Waters Corporation (Europe)

Waters makes scientific ambitions a reality through the application of HPLC, MS and TA instruments, consumables, and informatics as well as industry-leading scientific expertise.

WATREX Prague

WATREX Prague is the largest distributor and producer of HPLC techniques in the Czech Republic and Slovakia.

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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 <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>Field Analytical Chemistry Specialist - Midwest</strong></h3><h4><strong>Your Role:</strong></h4><p>You will be a field-based technical sales specialist within the Life Science Division of MilliporeSigma with focus on technical sales of the analytical workflow portfolio including chromatography, reference materials, sample preparation and other analytical techniques. Responsible for meeting a sales target across all industry segments such as Pharma, Testing, Academic and Industrial. You will be responsible for scientific discussions and developing relationships with customers with the main goal of driving the adoption of our vast analytical portfolio, discussing how our products are used in the customer's experiments and collecting feedback.&nbsp;You will be a subject matter expert in the analytical workflow and be able to become fully versed and support new product introductions in the adjacent workflows.</p><h4><strong>Additional responsibilities include:</strong></h4><ul><li>In coordination with the account manager, assist with support, sales plans and strategies for active and potential business for analytical workflows.</li><li>Lead customer conversations around MilliporeSigma’s analytical chemistry offering.</li><li>Develop technical solutions for customer applications and challenges.</li><li>Have intimate knowledge of research/testing applications to position our analytical product offering.</li><li>Assist Account Managers with account mapping by having a comprehensive understanding of the customer's research, business initiatives, R&amp;D organizational structure, and new technology evaluation/implementation processes.</li><li>Tailoring of technical content to the customer.&nbsp;</li><li>Deepen and broaden MilliporeSigma customer relationships with key scientific leaders.&nbsp;</li><li>Technical training for account managers.</li><li>Provide knowledge of competition and the current marketplace.</li><li>Ability to build scientific credibility with customers, the commercial organization, and marketing.</li><li>Partner with Commercial Marketing and Product Management to ensure the successful launch of innovative analytical products; generation and implementation of materials supporting strategic and tactical sales initiatives. &nbsp;</li></ul><h4><strong>Who You Are</strong></h4><h5><strong>Minimum Qualifications:</strong></h5><ul><li>Bachelor’s degree in analytical chemistry or related field with 5-7+ years combined laboratory or commercial experience</li><li>Ability to travel regularly (20-50%), overnight travel is dependent on home location</li><li><strong>Must live within the territory – ideally located in MN or adjacent state. No relocation packages are available</strong>&nbsp;</li></ul><h5><strong>Preferred Qualifications:</strong></h5><ul><li>M.S. or Ph.D. with 7+ years’ combined laboratory and commercial experience&nbsp;</li><li>3+ years chromatography lab experience</li><li>Prior field sales, marketing or customer facing experience</li><li>In depth knowledge of analytical techniques and workflows including sample prep, liquid and gas chromatography, LC-MS, GC-MS.&nbsp; Ideally measuring both small and large molecules.</li></ul><p>Pay Range for this position: $103,500 - $170,800. 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"><strong>here</strong></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>

Field Analytical Chemistry Specialist - Midwest

<p><strong>Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.</strong></p><p>The Technology and User Services (TUS) group in NX is driven to help users use tools effectively to improve productivity and foster innovation. We deliver the Technology and User Services (TUS) group in NX to help customers use tools effectively to improve productivity and foster innovation. Our organization is here providing the technology backbone and devices that enable users to work in an office, lab or mobile environment.</p><h3><strong>TRD QA Specialist</strong></h3><p><span style="color:rgb(22,22,22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;"><span style="font-style:normal;font-weight:400;letter-spacing:0.4px;text-align:left;text-indent:0px;text-transform:none;">During the pilot plant ramp up and operationalization support line units efforts in developing compliant manufacturing and QC-related quality system, with particular focus on master batch records, logbooks, forms, procedures. Oversee the manufacturing lines initial validation activities (e.g. water runs, engineering batches and eventually APSs) and QC laboratory instruments PQs.</span></span><br><br><span style="color:rgb(22,22,22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;"><span style="font-style:normal;font-weight:400;letter-spacing:0.4px;text-align:left;text-indent:0px;text-transform:none;">In routine will be responsible to coordinate the QA shopfloor team and perform manufacturing and QC oversight, deviation and OOX review/approval, batch record review and support QP for the release of phase I/II clinical products.</span></span></p><div><h4><strong>About the Role</strong></h4><div><h5><strong>Major Accountabilities:</strong></h5><ul style="border-width:0px;color:rgb(22, 22, 22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;font-style:normal;font-weight:400;letter-spacing:0.4px;line-height:24px !important;text-align:left;text-indent:0px;text-transform:none;vertical-align:baseline;"><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Support the pilot plant ramp‑up and operationalization by contributing to the development, implementation, and maintenance of a compliant manufacturing and QC quality system, with particular focus on master batch records, logbooks, forms, and GMP procedures.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Oversee and support initial manufacturing and QC validation activities, including water runs, engineering batches, APSs, and QC laboratory instrument Performance Qualifications (PQs), ensuring documentation completeness and GMP compliance.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">In routine operations, coordinate and provide leadership to the QA shopfloor team, ensuring continuous QA presence during manufacturing and QC activities.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Perform real‑time manufacturing and QC oversight, including review and approval of deviations, OOX/OOS events, and execution of immediate quality decisions on the shopfloor.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Review, approve, and ensure completeness and accuracy of batch manufacturing records, supporting the Qualified Person (QP) in the timely release of Phase I/II clinical trial radiopharmaceutical products.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Ensure timely collection, monitoring, and reporting of Quality KPIs, supporting management reporting and continuous performance monitoring of manufacturing and QC activities.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Actively support Health Authority inspections and internal audits, ensuring timely provision of accurate documentation, data, and subject‑matter expertise, and contributing to inspection readiness activities.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Manage and oversee GxP Quality System processes, including Change Control, Deviation Management and CAPA, ensuring full compliance with GxP requirements and the Novartis Quality Manual.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Ensure effective tracking, escalation, and timely closure of CAPAs, including proactive management of risks related to delayed or ineffective actions.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Prepare, review, approve, and manage GxP documentation lifecycle activities, including document issuance, filing, archiving, and controlled distribution.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Actively contribute to continuous improvement initiatives, including optimization of existing processes and implementation of enhanced quality practices aligned with operational maturity of the pilot plant.</li></ul><h5><br><strong>Key Performance Indicators:</strong></h5><ul style="border-width:0px;color:rgb(22, 22, 22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;font-style:normal;font-weight:400;letter-spacing:0.4px;line-height:24px !important;text-align:left;text-indent:0px;text-transform:none;vertical-align:baseline;"><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Successful support of projects and routine operations in line with agreed quality standards and delivery timelines.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Positive outcomes of internal and external inspections, with no critical compliance gaps attributable to QA oversight.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Demonstrated ability to maintain effective collaboration and sound working relationships with manufacturing, QC, technical operations, and QA teams.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Consistent role modeling of Novartis culture, values, and behaviors within the QA organization and cross‑functional teams.</li></ul><h5><br><strong>Work Experience:</strong></h5><ul style="border-width:0px;color:rgb(22, 22, 22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;font-style:normal;font-weight:400;letter-spacing:0.4px;line-height:24px !important;text-align:left;text-indent:0px;text-transform:none;vertical-align:baseline;"><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Quality Assurance in pharmaceutical sterile manufacturing environments</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Audit and Health Authority Inspection Management</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Quality Management Systems (QMS)</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Sterile Manufacturing Operations (DP or API)</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Aseptic Processing and Contamination Control</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Deviation, Incident, and Escalation Management</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">OOX/OOS and Investigation Management</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Corrective and Preventive Actions (CAPA)</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Change Control Management</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">SOP and Documentation Management</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Manufacturing and QC Oversight</li></ul><h5><br>Prerequisites:</h5><ul style="border-width:0px;color:rgb(22, 22, 22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;font-style:normal;font-weight:400;letter-spacing:0.4px;line-height:24px !important;text-align:left;text-indent:0px;text-transform:none;vertical-align:baseline;"><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Proven experience of minimum 3 years working on the shopfloor of a sterile pharmaceutical manufacturing site (Drug Product or API).</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Solid and demonstrable knowledge of Quality Systems, Data Integrity principles, and aseptic processing.</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;"><span style="font-size:16px;"><span style="border-width:0px;vertical-align:baseline;">Experience working with electronic quality systems (e.g. change controls, deviations, OOX, complaints, etc.)</span></span></li><li style="border-width:0px;font-size:16px;vertical-align:baseline;"><span style="font-size:16px;"><span style="border-width:0px;vertical-align:baseline;">Strong quality mindset, leadership and cross‑functional attitude</span></span></li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Proactive and continuous improvement mindset</li></ul><h5><strong>Languages:</strong></h5><ul style="border-width:0px;color:rgb(22, 22, 22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;font-style:normal;font-weight:400;letter-spacing:0.4px;line-height:24px !important;text-align:left;text-indent:0px;text-transform:none;vertical-align:baseline;"><li style="border-width:0px;font-size:16px;vertical-align:baseline;">Italian</li><li style="border-width:0px;font-size:16px;vertical-align:baseline;">English (intermediate level)</li></ul><p style="border-width:0px;color:rgb(22, 22, 22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;font-style:normal;font-weight:400;letter-spacing:0.4px;line-height:24px;text-align:left;text-indent:0px;text-transform:none;vertical-align:baseline;">&nbsp;</p><p style="border-width:0px;color:rgb(22, 22, 22);font-family:volta_modern_display55_roman, Arial, Verdana, Tahoma;font-size:16px;font-style:normal;font-weight:400;letter-spacing:0.4px;line-height:24px;text-align:left;text-indent:0px;text-transform:none;vertical-align:baseline;"><span style="font-size:16px;"><span style="border-width:0px;vertical-align:baseline;">Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.</span></span></p></div></div>

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