmacy #science #Hiring #vacancy #pharmaceuticals #pharmacist #pharmaceuticalmanufacturing #hospital_pharmacist #hospitals #qualitycontrol #quality_control #veterinarymedicine #qualitysystems #qualityassurance #quality_control_professional #egypt #sciencejobs #sciencejobs #pharmaceutical #pharmaceuticalindustry #pharmaceuticalmanufacturing #pharma #pharmacy #pharmacists #sciencejobs #biochemistry #agriculture #agriculturelife #fresherjobs #freshers2024 #freshers2023 up, mention and share please follow to see more jobs #antonious_fares

microbiology opportunity for freshers

فرصة لخريجين صيدلة فريش في شركة مينا فارم Minapharm Pharmaceuticals, 10th of Ramadan, Sharkia, Egypt Biotechnology Production Specialist Duties: 1.Perform mAB downstream processes according to production plan, and fulfil all duties required to ensure production (e.g. calibration of equipment, issuing materials and tools dispensing order, follow up of the stock). Strongly obey all GMP rules related to the field of employment. Comply with the IMS requirements, record all processes within the good documentation practice. 2. Comply with the annual objective of departments, Company's policy and the predetermined KPIs. 3. Supervise the technicians during the production process. 4. Issue new SOPs and revise approved SOP according to revision plan and current needs, initiate change controls according to instructions. 5. Notify timely supervisor and QA about all incidents, participate in investigation and assessment of incidents, deviations and changes, perform root cause analysis and contribute to SMART corrective and preventive actions for audit findings, implement CAPA, additional controls, change control actions, annual report actions and management review actions according to instructions. 6.Contribute to quality risk management projects, support continuous process improvements, report and support assessing environmental hazard aspects and impacts, report and support assessing health and safety risk assessment. 7.Strongly cooperate with other departments (for instance BMP, USP, QA, QC, R&D, engineering, purchasing, warehouse) aiming at smooth and efficient production andprocess flow. 8. Perform any additional tasks as requested related to the field of employment. Job Requirements: A. Experience: 0 - 2 years of Experience B. Education: Minimum Bachelor's degree in Biotechnology or Pharmaceutical Science. Work under pressure. • Ability to understand and follow written instructions. Computer literate. • Proficient in English Language. https://lnkd.in/dd4MdxJq #manufacturing #vacancy #pharmaceutical #recruiting #jobvacancy #jobalert #vacancy #qualitycontrol #qualitycontrolanalyst #qualityanalyst #Otsukapharmaceutical #Obourcity #QC #QCanalyst #regulatoryaffairs #pharmaceuticalindustry #pharmaceutical #CTD #cmc #Regulatory #Pharma #pharmacy #science #Hiring #vacancy #pharmaceuticals #pharmacist #pharmaceuticalmanufacturing #hospital_pharmacist #hospitals #qualitycontrol #quality_control #veterinarymedicine #qualitysystems #qualityassurance #quality_control_professional #egypt #sciencejobs #sciencejobs #pharmaceutical #pharmaceuticalindustry #pharmaceuticalmanufacturing #pharma #pharmacy #pharmacists #sciencejobs #biochemistry #agriculture #agriculturelife #fresherjobs #freshers2024 #freshers2023 up, mention and share please follow to see more jobs #antonious_fares

Updated CV : As a brief about me: ‎‏-QC Analyst at JPM-Delass Natural Products ‎‏Finished & Stability products ‎‏Raw materials Physical & chemical tests Perfectly perform more than 50 chemical & physical tests for over than 200 materials using more than 20 types of analytical instruments & manual procedures. ‎‏Finished,stability studies products and raw ‎‏materials analyst,all physical and chemical tests in pharmaceutical industry , sampling raw materials, very good practice on assay,related ,content uniformity and dissolution tests,good practice with Dionex,Waters,jasko HPLCs , and very good practice with handling the acid and base chemicals and very good knowledge in Good laboratory practice,Good manufacturing practice Perform maintenance, calibration and verification for laboratory instruments (such as Karl fisher,PH meter,Balances) to check if they meet the pharmacopoeia requirements. Pharmaceuticals standardizatin (Memo titor). Particle size analysis using Matersizer (Malvern). Have good experiences in chromatography softwires (Chromeleon, Mpower,lab solution ) and other analytical softwires which compatible with CFR 21. Training of new employees and trainees in QC labs. Sampling raw materials solids, liquids and gases, in addition perform all identification,and critical tests ‎‏QC Analyst Trainee at Dar Aldawa company ABDULLAH WAEL ESSA #updatedcv #chemist #talent #success #qualitycontrol #qualityassurance #researchanalyst #researchanddevelopment #officer ‎‏ #analyst #pharmaceutics #cv #jordan #humanresourceshr #qaanalyst #opportunity #work

#hiring QC Specialist I, Los Angeles, United States, $78K, fulltime #jobs #jobseekers #careers $78K #LosAngelesjobs #Californiajobs #ScienceTechnology Apply: https://lnkd.in/eM7wwrHp By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: To lead and implement key laboratory workflow, projects, and operations activities. As required, conduct biological, chemical and physical analyses by using sophisticated laboratory instrumentation and computer systems to collect and record data. Knowledge of analytical, biological, chemical and lean principles, GDP, cGMP, SOPs, FDA, and QSR regulations. Lead and participate in a team setting as lab representative for operational, project or investigational activities, to increase efficiency, solve problems, generate cost savings, improve quality and provide new product support. How you will contribute: To lead and implement key laboratory workflow, projects, and operations activities. As required, conduct biological, chemical and physical analyses on test samples following procedures; prepare and complete technical and lab investigational documentation. Provide technical and general GMP guidance to other lab personnel. Work under minimal Supervision. Use sophisticated laboratory instrumentation and computer systems to collect and record data. Perform advanced assays requiring precise analytical skills and understanding of biological and chemical principles.Perform review and evaluation of test data with application of GDP.Complete special project/protocol testing in a timely manner as needed. Prepare lab protocol studies/validations as required.Knowledge of the code of federal regulations, and compendia requirements.Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, QSR, and cGMP regulationsUse Global LIMS or other computerized systems for entering and approving test results as applicableLead and participate in a team setting as lab representative for operational, project or investigational activities to increase efficiency, solve problems, generate cost savings, improve quality, and provide new product support.Ensure area is maintained in a GMP state at all times while following all EHS and 5S guidelines. Prepare and update SOPs as required.Perform equipment maintenance and calibrations as requiredApply Lean principles such as 5S throughout daily work activitiesEnsure personal training requirements are met and that training records are current. Train staff per project needs.Perform Disposal of Hazardous Waste

Opening for Ahmedabad location