To write great resume for quality control chemist job, your resume must include: The section contact information is important in your quality control chemist resume. 4,499 open jobs for Quality control chemist. AMVAC’s Quality Control CHEMIST performs quality control evaluations of raw materials, process intermediate streams and finished products to assure conformity to established specifications. You’re about to see a chemist resume example you can change to fit any chemistry job. May be required to wear personal protective equipment including but not limited to: respiratory protection, safety glasses, hearing protection, safety shoes and protective clothing. Typically standing and/or walking. May require use of hands and use of arms. Güncel Reklamlar, Oyun Tanıtımı, Oyun İle İlgili Teknik Paylaşımlar Hizmetinizde. Moderate lifting or carrying 25-50 pounds. May be required to wear personal protective equipment including but not limited to: respiratory protection, safety glasses, hearing protection, safety shoes and protective clothing.   •  Environmental, Health, Safety & Quality: Is aware of ... •  Strong skills in multitasking, documentati... •  Excellent organizational skills, ability t... •  Strong organizational skills to be able to... •  %- Shape Food/Feed Safety, Quality and Regulatory Culture – Assists in the delivery of training materials for internal employees at various levels in the organization related to food/feed safety and quality issues, practices and risks. No need to think about design details. May be required to wear personal protective equipment including but not limited to: respiratory protection, safety glasses, hearing protection, safety shoes and protective clothing. By looking at the importance of the job, employers are very keen on hiring the best candidates for this position. Provided Quality Assurance/Quality Control (QA/QC) to ensure the data quality and analytical activities in compliance. Regular exposure to chemicals, solvents, fumes and/or gases. ASTM methods for: GC, AA, IC, XRF, elemental analysis, and wet chemistry), Demonstrated success delivering business value through laboratory innovation, Demonstrated ability to consult on analytical instrumentation and test methods, including method development and equipment/instrumentation repair and purchase, Experience working with data analytics tools (Spotfire, MS Power BI), Experience with chemometric modeling and analysis, Experience with the proper operation of laboratory instrumentation, troubleshooting, and the generation and revision of SOPs and test methods, Participate in validation and measurement system analysis of various testing methods, At least one-year experience in the production of reference material manufacturing, Lab experience in QC manufacturing environment, Performance of routine HPLC method development and validation of HPLC protocols of bulk APIs and new drug products required, Experience in a GMP or GLP Quality Contol (QC) lab, Complete visual inspection of product labeling prior to the issuance of the prepared labels to manufacturing, Performs raw material, in-process material and finished goods testing, Perform routine chemical testing of commercial, validation and stability samples in accordance to written methodology, Assure conformance to Good Laboratory Practice within the QC Group, Assist with the validation of analytical methods, Responsible for the quality release of goods in SAP QM system as well as product CoA creation, B.A. Organize work for completion according to timelines given. Typically bending, crouching, stooping. resume for quality control chemist VPS - VDS - Dedicated - Web Hosting Hizmeti Verilir. Key responsibilities of a Lab Chemist are conducting research, running tests, analyzing chemical compounds, finding applications for compounds, and compiling results. Total dedication to the [clients/staff] and to the accomplishment of targets of the division and the institute. Guide the recruiter to the conclusion that you are the best candidate for the quality control chemist job. Quality Control Data Review Chemist Resume Examples & Samples Independent execution of HPLC methods and preparation of sample, data packets, and data summaries Analysis of pharmaceutical products, including the set-up and execution of GMP in-process, release and stability testing using a variety of analytical techniques Approximately 8 years as a Research Scientist performing product development, formulations studies, research Pilot plant testing, and scale up to production. Lead QC Chemist Resume. Perform various chemical methods and procedures in the lab. Download Quality Control Chemist Resume Sample as Image file, Actively works in a team environment and participates in natural work groups and increases productivity, Provides technical input on observed issues with methods, procedures, and practices, Defines and works on resolving technical problems within defined scope and within level of expertise, Assists with method implementation and/or method transfer and equipment qualification activities as assigned, Conducts analysis and data collection necessary to support release of raw materials, parts, packaging components, in-process samples, and formulations produced, Proper use of analytical equipment, such as GC, HPLC, UV-Vis, FTNIR, IR, Titrations, USP Monograph Testing, Viscometer, Particle Size Analyzer, GPC, Conducts lab/ nonconformance investigations, and special projects as assigned, Participation in Out of Specification investigations and the writing of analytical variances, Stay current with analytical technology industry standards and equipment, Independent execution of HPLC methods and preparation of sample, data packets, and data summaries, Prepare documents and technical reports for clients, Conduct experiments and communicate results to supervisor, Interpret data and use conclusions to propose follow up experiments, Participate in technical discussions with supervisor and peers, Perform all work in a safe manner and maintain a clean and organized work environment, Perform elementary method analysis and development for troubleshooting purposes. Apply to Chemist, Quality Analyst, Shift Leader and more! Make your resume visible to recruiters. Quality Control Chemist Resume Examples & Samples Follow identified specifications and standard operating procedures regarding quality approvals of raw materials, mediums, and finished products Issue and proofread COA and SDS for the existing products, including generating templates for new customers, approving templates and creating documents It’s the one thing the recruiter really cares about and pays the most attention to. Quality Control Chemist I Oct 2014 - Present BD BIOSCIENCES- PHARMINGEN - San Diego, CA. Catalent Pharma San Diego is hiring for a Quality Control Chemist II. A well-written resume sample for Qc Analyst should focus on skills like quality control expertise, organizational skills, computer competences, time management, critical thinking, physical strength, and operation monitoring. Intermittently sitting, standing, stooping. An analytical science background strongly preferred. What salary does a Quality Control Chemist earn in your area? Ability to add, subtract, multiply, and divide, Intermittently sitting, standing, stooping. Notify me when a company views me, messages me or posts a job I might like. Typically standing and/or walking. This is one of those things that you can take it or leave it. Quality Control Chemist, QC Laboratory Responsible for the analysis of finished product In-process sample, Stability sample and raw material by USP, NF, In-house test method using HPLC, GC, UV, IR, KF, Dissolution and Wet Chemical Techniques. *Worked with fortune 500 companies thousands of test methods and over hundreds of OTC (Healthcare and Cosmetic) products for one of the top leading contract firm. Ridgeea در 5 روز، 5 ساعت پیش بروز شده است. Get the right Quality control chemist job with company ratings & salaries. Moderate lifting or carrying 25-50 pounds. View this resume sample for an entry-level chemist to see how you can formulate a resume to help launch your career. Chemist Quality Control Jobs in Ranchi, Jharkhand - Check out latest 191 available Chemist Quality Control Jobs openings in Ranchi, Jharkhand . Displayed here are job ads that match your query. Summary The Quality Control Chemist I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of … Climbing ladders or scaffolds. Customize Resume View Resume. One year of experience highly preferred. This way, you can position yourself in the best way to get hired.   •  Technical Knowledge and Ability: develops technical knowledge and ability within their functional areas May be required to stand; walk; stoop; bend; kneel; and climb steps. No manufacturing firm can function without a qualified team of quality control and quality assurance experts, and similarly, no job application is complete without a well-written resume. (You may update your preferences anytime.) Wet Chemist… A quality control chemist is one specialization available for laboratory chemists. This is why the Chronological is ideal for your Chemist resume format. Work Experience Chemist; 2015 to present Benninger Pharmaceuticals; Sarasota, FL. Must be able to distinguish colors. Must be accurate, detail oriented, possess the ability to multi-task and work in a fast paced, high output environment, Ability to solve problems with a variety of concrete variables through semi-standardized solutions that require some ingenuity and analysis. Search 20 Quality Control Chemist jobs now available on, the world's largest job site. is preferred, Knowledge of USP & cGMP procedures is required for higher-level chemist positions required, Potency assay testing, impurity testing, identification, content uniformity, drug release, binding capacity, dissolution, Karl Fisher titration to determine water content, loss on drying, Troubleshoot chemical and technical areas such as impurity in products and analytical instruments, Analyze specific products particularly for delayed-release capsules, delayed-release tablets and extended-release tablets and precursor and control substances, Perform method transfer from research and development department to QC department for product commercialization, Conduct cleaning verification tests on equipment to ensure fast turn-around time in manufacturing, Follow established test methods and USP monographs to perform analytical tests and document the analytical procedures in compliance with GMP, Investigate any “out of specification” conditions and conducting chemical analysis for incident reports investigation and completing corrective actions, Perform routine calibration and verification of lab instruments, Maintain inventories of chemicals and lab supplies for uninterrupted lab operation and safety compliance, Analytical analysis of a variety of drug substances and drug products with emphasis upon purity, content uniformity, and dissolution in a GMP-compliant manner using analytical instruments such as HPLC and GC, Analysis of bulk chemicals, active pharmaceutical ingredients, formulations and final drug products via Millennium software and Agilent Chemstation, Perform routine HPLC method development and validation of HPLC protocols of bulk APIs and new drug, 0-2 years of experience in a chemistry laboratory environment required, Experience in wet chemistry techniques, HPLC, GC, UV, IR, TLC and other instrumental techniques, preferred, Knowledge of USP & cGMP procedures, preferred, Computer skills: 1+ year of experience using Microsoft Word, Excel, Outlook is required, Good English and verbal communication skills are required; must be capable of using correct English spelling, grammar, and punctuation to write documentation, especially test procedures, Test samples in accordance with established procedures and using all instrumentation required in the procedures, including AA, LC, GC-FID, GC-EC, GC-MS, IR, UV-VIS, Test samples using wet chemistry technique, Review analytical and biological test results received from outside testing lab, Knowledge of analytical/biological/Microbiological testing required, Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified, Follows procedures at all times, adopting cGMP, cGDP practices, Follows supervisor directions at all times, Able to function independently, but asks questions as necessary, Actively participates in daily and weekly planning discussions with his/her teammates and supervision (as needed) offering suggestions to improve Right First Time and schedule adherence as needed, Consistently communicates work sequence status to supervisor in a timely manner, Demonstrates engagement in helping to achieve CQ laboratory, team, and individual goals, When faced with roadblocks and issues, routinely offers suggestions for improvements, Is a positive influence on the CQ laboratory, often going out of his/her way to support and assist teammates on the same shift wherever possible, Has understanding of basic non-instrumental wet chemistry techniques, Manual Titrations, pH, Conductivity, Autotitrations, UV-Vis, Polarimeter, For Incoming Material CQ lab analyst, has understanding of Assurance Quality Limit (AQL) and sampling procedures and tables for inspection by attributes, Completes documentation relating to material analysis and enters data into database/software systems; such as MES, SAP or LIMS, Completes and participates in training activities which maintain or improve laboratory skill sets and practices, Testing of raw materials, finished product, and stability samples while meeting deadlines and following an assigned schedule, Accurately documenting all tests/test materials/equipment used and all results obtained, Independently administrates assigned coordination functions, Capable of troubleshooting minor equipment issues, Responsible for safety and to protect themselves and fellow employees from harm, Follow the guidance and instruction of Supervisors and trainers, Work closely with Supervisor to monitor test progress and results, Support a culture of “quality” in the laboratory environment, Perform laboratory analysis on incoming raw materials, in-process samples, finished products and stability samples per established test methods, Prepare samples for chromatographic analysis, prepare standard and reagent solutions including buffers, mobile phase, diluents, etc, May perform cleaning validation using HPLC and UV methods, Must learn to perform Potency Assay, Blend Uniformity, Content Uniformity and Impurities testing by HPLC, May perform GC, FTIR, UV/Vis, Dissolution, IC, TLC, KF titration, LOD, Hardness and/or other wet chemistry techniques as instructed, Record test results in Lab Notebook; notes should be recorded promptly following a test and should be neat and accurate, Support projects as directed that lead to technical studies of the manufacture processes, Must organize work and budget the use of time in order to be efficient and results oriented, Perform and support 5S housekeeping duties (sort, straighten, sweep, standardize, sustain), Must have strong mathematical skills required, Must have computer skills; Microsoft Word, Excel required, Utilized company lab spreadsheets and databases for data collection, Performs lab duties in accordance with standard good laboratory practices (GLP), Performs various tests of production batches in accordance with specifications, producing results in a timely manner, Maintains quality tests record including manufacturing procedures and related test data, Applies fundamental technical skills to provide product and process support, Conducts assigned technical tasks, producing accurate timely results, Understands task scope, expectations and requirements, Participates in the areas of quality improvement process, Interacts with personnel at facility including laboratory staff, manufacturing, and customer service, and marketing business management, Utilizes available information resources and systems, developing working knowledge and understanding of various functions and interfaces, Develops understanding of customer processes and applications, Communicates results of assigned tasks to Quality Lead in a timely manner, Communicates findings to Technical Director, B.S.