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<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>Quality Specialist- 2nd shift</strong></h3><h4><strong>Your Role:</strong></h4><p>At MilliporeSigma, the QA Specialist will work various internal departments to improve and execute processes in compliance with cGMP regulations in 21CFR 210, 211, Part 11 and in ICH Q7.</p><ul><li><strong>Shift: Monday-Friday 4pm-12am.</strong></li><li>Participate in QA on the floor activities in manufacturing. Expectation for 70% of shift on the floor.</li><li>Review batch records while in process during manufacturing events.</li><li>Review batch records postproduction for completeness and accuracy based on GMP requirements to ensure acceptable product and process consistency.</li><li>Review and approval of QC data to support batch disposition.</li><li>Execution of batch and raw material disposition decisions.</li><li>Provide quality oversight and support for new product introductions as primary quality point of contact.</li><li>Write, review, and approve Operating Procedures, Manufacturing documents, Technical Transfer Protocols and other controlled documents under a Quality Managed System (QMS).</li><li>Release activities for cGMP product and raw materials.</li><li>Review and approval of master packaging formulas, master shipping records, and master manufacturing formulas.</li><li>Document and label issuance activities.</li><li>Interact with production and laboratory personnel regularly to ensure adequate communication and feedback for quality-related services to internal customers.</li><li>Monitor product for quality related issues and collaborate on resolution.</li><li>Respond to quality-related customer questions, as needed.</li></ul><h4><strong>Physical Attributes:</strong></h4><ul><li>Environmental conditions will vary depending on specific job responsibilities; typically, 10%-30% Office Environment, 70%-90% Production, QC, Packaging.</li></ul><h4><strong>Who You Are</strong></h4><h5><strong>Minimum Qualifications:</strong></h5><ul><li>Bachelor’s Degree in Life Sciences, Chemistry, Pharmacy, Chemical Engineering, Process Engineering, or other life science discipline.</li><li>5+ years quality experience.</li></ul><p><strong>OR</strong></p><ul><li>Master’s Degree in Life Sciences, Chemistry, Pharmacy, Chemical Engineering, Process Engineering, or other life science discipline.</li><li>2+ years quality experience.</li></ul><h5><strong>Preferred Qualifications:</strong></h5><ul><li>Knowledge of ICHQ7 and API knowledge and/or experience.</li><li>TrackWise and SAP experience.</li><li>Proficiency in MS Word, MS Excel, MS PowerPoint and the ability to learn and operate other specific application software.</li><li>Excellent communication (verbal &amp; written) and customer interfacing skills.</li><li>Experience writing technical documentation &amp; reports.</li><li>Ability to simultaneously manage multiple tasks/priorities.</li><li>Good problem-solving, time management and negotiating skills.</li><li>Capacity for independent work.</li><li>Data analysis, presentation, and experimental design knowledge.</li></ul><p>RSREMD</p><ul><li>Pay Range for this position: $62,500.00- $93,700.00.</li><li>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>.&nbsp;</li></ul><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 Specialist- 2nd 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>Field Analytical Chemistry Specialist - Southeast</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. 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><p>Additional responsibilities include:</p><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>Physical Attributes:</strong></h4><ul><li>Environmental conditions will vary depending on specific job responsibilities; typically, 10%-30% Office Environment, 70%-90% Production, QC, Packaging.</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 southeast territory – GA, FL or adjacent state. No relocation packages are available</strong></li></ul><h5><strong>Preferred Qualifications:</strong></h5><ul><li>M.S. or Ph.D. with 7+ years’ combined laboratory and commercial experience</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">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>

Field Analytical Chemistry Specialist - Southeast

<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 EMD Serono.</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>United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.</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 Operational Excellence Lead</strong></h3><h4><strong>Your Role:</strong></h4><p>We believe that effective processes are the backbone of our success, and we are looking for a talented <strong>Operational Excellence Quality Lead</strong> to join our team. In this role, you will be responsible for analyzing, and optimizing GLP, GCP, and GVP related processes across the organization in close collaboration with Business Process Owners and cross-functional stakeholders.</p><p>Evaluating current processes to identify inefficiencies and eliminate complexity will be a critical part of your responsibilities, along with creating detailed process maps and documentation to provide clarity for all involved parties. Collaboration will be essential as you engage with various teams to incorporate diverse perspectives into your designs.</p><p>Additionally, you will establish process metrics to monitor process performance and drive continuous improvement in partnership with Business Process Owners and stakeholders.</p><p>You will report to the Head of Central Quality Systems at R&amp;D Quality and Risk Management (RDQRM).</p><h4><strong>Who You Are</strong></h4><h5><strong>Minimum Qualifications:</strong></h5><ul><li>B.S. in a Life Science-related with 5+ years professional experience and expertise.</li><li>A minimum of 3 years of working knowledge of Good Clinical Practice (GCP), Good Vigilance Practice (GVP), and Good Laboratory Practice (GLP).</li><li>A comprehensive understanding of the drug development process and the regulatory environment, particularly in areas relevant to our Healthcare business.</li><li>Strong expertise in process design and optimization methodologies.</li></ul><h5><strong>Preferred Qualifications:</strong></h5><ul><li>Excellent analytical skills with the ability to identify inefficiencies and propose effective improvements.</li><li>Proficiency in creating process maps and flow charts.</li><li>Strong collaboration and communication skills to work effectively with Business Process Owners and cross-functional teams.</li><li>Experience in training and change management during process implementation.</li><li>Familiarity with establishing process metrics for performance monitoring.</li><li>Professional experience in multiple international pharmaceutical organizations is a plus.</li></ul><p><br>Pay Range for this position: $144,500 - 216,800<br>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>. &nbsp;</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 Operational Excellence Lead

<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>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>Site Quality Head, Florida (AD level)</strong></h3><p>As the Site Quality Head in Winter Park, Florida, you’ll shape the quality foundation for a new Radioligand Therapy manufacturing site—combining rigorous compliance with strong, visible leadership to help deliver time‑sensitive therapies reliably and safely. You’ll lead and develop a high-performing Quality organization, partner closely with site and global stakeholders, and set the standard for inspection readiness, robust management of product quality issues, and continuous improvement—so the site starts up strong and scales with confidence.</p><h4><strong>Key Responsibilities</strong></h4><ul><li>Lead site quality strategy and governance to meet Novartis standards and current Good Manufacturing Practice.</li><li>Build, coach, and develop the Quality team, strengthening capability, engagement, and safe working practices.</li><li>Drive plant startup, expansions, and technology transfer, ensuring compliant planning, commissioning, qualification, and validation activities.</li><li>Lead inspection readiness and represent the site during health authority, corporate, and internal audits.</li><li>Oversee deviations, investigations, out-of-specification events, and corrective and preventive actions through effective closure.</li><li>Partner with Manufacturing and cross-functional leaders to enable compliant, efficient operations and risk-based decision making.</li><li>Define and monitor site quality performance indicators, driving continuous improvement and timely escalation of risks.</li></ul><h4><strong>Essential Requirements</strong></h4><ul><li>Bachelor’s degree in life sciences or a related scientific discipline.</li><li>Ten years of experience in a GMP pharmaceutical manufacturing environment, including laboratory operations and Aseptic experience, and at least three years of combined relevant experience in Quality Assurance and/or Quality Control roles.</li><li>In-depth knowledge of cGMP and United States Food and Drug Administration regulations and International Council for Harmonization regulations. Understanding of US Pharmacopeia, European Pharmacopeia, and American Chemical Society standards.</li><li>Proven success leading health authority inspections and delivering robust remediation and sustained compliance improvements.</li><li>Demonstrated leadership in matrix organizations with excellent communication, organizational, and stakeholder management skills.</li><li>Experience applying continuous improvement methods such as Lean Six Sigma, Total Quality Management, and 5S workplace organization.</li></ul><h4><strong>Desirable Requirements</strong></h4><ul><li>Prior experience with site start-up or rapid site expansion</li><li>Experience or training in Radioligand Therapies, radiopharmaceuticals and/or radiation safety.</li></ul>

Site Quality Head, Florida (AD level)

<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>Senior Expert Container Closure Integrity (m/f/d)</strong></h3><p>As part of the Analytical Testing team within the Global Device &amp; Packaging Development (GDPD) organization, you will join a collaborative environment at our scenic site in Schaftenau / Tyrol, Austria. Here, you will contribute to defining, coordinating, developing, and implementing innovative container closure integrity testing and control strategies together with a small CCI expert team, supporting one of the most diverse and advanced portfolios in the pharmaceutical industry.</p><h4><strong>Key responsibilities</strong></h4><ul><li>Lead the development, validation and transfer of deterministic state-of-the-art methods for container closure integrity testing (CCIT), with a special focus on methods for sterile products (e.g. biopharmaceuticals and small molecule drugs in prefilled syringes, cartridges, vials; some assembled into drug-delivery devices like autoinjectors or needle safety devices) but also for non-steriles (e.g. blisters for pills), for global implementation at Novartis Technical Development and Manufacturing sites</li><li>Identify and evaluate respective test methods for primary packaging incoming control, drug product and final product in-process-control, release and stability testing; for example Helium leak detection, mass extraction, headspace analysis etc</li><li>Drive collaboration with universities and expert companies, attend conferences to understand state-of-the-art CCIT at pharmaceutical industry, contribute to external networks</li><li>Determine needed internal testing equipment and budget, convince stakeholders, organise equipment implementation and perform qualification</li><li>Trouble-shoot method implementation challenges across locations and support root-cause investigations in case of CCI failure</li><li>Strongly collaborate with laboratory colleagues, coach and work with students</li><li>Author test method and equipment documents and testing reports</li></ul><h4><strong>Essential Requirements:</strong></h4><ul><li>Bachelor’s, Master or PhD degree in engineering or natural sciences</li><li>Strong knowledge of / working experience with container closure integrity testing and sterile drug products filling</li><li>Interest and experience in working in state-of-the-art laboratory</li><li>Strong skills in cross-functional coordination / project management, leading and influencing in global matrix organization, actively reaching out, able to understand and connect across functions</li><li>Proficiency in English (oral and written), German skills are a plus</li></ul>

Senior Expert Container Closure Integrity (m/f/d)

<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>Stability Specialist</strong></h3><h4><strong>Your Role</strong></h4><p>MilliporeSigma is seeking a highly motivated and detail-oriented Stability Specialist to join our team. The Stability Specialist will be responsible for developing, executing and analyzing stability studies for IVD (In Vitro Diagnostic products). This role will ensure compliance to regulatory guidelines, such as ISO13485 and IVDR. Responsibilities include:</p><ul><li>Develop and implement stability protocols according to guidelines and internal SOPs</li><li>Execute testing for stability samples, ensuring accuracy and precision</li><li>Monitor and maintain stability chambers and associated equipment</li><li>Document all data accurately in electronic systems</li><li>Analyze stability data and generate reports</li><li>Interpret stability data to assess product shelf life and storage conditions</li><li>Identify and investigate stability trends and deviations</li><li>Prepare stability reports for regulatory submissions and internal documentation</li><li>Ensure stability studies are conducted in compliance with regulatory guidelines, such as IVDR, ISO 13485</li></ul><h4><strong>Who You Are</strong></h4><h4><strong>Minimum Qualifications:</strong></h4><ul><li>Bachelor's Degree in Biology, Chemistry, Biochemistry or other Life Science discipline</li><li>2+ years of laboratory or Quality experience</li></ul><h4><strong>Preferred Qualifications:</strong></h4><ul><li>Previous experience with IHC testing</li><li>Previous experience writing stability protocols and reports</li><li>Good communication, interpersonal, and collaboration skills</li><li>Ability to work effectively in a cross-functional team environment</li><li>Detail-oriented, organized, and able to manage multiple projects simultaneously</li><li>Problem-solving and analytical skills</li></ul><p>RSREMD</p><p>Pay Range for this position - $66,800 - $110,300 / annually</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&nbsp;<a target="_blank" rel="noopener noreferrer" href="https://careers.emdgroup.com/us/en/benefits"><strong>here.&nbsp;</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>

Stability Specialist

<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>Biomonitoring Account Manager</strong></h3><h4><strong>Your Role</strong></h4><p>An exciting opportunity to join a vibrant and technology company. You will be responsible for sales management of our BioMonitoring portfolio for our existing client portfolio and developing new segments for our product range dedicated to microbiological control.</p><p>If you are self-reliant with an entrepreneurial spirit and natural drive to be successful, then this position may be perfect for you.</p><ul><li>Establish and maintain a record of all customer details with contact names and other pertinent information through Customer Relationship Management System (CRM)</li><li>Regularly advise management regarding potential methods of business improvement.</li><li>Perform all work with consideration to the economical use of resources.</li></ul><h4><strong>What You Do</strong></h4><ul><li>Develop objectives, strategies and tactics to expand sales within your customer base.</li><li>Monitor sales results against budgets within the allocated customer base and take appropriate action.</li><li>Maintain an awareness of market trends and competitor activities and report these to the Sales Manager regularly.</li><li>Maintain a record of all customer visits, and feedback information to the Biomonitoring Sales and Marketing staff on Products promoted to these customers through the Customer Relationship Management System (CRM) on a regular basis.</li><li>Comply with the face to face call rate as requested by the Biomonitoring Sales Manager.</li><li>Provide monthly reports on activities and sales results to the Biomonitoring Sales Manager.</li><li>Prepare small quotes for customers and forward to the Quotes Officer.</li><li>Attend company meetings, exhibitions, sales conferences and training courses as requested.</li><li>Report on key achievements relating to objectives on a weekly basis.</li></ul><h4><strong>Who You Are</strong></h4><ul><li>Must have a Bachelor of Science or equivalent experience.</li><li>Must have previous scientific sales experience, preferably in pharmaceutical, environmental or food industries.</li><li>Experience in a laboratory will be well regarded.</li><li>Highly self-motivated and energetic individual with good interpersonal and communication skills.</li><li>Able to demonstrate excellent communication and negotiation skills.</li></ul><h4><strong>What we offer:&nbsp;</strong></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>

Biomonitoring Account Manager

<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>Sr. Associate Quality Control Chemist (Laboratory)</strong></h3><h4><strong>Your Role&nbsp;</strong></h4><p>As a Senior Associate Quality Control Chemist in the Sheboygan Quality Control lab, you will evaluate products according to established protocols, provide technical support to fellow chemists, and perform operations in support of the Quality Control department. Additional responsibilities, with a focus on the chemical identification lab, include the following:</p><ul><li>Perform routine assays and analytical evaluations of products and intermediates, ensuring results meet established specifications and unit operation requirements</li><li>Review stock suitability data in accordance with Quality Management System (QMS) guidelines to ensure all materials meet laboratory standards</li><li>Support general quality review functions and maintain meticulous, accurate records in logbooks consistent with cGMP and quality procedures</li><li>Manage laboratory support tasks, including equipment maintenance, reagent preparation, inventory restocking, and compliant waste disposal</li><li>Identify and implement process improvements by applying scientific knowledge and experience in compliance with change control procedures</li><li>Communicate operational status and deviations to management and relevant departments to maintain a focus on customer excellence and site-wide goals</li><li>Perform procedures accurately and independently, prioritizing responsibilities to stay aligned with established department objectives</li><li>Act as a technical resource by training personnel, resolving unsafe conditions, and participating in quality audits as needed</li><li>ACS compendial testing</li><li>Spectroscopy (ATR/IR, UV-vis, Fluorescence)</li><li>Water analysis by Karl Fisher (<a target="_blank" rel="noopener noreferrer" href="https://en.wikipedia.org/wiki/Coulometry">coulometric</a>, volumetric)</li><li>Hours/Days: 8:00 AM - 4:30 PM, Monday – Friday, on-site position</li></ul><h4><strong>Who You Are</strong></h4><h5><strong>Minimum Qualifications:</strong></h5><ul><li>Bachelor’s degree in Chemistry, Biochemistry or other Life Science discipline</li><li>3+ years of combined academic and professional laboratory experience</li></ul><h4><strong>Preferred Qualifications:</strong></h4><ul><li>Master’s Degree in Chemistry, Biochemistry, or other life science discipline</li><li>5+ years of experience in a laboratory or quality review environment</li><li>Proficiency in analytical techniques, chemical calculations, and safe laboratory practices</li><li>Strong critical thinking, decision-making, and problem-solving skills with meticulous attention to detail</li><li>Working knowledge of Data Integrity principles and proficiency with database software and the Microsoft Office Suite</li><li>Excellent communication and interpersonal skills, with a proven ability to collaborate effectively in a team setting</li><li>Demonstrated self-motivation, adaptability, and effective time-management abilities</li></ul><p>Pay Range for this position - $26.00-$46.00/hourly</p><p><strong>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.&nbsp;</strong>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&nbsp;<a target="_blank" rel="noopener noreferrer" href="https://careers.emdgroup.com/us/en/benefits">here.&nbsp;</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>

Sr. Associate Quality Control Chemist (Laboratory)

<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>Sales Specialist (Lab Water)</strong></h3><h4><strong>What You Do</strong></h4><ul><li>Responsible for selling, increasing market shares, achieving sales goal and profit growth.</li><li>Maintaining loyalty of existing customers &amp; dealers, also acquiring the new markets through the understanding of customers, business needs and consulting skills.</li><li>Developing overall strategies to approach existing and new customers in potential industries.&nbsp;</li><li>Identifying marketing opportunities by identifying consumer requirements, conducting competitor analysis, and establishing targeted market share.</li><li>Extracting customer’s data to analyzing Customers to understand, identifying Customer’s Segmentation, building customer needs and opportunities.</li><li>Looking for new markets and opportunities to further grow business.</li><li>Developing and implementing appropriate sales &amp; marketing activities with customers.</li><li>Develop new markets by collaboration with dealers, distributors, and partnership to expand products into their markets.</li><li>Managing the sale tender process together with customers.</li><li>Creating and initiating the new projects with key customers.</li><li>Providing the excellent services in to exceed sales targets.</li><li>Acting as an information channel between company and existing/potential partners</li><li>Coordinating with both internal and external relevant parties to ensure smooth &amp; effective cooperation.</li></ul><h4><strong>Who You Are</strong></h4><ul><li>Bachelor’s degree or higher in Chemistry, Chemical Engineer, Petrochemical or Engineering/Science, other related or equivalent work experience.&nbsp;</li><li>Experience in Sales for at least 2 years in field sales and marketing. Also having experience in life science business or equivalent work experience in laboratory equipment products and project management.</li><li>Strong interpersonal skills, ability to interact positively and constructively with all functions in matrix organization environment.</li><li>Able to work under pressure, be positive, having growth mindset and high flexibility of working hours.</li><li>80% working in field.</li><li>Able to communicate English on business level; both writing and speaking.</li></ul><h4><strong>What we offer:</strong></h4><p>We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team!</p>

Sales Specialist (Lab Water)

Lab technician

Liquid chromatography-mass spectrometry

Scientific and Research Fellow

Sales Representative

Academic staff

X-Ray

Laboratory services

Elementary analysis

Service engineer

Manager

Software

Product Specialist

Application Specialist

Gas chromatography

Gas chromatography-mass spectrometry

Molecular spectroscopy UV-Vis, RAMAN, FTIR

Marketing

Analytical chemist

Technologist/Engineer

Laboratory instruments

Spectroscopy

Chemist

Quality Control (QC)

Liquid chromatography

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Jobs - page 28

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