Senior Chemist QC

What we offerExplore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us.Click on the link below to learn what our employees have to say about Evonik:://careers.evonik.com/en/about/meet-the-team/JOB DESCRIPTION SUMMARYThe Senior Chemist provides technical leadership and scientific expertise to support Quality Control laboratory operations, with emphasis on advanced analytical techniques including NMR, LC-MS, and GC-MS. This role is responsible for reviewing and approving analytical data, leading laboratory investigations, supporting method development and validation activities, implementing new analytical technologies, and driving continuous improvement initiatives. The Senior Chemist serves as a technical resource to QC personnel, collaborates with cross-functional teams, supports regulatory inspections and customer projects, and ensures compliance with quality, safety, and laboratory standards.RESPONSIBILITIESProvide technical oversight for Quality Control laboratory operations, ensuring the accuracy, integrity, and compliance of analytical testing, protocols, methods, and change controls.Review and approve analytical data while leading investigations related to deviations, out-of-specification (OOS) results, and other laboratory issues.Develop, execute, and support protocol-driven studies, including method development, verification, validation, investigational studies, and method transfers.Serve as the technical subject matter expert for analytical methodologies and provide coaching, mentoring, and technical guidance to QC personnel.Lead or support the implementation of new analytical technologies, methodologies, and continuous improvement initiatives that enhance laboratory efficiency and performance.Partner with manufacturing, process development, project management, and cross-functional teams to support manufacturing investigations and new product introductions.Interface with customers and regulatory agencies to support technical discussions, inspections, audits, and project requirements as needed.Coordinate laboratory activities, contribute to internal and customer-driven projects, and provide project support for new product implementation into QC.Ensure compliance with quality systems, safety requirements, laboratory procedures, and regulatory standards while promoting operational excellence.Manage multiple priorities independently while maintaining effective communication and strong working relationships across technical and business functions.REQUIREMENTSPhD in Chemistry with 3–5 years of industrial laboratory experience; ORMaster's degree in Chemistry or a related scientific discipline with 5–10 years of industrial laboratory experience; ORBachelor's degree in Chemistry or a related scientific discipline with 10–15 years of industrial laboratory experience.Strong knowledge of analytical chemistry principles and laboratory techniques.Experience reviewing and approving analytical data, laboratory documentation, and change controls.Experience supporting method development, validation, verification, and technology transfer activities utilizing NMR, LC-MS, and/or GC-MS techniques.Demonstrated ability to independently manage laboratory investigations and technical projects.Strong communication, collaboration, and interpersonal skills with the ability to mentor and train technical staff.Ability to manage multiple projects while maintaining compliance with quality, safety, and regulatory requirements.Experience supporting regulatory inspections and customer audits.Experience implementing new analytical methodologies or laboratory technologies.Experience leading cross-functional technical projects or new product introductions.Knowledge of manufacturing investigations, root cause analysis, and deviation management.Experience serving as a technical subject matter expert within a Quality Control laboratory.Willingness to work non-core hours as needed to support 24/7 manufacturing operations.Evonik offers a comprehensive benefit package, subject to plan eligibility, terms, and guidelines. Benefits included, but not limited to:Medical, dental, and vision benefitsPaid time off plan401(k) savings plansHealth Savings Account (HSA)Flexible Spending Accounts (FSAs)Employee Assistance ProgramVoluntary Benefits and Employee DiscountsDisability benefitsLife InsuranceParental leaveTuition ReimbursementThe Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations. Your ApplicationTo ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at . Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations.Your Talent Acquisition Manager:Malika Carrington [C]Company isEvonik CorporationSummaryLocation: Lafayette, INType: Full time