Job Information

EMD MILLIPORE Quality Control Senior Analyst 1 in VERONA, Wisconsin

JOB REQUIREMENTS: A career with MilliporeSigma is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Scientist, Quality Associate, Srposition is responsible for the cGMP analyticallaboratory analysis in the raw material - quality control division of MilliporeSigma. Analysis may consist of all/some of the following; incoming raw material analysis, routine final product analysis, in-process tests,method validation/qualification, cleaning, environmental monitoringto support quality control activities at the Madison and Verona sites. Analysisincludes techniques specific to but not limited to HPLC, GC, KF, DSC, TGA, IR, MS, NMR and XRPD among other tests and instruments.Other responsibilities may include initiation an d review of deviations, OOS/OOT's, change controls, and CAPA's. Additionally, participation in process improvement initiatives, working in a team environment, maintaining a clean and safe work area, and supporting the department in maintaining the laboratory in an audit ready state are other duties. The Scientist, Quality Associate, Sr position will require a wil lingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties. Perform analytical data analysis of cGMP data in support of the quality control group to ensure accuracy and quality of data. * Work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. * Exercise judgment within generally defined procedures and practices * Solve problems and make decisions with assistance. * Meet with internal project groups to keep projects on track. * Support review of OOS and OOT investigations, deviations, change controls and C APA' s * Apply problem-solving skills to thoroughly investigate deviations, identify root causes, and propose appropriate corrective/preventive actions with assistance from supervisor. * Write and revise SOPs including raw material, intermediate, and final product specifications. * Work cooperatively within the QC department and with other departments to achieve project goals. * Work in compliance with effective procedures and regulatory requirements outlined in ICH Q7 and 21 CFR Parts 11, 210 and 211 as applicable. * Support all data integrity initiatives and strive for right first time * Work near moving mechanical parts. Physical Attributes: * Regularly sit, stand, walk, reach above the shoulder, stoop, kneel, twist, crouch, or crawl for at least 50% of the time. * Wear appropriate protective gear (hard hats, lab coats, safety glasses/goggles, chemical resistant sleeves, gloves, safety shoes, and half/full face respirators) and other personal protective equipm ent "P PE" to protect from toxic or corrosive chemicals in the forms of liquids, solids, vapors, or airborne particles. * Lift and/or move up to 25 pounds unassisted to complete assignments * Lift more poundage with assistance * Speak, hear, taste, and smell. * Utilize specific vision requirements include close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus. Who You Are: Minimum Requirements: * B.S. in Chemistry, BioChemistry or related biological sciences * 1+year(s)in a cGMP analytical laboratory environment, or equivalent industry ex To view the full job description please use the link below. ***** APPLICATION INSTRUCTIONS: Apply Online: https://www.aplitr