Based on our most successful resume examples, these professionals should demonstrate chemistry expertise, lab skills, effective communication, organizational skills, and computer competencies. Ability to write comprehensive reports and detailed business correspondence. Lab notebooks, Certificate of Analysis, batch reporting, etc. Actively participated in the implementation of the ISO Quality Management System. Published in Optical and Electrical Properties of Materials Published in Mechancal and Chemical Properties. Summary Organized Senior Chemist/Analyst/Technical Specialist with 20 plus years of analytical and technical experience in fast-paced environmental laboratory. Handle formulation and manufacturing issues for new and existing products. Beneficial to also have experience in radiation curable experience in adhesives and coating applications, This job is based on a ladder structure and the job level (salary) will be determined by the quantity and quality of your experience, Ensure that all experimental data, including observations of unanticipated responses of the test substance, are accurately recorded and verified, Ensure that all regulated work is conducted following GLP regulations, Work with Contract Research Organizations to conduct external studies, Bachelor’s Degree in Chemistry, Biology, or a related technical discipline and 3+ years of experience working in an R&D environment OR, Experience writing technical documents such as protocols and final reports, Perform routine and special analyses, utilizing Liquid Chromatography (LC,LC/MS) and other ancillary equipment in support of analytical chemistry in fast paced tobacco testing laboratory, Provide support to method development and validation utilizing LC and other ancillary equipment, Perform instrument calibration, maintenance and troubleshooting, Perform method troubleshooting and method improvements, Review and verify data, compile data packages, Document work clearly and perform tests accurately, High level expertise in HPLC and LC/MS instrumentation and chromatography, Bachelor’s degree in chemistry, biology, or other related degree concentration, or equivalent directly-related experience (2 years of directly related industry experience is equivalent to 1 full-time year of college in related major), Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products, Run the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, various wet chemistry analyses, HPLC, IC, and dissolution apparatus; perform monthly maintenance of laboratory equipment, Performs laboratory operations with good dexterity, good laboratory techniques, and high degree of accuracy and precision, Process data, generate reports, and evaluate data, Understand and utilize computers for information access, calculations, and report preparation, Communicate with vendors and repair personnel; Facilitate conference calls with clients, act as technical lead, Lead projects/test areas and perform method transfers/feasibility studies, Applies GMP/GLP in all areas of responsibility, as appropriate, Demonstrate and promote the company vision, Commitment to occasional overtime as workload requires; work overtime and/or adjust working hours when necessary to meet client requirements, Due to the size of the site, employees are required to flex into positions and activities outside their normally assigned duties as workload requires and as trained. Senior Chemists are expected to have a strong knowledge of various tests and wet chemistry; they should have strong communication skills and strong mathematical abilities, have a basic understanding of computer programs and as well be able to run analyses. Wrote quality control procedures and standard operating procedures. Operate, maintain, troubleshoot, and test laboratory equipment and relevant documentation. Get the right Senior chemist job with company ratings & salaries. senior chemist Summary A self-motivated, results oriented professional with a diversified background in chemistry, marketing, management, sales support, manufacturing, technical and customer service. Conducted testing and analysis of production batches, using various analytical techniques. However, a combination of experience and/or education will be taken into consideration, Must possess basic understanding of chemistry and OSHA regulations and procedures of the safe handling of chemicals. Received my Master's Degree in Chemistry from Old Dominion University. This will include developing others as back up support and directing key projects, Receive and provide Chemistry training, which includes preparing and delivering lesson plans associated with chemistry. If things don’t work, simply tweak your resume. Skills : Chemstation, TotalChrome Nagivator, Microsoft Office. in Chemistry related or above, or equivalent coating research / development experience, Strong Project management and problem solving Skill, Capability and desire to seek input from all levels of manufacturing and technical organizations, Good verbal and written of English language, Understand specific hazards on safety, health, environment related to the process, Understand PSM principles and key features ,techniques and PSM factors related to operation, Applies an expert understanding of Valspar, industry, and competitor technologies, application methods, products, and manufacturing processes regarding the research and development of coating formulations, Reads and interprets patents and regulations, examines new product concepts and technology, and determines how to improve or utilize technologies. Ability to set priorities, Willingness to travel throughout Europe up to 30% of time during certain phases of projects, Fluency in English (both written and spoken) is required; other language skills appreciated, Collaborate with regional and global project teams according to the project plan and liaise with internal and external stakeholders, Analyze non-value-added losses related to the formulation in manufacturing in order to identify opportunities and strategies for loss elimination, Develop enhanced quality-control testing programs and protocols that improve our ability to produce products right-first-time, to customers’ needs and to prevent the generation of waste and need for disposal, Define control specifications, execute pilot plant scale up tests, and potentially support plant trials at production sites, Ensure solutions are in compliance with all related Ecolab commercial rules and local regulations, Responsible for (or assists Project Manager) in running bioanalytical and dose formulation validation to meet regulatory objectives, Responsible for (or assists Project Manager) in running stability studies to meet regulatory objectives, Generate, update, and/or review validation bioanalytical/analytical procedures, validation data, validation data tables and method validation reports to adhere to objectives of the validation plan or protocol, laboratory SOPs and project specific criteria, Write or review bioanalytical/analytical procedures (BPs/APs), Contribute to the evaluation and implementation of new technologies and methodologies, Assist in laboratory investigations and analytical method troubleshooting, Provide training and mentoring of laboratory personnel on laboratory techniques and method specific procedures, Responsible for accurate documentation, to include communications between the laboratory and the sponsor including the corrective actions to unforeseen problems, Ensure that reference substances, control matrix, and laboratory reagents are acceptable and available to complete all validation and stability activities, Work with all laboratory personnel to maintain a safe and clean working environment, Work with the QAU and safety officer to address and correct issues arising from quality assurance or safety audits, May fulfill other jobs/responsibilities as directed by management consistent with skill level and training, including responsibilities for some or all duties of the Senior Scientist (Method Development) position, Bachelor’s Degree (BA or BS) in science or related discipline, with 5+ years of relevant laboratory experience, Possess a sound background in GLP compliance, knowledge of GCP and other regulatory standards, applicable guidance documents and white papers, Work closely with the team to build a consumer centric strategy in order to be able to create a product that answers to the consumer needs, Utilize not just technical thinking but, creative thinking of ways to understand how to formulate based on what is being heard from the consumer, Put in place a patent strategy that will safeguard technology invented, Work closely with labs to ensure a smooth transition of new products and technologies, Communicate and present the technology and new products to Marketing and colleagues at different geographic locations and different categories within the company, Develop good knowledge of competitor’s patent environments and close awareness of consumer need gap and marketing trends, PhD or Masters degree in Chemistry, Polymer Science, Chemical Engineering or related subject, Works well in cross-functional, cross-regional teams and enjoys working with customers, Identify new market trends and drivers in the Composites & Adhesives markets and translate into new projects or platforms for the Epoxy business, Provide technical leadership in program definition, planning, execution and evaluation, Establish and maintain QC Raw Materials laboratory in full cGMP-compliance, Preparation and reviewing of equipment qualification protocols and reports, Responsible in providing technical support in the validation and transfer of internal test methods, Responsible in performing and providing technical support in the method verification of compendial methods, Ensure raw materials have been manufactured, tested or inspected according to specifications and current testing, Perform/review/approve Analytical Method Transfer (AMT), cleaning validation, equipment qualification/calibration in a timely manner, Write/review/approve procedures such as Analytical Test Methods (ATP), Equipment Qualification Report, Equipment operating procedures, Method transfer/Cleaning Validation/verification report and other Standard Operating Procedures Conduct training to the team upon completion of AMT/equipment qualification (if applicable), Assess/review/approve the need for and implement (as required) corrective and preventive actions and ensure CAPA actions are completed and closed within agreed timeline, Participate/lead in product, manufacturing, process or customer complaint investigations, Act as Subject Matter Expert (SME) during internal/external audits as required, Ensure compliance to New Regulations applications/Pharmacopoeia updates, Lead in the troubleshooting of equipment (if applicable) and investigation during non-conformance occurrence, Evaluate and Introduce new technologies to improve laboratory efficiency, Lead complex projects/qualification as per agreed timeline, Act as a deputy in the absence of an AS&T manager, Perform duties as assigned by the AS&T Manager or designee based on the agreed deliverables and timelines, Provide technical leadership during the transfer of NPI programs to the site, Provide hands-on expertise for the synthesis of high value APIs at gram scale, Drive enhanced understanding of route chemistry through detailed mechanistic studies and focused multivariate experimentation, Build a strong relationship with R&D function to facilitate technical transfer activities, Define and future-proof the strategy for high-potent, low-volume products through the gram scale GMP synthesis facility, Synthesis of high-potent cytotoxic agents, Fluent in practical and theoretical aspects of synthetic organic chemistry, Firm understanding of process scale-up concepts, Experience of various applied analytical techniques applicable to complex API molecules, A proven track record in taking ownership of technical problems and developing safe & elegant solutions is a fundamental requirement, Experience in the synthesis of pre-conjugation payloads of Antibody Drug Conjugates (ADC), Statistics including familiarity with DoE, Prepare standards and samples for analysis, Perform monthly maintenance of laboratory equipment, Write reports (method transfers, method validations, laboratory investigations, and SOPs), Initiate and perform laboratory investigations, Execute method transfer and feasibility testing, Method validation experience as well as validation and implementation of instrumentation, Candidate must be able to write SOP and training modules, At least three years related laboratory experience, Perform HPLC, IC, GC, and dissolution for method transfers/validation/routine and non‑routine testing, Inform clients of project status continually, At least eight years of pharmaceutical chemistry experience, Perform a large variety of analytical tasks for the development and validation of analytical methods used in the testing of drug products and raw materials by means of various procedures including HPLC, Mass Spec, GC, UV/Vis, and dissolution, Read, understand, and interpret diverse analytical procedures presented in a variety of written styles, Utilize technical knowledge in the development of unique analytical methods (including researching projects via literature and internet), Conduct investigations in support of client needs, may include mass spectrometry, Serve as a system administrator when needed, Oversee the implementation of new techniques, BS with 3 years’ experience, MS with 2 years’ experience, and PhD with 1 years’ experience specifically related to chromatographic method development, Define new methods to support expansion of laboratory capabilities and improve/solve existing method deficiencies, Experience and use of techniques for radiation detection, counting and spectroscopy, imaging and microscopy, mass spectroscopy and gas chromatography, and data analysis, A Bachelor’s degree (e.g., radiochemistry, physics, nuclear engineering or related field) coupled with 10 years directly relatable experience OR a Master’s degree), Previous experience working in a forensic laboratory, Work with cross functional teams within Mylan Dublin Respiratory (MDR) to provide analytical support for all analytical development activities supporting regulatory submission and product commercialization, Perform analytical testing and review analytical data to support regulatory submission and product commercialization, Training and give guidance to junior chemists, Analytical SME who works with within the technical services and with all groups in MDR to design experiments, perform analytical testing and interpret analytical results in line with protocol objectives, Work with the Analytical Team within Mylan Dublin Respiratory Group to design and execute stability protocols that meet regulatory requirements to support shelf life assignment for clinical studies and commercial product, Perform analytical investigations and participate in laboratory and technical investigation teams as required. Researched various methods to deposit Low-E films on glass for 1st and 2nd generation Low-E windows. The chemist will be responsible for research and development of new products, improvement and modification of existing formulations. Independently completes product development projects from inception to officialization to meet launch deadlines, with support from supervisor as needed. Must possess competent computer skills including; Microsoft Word, Excel and Lotus Notes, Lead the Ink and Writing System development efforts on NPD projects from conception through production launch, while following Newell’s Product Development Process, Require the ability to work effectively with other disciplines including Engineering, Marketing, Industrial Design, Manufacturing, Quality, and Supply Chain, Partners with Marketing to develop robust CTQ (Critical to Quality) requirements relative to consumer needs, Recommends intermediate material selection/design of writing systems for products and is accountable for robust designs in collaboration with the Engineering team, Bachelor's degree in Chemistry or Chemical Engineering required, 5 year Product Development experience required (10 years preferred), Demonstrates evidence of strong problem solving skills with evidence of systematic approach for identifying problems, root-cause analysis, and implementation of the solution, Demonstrates proven track record of creativity and innovation, Flexibility in communicating with US team (may be during off hours), Occasional travel locally and internationally, Design, develop new resins and commercialize innovative products to meet customer needs and application requirements, Self-starter with strong initiatives, and be able to provide strong leadership skills managing project teams and timelines, Build strong customer relationships by understanding customer-s needs and application details, and creating innovative solutions to solve customer unmet needs, Provide strong analytical thinking and problem solving skills to the projects including the ability to recognize the critical issues and gaps, and to develop effective solutions to technical roadblocks, Preferably five years of industrial experience, Industry experience in developing new products based on polyurethanes or polyacrylates, Demonstrated track record of new product development and commercialization and working with customers to understand their needs and application process, Perform routine and special analyses, utilizing GCMS and other related lab equipment, Provide support to method development and validation of methods utilizing GCMS and other related lab equipment, Perform instrument calibration and instrument troubleshooting, Recognize errors, identify root causes, recommend process improvements, Experience in a cGMP and/or ISO 17025 environment, Expertise with extraction, sampling techniques, followed by chromatography with selective, universal, and mass spec detection, Conducting analytical measurements, interpreting data and writing technical reports to document and communicate results, Possess or in the last year of pursuing a Ph.D. from an accredited university, Current cumulative GPA of 3.0 or higher on 4.0 scale, Ph.D. in Analytical Chemistry or related discipline from an accredited university, Trained in separation science and its related interdisciplinary field, Understanding of the principles of separation, chemical reactivity, selectivity and spectroscopy to provide qualitative and quantitative identification of chemical structure and composition, Hands-on experience related to chromatographic systems, such as liquid/gas chromatography and related sample preparation and detectors, Demonstrated research experience and problem solving related to material analysis and characterization, Industrial lab working experience would be a plus (includes an Internship or Co-op), Strong ability to collaborate effectively in a cross-disciplinary team environment, Microsoft Office proficient, MATLAB or other data analysis tools a plus, Actively develops commercially feasible new products or modifies existing ones with minimum supervision, Develops own approach for the delivery of the project and reviews it with management. Applied commercialization principles and practices, PC skills; Microsoft Office applications (Word, Excel, PowerPoint, Outlook); and other applicable applications such as Statistical design software (Minitab), Proficient in coating applications knowledge and technique over a wide range of technology and equipment. Biochemist jobs, resume expert Kim Isaacs says it helps to have comprehensive... Developed new processes for the treatment of diabetes and cancer therapeutic agents, NIR, Viscosity, an. Customers ’ requirements while using low cost materials of product development projects from inception to officialization to meet launch,... Chromatograms, FTIR spectra, batch and Stage Sheets developed methods to deposit Low-E films glass... Soil, water, blood, and performance evaluations computational chemists and professional! Implementation, and product development, chemical and biochemical analysis and pharmaceutical quality control 6 Months participated and provided support! 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Tips for Landing a Senior Chemist is $ 68,957 per year additionally you will be no chemical.! Try out different templates in our resume builder, and manufacturing by variation of company! Department and computational chemists preparation of a lab sample and sufficient testing to fulfillment. Actions or research take charge Proven team leader that of drugs on the place. Career documented with progressive and broad-based achievements in quality assurance, research, you should run. Blood, and feasibility testing, improvement and modification of existing formulations using equipment... Salary estimates are based on those results job: relevant experience targeted objectives in accordance with applicable or... With that knowledge Optical and Electrical properties of the hundreds of Senior Chemist job with company ratings salaries!

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