Writing, optimizing, and validating SOPs and SOMs for a wide variety of analytical instrumentation and methods, A high level of technical knowledge in a broad range of fields such as metabolomics, proteomics, process analytics, and traditional analytical techniques, Ability to provide expert advice and innovation to develop solutions to complex technical issues, Design and execute experiments; interpretation of data from multiple sourcesMust be motivated, possess good interpersonal skills, communicate well within and between teams and be able to work to tight deadlines, Ability to prioritize responsibilities and work effectively in a multi-tasking and matrix environment, Participate in project strategy development and implementation, including developing intellectual property, Demonstrated commitment to safety in the work environment, Exhibit strong One Team behaviours: “Support those I work with and help to build the effectiveness of my team to achieve the best results”, “Lay the foundations for the future by helping people to develop their capabilities”, “Recognize and acknowledge the contribution of others”, “Enable others to trust me by delivering on my accountabilities and standing by decisions when they are made” and “Put the team first”, Exhibit strong Respect behaviours including “Respect the views and feelings of others and consider the impact of my words and actions”, “Build strong relationships based on trust and honest discussions”, “Listen carefully and consider different perspectives”, and “Create an inclusive and diverse workplace where everyone is treated with respect and dignity”, Experience with Agilent mass spectrometry, UHPLC, GC, and GC-MS equipment and software including OpenLab, Masshunter, Bioconfirm, and/or SpectrumMill, Previous experience of working with academic and 3rd party partners, Demonstrated experience at executing changes to existing laboratory set-ups through appropriate use of management of change processes, Ensure analytical methods are properly validated/qualified as appropriate in compliance with local and Group SOPs before routine use in QC, Ensure analytical instruments are properly qualified and calibrated in compliance with local and Group SOPs, Ensure all QC technicians are properly trained on all routine methods, Manage the instrument calibration program for the QC laboratory, Manage the QC Analytical Reference Standards program, Manage the QC laboratory supplies procurement process, Attention to detail and strict adherence to GMPs is a must, Wet Chemistry, Titration, HPLC, GC, IR, Data Integrity requirements, Effective problem solving/troubleshooting skills, Experience with analytical method validation per GMP requirements, Demonstrated ability to perform hands-on testing in a laboratory environment and summarize results, Problem solving capability in an R&D and/or production support organization, Experience in thermal analysis (DSC, TGA, thermal and mechanical properties measurement), combustion measurement, wet lab tests, chromatography and/or spectroscopy a plus, Demonstrated innovation and/or problem solving skills, Technical knowledge and expertise in the use and application of specialized analytical instrumentation to support Nutritional testing, pre-mix, pre-blends, mixer studies, raw ingredients, developmental products, and finished product analysis. or B.A. A knowledge of other European languages although not required is ideal, Communication Skills – Must be able to communicate experimental results clearly to peers & supervision through email, verbal communication and/or concise report. Maintain electronic databases, documenting results in laboratory notebooks and reports, 6) Troubleshooting existing laboratory processes and instrumentation, 7) Maintaining a safe and clean laboratory as well as all other assigned areas of responsibility, Run analyses as needed such as drug assay, Run and operate pharmaceutical formulation and bio-processing lab equipment, Plans and conducts chemical analysis of medical device manufacturing and design processes, materials, and products, Implements, refines and validates test methods for QC testing, Test method development and implementation using HPLC and GC through reports and protocols, Process control charting within manufacturing and quality processes, Complete internal audits of manufacturing processes, Perform testing and data review for HPLC/UPLC (high and ultra-high liquid chromatography), titre, ATOL purification using TECAN and plate reader, CE (capillary electrophoresis), CEX (cation exchange), HILIC (hydrophilic interaction), TOC (total organic carbon), LAL (endotoxin testing), ELISA, and DNA testing, Testing and purification of proteins and peptides, Utilize high-throughput, robotics sample handling and/or auto-sampler systems to manage samples, purify, and test, Demonstrate independence and ability to produce quality results under minimal direction, High energy individual who can multi-task and handle a fast-pace, dynamic work environment, Comply with safety guidelines and site specific procedures which include but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books, Interact with multiple functional areas in a highly matrixed-team environment, which may include Manufacturing, Process Development, IS, Facilities, Engineering, and Quality Control, Technical expertise for executing analytical test methods in one or more of the following areas, B.S., or M.S. Browse 3214 Analytical Chemist jobs on our job search engine. resumeOn a piece of paper, write your soft and hard skills down. Being a successful Chemist requires an exceptional education and analytical, problem-solving and scientific skills in order carry out experiments and research. ), Set-up and execute analytical method validation experiments per approved protocols, Maintain and troubleshoot lab instruments/lab problems, BS degree in chemistry or related discipline and have a minimum of 2-4 years of relevant background, Strong GMP compliance and documentation skills, Strong comprehension and facility in quantitative/qualitative analytical chemistry, Familiarity with Agilent ChemStation (HPLC, GC), Familiarity with compendial testing and OOS investigations, Data review experience in a compliance-oriented laboratory, Minimum of a Bachelor’s degree in Analytical Chemistry or a related field of study, Minimum of three or more years of related experience, Experience in analytical method development and validation, Hands-on experience with gas chromatography, gas chromatography-mass spectrometry, and sample preparation techniques, PhD in Analytical Chemistry or a related field of study, Experience with quantitative, low level analytical chemistry testing, Perform a range of routine analysis using chromatographic techniques under minimal supervision of a senior member of staff, Work as part of an efficient analytical team, Take responsibility as required for elements of specific projects and/or specific areas of general laboratory/sample administration, Responsibility to lead/participate in assigned RD&I development projects and assignments, and to report progress and results, Responsibility to order and perform method development, chemical analyses and other laboratory evaluations as part of project and assignments, Responsibility to initiate and support product development tasks in implementation stages, like production scale up, technical and analytical development and customer evaluation, Ensure progress in assigned projects through leading and coordinating team members, Ensure customer satisfaction through knowledge support and trouble shooting in customer related problems, Cooperate with other laboratories mainly in AkzoNobel, Master of Science in Chemistry / Chemical Technology, Experience within the area of Analytical Chemistry, Process Technology and Process Analytical Technology, Strong communication skills (both in writing and verbally), fluent in Swedish and English, Conduct laboratory testing in an accurate and timely manner on a variety of analytical instruments including particle distribution (by sedimentation, laser diffraction, and/or sieve analysis), BET surface area and porosity, density measurements, color/brightness analysis, and thermal analysis, Conduct or assist with analyses involving X-ray diffraction, X-ray fluorescence, FTIR spectroscopy, differential scanning calorimetry, optical microscopy, scanning electron microscopy, and transmission electron microscopy with emphasis on problem-solving, Complete sample preparation, which may include crushing and grinding of ore samples, polishing, working with chemicals, and various other sample preparation techniques.Coordinate submission of samples to external laboratories if needed, Assist with sample database log-in and organization of projects throughout stages of preparation, analysis, and reporting.Use electronic laboratory notebook to record and manipulate data.Assist with organization of raw data files, calculation files, reports, standard test methods, standard operating procedure, and/or work flow diagrams, according to ISO quality systems/good laboratory practices (GLP), Follow written test methods and standard operating procedures accurately during analysis; assist with updating existing or developing new test methods/operating procedures as needed.Organize inter-laboratory or intra-laboratory studies, calibrations, or other quality control related activities to validate results, Record and organize data in order to complete or assist with accurate interpretation of results, drawing conclusions, and communicating effectively by written standard internal reporting practices, Actively contribute to analytical method development, Coordinate with other Analytical scientists as needed to complete projects, Work within the Imerys Health, Safety and Environmental procedures, Sharing of laboratory administrative tasks, such as ordering supplies, organizing maintenance schedules, organizing sample inventory, filing, organization of equipment instructions, etc. Download Analytical Chemist Resume Sample as Image file, Scientist, Analytical Development Resume Sample, Leading the development and validation of both physical and analytical test methods in support of metered dose and transdermal products, Providing technical and analytical support for product and process improvement projects, Leading studies to support regulatory submissions and improvement projects, Writing of documents for regulatory submissions, Develop, evaluate, troubleshoot, validate, and transfer analytical methods, Author, review, and execute method validation and transfer protocols and reports, Manage the chromatography and mass spectrometry laboratory and provide timely analytical support to global R&D of the Silicones business, Technical and analytical support for product and process improvement projects, Development and validation of both physical and analytical test methods in support of reference standards, metered dose inhaler and transdermal products, Development and validation of both physical and analytical test methods, Develop new analytical techniques and methods that will be adapted in other labs within the company, Writing and routing of technical documents and change management requests, Develops, implements, and maintains analytical methods for use in lubricant product development, problem solving, and customer assistance, Provides analytical method development to the process development group, Assisting Application Development and Technical Service personnel in providing training and demonstrations, To identify and make recommendations for improvements as part of a team within or outside the department in order to ensure continuous improvement, Independently perform routine and complex analysis using established analytical methods and development of analytical methods when no SOP is in place, Data collection and experimentation assistance in support new product development, Perform routine performance checks on instruments that are being used for project support (e.g. It’s actually very simple. experiments, Assisted in preparing samples for Analytical Chemistry Resume Sample One is one of three resumes for this position that you may review or download. Applicants interested in expanding their knowledge into new areas of science would be welcomed, Knowledge of the analytical technologies required for the development of quantitative and qualitative methods for new agrochemical active ingredients and formulated products, Knowledge, gained through practical experience, of analytical methodologies available to apply to solving chemical characterisation problems, Knowledge of colloid and/or polymer science, analysis and characterisation using modern analytical techniques, Knowledge of extraction procedures and analytical technologies associated with the characterisation of agrochemicals, Experience of analytical techniques for the qualitative and quantitative analysis of active ingredients or polymers in one or more of the following techniques: GC, LC, CE, GC-MS, LC-MS, preparative chromatography, thermal techniques (inc. DSC) and spectrophotometry techniques, Good attention to detail, a high proficiency for multi-tasking & project planning, and flexibility to change, Effective oral and written communication, in a culturally diverse setting, including technical and non-technical audiences, Able to work effectively in a cross-functional team setting. Provide expertise on test methods as required to other Grace locations, Manage the correlation program between plants for the methods in their area and organize meetings and opportunities for lab staff to share best practices between locations, Lead specialized testing in their area of expertise as needed to support plant operations and troubleshooting, Keep up with equipment and method advances in their area of responsibility through vendor interaction, external training courses, and self-study, Provide thought leadership and drive continuous improvement in their lab looking for opportunities to improve workflow, equipment, automation and data handling, Demonstrated hands on experience in lab with responsibility for data quality and equipment operation, Bias for action and desire to delivery timely, correct analytical results, Prior experience with ICP equipment and methods, Good communication skills, conveying information both professionally and concisely, Actively champion and promote all safety related policies and programs to ensure colleague engagement and commitment to the benefits of working safe, Understands their role in food safety and quality systems, actively participates in food safety efforts and ensures all activities conform to good manufacturing practices, Perform analytical methods development, validation, and routine testing using a variety of analytical techniques (e.g. An Analytical Chemist analyzes chemical makeups of a variety of products while serving as specialized Scientists. Able to communicate across a range of scientific disciplines, Good knowledge of Physical Property techniques (e.g. Chemists are needed to help companies find solutions or to improve processes. The key to this section is keeping it short and sweet while summarizing the resume. IT and technology skills to work with advanced techniques. development. Experience with the identification of unknown compounds by GC-MS is preferred, Experience with sample analysis using FT-IR and/or EDXRF is preferred, Experience working in an ISO 17025 Accredited laboratory or other regulated laboratory environment is preferred, A Bachelor’s Degree in Chemistry or Polymer Science, 10 years minimum experience in a laboratory environment, or; a Master’s Degree in Chemistry or Polymer Science with 5 years minimum experience in a laboratory environment, The qualified candidate for this position will need to have the ability to function in both a team and an individual environment. Validates equipment and test methods, Identifies areas for improvement, suggests solutions, and submits idea records, May provide leadership, work direction, and technical oversight to Chromatography team members, May represent, coordinate work for, and report back from the analytical department to R&D project teams, Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures, Applies scientific principles and company policies and procedures, analyzes data or situations, and exercises judgment to recommend solutions to solve problems, Review of all laboratory Quality Systems to ensure compliance to GMP, Participate in Regulatory, Internal and Vendor audit programs as required, Provide technical guidance / trouble shooting where applicable, Review and approval of Laboratory results and documentation, 3-5 years industry experience in analytical chemistry in particular with chromatographic and pharmaceutical cGMP analysis; medical device or pharmaceutical experience preferred, Liquid chromatography experience with both routine testing and method development, Compliance experience in a regulated environment, Combination product analytical chemistry testing experience, Waters chromatographic equipment (e.g., Waters 2695 Separations Module with 2996/8 Diode Array Detector) and Empower software experience, Drug dissolution, content, or degradants analysis by chromatography experience, Experience with mass spectrometry detectors, Receive, log, analyze field samples and send out daily residue reports to customers, Prepare daily field sample analysis report and discuss the results with technical service personnel, Maintenance and upkeep analytical instruments and laboratory, Manage samples and waste generated from lab, Provide timely residue analysis reports to customers and filed personnel, Management of the analytical lab (instruments and seasonal temporary workers), Upkeep of Food safety certification (SQF) and logs, Design and execute experiments for analytical support of biotherapeutic proteins using HPLC, LCMS, and capillary electrophoresis, Troubleshoot and maintain analytical equipment in good working order, Experience analyzing proteins using HPLC, LCMS, and electrophoretic methods, Experience developing, qualifying, and testing analytical methods to characterize proteins, Strong analytical lab skills and technical knowledge of proteins and peptides, Excellent documentation skills, including an understanding of GxP requirements, Excellent communication (oral and written) skills and attention to detail, Strong computer and organizational skills, Ability to work independently and as part of a larger analytical team, Biotech/pharmaceutical industry experience preferred, B.S. Zipjob has over 100 professional resume writers with experience in all industries, ready to help you create your best resume. liquid:liquid extraction, solid phase extraction etc, Demonstrated ability to run high throughput analytical workflows requiring fast sample turnaround and consistent data quality, Excellent “teaming” skills. CHEMISTRY RÉSUMÉS 1. Reviews data for accuracy and completeness, Follows MRI safety and security policies and procedures and maintain labs and facilities in organized manner, Maintains equipment and ensures it is in working order. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. Prefer industrial experience with LC Mass Spectrometry (LCMS), HPLC, and UV-Vis, Must have computer skills including Microsoft Office (MS Excel, MS Word, and MS PowerPoint) and Microsoft Outlook, Knowledge of quality systems and laboratory safety. maintenance of analytical instruments as well as supervised and provided You will have opportunity to work in a high performance team environment and deliver against key project goals. following standard instructions and SOPs as well as utilized effective You want to keep it highly tailored to the job description. hydrofluoric) and performing wet chemistry testing, Become a subject matter expert in analytical test methods, procedures and instrumentation to run ICP-OES, IC, HPLC and auto-titration equipment, Preform routine analyses on raw materials and finished goods to endure proper QC, Participate in analytical method development and validation, Conduct occasional bench top experiments to simulate manufacturing processes, Ensure all data is generated in a timely and complaint fashion, Abide by all date input / output specifications, Perform routine maintenance or troubleshooting on laboratory equipment, Exercise a high regard for safety and chemical hygiene practice, Observe and promote exemplary housekeeping within the laboratory, Train junior chemist and technician to assist with the responsibilities listed above, Assignment will be a pre-defined rotating schedule to support continuous operations, BS or MS in chemistry or chemical engineering, with relevant bench-top chemistry experience, Working knowledge of and experience with analytical equipment including but not limited to ICP-OES, IC, HPLC and auto-titration, Ability to establish priorities, work independently and productively, and deliver results with minimal supervision, Ability to work in a fast-paced environment that may include rapidly shifting priorities, Ability to concentrate and perform quality work in a dynamic environment, Patience and leadership to train and oversee 1-3 chemical technicians per shift, 50 %- Utilize analytical knowledge to execute analytical methods that provide support to complex projects providing defined business value. Working in multidisciplinary teams is common, Develop gas chromatography methods for petroleum applications and provide troubleshooting support for manufacturing issues, Provide technical leadership/support for established methods (e.g. dedication and project management. Advanced knowledge of area of analytical chemistry is required. Drive development and validation of test method to support program schedule, Develop, characterize and validated test methods as needed, Support transfers of test methods to internal and external analytical labs as needed, Collaborate with other Renal Care Solutions analytical labs to ensure uniform application of lab procedures and best practices, Collaborate with company-wide analytical labs to develop laboratory metrics and best practices to measure continuous improvement in quality and productivity, Partner with manager to develop strategic hiring and equipment plan for analytical chemistry lab, BS in Chemistry, Analytical Chemistry or equivalent, 10+ years of analytical laboratory experience, including 5+ years in technical leadership and/or management role, 5+ years analytical chemistry experience in the medical device industry or other regulated industry (ISO or defense), Proficiency in laboratory software including Empower, ELN, LIMS, Expertise is developing methods for analytes in biologic fluids including blood, serum and urine, Self-starter with strong work ethic and initiative in accomplishing objectives, Design and conduct experiments using HPLC/UPLC/GC including HPLC-MS and GC-MS in support of method development and validation, Provide expertise in maintenance and usage of all analytical instrumentation, Act as a technical team member with cross functional project responsibilities on assigned projects, Provide expertise in the areas of analytical best practice, structure elucidation of impurities, state-of-the-art methodology and installation and qualification of equipment within AS&T, Support the network and lead activities related to extractable/leachable methods and instrumentation, as well as troubleshooting and resolving investigations to facilitate solutions to complex challenges, Collaborate with sites, R&D and Regulatory Affairs in the preparation, management and follow up of Health Authority documentation for extractable/leachable testing, analytical methodology, and equipment, Utilize proactive thinking to generate creative solutions to complex technical problems, Performs sample preparation and analysis of samples following prescribed procedures, Completes all paperwork associated with the analyses (ex., calibration logs, run logs, etc. New phd analytical chemist resume careers are added daily on SimplyHired.com. Experience with MS analysis of chemical warfare agents (CWAs) or pesticides is desired but not required, Candidate must have a PhD in Analytical Chemistry degree and a minimum of 3-5 years analytical chemistry working experience, Demonstrated experience in chemical analysis of small molecules, macromolecules, energetic materials and rubber products, Must have strong spectroscopic working experience with some chromatographic chemistry experience, Strong research and problem solving capability in an R&D and/or production support organization, Demonstrated experience and working knowledge of chemical analysis such as GC, GC/MS, HPLC, LC/MS, and Wetlab tests a plus, Experience with investigation and troubleshooting of Aerospace materials and processing a plus, Detail oriented but able to understand the big picture, Development of proficiency using analytical instrumentation to generate meaningful information in pursuit of problem solving solutions or material characterization goals, Education: Working toward Master or Ph.D. degree in either Analytical Chemistry or Materials Science focusing on Chemical / material Characterizations with various techniques and instrumentations, Demonstrated ability to apply technical skills and understanding of the fundamentals involved in analytical chemistry or materials science, Independently generate precise, reliable and reproducible data in a timely manner as part of the development, validation, and transfer of drug product analytical methods, including excipients, in-process and drug product testing, Independently or with coaching, design and conduct critical experiments to further project goals. Analytical Chemists examine chemical compounds to determine their construction. - Instantly download in PDF format or share a custom link. (LIMs, CDAS, Trackwise, PDOCs), Third level qualification preferably with a minimum of 2 years previous laboratory work experience in a cGMP pharmaceutical environment, Lead conduct work on analytical-based projects supporting all areas of the business involving beauty, cosmetic, and personal care products. chromatography for testing raw materials, and final pharmaceutical products as Strictly adhere to all necessary calibration requirements within all lab operations, Independently preparing and analyzing samples for analysis of e-vapor stability studies using UPLC-UV and QToF, Analyzing samples using the Waters AutoPurification System for collection and isolation of compounds, Tracking samples for stability projects, organizing work and documenting results in an electronic laboratory notebook, Organizing and reporting results from LC-Profiling in a clear and concise manner to meet the needs of our customers, Delivering high quality data to our customers, Collaborating with other scientists to provide additional insights to stability, Maintaining and managing the appropriate documentation for Analytical Sciences to be compliant with ISO 17025 Accreditation, Altria Quality System and Records Management policies, Participating in internal and external scientific meetings to maintain and expand scientific expertise, A Bachelor’s Degree in Chemistry, Forensic Science or closely related field with demonstrated experience in an analytical testing laboratory, Demonstrated experience with UPLC-UV, UPLC-MS and with prep LC collections, Demonstrated experience working with Waters AutoPurification System and FractionLynx for collection and isolation of compounds, A minimum of 3 years of experience working with liquid chromatography-mass spectrometry for the analysis of compounds in complex matrices, Experience working in a regulated environment under ISO 17025 Accredited laboratory or other regulated laboratory environment is preferred, Experience with sample preparation and extraction techniques (LL, SPE, etc.) presenting at numerous conferences. Establish schedules, define priorities, and direct activities of other scientists and non-scientists as well as provide training and development for others, Minimum of 5 years of pharmaceutical laboratory experience in analytical R&D, Extensive knowledge of cGMPs, GLPs, and FDA/ICH guidelines and their application to drug development, Technical expertise in developing and running analytical methods using common quantitative techniques including UPLC/HPLC-UV/FL/ELSD/MS, UV/Vis, GC, and wet chemistry. The template is set up with an easy to read layout like the example above: clear section headings, modern font, and follows a reverse-chronological resume format (preferred by both hiring managers and ATS scans). Still have questions? Ability to work on different projects in parallel is required, Supervise activities in the analytical laboratory in order to assure acceptability of raw materials, active ingredients and preservative levels in cosmetic drug products, assures test methods, specifications and standards are available, Provides training in analytical techniques such as wet chemical and instrumental analysis, Perform analytical/instrumentation analysis of raw materials, bulks and finished goods, Review new and innovative instrumentation/test methods and operating procedures to improve the efficiency and accuracy of the lab, Supervise activities in the Analytical Laboratory for timely evaluation of raw ingredients, cosmetic drug bulk batches and finished goods. Strong job applicants should have a mix of hard skills and soft skills. ANALYTICAL CHEMIST. What steps to follow when adding skills to your chemist. You may also want to include a headline or summary statement that clearly communicates your goals and qualifications. This section should change slightly for almost every job you apply for. Consistently makes sound decisions based on data and anticipates problems, Technical Skills – Good knowledge of a broad range of analytical chemistry and techniques. Recommend revisions to standards and/or specifications as necessary, Review and establish procedures to maintain all analytical instruments in proper calibration. Soft skills include collaboration, communication, emotional intelligence, and creativity. Maintain instrument logs and records, Maintain supplies and materials for the GAATS area, Assist in the evaluation and cost estimates for new projects, Document and record work observation and results according to written SOP’s, Implement analytical methods to elucidate the types and quantities of impurities present in reaction mixtures, process streams, waste streams, intermediates and finished products, Work with CRD staff to develop impurity profiles for Active Pharmaceutical Ingredients and regulated intermediates, Ensure that work in the analytical development laboratories is done safely and in accordance with the site chemical hygiene plan, following any additional regulatory requirements that may apply, Conduct all job responsibilities in a manner consistent with all applicable safety and environmental laws and regulations, company policies and procedures, regulations and commit to continuously improve safety and environmental performance, Develop and validate chromatographic (HPLC, GC, and IC) methods for the analysis of pharmaceutical active ingredients and their precursors (intermediates), Develop and validate as needed other analytical methods required by regulatory agencies for a pharmaceutical active ingredient and its precursors, Develop and qualify in-process controls (HPLC, GC, etc) for processes, Validate analytical methods for cleaning verification, raw material assay, stability testing, waste streams, and final product release, Modernize analytical methods for existing products and processes, Develop validation protocols, conduct validation work and write validation reports, Perform appropriate testing for specification development, Ensure that all IPC’s are performed on laboratory experiments before they are used to monitor a kilo lab, pilot plant or manufacturing run, Provide analytical support for CRD and Pilot Plant projects. This would involve DoEs and accelerated stability studies, Development of assay/purity methods and assessment of method robustness/ruggedness, Development and execution of method validation protocols, Transfer of analytical methods to other laboratories and remote sites, Hands-on generation of data in support of accelerated and registration stability studies, At least one year experience in product development analytical chemistry, Perform assays on vaccine products, process intermediates, and related experimental samples using ELISA, HPLC and other biochemical/analytical tests (e.g., spectrophotometric, electrophoretic, immunochemical methods), General laboratory skills, experience with pipettes, plate washers, plate readers, electrophoresis equipment, and automated instrumentation, Bachelor's degree in Biochemistry, Biology, Chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major), Minimum of 2-5 year related laboratory experience, Function as a team member with other scientists in, testing, developing and transitioning chemical / biological detection / identification technologies, Generates test data and contributes to technical report development, Performs the operation, maintenance, and troubleshooting of various mass spectrometers including a Thermo Fisher Orbitrap, Performs analytical practices including the generation of a calibration curve with the application of isotopically labelled internal standards. analyzing drugs and related chemicals, Using instruments such as testing new forms of virtual delivery, BS degree with a minimum of 1 year of relevant experience OR a MS degree with no more than 3 years of experience in biotech or pharmaceutical industry, Experience with analytical and protein chemistry, Working experience with other routine analytical and biophysical techniques such as capillary electrophoresis and spectroscopy, BS degree focused in chemistry, biochemistry or biology is preferred, Some experience with HPLC and/or LC/MS and LC/MS/MS analysis of protein therapeutics would be desirable, A good understanding of protein structure and function relationships, Knowledge and hands-on experience in various protein and oligosaccharide separation and characterization techniques would be a plus, A highly motivated individual with excellent communication skills, both written and verbal, An instinctive team player with excellent people skills, Looking for a highly motivated individual who will support the analytical testing for vaccine development, This involves the chemical labeling of biological samples, HPLC separation, and data analysis, This individual needs to ensure that the analytical results are of high quality and all work is documented in a clear, concise and timely manner, A BS or MS degree or equivalent in Biochemistry, Analytical Chemistry or a related field is required, The successful candidate should show ability to work independently, follow procedures precisely, and generate analytical data consistently, Experience in HPLC separation and using Empower would be an advantage. Attend weekly plant production meetings. contract laboratories), Well versed in a broad range of standard tests and have hands on experience with a variety of instruments, Perform chemical analysis and research for projects involving trace analysis of components in environmental samples and complex matrices, Perform a variety of standard preparation, sample preparation, and analysis using LC-MS and/or GC-MS systems in compliance with applicable methods, test plans, and SOPs, Perform aspects of equipment operation and maintenance including calibration, operation and maintenance of GC-MS and LC-MS systems, Perform calculations and conversions, and compile the data generated. Coordinate activities to assure that information is provided on a timely basis to service international production requirements, Compile data and report information to support the raw material vendor certification program, Perform special projects as requested by management, reporting results and recommending solution/corrective actions, Science degree in applicable scientific discipline, or equivalent on-the-job experience, Working laboratory experience, preferably with FMCG experience, Working knowledge of GSK Quality standards, GLP and GMP requirements, Working knowledge of validations, calibration systems, and instrumentation, Working knowledge of applicable GSK policies and procedures, Problem solving/continuous improvement skills, Developed skills in coaching, interpersonal communications, team building and training facilitation, Ability to interact with all levels of the organization, Experience in writing, reviewing and revising SOPs, Working knowledge of Microsoft Word, Microsoft Excel and Laboratory Information Management System (LIMS), Ability to work and succeed in a team based environment, Flexibility to work extended hours (including weekends) to achieve results as needed, 1) Support Operations by analyzing raw materials, intermediate batches, packaging and finished products as required, 2) Responsible for trouble shooting and investigating out of specification results. Coordinate and perform data analysis and prepare data reports, Experience with analytical method development, Previous research experience related to chemical, biological, radiological, nuclear, and/or explosive (CBRNE) threats, Experience operating in GLP/GMP/ISO environments including the preparation and validation of standard operating procedures, Minimum of a Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field of study, Experience working in an analytically diverse environment, Familiarity with method validation procedures, SOPs, and electronic systems, Hands-on experience with the following: HPLC, GC, FTIR, and NIR, Self-motivation, good interpersonal and communication skills, and strong customer orientation, Prior work experience in a manufacturing analytical laboratory, Hands-on experience with the following: ICP-OES, ICP-MS, LC-MS, GC-MS, and IC, Working knowledge of other analytical methods (including wet chemical procedures), Familiarity/experience with manufacturing sampling planning, Experience in communicating with manufacturing chemists and/or unit operators, Minimum of a PhD degree in Analytical Chemistry or a related field of study, Experience in analytical method development and validation (industrial or academic), Hands-on experience with chromatography, mass spectrometry, and NMR, Self-motivated with good interpersonal and communication skills, and strong customer orientation, Experience working with process chemists and engineers, Experience in the field of phosphorus chemistry analytics, Working knowledge of the following: FTIR, multivariate statistics, thermal analysis, particle size measurements, scanning electron microscopy (SEM), Minimum of one or more years of experience in industry, Hands-on experience with all of the following: HPLC, ICP-OES, ICP-MS, Hands-on experience with GC, LC-MS, GC-MS, and/or IC, Working knowledge of other analytical methods such as wet chemical procedures, UV/Vis, and/or FTIR, Familiarity/experience with manufacturing sample analysis, Prior experience working for a global organization, Prior experience in the agricultural industry, Minimum of a Bachelor’s degree (or higher) in Analytical Chemistry or a related field of study, Minimum of three or more years of related industrial experience, Experience in development and validation of GC-MS/MS methods, Hands-on experience in analytical method development and validation with emphasis on liquid chromatography - mass spectrometry (LC-MS/MS) based techniques, Demonstrated ability to troubleshoot analytical methods and equipment, Excellent oral/ written communication and interpersonal skills, Agility to work on and balance multiple projects, while maintaining the focus to meet business objectives, Ph.D. degree in analytical chemistry or closely related field, Experience developing, validating and executing residue analytical methods in two or more matrices (i.e.
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