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<p><strong>Restek is a world leader in the development and manufacturing of chromatography products — designed by chromatographers — that offer increased sample throughput, faster separations, and reduced cycle times. The Restek portfolio includes gas chromatography (capillary) columns, columns for high-performance and ultra-high-performance liquid chromatography (HPLC and UHPLC), reference standards and other chromatography standards and accessories. Their products are designed by chromatographers for chromatographers, engineered for durability and performance, and supported by a database of applications data.</strong></p><h3><strong>Operations Technician I - Reference Standards QC</strong></h3><h4><strong>Join the Team That Powers Innovation in Chromatography</strong></h4><p>Are you looking for a hands-on role in a dynamic, clean, and team-oriented manufacturing environment? At <strong>Restek</strong>, we're more than just a place to work, we’re a place where science, innovation, and people come together to make a difference. We’re currently hiring an <strong>Operations Technician I</strong> for our ARMQC department, where you’ll help ensure the quality and consistency of our trusted chromatography products.</p><p>We prioritize work-life balance and well-being with offerings like generous PTO, unlimited sick time, onsite fitness center and wellness program with incentives, childcare reimbursement, and adoption assistance—giving you the tools to <strong>Own Your Well-Being</strong>. Through our Employee Stock Ownership Plan (ESOP) and robust 8% retirement contributions, you can <strong>Own Your Financial Future</strong> while sharing in the success you help create. Our commitment to development ensures you can <strong>Own Your Growth</strong> through learning opportunities, career advancement programs, and a collaborative culture that values innovation and teamwork.</p><h4><strong>What You'll Do</strong></h4><p>The Manufacturing ARMQC Technician I is responsible for the preparation, processing and manufacture of products directly associated with the assigned department.&nbsp;</p><p>The hours for this position are Monday through Friday 7:00am- 3:30pm.</p><h4><strong>What You'll Do</strong></h4><div><ul><li>Process and manufacture products in assigned area to maintain appropriate inventory levels and service back orders in a timely manner as determined by operation requirements. May provide technical training and “hands on” support to others in assigned area when a sufficient level of expertise is attained.&nbsp;</li><li>Track and maintain raw materials as necessary to facilitate their respective process.</li><li>Adhere to Standard Operating Procedures (SOP) within their assigned area.&nbsp;</li><li>Maintain records and databases as required in their respective process, including Statistical Product Control (SPC) or other quality records. Has a basic understanding of the data in order to recognize problems.</li><li>Maintain equipment within assigned area, including making basic repairs or performing equipment installation as directed.</li><li>Review product requirements and determine basic performance to quality standards.</li><li>Understand and follow safe handling procedures for all chemicals and equipment and consult EHS, SOPs, Supervisor, or SDS when safety is in question.&nbsp;Adhere to Restek’s safety codes and regulations.</li><li>Participate in JSA and CAPA activities.</li><li>Ability to order inventory materials and supplies.</li><li>Attend and participate in departmental /team meetings.</li><li>Observe and adhere to Core Values.</li><li>Perform other duties as assigned.</li></ul></div><h4><strong>What You'll Bring</strong></h4><h5><strong>Education &amp; Skills</strong></h5><ul><li>Minimum of high school diploma/GED</li><li>Prefer 2 years specialized training in a science-related technology or relevant experience</li><li>Ability to perform basic level job responsibilities, including problem solving using basic math and scientific rules&nbsp;</li><li>Must obtain required certifications upon hire</li></ul><h5><strong>Knowledge, Skills, Abilities</strong></h5><ul><li>Exhibits a friendly and helpful manner and is able to work well with others in a team environment.</li><li>Good attention to detail and accuracy</li><li>Good problem-solving skills</li><li>Working knowledge of Microsoft Office Suite and basic ERP system</li><li>Ability to understand basic business concepts and technical details.</li><li>Knowledge of all EHS requirements for products housed in area.</li><li>Ability to understand and follow basic oral and written instructions&nbsp;</li><li>Ability to communicate both oral and written instruction to other functions in the manufacturing area&nbsp;</li><li>Ability to provide basic system and process training.</li><li>General understanding of metrics for primary discipline</li></ul><p>This position will require the successful completion of a standard background check in accordance with Restek policy. Employment with Restek will require successful completion of a pre-employment drug screen.</p><p>At Restek, our core values—<strong>We Care, Better Every Day, Respect for All, and Win Together</strong>—are at the heart of everything we do. <strong>We care</strong> deeply about our employee-owners, our customers, and the communities we serve around the world. We strive to be <strong>better every day</strong> by fostering personal and professional growth while delivering solutions that drive positive global change. We value <strong>respect for all</strong>, creating a workplace where every voice matters and diverse perspectives drive innovation. And we believe we <strong>win together</strong>, celebrating shared success as a 100% employee-owned company.</p><p>We are an equal opportunity employer, considering applicants without regard to race, ethnicity, national origin, sex, sexual orientation, gender identity or expression, age, disability, religion, military or veteran status, or any other protected characteristic. Restek provides reasonable accommodations for individuals with disabilities in accordance with the Americans with Disabilities Act and applicable laws.</p><p>If you’re ready to join a team that lives its values and empowers you to <strong>Own Your Future</strong>, we’d love to hear your story. Apply today.</p>

Operations Technician I - Reference Standards QC

<p><strong>Our passion for science and technology is what drives our more than 64,000 employees across 66 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live.</strong></p><p>Work Your Magic with us! Start your next chapter and join MilliporeSigma.</p><p>Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. &nbsp;</p><p>This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.&nbsp;</p><h3><strong>Quality Associate Scientist -3rd Shift</strong></h3><h4><strong>Your Role:</strong></h4><p>The Scientist, Quality Associate position is responsible for the cGMP analytical laboratory analysis in the Quality Control department of MilliporeSigma. Analysis may consist of all/some of the following: incoming raw material analysis, in-process testing, final product analysis, method validation/qualification, cleaning, reference standard requalification, and environmental monitoring to support Quality Control activities at the Madison and Verona sites. Analysis includes 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 and 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 You will exhibit a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.</p><h5><strong>Physical attributes:</strong></h5><ul><li>Work in analytical testing lab with hazardous and toxic chemicals</li><li>Utilize proper personal protective equipment (PPE), including respiratory protection, lab coats, and full body protection.</li></ul><h4><strong>Who You Are</strong></h4><h5><strong>Minimum Qualifications:</strong></h5><ul><li>Bachelor’s Degree in Chemistry, Biology, or other Life Science discipline</li></ul><h5><strong>Preferred Qualifications:</strong></h5><ul><li>1+ years of experience in a GMP manufacturing or testing laboratory</li><li>Understanding of 21 CFR Part 11, 210 and 211, and ICH Q7</li><li>Experience with chemical analyses including HPLC, GC, KF, DSC, TGA, IR, MS, NMR, and/or XRPD</li><li>Good written and verbal communication skills and good documentation practices and attention to detail&nbsp;</li><li>Knowledge and understanding of analytical chemistry techniques</li></ul><p>Pay Range for this position: $25-$39 per hour.</p><p>The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click <a target="_blank" rel="noopener noreferrer" href="https://careers.emdgroup.com/us/en/benefits">here</a></p><h4><strong>What we offer:</strong>&nbsp;</h4><p>We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!</p><p>Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</p><p>Money makes the world go round. But at Merck there’s more than just financial rewards. We offer a range of attractive benefits to help you work your magic.</p><ul><li>Financial &amp; Protection: <span style="line-height:inherit !important;">These core benefits help to provide long-term financial stability for you and your family.</span></li><li>Health and Wellbeing: This pillar is important to us. Therefore, our health benefits are designed to support employees physical and mental wellbeing, e.g. health checkups or medical insurance.</li><li>Family: From our Fertility Benefit, to helping support your family life through all its different stages.</li><li>Time Away: Time to recharge and specific Leaves to support life events and choices</li><li>Life-style: Such as flexible working, gyms, car benefits, shopping discounts.</li></ul>

Quality Associate Scientist -3rd Shift

<p><strong>Our passion for science and technology is what drives our more than 64,000 employees across 66 countries to find solutions to some of today’s toughest challenges and create more sustainable ways to live.</strong></p><p>Work Your Magic with us! Start your next chapter and join <i>MilliporeSigma</i>.</p><p>Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.</p><p>This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.</p><h3><strong>Senior Associate Quality Control Scientist</strong></h3><h4><strong>Your Role:</strong></h4><p>MilliporeSigma is seeking a skilled and motivated Analytical Chemist with HPLC experience for analysis of cleaning samples taken from &nbsp;GMP manufacturing equipment and to support a multidisciplinary CDMO center in Madison/Verona WI. The successful candidate will be responsible for performing analytical testing, collecting samples from GMP manufacturing equipment, and reporting of analyzed data. The Quality Associate Senior Scientist position, like all positions at SAFC, will have a willingness to contribute to the overall success of the company by assisting in many areas beyond specific job duties.</p><ul><li>Perform analytical testing of cGMP materials (cleaning samples from GMP Manufacturing equipment) and ensure accuracy and quality of data by using proper laboratory techniques and documentation</li><li>Coordinate with Manufacturing Department for the collection of samples of GMP Manufacturing equipment</li><li>Perform analytical testing of cGMP materials, guaranteeing data accuracy and quality through proper laboratory techniques while managing tight project deadlines</li><li>Maintain and troubleshoot instruments, conducting performance verifications and operational qualifications as needed</li><li>Work cooperatively within the QC department and with other departments to achieve project goals.</li><li>Document and investigate out-of-specification (OOS) and out-of-trend (OOT) results, applying critical thinking to identify root causes and corrective actions</li><li>Ensure laboratory safety and cleanliness, managing supplies and housekeeping tasks to maintain an audit-ready environment</li><li>Author and revise standard operating procedures (SOPs) in compliance with regulatory requirements, supporting data integrity initiatives</li></ul><h5><strong>Physical Attributes:</strong></h5><ul><li>Work in analytical testing lab with hazardous and toxic chemicals</li><li>Bend, stoop, squat, crawl, kneel, climb, or reach overhead</li><li>Wear PPE such as safety glasses, gloves, masks, and steel-toed shoes</li></ul><h4><strong>Who You Are</strong></h4><h5><strong>Minimum Qualifications:</strong></h5><ul><li>Bachelor’s Degree in Chemistry, Biology, or other Life Sciences discipline</li><li>3+ years &nbsp;experience in a cGMP analytical laboratory environment</li></ul><h5><strong>Preferred Qualifications:</strong></h5><ul><li>Thorough understanding of 21 CFR Part 11, 210 and 211, and ICH Q7</li><li>Experience with HPLC/UPLC Analytical Techniques, and preferred experience with LC/MS-MS instrumentation</li><li>Excellent written and verbal communication skills, as well as excellent documentation practices and attention to detail</li><li>Knowledge and understanding of analytical chemistry</li><li>Adequate technical writing skills to author reports and operating procedures</li><li>Strong team player and willing to adapt to changes / be flexible</li><li>Proven problem-solving skills and attention to detail</li></ul><p>Pay Range for this position: <strong>$25.00-$39.00 per hour</strong>.</p><p>The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click <a target="_blank" rel="noopener noreferrer" href="https://careers.emdgroup.com/us/en/benefits">here</a>.</p><h4><strong>What we offer:</strong>&nbsp;</h4><p>We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!</p><p>Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!</p><p>Money makes the world go round. But at Merck there’s more than just financial rewards. We offer a range of attractive benefits to help you work your magic.</p><ul><li><strong>Financial &amp; Protection:</strong> <span style="line-height:inherit !important;">These core benefits help to provide long-term financial stability for you and your family.</span></li><li><strong>Health and Wellbeing:</strong> This pillar is important to us. Therefore, our health benefits are designed to support employees physical and mental wellbeing, e.g. health checkups or medical insurance.</li><li><strong>Family:</strong> From our Fertility Benefit, to helping support your family life through all its different stages.</li><li><strong>Time Away: </strong>Time to recharge and specific Leaves to support life events and choices</li><li><strong>Life-style:</strong> Such as flexible working, gyms, car benefits, shopping discounts.</li></ul>

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