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<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>Speciality Laboratory Assistant</strong></h3><p>ALS Minerals is internationally recognised as the global leader in providing geochemical sample preparation, analytical procedures and data management solutions, with its European hub lab based in Loughrea, Co. Galway.</p><p>We are currently seeking motivated individuals to join our team as Speciality Laboratory Assistants with an immediate start.</p><h4><strong>Duties / Responsibilities (non-exhaustive list):</strong></h4><ul><li>Follow safety rules and practices at all times.</li><li>Wear protective equipment specified for each task.</li><li>Advise Supervisor if you see anything suspicious or potentially hazardous or if you see possibilities for improvement.</li><li>Perform work as per assignment given by the Laboratory Manager or other supervisor. Report completion of the work.</li><li>Follow written methods and procedures when carrying out work. When written instructions are not available follow oral instructions given by the Laboratory Manager or other Supervisor.</li><li>Check and maintain order of the samples being processed and samples identification. Report any deviations to the Laboratory Manager or other Supervisor.</li><li>Handle the samples so as to preserve their identification and prevent their loss, contamination or confusion. Report any accidents to the Laboratory Manager or other Supervisor.</li><li>Monitor quality of work being performed, make notes of any anomalies, e.g. reactive samples, boil overs and incomplete dissolution. Report to the Laboratory Manager or Supervisor if necessary.</li><li>Fill in appropriate forms and worksheets and sign/initial records.</li><li>Operate equipment according to instructions/manuals and follow safety rules at all times. If applicable (e.g. balances, dispensers, dilutors) check calibration status of the equipment daily or before use. Report any anomalies/deviations in equipment performance to the Laboratory Manager or Supervisor. Do not use equipment that is out of order, misbehaving or giving suspicious results. Perform routine maintenance of the equipment (e.g. lubrication, changing/cleaning parts) as per equipment <span style="text-decoration:inherit;">manuals/instructions.</span> Keep equipment and workplace clean. When work is finished, tidy up the work area, clean equipment used and get everything ready for the next use.</li><li>Bring considerations regarding possible method or operation improvements to the Laboratory Manager or Quality Manager.</li><li>Complete all required records as per ISO 17025, INAB requirements and the laboratory’s quality management system.</li></ul><h4><strong>Experience &amp; Expertise:</strong></h4><p>Generally, none required as full training is provided, however previous laboratory experience is desirable.</p><h4><strong>Qualification &amp; Training:</strong></h4><p>Full or partial secondary education with the ability to understand and follow oral and written instructions.</p><p>These roles are primarily Monday to Friday but will require overtime to be carried out on weekends from time to time.</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. <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>

Speciality Laboratory Assistant

<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><span><strong>Laboratory Technician 1</strong></span></h3><p><span><strong>Imagine your future with us!</strong></span></p><p><span>At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world’s most complex problems for a safer, healthier world.&nbsp;</span></p><h4><span><strong>About the role:</strong></span></h4><p><span>We are seeking a full time Laboratory Technician who will be responsible for various laboratory testing This individual will be responsible for following all safety and quality guidelines while maintaining a satisfactory production level.&nbsp; The requirements listed below are representative of the knowledge, skill, and/or ability required.</span></p><h4><span><strong>About you:</strong></span></h4><ul><li><span>Performing laboratory tests as outlined by the SOPs.</span></li><li><span>Performing all scheduled calibrations, standardization and SPC tests.</span></li><li><span>Routine maintenance of testing instrumentation.</span></li><li><span>Properly completing all paperwork used to track tests and their validity.</span></li><li><span>Loading data for tests performed.</span></li><li><span>Maintaining a clean, safe work area.</span></li><li><span>Accurately recording personal production and meeting production requirements.</span></li><li><span>Routing samples for additional testing as outlined by SOPs.</span></li><li><span>Storing and disposing of samples properly.</span></li><li><span>Complying with local and corporate quality assurance policies, as well as ISO 17025 lab accreditation requirements.</span></li><li><span>Other duties and responsibilities may be assigned from time to time, as required</span></li></ul><h4><span><strong>Required Qualifications:</strong></span></h4><ul><li><span>High School diploma or laboratory experience preferred.</span></li><li><span>Working knowledge of good laboratory practice.</span></li><li><span>Comfortable in high paced production environment.</span></li></ul><h4><span><strong>Physical Demands:</strong></span></h4><ul><li><span>The ability to stand for intervals of up to 8 hours while working.</span></li><li><span>Able to speak and hear clearly while communicating with co-workers and managers.</span></li><li><span>Dexterity in hands and fingers to operate equipment and handle glassware.</span></li><li><span>Must have average vision and able to see to read reports and operate equipment.</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>

Laboratory Technician 1

<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>Engineer I, QA</strong></h3><div><div><section><div><h4><strong>Work Schedule</strong></h4><p>Standard Office Hours (40/wk)</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><p>At Thermo Fisher Scientific, you'll join a quality assurance team focused on ensuring consistent execution of quality standards and regulatory compliance. You'll play a vital role in enabling our customers to make breakthrough discoveries and innovations that make the world healthier, cleaner and safer. You'll ensure product quality, drive continuous improvement initiatives, and collaborate with cross-functional teams to maintain the highest standards of quality and compliance in a GMP environment.</p><h4><strong>REQUIREMENTS:</strong></h4><ul><li>Bachelor's Degree required</li><li>Preferred Fields of Study: Chemistry, Biology, Biotechnology, Engineering, or related scientific/technical field</li><li>Additional certifications in Quality Systems or GMP preferred</li><li>Strong knowledge of cGMP, ISO standards (13485/9001), and international regulatory requirements</li><li>Experience with quality systems and documentation including batch records, SOPs, deviations, CAPA</li><li>Proficiency in quality management software systems (TrackWise, SAP, OCPLM, etc)</li><li>Demonstrated ability to perform detailed documentation review and quality assessments</li><li>Strong analytical and problem-solving skills for quality investigations and root cause analysis</li><li>Excellent written and verbal communication skills</li><li>Ability to work independently and collaborate effectively with cross-functional teams</li><li>Proficient computer skills including Microsoft Office applications</li><li>Strong attention to detail and commitment to accuracy</li><li>Ability to prioritize and adapt in a changing environment</li><li>Good knowledge of using AI Tools and/or programming macros preferred</li></ul></div></section></div></div>

Engineer I, QA

<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>Scientist – QC Lab Systems &amp; CSV (GMP)</strong></h3><div><div><section><div><h4><strong>Work Schedule</strong></h4><p>Standard (Mon-Fri)</p><h4><strong>Environmental Conditions</strong></h4><p>Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)</p><h4><strong>Job Description</strong></h4><p>Join Thermo Fisher Scientific at our Lengnau site as a <strong>Scientist – QC Lab Systems &amp; CSV (GMP)</strong> in the Quality Control department. In this role, you will contribute to ensuring GMP compliance, data integrity, and operational excellence of electronic laboratory systems and analytical equipment. You will support the lifecycle management, validation, and continuous improvement of QC applications, directly contributing to reliable product quality and regulatory compliance.</p><h4><strong>Key Responsibilities</strong></h4><ul><li>Ensure lifecycle management of QC applications (e.g., SM LIMS, Empower, LabX, Tiamo), including administration and first- and second-level support</li><li>Support qualification of analytical equipment, including Computerized System Validation (CSV) of electronic laboratory systems</li><li>Coordinate activities between QC, QA, IT, and external vendors for system implementation, maintenance, and enhancements</li><li>Create, review, and maintain GxP lifecycle documentation to ensure compliance with regulatory requirements</li><li>Ensure compliant storage, handling, and integrity of laboratory raw data</li><li>Support QC laboratories in deviation, change controls, and troubleshooting activities</li><li>Participate in gap assessments and support actions to ensure inspection and audit readiness; actively contribute during audits</li><li>Contribute to automation and digitalization initiatives, including implementation of automated data flows</li><li>Collaborate with local and global teams to support continuous improvement (PPI) and system optimization</li><li>Ensure adherence to cGMP, quality, and EHSS requirements</li></ul><h4><strong>Qualifications</strong></h4><p>Bachelor’s or Master’s degree in Life Sciences (e.g., Chemistry, Biochemistry, Microbiology, Physics) or an IT/Automation background with experience in a GMP-regulated environment or similar education with experience in maintaining QC laboratory applications.</p><h4><strong>Experience</strong></h4><p>Minimum 3+ years of experience in a GMP-regulated laboratory or pharmaceutical environment. Hands-on experience with Computerized System Validation (CSV) and electronic laboratory systems is required. Experience with systems such as LIMS, Empower, Tiamo, LabXChromeleon, or similar platforms is advantageous. Basic knowledge of IT systems, databases is beneficial.</p><h4><strong>Skills &amp; Competencies</strong></h4><ul><li>Strong understanding of GMP, data integrity, and regulatory requirements for computerized systems</li><li>Structured, detail-oriented, and risk-based approach to work</li><li>Ability to work independently while collaborating across cross-functional teams</li><li>Strong communication, organization, and prioritization skills</li><li>Customer-focused mindset with a proactive approach to problem solving</li><li>Interest in digitalization, automation, and continuous improvement (PPI)</li><li>Fluency in technical English; German language skills are an advantage</li></ul><p>Thermo Fisher Scientific is an equal opportunity employer and values diversity and inclusion in the workplace.</p></div></section></div></div>

Scientist – QC Lab Systems & CSV (GMP)

<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>QC Scientist I</strong></h3><div><div><h4><strong>Work Schedule</strong></h4><p>Standard (Mon-Fri)</p><h4><strong>Environmental Conditions</strong></h4><p>Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)</p><h4><strong><u>Job Description</u></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 us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of <strong>pharmaceutical products</strong>. You will perform chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments, you'll conduct testing of raw materials, in-process samples, finished products, and stability samples. Our collaborative environment provides opportunities for continuous learning and career growth as you help deliver vital therapies to patients</p><h4><strong>Education:</strong></h4><ul><li>Bachelor's degree required, no prior experience required</li><li>Preferred Fields of Study: Chemistry, Biology, Biochemistry or related scientific field</li></ul><h4><strong>Experience:</strong></h4><ul><li>Proficiency with analytical techniques including <strong>HPLC, GC, spectroscopy</strong>, dissolution testing, and wet chemistry methods</li><li>Experience with microbiological testing, environmental monitoring, and aseptic techniques</li><li>Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards</li></ul><h4><strong>&nbsp;Knowledge, Skills, Abilities:</strong></h4><ul><li>Strong attention to detail with ability to follow standard procedures and maintain data integrity</li><li>Excellent problem-solving skills and logical approach to scientific challenges</li><li>Proficient computer skills including Microsoft Office and laboratory information systems</li><li>Strong written and verbal communication abilities</li><li>Ability to work both independently and collaboratively in a dynamic environment</li><li>Physical requirements include standing/walking for extended periods, lifting up to 50 lbs, and manual dexterity</li><li>Must be able to work in cleanroom environments wearing required PPE</li><li>Ability to work various shifts including nights, weekends, and holidays as needed</li><li>Experience in pharmaceutical/regulated environment preferred but not required</li></ul></div></div>

QC Scientist I

<p><strong>Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek - so they can do what they do best: improve the world around us. Information about </strong><a target="_blank" rel="noopener noreferrer" href="https://www.agilent.com/"><strong>Agilent</strong></a><strong>.</strong></p><h3><strong>QC Supervisor - Second Shift</strong></h3><div><div><h4><strong>Job Description</strong></h4><div><div><div><div><div><div><div><div><p>The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines.</p><p>The <strong>QC Supervisor</strong> will oversee activities assigned to Quality Control (QC) and supervise a group of QC analysts. They will ensure workload and priorities are met and will be required to supervise staff and perform Laboratory testing and review in support of the workload. The supervisor will also ensure QC operations are in compliance with current Good Manufacturing Practices (cGMP) and other regulatory guidance.</p><h4><strong>Essential Job Responsibilities:</strong></h4><ul><li><span>Supervise QC personnel to support in-process testing</span></li><li><span>Exercises judgment within defined procedures and policies to determine appropriate action</span></li><li><span>Acts as the shift supervisor and becomes actively involved as an analyst as required to meet schedules and resolve problems.</span></li><li><span>Prioritizes and arranges the workload to ensure in-process testing timelines are met</span></li><li><span>Delegates effectively and exercises judgment when escalating issues to QC upper Management</span></li><li><span>Writes, reviews and revises standard operating procedures. associated Quality Control functions, and analytical test methods</span></li><li><span>Generates, processes and/or reviews analytical data</span></li><li><span>Reviews data for compliance to specifications and reports anomalous results to the Quality Manager and Quality Assurance, as appropriate</span></li><li><span>Assists with QC related deviations, </span><span style="text-decoration:inherit;">inquiries/investigations,</span><span> and </span><span style="text-decoration:inherit;">corrective/preventative</span><span> actions (CAPAs)</span></li><li><span>Will be directly involved in client Audits and regulatory inspections</span></li><li><span>Ensures that quality products are designed and manufactured by Agilent, and are in alignment and compliance with national, regional and global regulations, company policies and business objectives</span></li><li><span>Develops and implements programs and processes to ensure that Agilent products are safe, legal, and meet or exceed customer expectations for regulatory compliance</span></li><li><span>Oversees and advises quality and/or regulatory activities and drives key strategic programs within assigned area of responsibility</span></li><li><span>Acts as a change agent to help establish a customer-centered culture</span></li><li><span>Ensures quality management system procedures were accurate and current</span></li><li><span>Provides expertise in translating regulatory requirements into practical, workable plans</span></li><li><span>Represents the company in industry associations and standards bodies and may work with regulatory agencies</span></li><li><span>May lead development and implementation of standards, methods and procedures for inspecting, testing and evaluating the precision, accuracy and reliability of company products</span></li><li><span>May lead generation and review of documentation used in good manufacturing practices</span></li><li><span>May supervise audits of production and quality control areas and raw material vendors</span></li><li><span>Selects, develops and evaluates personnel to ensure the efficient operation of the function</span></li><li><span>Supervises individual contributors responsible for routine tasks</span></li><li><span>Assign and direct implementation of tasks and processes</span></li><li><span>Establishes, maintains business controls and process</span></li></ul><p>Second Shift - 2:30 pm - 11 pm</p><h4><strong>Qualifications</strong></h4><h5><strong>Required:</strong></h5><ul><li>Secondary Education with relevant experience</li><li>Two years of QC experience</li><li><span>Knowledge and skill using basic computer software and hardware applications, including Microsoft Word and Excel</span></li><li><span>Excellent written and oral communication skills</span></li><li><span>Ability to multi-task and lead various projects and competing priorities</span></li></ul><h5><strong>​</strong><span><strong>Desired:</strong></span></h5><ul><li>Bachelors of Science preferred</li><li>Experience in a cGMP environment</li><li>One year of experience formally or informally leading people</li><li>Experience with lab equipment: HPLC, LCMS, UV, GC</li><li>​<span>Ability to write and review protocols, reports, and procedures</span></li></ul><h4><strong>Additional Details</strong></h4><p>This job has a full time weekly schedule. Applications for this job will be accepted until at least April 15, 2026 or until the job is no longer posted.</p><p>The full-time equivalent pay range for this position is <strong>$105,280.00 - $164,500.00/yr plus eligibility for bonus, stock and benefits.</strong> Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: <span style="text-decoration:inherit;">https://careers.agilent.com/locations</span></p><p>Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email <span style="text-decoration:inherit;">job_posting@agilent.com</span> or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit <span style="text-decoration:inherit;">www.agilent.com/en/accessibility.</span></p></div></div></div></div></div></div></div></div><h4><strong>Travel Required:</strong></h4><p>No</p><h4><strong>Shift:</strong></h4><p>Day</p><h4><strong>Duration:</strong></h4><p>No End Date</p><h4><strong>Job Function:</strong></h4><p>Quality/Regulatory</p></div></div>

QC Supervisor - Second Shift

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

Operations Technician I - Reference Standards QC

<p><strong>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>QC Technician (2nd shift, weekends)</strong></h3><p>Are you driven by precision, quality, and the knowledge that your work directly impacts patient safety? As a QC Technician at Novartis, you’ll play a critical role in ensuring our products meet the highest standards of quality and compliance. Working hands-on in a chemistry laboratory environment, you’ll apply your analytical expertise to test, evaluate, and document materials and finished products, supporting reliable supply and inspection readiness. This role offers the opportunity to contribute meaningfully to life‑changing medicines while growing your skills in a collaborative, quality‑focused environment.</p><h4><strong>Key Responsibilities</strong></h4><ul><li>Perform analytical testing of drug products, stability samples, and materials in compliance with quality and regulatory standards</li><li>Manage sample receipt, storage, tracking, and disposition to ensure integrity and inspection readiness</li><li>Document test results accurately using approved methods, procedures, and quality systems</li><li>Execute stability testing activities and maintain complete, audit‑ready documentation</li><li>Identify, document, and escalate technical complaints or adverse events within required timelines</li><li>Support inspection preparedness by adhering to Good Manufacturing Practice and internal quality guidelines</li><li>Contribute to continuous improvement initiatives, including efficiency, cost optimization, and laboratory excellence</li></ul><h4><strong>Essential Requirements</strong></h4><ul><li>High school diploma with at least one year of experience working in a laboratory or quality control environment or bachelor’s degree in biochemistry, chemistry or another scientific discipline with no prior experience required. Biochemistry degree preferred.</li><li>Experience using quality control laboratory instrumentation and equipment</li></ul><h4><strong>Desirable Requirements</strong></h4><ul><li>Experience working in pharmaceutical, biotechnology, or radiopharmaceutical environments</li><li>Familiarity with microbiological aseptic techniques</li></ul>

QC Technician (2nd shift, weekends)

<p><strong>At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic &amp; consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries.</strong></p><p><strong>PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.</strong></p><p><strong>Life at Eurofins is a meritocracy, where people are empowered to make decisions and are rewarded for their success, allowing them to advance quickly. Become your most extraordinary self with support and development throughout your career.</strong></p><h3><strong>QC Raw Materials Sampling Analyst</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><section><div><section><div><div><section><div><div><section><div><div><section><div><section><div><section><div><section><div><div><section><div><h4><strong>Job Description</strong></h4><section><div><section><div><p><strong><u>What You’ll Do</u></strong></p><ul><li>Follow all regulatory and safety requirements in a GMP environment</li><li>Work hands‑on in a cleanroom environment, aseptically gowning and sampling raw materials</li><li>Inspect containers, components, and consumables to support high‑quality manufacturing</li><li>Receive, label, handle, and safely dispose of samples</li><li>Calibrate or verify calibration of instruments before use</li><li>Record test results accurately and report any unusual findings</li><li>Maintain lab supplies and keep work areas clean and organized</li><li>Provide reliable, professional support to internal clients and manufacturing teams</li><li>Complete required training and follow all regulatory and safety procedures</li><li>Gain cross‑training experience in sampling and testing compressed gas systems and tankers</li></ul><p><strong><u>Opportunities You'll Gain</u></strong></p><ul><li>Build <strong>real cleanroom experience</strong> — a major advantage in biotech and pharma</li><li>Learn <strong>industry‑standard testing and calibration skills</strong></li><li>Work in <strong>regulated environments</strong> that strengthen your scientific discipline</li><li>Gain <strong>cross‑functional exposure</strong> to sampling, testing, and quality operations</li><li>Develop a strong foundation for future roles in QC, manufacturing, or analytical labs</li></ul><p><strong><u>Work Environment &amp; Cleanroom Requirements</u></strong></p><p>This is a fully onsite, lab‑based role in biopharmaceutical cleanrooms and lab spaces. You’ll spend significant time in <strong>ISO 8 cleanrooms</strong>, which require specific gowning and hygiene standards:</p><ul><li><i>No cosmetics (makeup, false lashes, spray tans, etc.)</i></li><li><i>Nails must be short, trimmed, and unpolished</i></li><li><i>No jewelry (except medical alert items or a simple band that fits under gloves)</i></li><li><i>Hair must be fully contained in a hairnet; facial hair must be neatly trimmed and coverable</i></li></ul><p>These standards protect product quality and ensure a safe, controlled environment.</p></div></section><section><div><h4><strong>Qualifications</strong></h4></div><div><p><strong><u>Ideal Qualifications</u></strong></p><ul><li>Positive, adaptable, team‑oriented mindset with strong attention to detail</li><li>Able to learn new techniques quickly and follow procedures accurately</li><li>Familiar with basic aseptic practices or cleanroom concepts</li><li>Clear written and verbal communication skills</li><li>Comfortable with a moderately physical role involving extended standing</li></ul><p><strong><u>Minimum Qualifications</u></strong></p><ul><li>Bachelor’s degree in chemistry or a related scientific field, <strong>or</strong> equivalent hands‑on experience</li><li>Authorization to work in the United States indefinitely without restriction or sponsorship</li></ul></div></section><section><div><h4><strong>Additional Information</strong></h4></div><div><ul><li>Hourly pay range: $22.50 - $28.50</li><li>Schedule: Monday - Friday, 8:00 AM - 4:30 PM&nbsp;</li></ul><p><strong>Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.</strong></p></div></section></div></section></div></section></div></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></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>

QC Raw Materials Sampling Analyst

Lab technician

Liquid chromatography-mass spectrometry

Scientific and Research Fellow

Sales Representative

Sample collector

Academic staff

Laboratory services

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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