Develops plans for moderately sized projects or portions of large projects. Salary can vary based on factors such as location, company, and industry. Coty Llc Senior Chemist Resume Sample Resumehelp . 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.) Analytical Chemist Resume. degree in Chemistry or similar science required, Experience in the chemical or petrochemical industry is preferred but not required, Previous experience with liquid chromatography (LC or HPLC), gas chromatography (GC), and gas chromatography mass spectrometry (GC-MS) is highly desirable, Strong interpersonal and teamwork skills with the ability to influence leadership, peers, and Quality Control Technicians; able to take a "hands-on" approach to drive change and get results, Prioritize and manage multiple, complex, time-sensitive projects, Manage and lead both strategic long-term programs/projects as well as address short-term operational issues, Drive the qualification of new analytical equipment, Leads improvements quality control analytical processes, either through technology, process, and equipment upgrades, Maintains laboratory standards and equipment in accordance with quality certifications, Supervises a staff of 6 laboratory employees providing testing support across three operational shifts, Chromatography experience including HPLC, GC, as well as GPC is required, Strong technical, analytical and functional skills, Demonstrated computer skills including proficiency in Microsoft Office, Executing analytical tests in compliance with GMP and in-house procedures. Candidates currently living within a commutable distance of West Greenwich, RI are encouraged to apply, Masters or PhD in analytical or organic chemistry. Provide interpretation of results, Perform scanning electron microscopy with energy dispersive spectroscopy (SEM/EDS) on both non-metallic and metallic samples for fractography, general sample characterization, and chemistry, Lead minor failure analysis and analytical technical service jobs. degree with a minimum of four (4) years of experience in analytical chemistry, Demonstrated ability to impact multiple project goals by utilizing technical knowledge and techniques in projects regarding organization, research, production and operation, Demonstrated independent judgment in selecting methods and techniques for creating solutions to a wide range of challenging chemical processes, Demonstrated ability for launching, overseeing, and carrying out projects in Process Development, Lead lab configuration for new project testing requirements, Aid in the determination of specific lab equipment needed for project testing and work with vendors to obtain quotes, Responsible for working with site personnel to order equipment necessary, Must be willing to study and understand the new chemicals coming into the lab and train current lab technicians on proper handling and PPE, Support installation and set-up of new instrumentation in lab for project testing, Demonstrated work with Gas Chromatography instrumentation, Experience with a variety of laboratory instrumentation and equipment including, but not limited to, Provide chromatography support to R&D and manufacturing, Develop chromatography methods and solve chemical and process problems, Analyze samples, report results and document methods, Maintain and operate chromatography instruments, Maintain excellence in safety, health and environment practices, B.S. This includes method development, optimization and validation, Identify and support introduction of systems & testing improvements, Support the implementation of quality systems, Management of the Biomaterials Laboratory including testing, documentation and laboratory maintenance, Maintain laboratory test/validation records in compliance with regulatory requirements, Lead laboratory chemical risk assessment and introduction of appropriate engineering controls, Participate in the planning and running of DOE’s and test plans, Perform trending and analysis of data, and compiling of associated technical reports, Participate in brainstorming and problem solving sessions, Maintain appropriate laboratory supplies and equipment to ensure efficient operation of the Biomaterials Test Laboratories, Independently determines and develops approach to resolving end customers product related issues, through problem solving and troubleshooting test issues, product training and relationship building, Prepares and accurately determines metal content and other properties of matrix materials, applying approved analytical and/or instrumentation test methods to support refining, catalyst and chemical production, development or other JM department, Prepares and maintains proper analysis documentation, including summarized test data and procedures, Develops a basic understanding of production processes and an ongoing proficiency with all analytical test methods related to customer specifications, Operates in accordance with all JM safety procedures and SOPs at all times, Post-secondary major in chemistry or related science required, Lab experience including commercial analytical/quality control laboratory experience needed, Instrumentation techniques, for inorganic, elemental analysis, and physical characteristics preferred, Solid working knowledge of Microsoft Office and strong attention to detail required, Requires sound communication skills both verbal and written and ability to work successfully in a team environment, Define and establish the target of analytical team, review and assess its progress and fulfillment, Define and follow quality procedure, test method development, and coordination with global analytical team, Based on effective communication, coordinate the suitable analytical resource to support global business technology (GBT) team, technical service team and colleagues from manufacturing/process technology team, establish good work relationships with kinds of partners, Review the work-flow of analytical lab, record test procedure and lab activity, summarize general report on time, Lead and organize the analytical support to new projects, Keep connection with collaborated universities and institutes to support internal unsatisfied analytical needs, Management of overall analytical lab and showcase display, Master or above in analytical chemistry, organic chemistry, polymer chemistry or other related majors with minimum 5 years working experiences and 1-3 years automotive coating R&D experience is plus, Very familiar with modern analytical techniques, including but not limited to Spectroscopy (IR, Microscopy IR, UV-VIS, XRD), Chromatography (GPC, GCs, Pyrolysis-GC/MS), Thermal analysis (TGA, DSC) and Physical properties technology (Surface tension, Contact angle, Optical microscopy, Water content by Karl-Fisher, etc. Senior Analytical Chemist. Experience must be proven by a solid track record of publications and/or patents, Experience developing and optimizing fit-for-purpose analytical methods for analysis of a wide range of analytes (small molecules, proteins, lubricants, fatty acids, fermentation products, anions, cations, and metals) in complex matrices using a wide variety of analytical instrumentation including LC-MS (QTOF and QQQ), UHPLC, GC, GC-MS, IC, ICP, and MIR, Generating, recording, interpreting, and reporting high quality and accurate analytical chemistry data and information, Openness to train others on a variety of instrumentation and methods, Courage to constructively challenge and discuss the analytical results of others, Ability to communicate effectively with project team leaders to anticipate analytical needs and estimate resource requirements to develop required methodology and execute testing. A good standard of numeracy and skills in data analysis. in Chemistry, with a minimum of 5 years’ industry experience working in a GMP/GLP environment, Testing of Raw Materials/Excipients/Components/Intermediates/Drug Substance/Drug Product in accordance with site schedules and company policies, procedures and guidelines, Support the introduction of new products to the site, Aid in the resolution of issues that may arise during testing, B.S. Some examples are HPLC, GC, TLC, Dissolution Baths and Titrators, Design and coordinate chromatography experiments as a member of a corporate engineering services analytical laboratory, Participate in development of analytical test methodology and strategies for R&D medical device products, Perform hands-on testing in the chromatography and analytical chemistry lab, Prepare test data summary reports/documentation to communicate results to lab customers and the technical community. 79 83 note how hoy and sweetland reconciled conflicting theories concerning an important study that shows which approaches to writing in english. Seasoned professional with Master’s degree in Biochemistry. Experienced Analytical Chemist resume in Oakdale, NY, 11769 - December 2011 : chemist, gc, hplc, scientist, polymer, safety officer, soil, chemistry, russian This may include but not limited to developing methods and performing method validation and verifications, Operate and maintain/calibrate laboratory equipment as per manufacturer’s recommendations and company’s Preventive Maintenance program, Maintain laboratory records related to all testing activities assuring that they are accurate and up to date, Perform all analysis and lab related duties as per cGMP, B.S. This is a real resume for a Analytical Chemist in CANA, Virginia with experience working for such companies as American Environmental Testing Lab, Applied Physic & Chemistry Lab, Calscience Analytical Lab. Solutions require creativity, critical thinking, and collaboration, considering a broad range of potential impacts, including those that are downstream, .Extensive experience in preparing regulatory submissions, Develop and validate new analytical methods and implement improvements to existing methods to support both new and existing products. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. Format your chemistry resume template with a respected resume font and 1-inch margins. May contribute to the development of new concepts, practices and standards, Directly or indirectly supervises/mentors others; delegates activities appropriately, Develops alternatives and solutions for a range of complex problems. Organize inter-laboratory or intra-laboratory studies, calibrations, or other quality control related activities to validate results, Required 3+ years of direct experience with working in a laboratory environment, Required experience X-ray diffraction, X-ray fluorescence, FTIR spectroscopy, differential scanning calorimetry, optical microscopy, scanning electron microscopy, and transmission electron microscopy, Preferred background from mineral or mining company, Organizes and conducts routine analyses independently and in compliance with applicable methods, protocols, SOPs and regulatory agency guidelines, Independently able to use and perform basic troubleshooting of laboratory equipment and software appropriate for assigned tasks, while learning to perform routine and non-routine maintenance, Provides input and participates in project meetings, Performs assigned workload on a daily basis and effectively completes multiple assignments, Contributes to a cohesive team environment and maintains a positive attitude. Material scope includes but is not limited to API, in process testing and finished drug products of the product forms noted in the company summary, In coordination with other Technical Service personnel design investigation schemes to support commercial product troubleshooting and execute designed lab experiments, Troubleshoot and remediate analytical test methods for a wide range of API, excipients and finished products, Perform the analytical laboratory work to serve as the sending lab for test method transfer as needed within Akorn sites, contract manufacturing facilities and contract laboratories, Operate and maintain the Technical Service Laboratory within GLP/GMP and SOP requirements and within budget, Perform other duties as deemed necessary by department management, Participate in Technical Service and Operation’s management staff meetings, The individual must have strong verbal communication and writing skills in English, Some synthetic organic experience is desired, Strong project management and organizational skills, prioritizes and plans work activities; uses time efficiently; plans for additional resources; sets goals and objectives; organizes or schedules efficiently; and develops realistic plans, Demonstrates accuracy and thoroughness; looks for ways to improve and promote quality; applies feedback to improve performance; monitors own work to ensure high quality, Strong chromatography and other separations science knowledge, Strong MS knowledge and hands-on applications method development, Sample preparation for trace analyte determination, Use of stable-isotope-internal standards for trace determinations, Maintaining a safe work place, good housekeeping, safe lab practices, and compliance with all site-wide safety regulations, Analytical Methods development, substantially but not limited to chromatography, and validation of technical and formulated goods, Analytical equipment/instrument troubleshooting and maintenance skills are a requirement, Be comfortable working within a lab setting at a minimum of 75% of the time, Perform the analytical phase of projects, analysis and stability testing, relating to formulations development, Execute analytical tasks in support of product development projects within agreed upon timelines, Provide analytical support relevant to the investigation of product performance issues, Provide technical support to implement appropriate analytical methodologies, The interpretation of analytical results to formulation chemists/engineers, biology staff, and others as appropriate, Report writing will include formal documentation of study results, test methods, validation studies, etc, When appropriate perform and report upon analytical work requiring compliance with GLP regulations. Chemistry, Material Science or related field with 3-5 years' experience, Experience with analytical equipment and testing methods. Since we've looked over 6108 Analytical Chemist resumes, we're close to being experts to knowing exactly what you need on your resume. Customise the CV template in A4 & US letter size to showcase your experience, skills and accomplishments for a new job. Work independently, utilizing a broad range of analytical techniques and scientific knowledge, to arrive at conclusions that guide business decisions, Understand big picture and in-depth technical details related to projects, Communicate results clearly and concisely to associates of all levels across R&D in oral and written form, Develop new and improve existing analytical methods to increase accuracy, efficiency, and robustness, Explore and evaluate new analytical technology and methodology for potential application to innovative research, Set specifications for raw ingredients and finished products, BA/BS or MS degree in chemistry or equivalent scientific discipline with 2-10 years experience, Self-starter able to see projects through to conclusion, Broad and in-depth knowledge of analytical chemistry techniques, including chromatography (HPLC, GC), spectroscopy (IR, UV/VIS), DSC, Wet chemistry techniques, Strong problem solving skills and the ability to develop creative and scientifically sound solutions, Highly flexible, adaptive to changing business priorities, completing projects in a fast-paced work environment, Bachelors Degree or higher in Chemistry/ Life Sciences, Strong background in method development and validation for HPLC, GC-MS and NMR, 5+ years relevant experience in GMP Manufacturing/Testing environment in FDA Regulated Medical Device/Pharmaceutical Industry, particularly analytical testing associated with combination product development, To troubleshoot, develop and validate robust, sound analytical methods, To prepare Submission documentation in support of license applications, To take part in/ lead laboratory analytical investigations, To liaise directly with customers and attending conference calls, To attend internal project review meetings, To draft Test Methods, Protocols and Reports, To support all other on-going laboratory functions & requirements, To ensure that all work carried out is in compliance with the required standards conforming to company, cGxP, SOPs, regulatory regulations and guidelines, safety and environmental guidelines, To test and analyse raw materials & finished products in a timely and efficient manner, To perform additional team tasks as agreed to support effective running of the Business, At least two years experience working in a related technical environment, Instrumentation experience including any of the following: HPLC, GC, Wet Chemistry, 4+ years of experience as an Analytical Chemist, 2+ years of experience in Gas Chromatography or Gas Chromatography-Mass Spectroscopy or Liquid Chromatography experience, 2+ years of experience writing technical reports, Career goal to work as an Analytical Chemist in the Laboratory, Experience developing methods and macros using Agilent and Perkin Elmer Chromatography software, Minimum of six (6) years of good manufacturing practice (GMP) laboratory experience in an analytical capacity including method development and validation experience, Bachelor’s degree or higher in Chemistry from an accredited university, Experience with metered dose inhaler and transdermal products, Strong working knowledge of High Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC), Strong knowledge of FDA and USP requirements for metered dose inhaler and transdermal products, Self-driven with excellent organizational and leadership skills, Strong data analysis and statistical skills, Empower chromatographic data system experience, Analysis of registration stability samples, collation of data, stability data analysis, Addressing additional studies to support preparation of regulatory submissions, Minimum of three (3) years regulated environment laboratory experience, 3M experience working across multiple disciplines, businesses and/or departments, Strong working knowledge of Gas Chromatography (GC) and/or High Performance Liquid Chromatography (HPLC), Meticulous data collection and ability to maintain a laboratory notebook, Ability to adhere strictly to SOPs, good technical skills and working familiarity with laboratory procedures and processes, StarLIMS Lab Information Systems software experience, Basic understanding of statistical techniques, data analysis and variability, Conduct raw material, in process and final product testing in GMP Analytical labs, Analyze and interpret results of technical work and testing, Identify and implement improvements to daily lab operations, standard work, testing work flow/cycle time, test methods and lab capability using Lean Six Sigma methodologies, Bachelor's degree or higher in a Science or Engineering discipline from an accredited institution, Minimum of one (1) year of experience in a laboratory environment (an Internship or Co-op is considered qualifying), Bachelor’s degree or higher in Chemistry, Analytical Chemistry, Engineering or related discipline from an accredited institution, Experience performing analysis of drug, combination product and medical device products and materials in GMP lab setting [Food and Drug Administration (FDA) Drug GMP, U.S. Pharmacopia (USP), International Council on Harmonisation (ICH) guidelines relevant to drug and combination products industry), Functioning knowledge of High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Fournier Transform Infrared (FTIR) Chromatography, wet chemistry, and analytical laboratory techniques, Experience in successfully leading projects. 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