A2W Pharma Limited A2W Pharma. is part of ABA Chemicals Corporation, Shanghai which provide custom manufacturing services to the pharmaceutical, biotechnological and agrochemical industries worldwide. A vacancy has arisen in the Production Department for the position of Production Assistant The ideal candidate should: -Be meticulous in the following steps/checklists with a good eye for detail, highly organised, accurate and methodical. Good communication, documentation, and time management skills are necessary -Be able to work in a small team. -Be willing to work overtime and night shift for specific production campaigns. -Preferably have certificates/diplomas in either applied science, pharmaceutical technology or operations and maintenance. -Advanced/Ordinary levels in Physics, Chemistry, Biology or Mathematics are also considered an asset. -Have experience and knowledge in pharmaceutical manufacturing and Good Manufacturing Practices (GMP), preferably in the field of liquid medication. -Be proficient in using Microsoft Word with good documentation drafting/review skills. In addition, the candidate will be expected to use computerized web-based systems, Enterprise Resource Planning (ERP) software and to operate machines via Human-Machine Interfaces (HMIs). -Be fluent in English with proficiency in Technical English considered an asset. Main Tasks -Reports to the Production Manager. Amongst other Production duties, the incumbent will be responsible for: -Adhering to Standard Operating Procedures (SOPs), Batch Records (BRs) and Cleaning Records (CRs) to execute manufacturing and cleaning tasks. -Drafting or review drafts of the above document types (new/revisions). -Carrying out day-of-use, daily, weekly and monthly tasks. -Following Environmental, Health, Safety and Security procedures. -Reporting deviations, malfunctions or faults to superior or relevant personnel. -Executing Research and Development batches in Production. -Supervising contractors (cleaners. pest-control, calibration/qualification etc.). We are offering a full-time position, with an attractive remuneration package according to qualifications/experience along with training and opportunities for professional growth in line with company growth to shift-leader or documentation. Please send your Curriculum Vitae by email to hr@aminochemicals.com A2W Pharma. Industial Estate Marsa MRS 3000 – Tel. 21249223/4/5
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Nerhadou International, 6th of October, Giza QC Supervisor Raw material & Packaging material. Job Description Review, Check & follow up on all activities in the QC lab (Chemist lab). Responsible for ensuring that all new hires in the QC lab (Chemist lab) are well qualified through the reports of senior analysts. Reviewing & Checking of the protocols & Reports. Volumetric solution Preparation. Standard management system. Aware references (ICH – FDA – ISO17025 - Reference pharmacopoeia) & any reference update. Reviewing & Checking 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/dcdgbQ72 #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
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Open to work! Hello Connections! I am looking for a job change as a QC Officer, Experience: 11 Months Job role: Raw material analysis, Packing material analysis, Prepared - COA, SOP, RDS Industry: Pharmaceutical Industry Here are some skills highlights Analytical Chemistry: Proficiency in HPLC, GC, FTIR, and UV-Vis spectroscopy. Pharmacopeial Standards: Knowledge of USP, EP, and BP standards. QC: Understanding of GMP and GLP guidelines. Documentation: Ability to prepare COAs, SOPs, and RDS accurately. Data Analysis: Proficiency in analyzing and interpreting analytical data. Problem-Solving: Ability to troubleshoot issues and propose solutions. Communication: Effective communication skills for collaboration and reporting. Attention to Detail: Ensuring accuracy in testing and documentation. Regulatory Knowledge: Understanding of relevant regulations. Teamwork: Collaboration in cross-functional teams to achieve objectives. Kindly connect and provide references. #pharmaceutical #pharmaceuticalindustry #pharmaceuticalmanufacturing #analyticalchemistry #qc #gmp #dataanalysis #documentation #teamwork #careerempowerment #professionalgrowth #careergrowth #openforwork #lookingforjobchange #connect #share
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What is a #Sonicator in Quality Control laboratory 🧪 A sonicator is a laboratory instrument used in Quality Control (#QC) to disintegrate, disrupt, or extract samples using high-frequency sound waves. What is a Sonicator?🤔 A sonicator, also known as an ultrasonic homogenizer or ultrasonic disruptor, uses #high-frequency sound waves (typically between 20 kHz to 40 kHz) to create intense mechanical vibrations. These vibrations generate cavitation bubbles that collapse with immense force, causing disruption or disintegration of the sample. Uses of Sonicator in QC:✍️ 1. *Sample #Preparation*: Sonicators are used to prepare samples for analysis by breaking down particles, cells, or tissues. 2. *#Extraction*: Sonicators can be used to extract active ingredients or analytes from samples, such as plant extracts or pharmaceuticals. 3. *#Homogenization*: Sonicators can homogenize samples, ensuring uniform distribution of particles or components. 4. *Cell #Disruption*: Sonicators can disrupt cells, releasing their contents for further analysis. 5. *#Cleaning*: Sonicators can be used to clean laboratory equipment, such as pipettes and glassware. Advantages of Sonicator in QC:📈 1. *#Efficient Sample Preparation*: Sonicators can quickly and efficiently prepare samples for analysis. 2. *Gentle or #Aggressive Disruption*: Sonicators can be adjusted to provide gentle or aggressive disruption, depending on the sample requirements. 3. *Reduced #Sample Contamination*: Sonicators can minimize sample contamination by reducing the need for manual handling. 4. *Improved #Analytical Results*: Sonicators can help improve analytical results by ensuring consistent sample preparation. Common Applications in QC: ✍️ 1. #Pharmaceutical analysis 2. #Biotechnology research 3. #Food and beverage testing 4. #Environmental monitoring 5. #Cosmetic testing In summary, sonicators are versatile laboratory instruments used in QC to prepare samples, extract analytes, homogenize samples, disrupt cells, and clean equipment. #Qualitycontrol #QC #analyticalchemistry #QA #Qualityassurance #chemistry #lab
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good opportunity
فرصة لخريجين علوم و صيدلة VIATRIS,Cairo,Egypt Quality Control Analyst (Stability and Methodology) Experience and Knowledge Good command of English in both written and spoken. Excellent in Microsoft office (word, excel & PowerPoint) Knowledgeable with interpersonal, good communication and presentation skills. cGMP & cGLP knowledge is preferred with particular emphasis on Quality Control. Knowledgeable with Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation. Essential Personal Qualifications Bachelor’s degree in pharmacy or science. 1-5 years’ experience in a related area. Demonstrated ability to work independently. Excellent documentation and technical writing skills. Able to work in a team, interact with various priorities and meet deadlines. Active, organized and planner with high attention to details. High observation skills. Self-motivated and able to consistently meet timelines. https://lnkd.in/dWmFYBMv #manufacturing #vacancy #pharmaceutical #recruiting #jobvacancy #jobalert #vacancy #qualitycontrol #qualitycontrolanalyst #qualityanalyst #QC #QCanalyst #Pharma #pharmacy #science #Hiring #vacancy #pharmaceuticals #pharmacist #pharmaceuticalmanufacturing #quality_control #quality_control #qualitysystems #qualityassurance #quality_control_professional #egypt #sciencejobs #sciencejobs #pharmaceutical #pharmaceuticalindustry #pharmaceuticalmanufacturing #pharma #pharmacy #pharmacists #sciencejobs #biochemistry up, mention and share please follow to see more jobs #antonious_fares
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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
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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
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Microbiology skills needed
Hello LinkedIn connections, We are #hiring for #Microbiologist; 9 -10 years of experience. Location: Pithampur, Madhya Pradesh API Plant Responsibilities: 1. Plan and coordinate environmental monitoring activities during batch manufacturing, filling, and media fill operations in sterile facilities. 2. Manage Out-of-Action/Out-of-Alert-Limits (OOAC/OOAL), incidents, deviations, and non-conformances in the microbiology laboratory. 3. Perform and oversee a range of tests including MLT, EM, Antibiotic Assay, Sterility, GPT, Sub Culturing, BET, and DET tests. 4. Conduct validation studies including method validation, media fill activities, hold time studies, water and area qualifications, and autoclave validations. 5. Oversee the qualification of new instruments and equipment in the Quality Control Microbiology Laboratory. 6. Lead the Green Land project for new facility installation. 7. Manage consumable items qualification including bio balls, biological indicators, gloves, and IPA 70% qualification. 8. Oversee GLP section operations and ensure compliance. 9. Conduct equipment swab tests and drain swab analysis in FFS facilities. 10. Conduct water testing, compressed gas, and nitrogen sampling in sterile and non-sterile facilities. Additional Responsibilities: 1. Lead GLP team and manage work distribution. 2. Review GLP and analytical documents. 3. Install and execute instrument qualifications. 4. Prepare specifications and SOPs. 5. Ensure compliance with GLP and GDP. 6. Prepare and review validation protocols and reports. 7. Conduct calibration and water testing. 8. Qualify areas and monitor microbial activity. 9. Prepare media and conduct sterility testing. 10. Handle quality performance indicators. 11. Investigate laboratory incidents. 12. Maintain documentation and training records. 13. Manage stock of microbiology materials. 14. Verify instrument logbooks and calibration. 15. Conduct trainings and ensure GLP compliance. Instrument Handling: Calibration of incubators, BOD incubators, colony counters, autoclaves, LAF, UV lights, antibiotic zone readers, micro pipettes, pH meters, analytical balances, digital microscopes, foggers, and air samplers. Interested candidate can share their profile at poonam.lahire@thinqcro.com #microlab #microbiologist #pharma #pharmaceutical
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Dear all valued connections, Our client is calling out talents in #Pharmaceutical industry as below: • Business: Pharmaceutical 💊 • Location: #CanGiuoc, #LongAn 🚌 There is shuttle bus from Go Vap, District 7. • Salary: negotiable based on ability and experience ------------------------------------- 💊 Position: 𝗤𝗔 𝗟𝗲𝗮𝗱𝗲𝗿 - Open for local candidates ✅𝗤𝘂𝗮𝗹𝗶𝗳𝗶𝗰𝗮𝘁𝗶𝗼𝗻𝘀 - University graduation, major in Pharmacy - 3+ years of experience in QA Lead. - Proficient in English communication and reading comprehension. - Experience with #liquid and #sterile medicine - Experience with #GMP approval of pharmaceutical factories. 🔵𝗥𝗼𝗹𝗲 𝗗𝗲𝘀𝗰𝗿𝗶𝗽𝘁𝗶𝗼𝗻 • Implement and report to the Factory Director and Board of General Directors. • Develop and implement GMP training plans for factory-wide staff • Plan and arrange evaluation work (in collaboration with other departments) for manufacturing processes, equipment cleaning, and auxiliary systems (HVAC, RO water, distilled water, compressed air). • Regularly control and monitor the environment, including water and compressed air. • Oversee and monitor the calibration, inspection, and maintenance of equipment and auxiliary systems. • Prior to approval by the Factory Director, review standard operating procedures (SOPs), original production documents/processes, and job descriptions. • Monitor the drug production process from the time raw materials are imported, through packing, and until the finished product is dispatched. 💊 Position: 𝗤𝗖 𝗟𝗲𝗮𝗱𝗲𝗿 - Open for local candidates ✅𝗤𝘂𝗮𝗹𝗶𝗳𝗶𝗰𝗮𝘁𝗶𝗼𝗻𝘀 - University graduation, major in Pharmacy - 3+ years of experience in same role - Trained in #GMP, #GLP. - Working experience in pharmaceutical manufacturing company 🔵𝗥𝗼𝗹𝗲 𝗗𝗲𝘀𝗰𝗿𝗶𝗽𝘁𝗶𝗼𝗻 • Understand, implement, and check the work of the hashtag #microbiology department: • Sample testing by microbiological methods: Sterility test, bacterial contamination test, bacterial identification isolation, antibiotic potency quantification, endotoxin determination • Manage chemicals, standards, microbial strains, tools, and equipment of the Microbiology department • Prepare the specification, method for raw materials and excipients, updated according to the current pharmacopeia version. • Set up analytical records according to #ACTD, #GLP, #ISO • Manage risk assessment to prevent incidents from occurring and improve the system. • Directly report to #QC_Manager on the situation and results. ------------------------------------------ 𝗖𝗢𝗡𝗧𝗔𝗖𝗧 𝗙𝗢𝗥 𝗔𝗣𝗣𝗟𝗜𝗖𝗔𝗧𝗜𝗢𝗡: Please kindly share your CV (in English) to email: Ms. Mai - Email: mai.huynh@iconic-intl.com Due to the significant number of applications received, we will only be able to contact those candidates who are being most actively considered for the position. Thank you #hiring #pharmaceutical #infusion #qualitycontrol #qualityassurance #Japanesecompany #myconnect
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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
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