Sr. Lab Analyst

Company Overview Aurorium is the materials innovation partner that helps global manufacturers harness the power of possibility making the world a better place. Their specialty ingredients and high-performance materials enhance quality of life, support health and wellness, and enable customers to deliver value-added solutions. Key industries served include healthcare, personal & home care, mobility, infrastructure, and specialty paper & packaging. A Responsible Care company, Aurorium follows the highest regulatory standards across all manufacturing facilities. The company's global integrated supply chain offers the customer product consistency, easy access, supply security, and reasonable turnaround on delivery. Aurorium is committed to operating at the highest levels of manufacturing consistency, quality control, and safety. Job Description The Senior Analyst serves as the primary subject matter expert (SME) for high complexity analytical and wet chemistry in a CGMP environment. This role is responsible for the entire analytical lifecycle—from method development and validation to routine testing and equipment lifecycle management. Beyond technical execution, the Senior Analyst provides mentorship, training, and technical oversight to laboratory staff to ensure high-quality data in compliance with global regulatory standards. Role Specific Responsibilities Lead the setup, daily tuning, and routine operation of ICP-MS and other specialized analytical equipment such as AA, GC, HPLC, etc. Perform analytical and wet chemistry testing in accordance with approved methods and specifications. Design and develop robust analytical methods for trace elemental analysis using ICP-MS across various matrices. Author and execute validation protocols in accordance with ICH and USP guidelines. Establish appropriate digestion techniques (e.g., microwave‑assisted, open‑vessel) and optimize collision/reaction cell parameters (KED/CRI) to mitigate polyatomic interferences. Prioritize and coordinate daily QC laboratory activities with the Quality Unit including sample testing, data review, documentation and timely batch release. Perform complex troubleshooting of instrument hardware and software. Review and approve analytical data batches for accuracy, ensuring full adherence to data integrity principles and CGMP. Oversee the preventive maintenance schedule and calibration programs for laboratory instrumentation to ensure zero downtime. Oversee the stability testing program and ensure compliance with required standards. Manage relationships with external service providers and coordinate equipment qualification activities (IQ/OQ/PQ) for new equipment installations. Maintain inventory of NIST standards and reagents for calibration. Develop and deliver technical training programs for Lab Analysts on elemental testing, equipment maintenance, and sample preparation techniques. Serve as the technical lead during internal and external audits (e.g., FDA, ISO, Customer Audits). Mentor staff on proper laboratory safety and hygiene and the “trace‑metal mindset” required for ppb/ppt‑level analysis. Support investigations related to out‑of‑specification (OOS), out‑of‑trend (OOT), deviations, and corrective and preventive actions (CAPAs). Collaborate effectively with cross‑functional teams including Manufacturing, QA, Supply Chain, Warehouse and EH&S. Compliance Complies with company Health, Safety and Environmental policies, procedures and arrangements. Reports all Health, Safety and Environmental accidents, incidents and near misses promptly. Acts in a safe and responsible manner at all times. Problem Solving and Innovation Active participation within continuous improvement activities. Participates in problem solving. Takes responsibility and ownership for own learning and development in the spirit of continuous improvement of both self and the business. Assists in the training, mentoring and assessment of other team members.Exercises autonomy and judgement subject to overall direction or guidance. Education and Qualifications B.S./M.S. in Chemistry, Analytical Chemistry, or a related scientific field. Strong working knowledge of cGMP regulations and laboratory compliance. Demonstrated ability to operate independently or in a team environment. Experience 5-8 years in an analytical laboratory environment, with a minimum of 3 years of hands‑on expertise specifically in ICP-MS, HPLC, GC, AA and wet chemistry testing. Deep understanding of cGMP and pharmacopeial requirements (USP, EP, JP) for elemental impurities. Familiarity with method development, validation and stability testing activities. Knowledge, Skills, and Abilities Strong communication and interpersonal skills, with the ability to work effectively across teams. Excellent attention to detail and strong problem‑solving abilities. Ability to prioritize tasks and manage multiple responsibilities. Proficient in laboratory documentation, data review, and electronic systems (e.g., SAP, LIMS). Capable of making sound technical decisions and escalating issues appropriately. Core Values credible: keeps their word and honors their commitments, acts with integrity, and holds themselves accountable to their decisions and actions outcome‑oriented: adheres to an unparalleled standard of excellence in everything they do, to deliver results with real impact driven: passionate about delivering authentic, world‑class experiences that engage customers and inspire greatness empowered accountability: empowered to achieve common goals and accountable for delivering performances and results that exceed standard. Benefits Aurorium offers competitive total compensation packages, including benefits such as medical, dental, vision, life, 401(k), disability insurance, flexible spending accounts, health savings accounts, paid time off, and paid holidays. Equal Opportunity Employer Statement Aurorium is a global Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of gender, sexual orientation, gender identity, race, ethnicity, religion, age, veteran status, disability status, genetic information, or any other protected category. #J-18808-Ljbffr Vertellus