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<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, Texas (AD level)</strong></h3><p>As the Site Quality Head Texas, 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, Texas (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>Site Quality Head (m/w/d)</strong></h3><p>In this role you will provide quality assurance oversight and be accountable for supporting Quality operations and provide technical and strategic leadership for all quality-related matters. Accountable to ensure compliance to GxP standards including product manufacturing and testing. You will also ensure Compliance with cGMP requirements and with the Novartis Quality Manual and policies.</p><h4><strong>Major Accountabilities:</strong></h4><ul><li>Provide leadership for strategic site initiatives, and represent site SLT quality in local cross-functional and global projects teams as team member or team leader that represent site quality.</li><li>Ensure all facilities, utilities and equipment are designed and installed to be operated in a safe and effective manner and are compliant with applicable standards</li><li>Ensure that during project phase planning, construction, commissioning, qualification (IQ, OQ and PQ) including any other validation activity complies with cGMP.</li><li>Timely escalation of risks in meeting timelines and / or budget incorporating site master planning and the long-term strategic plan.</li><li>Ensure adequate management of product critical quality issues (deviations, out of specifications). Ensure investigations are correctly executed and adequate CAPAs are defined, and proper follow up of CAPAs effectiveness. Review, provide guidance for, escalate where appropriate, and approve HA notifications (compliance related such as Exception requests, other).</li><li>Define, implement, monitor, consolidate and analyse Site Quality KPIs. Ensure Site Quality Committee is established, ensure relevant corrective and preventive actions are endorsed and implemented.</li><li>Drive for Site management team accountability. Coordinate the generation and monitor the execution of the Site Quality Plans, DI Plan, Site Quality Risk Assessments and other relevant gap assessments.</li><li>Hiring people, team building, people development and talent retention.</li></ul><h4><strong>Obligatory Requirements:</strong></h4><ul><li>Education: BS/MSc in Life Sciences and/or related experience.</li><li>10+ years of experience in GMP Pharmaceutical Manufacturing (including laboratory operations and Aseptic experience), at least 3 years combined of relevant experience in Quality Control and/or Quality Assurance covering quality areas.</li><li>Proven track record and practical experience in supporting a Quality Control operations unit and operating in full compliance with global cGMP requirements.</li><li>In-depth knowledge of cGMP regulations. Successfully managed inspections from major Health Authorities</li><li>Proven ability to manage multiple projects with moderate resource requirements, risk and/or complexity.</li><li>Fluent German and English, written and spoken.</li></ul>

Site Quality Head (m/w/d)

<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>Global Quality Control/Analytical Science and Technology Head</strong></h3><p>The Global Head RLT QC / AS&amp;T plays a crucial role in ensuring the quality and consistency of our products throughout their lifecycle. This role encompasses a wide range of responsibilities for the execution of strategy and the integration of all strategic and operational initiatives to ensure consistent and aligned standards across all laboratories, laboratory performance ("lean labs") and compliant analytical systems with competent and effective AS&amp;T and QC organizations in the RLT Platform. Acting in accordance with legislation, internal regulations, good practices and business goals. It is a key leadership position as part of the RLT Quality leadership team working closely with Site QC heads as well as other platform QC / AS&amp;T communities.</p><h4><strong>Major Accountabilities:</strong></h4><ul><li>Leading the implementation of a QC strategy, including method lifecycle strategy, global laboratory digital strategy, new method strategy, to increase the compliance and efficiency of QC laboratories in the RLT organization.</li><li>Enforcing global standardization/integration of business processes and information, data, global equipment standards and application architecture.</li><li>Enforcing the QC/AS&amp;T action plan by defining and implementing appropriate roadmaps for QC/AS&amp;T teams across the platform, ensuring compliance, continuous improvement and increasing the effectiveness of all types of QC testing. Initiating, implementing and sustaining initiatives defined by global QC/AS&amp;T.</li><li>Ensuring and promoting cross-site collaboration and transparency of joint initiatives, problems and lessons learned.</li><li>​ Supporting the development of on-site platform/team members in technical and leadership skills. Coaching and people development. Delivering training programs developed by the global QC/AS&amp;T function and actively participating in the development of relevant learning materials.</li><li>Proactively provide strong QA leadership to the business by ensuring considerable quality and organization awareness</li><li>Ensure adherence to global and local safety and regulatory internal and health authority standards.</li></ul><h4><strong>Requirements:</strong></h4><ul><li>Minimum degree in Pharmacy, Chemistry, Biology or related subject; higher level degree: MS, preferred but not required. Additional knowledge in Quality Assurance / Compliance</li><li>10+ years’ experience in GMP-regulated industries incl. QA/QC in Biotech area.</li><li>Solid working knowledge of FDA/EMA/ICH regulatory requirements</li><li>Broad cGMP experience with knowledge and understanding of manufacturing, quality control, and validation requirements and activities.</li><li>Ability to synthesize detailed information and provide clear communication and messaging across quality, manufacturing and supply chain.</li><li>English Fluent, written and spoken. Other languages are a plus.</li></ul>

Global Quality Control/Analytical Science and Technology Head

<p><strong>Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.</strong><br><strong>Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.</strong><br><strong>With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients—including DoD, DOE, and municipalities—through robust logistics and continuous investment in people, technology, and infrastructure.</strong><br><strong>We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more.</strong></p><h3><strong>Support Services Group Leader, Eurofins Environment Testing - Air Toxics, Folsom, CA</strong></h3><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><section><div><h4><strong>Job Description</strong></h4></div><div><section><div><section><div><p>Eurofins Environment Testing is seeking a Support Services Group Leader to join our team!&nbsp;</p><p>The Support Services Group Leader is responsible for managing and directing all aspects of the canister preparation department, including staffing, workflow planning, quality standards, and resource allocation. The Group Lead ensures that departmental goals align with organizational objectives and drives operational efficiency through strategic oversight rather than hands-on task execution.</p><p>As the first-level front-line leader, the Group Lead sets performance expectations, coaches and develops staff, and exercises independent judgment in operational decisions, including process improvements, scheduling, and allocation of resources. This role represents senior management in the department, translating company goals, policies, and culture into actionable strategies, and ensuring compliance with safety, quality, and regulatory standards.</p><p><strong>Essential Duties and Responsibilities</strong></p><p><strong>Safety &amp; Compliance</strong></p><ul><li>Lead and enforce a strong safety culture, ensuring all departmental activities comply with company policies, SOPs, and regulatory requirements.</li><li>Oversee staff training programs to ensure team members consistently follow safety protocols.</li><li>Support and help resolve safety and compliance issues while maintaining accountability to senior management.</li></ul><p><strong>Operations &amp; Productivity</strong></p><ul><li>Manage and direct daily departmental operations, including workflow planning, staffing allocation, and scheduling to ensure efficiency and timely delivery.</li><li>Supervise and perform tasks, including:<ul><li>Canister cleaning and certification</li><li>Assembly of sampling equipment</li><li>High-volume media preparation</li><li>Equipment handling and readiness</li></ul></li><li>Monitor and drive productivity to meet operational targets while controlling costs.</li><li>Ensure shipment orders are fulfilled accurately and on time, aligning with client schedules and project requirements.</li><li>Identify and implement workflow optimizations to scale operations and support business growth.</li></ul><p><strong>Quality &amp; Continuous Improvement</strong></p><ul><li>Establish and enforce departmental quality standards, including proper canister/media preparation, certification, and equipment readiness.</li><li>Identify process inefficiencies and implement improvements to enhance workflow, quality, and operational performance.</li><li>Communicate production or technical issues to senior management and drive timely resolution.</li></ul><p><strong>Customer Focus</strong></p><ul><li>Act as the primary departmental point of contact for client concerns, coordinating staff to ensure timely and effective resolution.</li><li>Support project planning by understanding client needs and aligning operations to meet expectations.</li><li>Ensure a high level of service through accuracy, responsiveness, and reliability.</li></ul><p><strong>Inventory &amp; Asset Management</strong></p><ul><li>Maintain optimal inventory levels of canisters, sampling equipment, and supplies to support uninterrupted operations.</li><li>Monitor usage of spare parts and maintenance supplies, initiating reorders as needed.</li><li>Ensure proper maintenance, repair, and readiness of sampling equipment.</li><li>Participate as needed in equipment handling and preparation to support operational continuity.</li></ul><p><strong>People &amp; Leadership</strong></p><ul><li>Lead, supervise, coach, and develop departmental staff, establishing clear performance expectations and accountability standards.</li><li>Conduct performance evaluations, identify talent development opportunities, and implement strategies to strengthen team capability.</li><li>Make staffing, hiring, and disciplinary decisions, exercising independent judgment and managerial authority.</li><li>Foster a collaborative, professional, and results-driven team environment.</li><li>Maintain the ability to perform physical aspects of the role when necessary, while prioritizing leadership and oversight responsibilities.</li></ul><p><strong>Additional Duties</strong></p><ul><li>Perform general or other duties as assigned by senior management based on business needs.</li><li>Use discretion and independent judgment to carry out additional responsibilities that support departmental objectives and organizational priorities.</li><li>Demonstrate a hands-on approach in supervising and occasionally performing operational tasks to support the team and ensure high-quality results.</li></ul></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><p><strong>Basic Qualifications</strong></p><ul><li>Minimum of 4 years of relevant experience in environmental or laboratory operations, including supervisory/leadership responsibilities.</li><li>Strong understanding of canister/media preparation, cleaning, certification, and sampling equipment operations.</li><li>Familiarity with TO-15 methods and related sampling equipment (e.g., canisters, regulators, flow controllers) preferred.</li><li>Experience with inventory management systems and processes, including tracking of canisters, parts, and consumables.</li><li>Strong mechanical aptitude, with experience supervising assembly, maintenance, and troubleshooting of sampling equipment.</li><li>Proficiency in computer applications, including MS Word, Excel, and LIMS systems.</li><li>Excellent organizational and time management skills, with the ability to prioritize and manage multiple projects and deadlines.</li><li>Strong decision-making, problem-solving, and troubleshooting skills, with the ability to exercise sound judgment.</li><li>Ability to effectively communicate technical information to staff and support client needs.</li><li>Commitment to safety, quality, and promoting company values.</li><li>Demonstrated ability to supervise and occasionally perform operational tasks when necessary, while maintaining primary responsibility for management and oversight.</li><li>Authorization to work in the United States without restriction or sponsorship.</li><li>Regular and reliable attendance and punctuality.</li><li>Ability to work a full-time schedule (Monday–Friday), with flexibility for weekends and overtime as needed.</li><li>Professional working proficiency in English is a requirement, including the ability to read, write and speak in English</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><p><strong>Compensation Range</strong>: $70,304 - $75,000 per year depending on level of experience and qualifications.</p><p>Position is Full-time, exempt from overtime pay. Candidate must be able to work Monday thru Friday 8am - 5pm and other hours as needed.</p><p>Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation of internal peers, business sector, and geographic location.</p><p>We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.</p><p><strong>We support your development!&nbsp;</strong>Do you feel you don’t match 100% of the requirements? Don’t hesitate to apply anyway! Eurofins companies are committed to supporting your career development.</p><p><strong>We embrace diversity!&nbsp;</strong>Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique.</p><p><strong>Sustainability matters to us!</strong>&nbsp;At Eurofins, we believe sustainability is at the heart of everything we do. Guided by our vision to be the Global Leader in “Testing for Life,” our mission to contribute to a healthier and safer world, and our core values, we are building a strong foundation for Environmental, Social, and Governance (ESG) initiatives. Eurofins’ commitment to sustainability begins within our own companies through a shared responsibility to people and the planet. With climate change posing an imminent threat, Eurofins and its many companies recognize their duty to proactively reduce or offset the environmental impact of essential operations while also helping our clients do the same—serving as a true ESG Enabler.</p><p>Find out more in our career page: https://careers.eurofins.com/</p><p><strong>Company description</strong>: Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.</p><p>The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.</p><p>In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.</p><p>In 2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.</p><p><strong>Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></div></section></div></div></section></div></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section></div></section>

Support Services Group Leader

<p><strong>Chromatography, the science of separation, affects the lives of almost everyone. Phenomenex’s chromatography products advance the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. We strive to provide the best tools and resources possible to help scientists improve global health and well-being, including award-winning liquid chromatography, gas chromatography, and sample preparation products. Be part of our global success, centered on a commitment to developing novel analytical chemistry solutions, unique marketing, and exceptional customer service and support.</strong></p><p><strong>Bring more to life.</strong></p><p>Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?</p><p>At Phenomenex, one of <a target="_blank" rel="noopener noreferrer" href="https://danaher.com/our-businesses">Danaher’s</a> 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.&nbsp;</p><p>You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.</p><p>Phenomenex isn’t your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health.</p><p>Learn about the <a target="_blank" rel="noopener noreferrer" href="https://www.danaher.com/how-we-work/danaher-business-system">Danaher Business System</a> which makes everything possible.</p><h3><strong>Project Manager (Chromatography Solutions, Medical Device, NPD)</strong></h3><div><p>The <strong>Project Manager</strong> is responsible for end-to-end delivery of New Product Development (NPD) and value engineering initiatives for separations consumables, leading cross-functional teams through scope definition, integrated planning, execution, and risk management to achieve timeline, budget, quality, and regulatory/design control requirements. This role operates in a matrix environment, drives stage-gate/tollgate rigor, and communicates clear status, risks, and decisions to functional and senior leaders.&nbsp; Partners daily with R&amp;D, Product Management, Marketing, Manufacturing/Operations, Quality, Supply Chain, and Finance to plan and deliver programs; interfaces with senior leadership to align priorities, escalate decisions, and maintain execution discipline.</p><p><strong>This position reports to the Senior Manager, PMO and is part of the R&amp;D Department located in Torrance, CA.&nbsp;This role is designated as U.S.-Remote.</strong></p><h4><strong>In this role, you will have the opportunity to:</strong></h4><ul><li>Lead cross-functional teams to deliver NPD and value engineering programs from concept through launch, meeting scope, schedule, budget, and QMS requirements.</li><li>Drive stage-gate / tollgate execution by defining clear deliverables, ensuring decision readiness, and documenting outcomes.</li><li>Build and run the integrated project plan (schedule, critical path, resources, dependencies), proactively managing risks/issues with countermeasures to protect on-time delivery.</li><li>Establish project governance &amp; stakeholder alignment (cadence, action tracking, decision logs, comms), including coordination of external vendors/partners as needed.</li><li>Own performance reporting &amp; continuous improvement (RAG, milestones, cost/capex forecasts, escalations), applying DBS/structured problem-solving and ensuring design control/compliant documentation.</li></ul><h4><strong>The essential requirements of the job include</strong></h4><ul><li>Education: Bachelor’s degree in life science, chemistry, chemical engineering, or related field (advanced degree a plus) along with preference for 5+ years of experience in one of the following disciplines: product development, R&amp;D, operations, and/or life science consumables environment (hands on exposure to experimental workflows/data-driven development).</li><li>Project management experience: Prefer 3+ years in project management, including at least one product development program delivered to launch (or equivalent lifecycle release).</li><li>Regulated / design control: Experience running stage‑gate/design control in a regulated development/manufacturing environment (e.g., ISO‑based QMS).</li><li>Tools / methods: Proficiency with Microsoft 365 (Word/Excel/PowerPoint) plus MS Project (or equivalent scheduling tool); demonstrated use of risk management methods to translate technical uncertainty into executable plans.</li><li>On-site attendance will be required as business needs dictate (e.g., onboarding programs, key team meetings, program workshops, kaizen/training events, and milestone reviews).</li></ul><h4><strong>It would be a plus if you also possess previous experience in:</strong></h4><ul><li>PMP certification (or equivalent formal PM training) and experience applying Lean / DBS tools (e.g., VPM and PSP).</li><li>Demonstrated project delivery experience within life sciences/diagnostics and/or separations/chromatography consumables.</li><li>Experience with risk management / risk reduction and translating VOC into clear product requirement specifications (PRS) and executable plans.</li></ul><p>Phenomenex, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at <a target="_blank" rel="noopener noreferrer" href="https://leplb1040.upoint.alight.com/ah-angular-afirst-web/#/web/danaher/cp/preauth-home">Danaher Benefits Info</a>.</p><p>At Phenomenex we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Phenomenex can provide.</p><p>The salary range for this role is 92,500-120,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.</p><p>This job is also eligible for bonus/incentive pay.</p><p>We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.</p><p>Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.</p><p>#LI-ND19</p><p>#thisisbelonging</p><p>#thebestteamisdiverse</p><p><span>Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.</span></p><p><span>For more information, visit </span><a target="_blank" rel="noopener noreferrer" href="http://www.danaher.com/"><span>www.danaher.com</span></a><span>.</span></p><p><span>Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.</span></p><p><span>The U.S. EEO posters are available </span><a target="_blank" rel="noopener noreferrer" href="http://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12ScreenRdr.pdf"><span>here</span></a><span>.</span></p><p><span>We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or </span><a href="mailto:applyassistance@danaher.com"><span>applyassistance@danaher.com</span></a><span>.</span></p></div>

Project Manager (Chromatography Solutions, Medical Device, NPD)

<p><strong>ALS is a global leader in testing, providing comprehensive testing solutions to clients in a wide range of industries around the world. Using advanced technologies and innovative methods, we help our clients leverage data-driven insights for a safer and healthier world.</strong></p><p><strong>Our people are the heart of our business, driving testing solutions and innovations to solve complex challenges and create lasting value for our clients. But most importantly, our people care – for each other and for the work we do. With over 20,000 team members across 70 countries, you’ll be part of a global network. Learn more about what makes our workplace great here.</strong></p><p>At ALS, we encourage you to dream big.</p><p>When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.</p><h3><strong>Assistant Laboratory Manager</strong></h3><p>We are seeking an experienced <strong>Assistant Laboratory Manager</strong> to support the efficient, safe, and high‑quality operation of our Hamilton laboratory. This is a hands‑on leadership role suited to a technically strong professional with proven supervisory experience and a strong customer and quality focus.</p><p>Working closely with the Laboratory Manager and Production team, you will help manage workflow priorities, staffing levels, turnaround times, and technical reporting, while ensuring quality, safety, and compliance standards are consistently met.</p><h4><strong>Key Responsibilities</strong></h4><ul><li>Support workflow prioritisation, turnaround time management, and load balancing</li><li>Manage staff resourcing, cross‑training, and day‑to‑day supervision</li><li>Provide technical support to clients and internal teams</li><li>Resolve sample, reporting, and turnaround issues across ALS sites</li><li>Maintain quality systems, audit outcomes, and continuous improvement initiatives</li><li>Ensure compliance with Health, Safety, and Environmental requirements</li></ul><h4><strong>About You</strong></h4><ul><li>Tertiary qualification in science (preferably Chemistry or related field)</li><li>Minimum 5 years’ laboratory experience, including 2 years in a supervisory role</li><li>Strong communication, organisational, and leadership skills</li><li>High level of computer literacy and attention to detail</li><li>Strong customer focus with sound understanding of business principles</li><li>Commitment to quality, safety, teamwork, and ALS values</li></ul><h4><strong>Quality Responsibilities</strong></h4><ul><li>Ensure all testing and tasks comply with ALS quality systems and procedures.</li><li>Maintain accurate records and ensure instrument maintenance is up to date.</li><li>Always uphold the integrity of data and laboratory processes.</li></ul><h4><strong>Health, Safety &amp; Environment (HSE)</strong></h4><ul><li>Understand and comply with ALS HSE policies and laboratory safety procedures.</li><li>Follow appropriate precautions when working with samples of unknown hazard.</li><li>Report and address unsafe practices or environmental risks.</li><li>Actively contribute to a strong safety and sustainability culture.</li><li>Comply with all applicable OHS legislation.</li></ul><p>Join ALS and play a key leadership role within a global organisation committed to scientific excellence, safety, and service.</p><h4><strong>Working at ALS</strong></h4><p>The ALS team is a diverse and dedicated community united by our passion to make a difference in the world.</p><p>Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence.&nbsp;</p><p>At ALS, you’ll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us.&nbsp;</p><p>We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities.</p><h4><strong>Everyone Matters</strong></h4><p>ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued.</p><p>ALS also welcomes applications from people with all levels of ability. Reasonable adjustments to support candidates throughout the recruitment process are available upon request. </p><h4><strong>Eligibility</strong></h4><p style="text-align:left;">To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa.</p><h4><strong>How to apply</strong></h4><p>Please apply on-line and provide a resume &amp; cover letter that best demonstrate your motivation and ability to meet the requirements of this role.</p>

Assistant Laboratory Manager

<p><strong>ALS is a global leader in testing, providing comprehensive testing solutions to clients in a wide range of industries around the world. Using advanced technologies and innovative methods, we help our clients leverage data-driven insights for a safer and healthier world.</strong></p><p><strong>Our people are the heart of our business, driving testing solutions and innovations to solve complex challenges and create lasting value for our clients. But most importantly, our people care – for each other and for the work we do. With over 20,000 team members across 70 countries, you’ll be part of a global network. Learn more about what makes our workplace great here.</strong></p><p>At ALS, we encourage you to dream big.</p><p>When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.</p><h3><strong>Regional Sample Preparation Manager - USA</strong></h3><p>The Regional Sample Preparation Manager, USA plays a critical role in ALS’s hub-and-spoke operational model, overseeing six strategically located sample preparation laboratories (spokes) located in Twin Falls, Elko, Tucson, Las Vegas and Reno. These spoke labs are directly supported by and integrated with the Reno facility that centralizes sample preparation, warehousing, analytical services, quality and HSE functions and coordinates with the North America Hub in North Vancouver, Canada.</p><p>Reporting to the General Manager, Geochemistry North America, the Regional Manager ensures seamless coordination between the spokes and the hub, driving operational consistency, optimizing sample flow logistics, and maintaining high standards of service quality and compliance. This role is instrumental in aligning regional operations with corporate strategy, leveraging the centralized capabilities of the hub to enhance efficiency, responsiveness, and scalability across the region.</p><h4><strong>Specific Responsibilities:</strong></h4><ul><li>Lead and support branch managers and regional teams across all spoke locations.</li><li>Foster a high-performance culture aligned with ALS core values.</li><li>Collaborate with HR to mentor and develop high-potential employees.</li><li>Ensure consistent implementation of SOPs, systems, and documentation across all sample preparation sites.</li><li>Oversee workflow coordination, logistics, and quality assurance to maintain operational efficiency and compliance.</li><li>Coordinate the efficient movement of samples from spoke labs to the Reno and Vancouver Hub labs.</li><li>Leverage Reno and Vancouver Hub’s high-capacity capabilities to optimize regional throughput and turnaround times.</li><li>Maintain strong client relationships and ensure timely, high-quality service delivery.</li><li>Identify and support business expansion opportunities in the USA.</li><li>Manage regional budgets and cost controls in collaboration with North America regional teams.</li><li>Monitor financial performance and contribute to achieving revenue and profitability targets.</li><li>Promote a strong safety culture and ensure adherence to ALS health, safety, and environmental policies.</li><li>Champion ALS values and foster a positive, inclusive workplace culture.</li><li>Support employee engagement through recognition, development, and communication initiatives.</li><li>Ensure effective use of centralized systems (e.g., Webview) for data integrity and operational visibility.</li><li>Support continuous improvement through data-driven decision-making.</li><li>Conduct regular site visits and audits to evaluate operational performance, ensure compliance with corporate and regulatory standards, provide coaching to local teams, and drive alignment with company policies and laboratory best practices.</li><li>Perform additional responsibilities as assigned by the General Manager.</li></ul><h4><strong>Required Knowledge, Skills &amp; Abilities:</strong></h4><ul><li>Excellent English communication (written &amp; verbal), public speaking, and ability to build client relationships.</li><li>Proficiency in analyzing Profit &amp; Loss statements, identifying trends, and making data-driven decisions to improve performance.</li><li>Experience managing large-scale production or laboratory operations, meeting budgets, and achieving business targets.</li><li>Strong judgment, integrity, adaptability, and ability to manage escalations in a fast-paced environment.</li><li>Industry Knowledge: Understanding of analytical chemistry principles and client needs in Geological Sciences and Engineering.</li><li>Advanced proficiency in Microsoft Word, Excel, PowerPoint, and Visio.</li><li>Ability to set direction, inspire teams, and drive results in a dynamic, service-oriented business.</li><li>Ability to manage change, work under pressure, and meet strict deadlines while maintaining a professional demeanor.</li></ul><h4><strong>Required Qualifications:</strong></h4><ul><li>5+ years of experience in logistics, analytical testing or consulting in environmental or geological fields.</li><li>5+ years of supervisory experience in production, manufacturing, industrial, or laboratory environments.</li><li>Experience in the mining, minerals analysis, or geology industries (preferred).</li><li>Strong computer skills, including proficiency in MS Word and Excel.</li><li>University degree in Chemistry, Geology, or a related scientific field (preferred).</li><li>Experience in laboratory or geological preparation facilities is an asset.</li></ul><h4><strong>Working at ALS</strong></h4><p>The ALS team is a diverse and dedicated community united by our passion to make a difference in the world.</p><p>Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence.&nbsp;</p><p>At ALS, you’ll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us.&nbsp;</p><p>We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities.</p><h4><strong>Everyone Matters</strong></h4><p>ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued.</p><p>Qualified candidates will be considered without regard to race, colour, religion, national origin, military or veteran status, gender, age, disabilities, sexual orientation, gender identity, pregnancy and pregnancy-related conditions, genetic information and any other characteristics protected by the law. We invite resumes from all interested parties, including women, members of minority groups, and persons living with disabilities.  </p><p>ALS also welcomes applications from people with all levels of ability. Reasonable adjustments to support candidates throughout the recruitment process are available upon request. </p><h4><strong>Eligibility</strong></h4><p style="text-align:left;">To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa.</p><h4><strong>How to apply</strong></h4><p>Please apply on-line and provide a resume &amp; cover letter that best demonstrate your motivation and ability to meet the requirements of this role.</p>

Regional Sample Preparation Manager - USA

<p><strong>As the world leader in serving science, our work is more than something that fills our days – what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.</strong></p><h3><strong>Laboratory Chemicals Division Sales Development Manager - Southeast Asia</strong></h3><div><div><section><div><div><div><div><div><div><div><div><div><div><ppc-container><span><ppc-content></ppc-content></span></ppc-container></div></div></div></div></div></div></div></div></div></div></section><section><div><section><div><h4><strong>Work Schedule</strong></h4><p>Standard (Mon-Fri)</p><h4><strong>Environmental Conditions</strong></h4><p>Office</p><h4><strong>Job Description</strong></h4><p>As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.</p><h4><strong>DESCRIPTION:</strong></h4><p>Join our team at Thermo Fisher Scientific where you'll contribute to business growth and strategic partnerships across key markets. As Sales Development Manager, you'll identify opportunities while building strong relationships with customers in sectors including pharmaceuticals, biotechnology, semiconductors, and academic research. You'll develop and implement comprehensive market strategies, coordinate cross-functional initiatives, and provide solutions that help our customers make the world healthier, cleaner and safer. This role offers the opportunity to work with advanced scientific technologies while collaborating with colleagues across our organization.</p><h4><strong>REQUIREMENTS:</strong></h4><ul><li>Master's Degree plus 8 years of sales or business development experience in relevant industries. Candidates with a bachelor’s degree are also encouraged to apply.</li><li>Preferred Fields of Study: Life Sciences, Chemistry, Engineering, Business or related field</li><li>Demonstrated ability to develop and implement strategic sales plans to achieve revenue targets</li><li>Strong understanding of customer workflows, applications and market dynamics</li><li>Excellence in building and maintaining relationships with key stakeholders and decision makers</li><li>Advanced communication, presentation and negotiation skills</li><li>Ability to work effectively in a complex, matrix organization</li><li>Experience with CRM systems and Microsoft Office suite</li><li>Strong analytical and problem-solving capabilities</li><li>Fluency in English required</li><li>Ability to travel up to 50% of time</li><li>Experience coordinating cross-functional projects and initiatives</li><li>Demonstrated leadership abilities and strategic thinking skills</li><li>Strong organizational and time management abilities</li><li>Knowledge of scientific instrumentation and laboratory operations preferred</li></ul></div></section></div></section></div></div>

Laboratory Chemicals Division Sales Development Manager - Southeast Asia

<p><strong>Just – Evotec Biologics, wholly-owned by Evotec SE, is a unique platform company that integrates the design, engineering, development, and manufacture of biologics. With deep experience in the fields of protein, process and manufacturing sciences, the Just team came together to solve the scientific and technical hurdles that block access to life-changing protein therapeutics; from the design of therapeutic molecules to the design of the manufacturing plants used to produce them. Just's focus is to create access and value for a global market through scientific and technological innovation.</strong></p><h3><strong>QC Manager, Raw Materials - Site Based, Redmond, WA</strong></h3><p>We’re looking for a passionate and curious <strong>QC Manager, Raw Materials</strong> to join our team. If you’re excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you’ll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories.</p><p>As a <strong>QC Manager, Raw Materials</strong> at <strong>Just Evotec Biologics</strong>, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It’s a role where your curiosity will fuel both your personal growth and the success of the team.</p><h4><strong>Position</strong></h4><p><span>This position oversees and participates in the sampling and testing of incoming raw materials prior to their use in cGMP manufacturing. This role works collaboratively with other teams to ensure that raw materials are released in a compliant manner prior to their need-by dates. The role requires extensive cGMP compliance experience, exceptional attention to detail, and experience designing and implementing efficiency improvements.</span></p><h4><strong>What You’ll Do:</strong></h4><ul><li><span>Lead a QC raw materials testing program to support commercial manufacturing.</span></li><li><span>Oversee the inspection, sampling, and testing of incoming raw materials prior to use in manufacturing, according to US and EU GMP requirements.</span></li><li><span>Ensure materials are sampled in accordance with SOPs, entered into the data management systems, and are available for use on time.</span></li><li><span>Participate in the qualification of raw materials via external and in-house testing.</span></li><li><span>Serve as subject matter expert in review of raw material specifications.</span></li><li><span>Participate in vendor audits as a technical advisor.</span></li><li><span>Oversee the daily routine activities of the raw materials group, provide data review, and ensure the operation remains compliant at all times.</span></li><li><span>Collaborate with Quality Assurance, Manufacturing, Materials Management, external vendors, and other functions to ensure internal timelines, testing TAT, and team milestones are achieved.</span></li><li><span>Author and maintain required cGMP documentation such as SOPs and guidance documents.</span></li><li><span>Oversee verification of assays at external testing labs.</span></li><li><span>Identify gaps, design collaborative solutions, and implement improvements.</span></li><li><span>Participate in external testing labs QC laboratory investigations, deviations, OOS, and CAPAs.</span></li><li><span>Support onboarding and qualification of analytical equipment.</span></li></ul><h4><strong>Who You Are:</strong></h4><ul><li><span>BS in Chemistry, or related field with a minimum of 5+ years of relevant experience within the pharmaceutical industry and a minimum of 3+ years of hands-on, industry experience managing in a cGMP QC laboratory.</span></li><li><span>Extensive experience with raw material sampling, including handling of powders and liquids, using aseptic techniques.</span></li><li><span>Knowledge of cGMP raw materials tests including pH, conductivity, osmolality, moisture, appearance, FTIR, HPLC, etc.</span></li><li><span>Knowledge of verification and validation of assays required for raw material testing.</span></li><li><span>Extensive knowledge of regulatory requirements and guidelines (ICH, CFR, FDA).</span></li><li><span>Extensive knowledge of GDPs, GMPs multi-compendial assays (USP, EP, JP).</span></li><li><span>Excellent communication and collaboration skills.</span></li><li><span>Attention to detail, highly organized, able to meet schedules and timelines and handle multiple priorities.</span></li></ul><h4><strong>Why Join Us:</strong></h4><ul><li><strong>Growth Opportunities</strong>: We’re a company that believes in continuous learning and development. Whether it’s professional courses, mentorship, or new projects, we’ll help you grow.</li><li><strong>Flexible Work Environment</strong>: We offer flexible work options to help you balance your professional and personal life. This is a site role.</li><li><strong>Inclusive Culture</strong>: We’re committed to building a diverse and inclusive environment where everyone’s voice is valued, and curiosity is encouraged.</li><li><strong>Innovative Projects</strong>: You’ll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success.</li><li><strong>A Place for Big Ideas</strong>: We don’t just talk about thinking outside the box—we throw the box away. If you’ve got ideas, we want to hear them.</li></ul><h4><strong>Are You Still Curious?</strong></h4><p>If you’ve read this far, then chances are you’ve got a curious mind—just like us. So, what are you waiting for? Take the leap and apply today. We can’t wait to see where your curiosity leads you—and how it will shape the future of <strong>Just Evotec Biologics</strong>.</p><p>Let your curiosity guide your career—<strong>#BeCurious</strong> and explore the endless possibilities at <strong>Just Evotec Biologics</strong>!</p><p><span>The base pay range for this position at commencement of employment is expected to be $92,400 to $126,500;&nbsp;<strong>this is a salary exempt role</strong>. Base salary offered may vary depending on the individual’s skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, generous paid time off and paid holiday, wellness and transportation benefits.</span></p><p><span>Evotec (US) Inc. is an Equal Opportunity Employer.&nbsp; All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.</span></p>

QC Manager, Raw Materials

<p><strong>ALS is a global leader in testing, providing comprehensive testing solutions to clients in a wide range of industries around the world. Using advanced technologies and innovative methods, we help our clients leverage data-driven insights for a safer and healthier world.</strong></p><p><strong>Our people are the heart of our business, driving testing solutions and innovations to solve complex challenges and create lasting value for our clients. But most importantly, our people care – for each other and for the work we do. With over 20,000 team members across 70 countries, you’ll be part of a global network. Learn more about what makes our workplace great here.</strong></p><p>At ALS, we encourage you to dream big.</p><p>When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future.</p><h3><strong>Clinical Research Coordinator</strong></h3><h4><span><strong>About the role</strong></span></h4><p><span>ALS global company, is a leader in the field of clinical testing with an opening for full-time Clinical Research Coordinator (CRC) in Phoenix, AZ. The successful candidate will join a team that provides clinical testing services to many of the world's best-known consumer product companies.&nbsp;</span></p><h4><span><strong>The Study Coordinator will be responsible for:</strong></span></h4><p><span>Plans, develops, and coordinates the safety and efficacy research studies under the supervision of the Principal Investigator and in accordance to protocol, company SOP’s and Good Clinical Practices.</span></p><h4><span><strong>Duties include but not limited to:</strong></span></h4><p><span>The Study Coordinator has the following duties:</span></p><ul><li><span>Participates and coordinates the planning, development and implementation of clinical protocols, logistical procedures, and operating systems in accordance with parameters set out by the study sponsor and Principal Investigator.</span></li><li><span>Supervises, evaluates, and coordinates the activities of a team of Clinical Research Assistants; ensures that all clinical activities are carried out in accordance with Company SOP's and guidelines of Good Clinical Practices.</span></li><li><span>Oversees the planning, scheduling, and carrying out of day-to-day clinical activities, maximizing on study workflow, and associated availability of research subjects.</span></li><li><span>Works closely with Recruitment Department ensuring specific research subject entrance criteria is observed prior to conducting study.</span></li><li><span>Monitors test subjects’ response to treatment and communicates study data and results to investigators in a timely fashion.</span></li><li><span>Works in conjunction with Clinical Management on generation of protocols, interim reports, and final reports for Company sponsors.</span></li><li><span>Order and maintain inventory of laboratory supplies</span></li><li><span>Other duties as assigned.</span></li></ul><h4><span><strong>About you:</strong></span></h4><ul><li><span>Bachelor of Science or Arts degree in life sciences preferred.</span></li><li><span>1 – 2 years’ experience in clinical industry experience (substitute for BS or BA).</span></li></ul><h4><span><strong>Working conditions:</strong></span></h4><ul><li><span>Sitting and/or standing for extended periods of time, up to eight (8) hours per business day</span></li><li><span>Must be able to stand, bend, push, pull, stoop and crouch frequently while performing the duties of this position</span></li><li><span>Must be able to lift (with both hands) and/or move up to 50 pounds and occasionally lift and/or move heavier loads with assistance</span></li><li><span>Must be able to interact and communicate effectively with panelist</span></li></ul><h4><strong>Working at ALS</strong></h4><p>The ALS team is a diverse and dedicated community united by our passion to make a difference in the world.</p><p>Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence.&nbsp;</p><p>At ALS, you’ll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us.&nbsp;</p><p>We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities.</p><h4><strong>Everyone Matters</strong></h4><p>ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued.</p><p>Qualified candidates will be considered without regard to race, colour, religion, national origin, military or veteran status, gender, age, disabilities, sexual orientation, gender identity, pregnancy and pregnancy-related conditions, genetic information and any other characteristics protected by the law. We invite resumes from all interested parties, including women, members of minority groups, and persons living with disabilities.  </p><p>ALS also welcomes applications from people with all levels of ability. <span style="font-size:14px;">Reasonable adjustments to support candidates throughout the recruitment process are available upon request.</span> </p><h4><strong>Eligibility</strong></h4><p style="text-align:left;">To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa.</p><h4><strong>How to apply</strong></h4><p>Please apply on-line and provide a resume &amp; cover letter that best demonstrate your motivation and ability to meet the requirements of this role.</p>

Clinical Research Coordinator

Lab technician

Scientific and Research Fellow

Sales Representative

Sample collector

Academic staff

Laboratory services

Service engineer

Manager

Software

Administrative Assistant

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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