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<p><strong>Waters Corporation (NYSE: WAT), the world's leading specialty measurement company, has pioneered chromatography, mass spectrometry and thermal analysis innovations serving the life, materials, and food sciences for over 60 years. With approximately 8,000 employees worldwide, Waters operates directly in 35 countries, including 15 manufacturing facilities, with products available in more than 100 countries. Our team focuses on creating business advantages for laboratory-dependent organizations to enable significant advancement in healthcare delivery, environmental management, food safety, and water quality.</strong></p><p>Working at Waters and TA Instruments enables our employees to unlock the potential of their careers. Our global team is driven by purpose. We strive to be better, learn and improve every day in everything we do. We’re the problem solvers and innovators that aren’t afraid to take risks to transform the world of human health and well-being. We’re all in it together delivering benefit as one to provide the insights needed today in order to solve the challenges of tomorrow. &nbsp;</p><h3><strong>Software Engineer</strong></h3><h4><strong>Overview</strong></h4><p>This is a great opportunity to come and join the Biologics software engineering group. We’re looking for a Software Engineer to join an agile team focused on full-stack development. In this role, you'll play a key role in developing software which makes a real impact to people’s lives, whether its developing COVID tests and vaccines, helping scientists detect cancer, ensuring food safety or helping scientists develop biodegradable plastics – our work has a real benefit to the world!</p><h4><strong>What can we offer you?</strong></h4><ul><li>A&nbsp;plan for your personal development in your own area of specialism, pursuing this with the support of your manager to undertake the training and learning to progress.</li><li>Competitive salary</li><li>Flexible working hours and a hybrid approach</li><li>25 days annual leave</li><li>Private health and dental insurance</li><li>Contributory based pension scheme</li><li>EAP (Employee Assistance Program)</li></ul><h4><strong>Responsibilities</strong></h4><p>As a Software Engineer, your main responsibilities would include:</p><ul><li>Developing software across our technology stack and contributing to team delivery</li><li>Contributing to the team's automated tests and pipeline automation</li><li>Reviewing pull requests from other team members</li><li>Working collaboratively as part of a cross-discipline agile team to incrementally deliver software</li><li>Contributing to team and technical continuous improvement activities</li><li>Continually learning, to stay up-to-date with the latest techniques and technologies in software development</li></ul><h4><strong>Qualifications</strong></h4><p>We would love to hear from you if you:&nbsp;</p><ul><li>Have experience with C# and .Net / .Net Core.</li><li>Have experience with Python (desirable - don't worry if you don't have this).</li><li>Have knowledge and experience in some other elements of our technology stack: TypeScript, Angular, NgRx, Javascript, HTML &amp; CSS.</li><li>A passion for full-stack, web application development</li><li>Practice and pursue good software engineering practices (e.g., Unit testing, TDD, refactoring, CI/CD, BDD)</li></ul><p>Don't be put off if you don't feel you match all of the skills or technologies. C# is important, but we don't expect a complete match with the rest. Mostly, we're looking for talented software engineers with a passion for making good products.</p><p><strong>Working pattern and location</strong>. We offer hybrid working, which means some working in the office each week. This role is based at our Wilmslow office; candidates should be within a reasonable commutable distance from Wilmslow.</p><p><strong>Experience</strong>. We're looking for a mid-level software engineer.</p>

Software Engineer

<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>Lead Manufacturing Technician</strong></h3><div><div><div><section><div><div><div><div><div><h4><strong><u>Job Description</u></strong></h4><h4><strong>Responsibilities</strong><span style="font-family:&quot;Arial&quot;,sans-serif;"><strong>​</strong></span></h4><ul><li><strong>Production Operations</strong>: Execute the synthesis, ammonolysis, purification, and other key processes of oligonucleotides with precision, following strict standard operating procedures (SOPs) and quality control guidelines. Monitor and record process parameters in real - time to ensure consistency and traceability of production batches.<span style="font-family:&quot;Arial&quot;,sans-serif;">​</span></li><li><strong>Process Optimization</strong>: Actively participate in the optimization of oligo synthesis processes, including but not limited to reaction conditions, purification methods, and reagent usage. Analyze production data, identify bottlenecks, and propose innovative solutions to enhance process efficiency, reduce costs, and improve product quality. Collaborate with cross - functional teams, such as R&amp;D and quality assurance, to implement process improvements.<span style="font-family:&quot;Arial&quot;,sans-serif;">​</span></li><li><strong>Troubleshooting</strong>: Quickly diagnose and resolve technical issues that may arise during the production process. Develop and maintain a troubleshooting guide for common problems in oligo synthesis, ammonolysis, and purification, ensuring minimal disruption to production schedules.<span style="font-family:&quot;Arial&quot;,sans-serif;">​</span></li><li><strong>Documentation</strong>: Prepare detailed production reports, process records, and technical documentation in accordance with regulatory requirements and internal standards. Keep abreast of industry best practices and relevant regulations, and ensure compliance in all aspects of production operations.<span style="font-family:&quot;Arial&quot;,sans-serif;">​</span></li></ul><h4><strong>Requirements</strong><span style="font-family:&quot;Arial&quot;,sans-serif;"><strong>​</strong></span></h4><ul><li><strong>Education</strong>:&nbsp;A minimum of a Master's degree in Organic Chemistry</li><li><strong>Experience</strong>: At least 1 years of hands - on experience in oligo chemical synthesis production, with in-depth knowledge of synthesis, ammonolysis, and purification techniques.</li><li><strong>Technical Skills</strong>: Proficiency in operating oligo synthesis instruments, purification equipment (such as HPLC), and related analytical tools. Strong understanding of organic chemistry principles, reaction mechanisms, and purification methods applicable to oligonucleotides.<span style="font-family:&quot;Arial&quot;,sans-serif;">​</span></li><li><strong>Problem - Solving and Analytical Skills</strong>: Excellent analytical and problem - solving abilities, with the capacity to interpret complex data and make informed decisions. A logical and systematic approach to troubleshooting production issues.<span style="font-family:&quot;Arial&quot;,sans-serif;">​</span></li><li><strong>Teamwork and Communication</strong>: Strong teamwork skills, with the ability to collaborate effectively with colleagues from different departments. Excellent communication skills, both written and verbal, to clearly convey technical information and contribute to team discussions.<span style="font-family:&quot;Arial&quot;,sans-serif;">​</span></li><li><strong>Dedication and Initiative</strong>: A high level of dedication to continuous learning and professional development. Self - motivated with a strong sense of initiative, and a willingness to take on new challenges and responsibilities. A passion for research and a spirit of exploration, with the drive to push the boundaries of existing processes and technologies.</li><li>Join us to play a pivotal role in ensuring our products meet the highest standards. Our team is driven by a shared purpose to make the world healthier, cleaner, and safer. We look forward to welcoming you to our collaborative and innovative environment!</li></ul><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.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials</p></div></div></div></div></div></section></div></div></div>

Lead Manufacturing Technician

<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>Sr. technician</strong></h3><div><div><div><section><div><div><div><div><div><h4><strong><u>Job Description</u></strong></h4><p>Job Description - operation(Oligo Synthesis)</p><p>Job Title: Sr.technician Department: Oligo Probe &amp; Primer Production Location: [Suzhou]</p><h4>Responsibilities</h4><ul><li>Production Operations: Execute the synthesis, ammonolysis, purification, and other key processes of oligonucleotides with precision, following strict standard operating procedures (SOPs) and quality control guidelines. Monitor and record process parameters in real - time to ensure consistency and traceability of production batches.</li><li>Process Optimization: Actively participate in the optimization of oligo synthesis processes, including but not limited to reaction conditions, purification methods, and reagent usage. Analyze production data, identify bottlenecks, and propose innovative solutions to enhance process efficiency, reduce costs, and improve product quality. Collaborate with cross - functional teams, such as R&amp;D and quality assurance, to implement process improvements.</li><li>Troubleshooting: Quickly diagnose and resolve technical issues that may arise during the production process. Develop and maintain a troubleshooting guide for common problems in oligo synthesis, ammonolysis, and purification, ensuring minimal disruption to production schedules.</li><li>Documentation: Prepare detailed production reports, process records, and technical documentation in accordance with regulatory requirements and internal standards. Keep abreast of industry best practices and relevant regulations, and ensure compliance in all aspects of production operations.</li></ul><h4>Requirements</h4><ul><li>Education: A minimum of a Bachelor's degree in Organic Chemistry or a related field. A Master's degree or higher is preferred.</li><li>Experience: At least 1 years of hands - on experience in oligo chemical synthesis production, with in-depth knowledge of synthesis, ammonolysis, and purification techniques.</li><li>Technical Skills: Proficiency in operating oligo synthesis instruments, purification equipment (such as HPLC), and related analytical tools. Strong understanding of organic chemistry principles, reaction mechanisms, and purification methods applicable to oligonucleotides.</li><li>Problem - Solving and Analytical Skills: Excellent analytical and problem - solving abilities, with the capacity to interpret complex data and make informed decisions. A logical and systematic approach to troubleshooting production issues.</li><li>Teamwork and Communication: Strong teamwork skills, with the ability to collaborate effectively with colleagues from different departments. Excellent communication skills, both written and verbal, to clearly convey technical information and contribute to team discussions.</li><li>Dedication and Initiative: A high level of dedication to continuous learning and professional development. Self - motivated with a strong sense of initiative, and a willingness to take on new challenges and responsibilities. A passion for research and a spirit of exploration, with the drive to push the boundaries of existing processes and technologies.</li></ul><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></div></div></div></div></div></section></div></div></div>

Sr. technician

<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>(Senior) Electrical Design Engineer Mass Spectrometry Developement (m/f/d) - Join our exclusive Talent Community</strong></h3><div><div><div><section><div><div><div><div><div><h4><strong><u>Job Description</u></strong></h4><p>Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.</p><h4><strong>Location/Division Specific Information</strong></h4><p>We are a research, development, and production site in Bremen currently, with about 500 employees, whose “high-end” measurement and analysis instruments (mass spectrometers) are used in research and science worldwide. Our innovative products in the fields of Life Sciences MS and Inorganic MS, as well as Trace Elemental Analysis, are among the leading products globally in their respective markets.&nbsp;</p><h4><strong>Discover Impactful Work:</strong></h4><p>To strengthen our agile Life Science R&amp;D department, we are seeking a highly experienced and motivated Electrical Design Engineer who will be responsible for developing electrical circuits for mass spectrometers. In this role, you will oversee the entire process from idea conception to design and the creation of necessary production documentation, ensuring a successful transition to series production. You will join a team of experts in an innovative R&amp;D environment, constantly translating new ideas into robust designs. As an Electrical Design Engineer, you will play a crucial role in developing electrical components for the next generation of life science mass spectrometers and their accessories, contributing to a healthier, cleaner, and safer world.</p><h4><strong>A day in the Life:</strong></h4><ul><li>Design and development of complex electronics (including high frequency and high voltage circuits) in a highly motivated, multinational and interdisciplinary team in Bremen</li><li>Participation in product development teams and project planning</li><li>Preparation of production documentation and test procedures to ensure a smooth and timely transfer to series production</li><li>Installation and test of developed Electronics on mass spectrometers</li><li>On-the-bench and in-system design verification</li><li>Calculation of product and process costs</li><li>Technical support of suppliers and their qualification</li><li>Change Management (ECO) and Quality Control during product commercialization phase</li><li>Your tasks and responsibilities will be diverse and exciting, with the opportunity to participate in product development projects across multiple sites worldwide. </li></ul><h4><strong>Keys to Success:</strong><br><strong>Education</strong></h4><ul><li>University degree in electrical engineering, or related fields</li></ul><h4><strong>Experience</strong></h4><ul><li>Several years of professional experience of designing analog electronics, preferably including high voltage and/or high frequency electronics</li><li>Experience in Product Development Practices, Processes and Tools, preferably in the context of sophisticated analytical instruments</li><li>Experience in low volume, high-value large complex systems such as scientific instrumentation, medical devices, or semiconductor process systems is highly preferred</li><li>Experience in troubleshooting electronic circuits and in conducting root cause analysis on PCBA and system level&nbsp;</li><li>Experience in lateral leadership desirable</li></ul><h4><strong>Knowledge, Skills, Abilities</strong></h4><ul><li>Strong desire to push the limits of science and technology</li><li>Working cost-conscious, effective, and autonomous</li><li>Good written and oral communication skills in German and English language</li><li>Good knowledge of Windows and Office programs</li></ul><h4><strong>What we offer:</strong></h4><ul><li>Employment with an innovative, future-oriented organization</li><li>Outstanding career and development prospects</li><li>Company pension scheme and other fringe benefits</li><li>Exciting company culture which stands for integrity, intensity, involvement and innovation</li></ul><h4><strong>Join Our Exclusive Talent Community</strong></h4><p>Are you passionate about Electronics? We are always on the lookout for talented individuals to join our team. If you are interested, please apply online with your CV and Motivation Letter to become a part of our exclusive Talent Community.</p><p>By joining our Talent Community, you will be among the first to be considered for new opportunities as they arise. We will review your application and provide feedback if your profile matches our needs. When a suitable position opens up, we will reach out to schedule interviews.</p><h4><strong>Work Schedule</strong></h4><p>Standard (Mon-Fri)</p><h4><strong>Environmental Conditions</strong></h4><p>Laboratory Setting, Office</p></div></div></div></div></div></section></div></div></div>

(Senior) Electrical Design Engineer Mass Spectrometry Developement (m/f/d) - Join our exclusive Talent Community

<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>Junior R&amp;D Software/Firmware Engineer (C++ and Data Structures)</strong></h3><p>We are looking for a Junior R&amp;D Software/Firmware Engineer (C++ and Data Structures) to join our Automation Solutions Business team in Craven Arms, Shropshire. This is a great opportunity to create the next generation technology solutions in the lab environment. Our aim is to investigate, identify and develop new products, processes, and technology that will enable a smoother laboratory workflow operation for our customers, connecting software applications and instruments.</p><p>If you are a person who thrives through new challenges, passionate about making a positive impact that will improve quality of life, then apply to this position!</p><p>In order to succeed you will be expected to learn and apply a variety of software development knowledge including system design, project management, and hands-on development.&nbsp;</p><h4>Your key responsibilities will include:</h4><ul><li>Work with the R&amp;D team to test and develop products, components, processes, and systems using broad engineering principles and research methodologies.</li><li>Solving complex and high-impact design and development problems, including customer application issues of varying scope and complexity.</li></ul><h4>About Craven Arms</h4><p>Craven Arms is located in the heart of the South Shropshire Area of Outstanding Natural Beauty, within easy reach of Shrewsbury, Telford, Wolverhampton, and Hereford. The area offers a high quality of life with excellent outdoor recreation opportunities. House prices are below the national average while local schools outperform the UK average -- with many State schools achieving excellent results. The successful candidate can expect a fun place to work, exposure to new technologies, and good career progression prospects. In addition, the thing we value is work-life balance, encouraging people to leave work when they should.</p><h4>Qualifications</h4><p>We are seeking a motivated individual with the following background:</p><ul><li>A University degree in Computer Science, Software Engineering or a related field</li><li>Excellent understanding of Data Structures</li><li>1 year of experience working with OOP languages and frameworks such as C++, C# and .NET (This can include experience gained through internships, academic projects, or personal projects)</li><li>Working knowledge of JavaScript scripting language</li><li>Familiarity with ActiveX</li></ul><p>We are committed to making Agilent the best place to work for everyone by providing a truly inclusive work experience. Together, through collaboration, as One Agilent, we are better able to deliver trusted answers to our customer's critical questions because we know there is work to be done.&nbsp;</p><h4>We offer:</h4><ul><li>Exciting projects in a dynamic collaborative team grounded on an Agile Culture and Mindset</li><li>Career development opportunities in an international company</li><li>Competitive compensation and benefits package</li><li>Work-Life-Balance programs</li><li>Permanent contract in a fast-growing global company</li><li>Company pension scheme</li><li>Private health care</li></ul><p>We will make sure you get all the training and development opportunities you need to become the best in your field!</p><h4>Additional Details</h4><p>This job has a full time weekly schedule.</p><p>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: https://careers.agilent.com/locations</p><p>Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.</p><p><strong>Travel Required:</strong> Occasional</p><p><strong>Shift:</strong> Day</p><p><strong>Duration:</strong> No End Date</p><p><strong>Job Function:</strong> R&amp;D</p>

Junior R&D Software/Firmware Engineer (C++ and Data Structures)

<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>LabVIEW Software Engineer</strong></h3><p>Are you our new LabVIEW Software Engineer? We are looking for an additional permanent member of our team to develop software for Agilent’s Raman Spectroscopy products. The position will be based at our Harwell office near Oxford in the United Kingdom, with options for hybrid working. You will be working as part of a cross-functional R&amp;D and product development team to develop high-quality software and products for our Pharmaceutical and Field Detection markets - delivering trusted answers, differentiated workflows and a common Agilent user experience.</p><p>As a LabVIEW Software Engineer, you will join a small team (of around 10 employees and contractors), which has recently been certified as an NI Centre of Excellence, to demonstrate our ability as a world-class software team as part of the larger R&amp;D function that includes hardware development, data science, optics, software quality and marketing. You will be developing software as part of a team using Agile methodologies to meet customer requirements, with a high-level of quality and consideration for regulatory and product security requirements.</p><p>This is an excellent opportunity for an experienced LabVIEW Software Engineer to work with a premier LabVIEW software team developing products making a difference in the world - from airport security screening and pharmaceutical quality control to hazardous chemical identification!</p><h4>Your main responsibilities will be:</h4><ul><li>Design, develop, test and debug LabVIEW Software for Raman Spectroscopy products to a high-level of quality as part of a small project development team</li><li>Working on new products, product improvement projects and supporting/maintaining existing products to add new features and address defects</li><li>Follow our Agile software development process using Jira for implementing new features and resolving defects across our portfolio of products</li><li>Work with the wider cross-functional team to define requirements, troubleshoot software &amp; hardware integration issues and work with software quality team on software testing</li><li>Ensuring code is maintainable – writing good software documentation and writing unit tests</li><li>Contribute to our continuous improvement activities, internal user group and ongoing learning and development</li><li>Ensuring software meets regulatory (pharmaceutical or government) and product security requirements</li><li>Working on Aviation Security products</li></ul><p>This position is based in Harwell, Oxford (UK) with the flexibility to work on a hybrid model (3 days in the office, 2 days from home). You will report to the R&amp;D Software Manager (LabVIEW).</p><h4>Qualifications</h4><ul><li>Bachelor’s or master’s degree or equivalent in Software, Engineering or Life Sciences</li><li>Experienced LabVIEW Software Engineer – Certified LabVIEW Architect or Developer desirable, but certification is not crucial</li><li>Broad LabVIEW experience including working with hardware, databases, user interface development, object-oriented programming (LVOOP) and design, unit testing and source code control (Git) is all beneficial</li><li>Experience of agile software development as part of a development and cross-functional team is desirable</li><li>Experience of Spectroscopy and/or laboratory instrumentation/product development is desirable</li><li>Experience in a regulated environment (e.g. Pharma / Aerospace / Defence) is desirable</li><li>Experience with government-focussed software development for Aviation Security products</li><li>Must be capable of obtaining security clearances</li></ul><p>On a personal level, you should be able to work well independently and as part of a product development team, have creative and good problem-solving and research skills – seeking simple and effective solutions to interesting problems using LabVIEW.</p><h4>We offer:</h4><ul><li>Exciting projects in a multifaceted collaborative team grounded on an Agile Culture and Approach</li><li>Career development opportunities in an international company</li><li>Competitive compensation and benefits package</li><li>Work-Life-Balance programs</li><li>Permanent contract in a fast-growing global company</li><li>Company pension scheme</li><li>Private health care</li></ul><h4>Additional Details</h4><p>This job has a full time weekly schedule.</p><p>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: https://careers.agilent.com/locations</p><p>Agilent Technologies Inc. is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other protected categories under all applicable laws.</p><p><strong>Travel Required:</strong> No</p><p><strong>Shift:</strong> Day</p><p><strong>Duration:</strong> No End Date</p><p><strong>Job Function:</strong> R&amp;D</p>

LabVIEW Software Engineer

<p><strong>Metrohm is one of the world’s most trusted manufacturers of high-precision instruments for chemical analysis. Founded in 1943 by Bertold Suhner in Herisau, Switzerland, Metrohm has grown to an international company that supplies its products in more than 80 countries through more than 37 own subsidiaries and numerous exclusive distributors.</strong></p><p><strong>We are the North American division of world-renown Metrohm AG (Herisau, Switzerland), an industry leader in laboratory instruments and accessories for analytical testing/research. We are looking for an experienced Field Service Specialist – Chemical Instrumentation Equipment to join our team in the Southern Greater Houston area. This position will be responsible for a territory that includes Freeport, Bryan/College Station, Katy, Bay City, and surrounding areas.</strong></p><h3><strong>Senior Software Engineer&nbsp;</strong></h3><p><strong>Job Openings for Senior software engineer in Metrohm Research India Private Limited (Formerly named as Ohmic Research India) (Metrohm Group Company)</strong></p><p><strong>Location - Pune, India.</strong></p><h4><strong>Experience</strong></h4><ul><li>8+ years</li></ul><h4><strong>Reporting To</strong></h4><ul><li>Team Lead</li></ul><h4><strong>Skills required</strong></h4><ul><li>8+ years of previous experience as a C++ product developer for frontend and backend as per Object oriented programming (OOPS) concepts.</li><li>Experience in QT application Development (familiar with QT Core, QT GUI, QT Widgets, QT Creator IDE).</li><li>Experience in QT QML based application Development.</li><li>Strong experience working with design patterns and following SOLID principles.</li><li>Deep understanding of quality aspects such as Static, Dynamic code review, unit, integration, and system testing.</li><li>Hands-on experience on UML diagrams.</li><li>Must have a strong debugging and problem-solving skills.</li><li>Working experience with test framework and automation projects</li></ul><h4><strong>Responsibilities</strong></h4><ul><li>Software design &amp; development along with functional testing of business requirements.</li><li>Will be working on development of source code as per architecture, Unit test, Integration test, and system-level test implementation.</li><li>Responsible for ensuring code quality as per Coding standards, best coding practices.</li><li>Diagnose and resolve highly complex level issues of application.</li><li>Use cases and design to quickly deliver new features and fixes for the applications.</li><li>Participate in interactions with all levels of personnel in a scrum team.</li></ul><h4><strong>Secondary skills</strong></h4><ul><li>Good understanding of communication protocols (UART, SPI, I2C, USB, Ethernet).</li><li>Expertise with different peripherals such as ADC, PWM, Timer, Counters, GPIO, Interrupts.</li><li>Experience in programming for microprocessor/microcontroller based embedded devices.</li><li>Experience of RDBMS like SQLite, MySQL.</li><li>Experience on agile software development process during product development.</li><li>Experience in Linux programming concepts (Process, Threads, Semaphore, Mutex, IPC, signal handling, exception handling, networking protocols).</li><li>Hands-on experience on Python scripting</li></ul><h4><strong>Behaviours &amp; Aptitude</strong></h4><ul><li>Excellent interpersonal and written communication skills in English.</li><li>Good time-management skills.</li></ul><h4><strong>We are Looking for You with</strong></h4><ul><li>Qualification - B.E. / M.E (Computer Science/ IT /Electronics) or equivalent higher level degree.</li></ul>

Senior Software Engineer

<p><strong>Metrohm is one of the world’s most trusted manufacturers of high-precision instruments for chemical analysis. Founded in 1943 by Bertold Suhner in Herisau, Switzerland, Metrohm has grown to an international company that supplies its products in more than 80 countries through more than 37 own subsidiaries and numerous exclusive distributors.</strong></p><p><strong>We are the North American division of world-renown Metrohm AG (Herisau, Switzerland), an industry leader in laboratory instruments and accessories for analytical testing/research. We are looking for an experienced Field Service Specialist – Chemical Instrumentation Equipment to join our team in the Southern Greater Houston area. This position will be responsible for a territory that includes Freeport, Bryan/College Station, Katy, Bay City, and surrounding areas.</strong></p><h3><strong>Software Architect- C++</strong></h3><p><strong>Job Openings for Software Architect- C++ in Metrohm Research India Private Limited (Formerly named as Ohmic Research India) (Metrohm Group Company)</strong></p><p><strong>Location - Pune, India.</strong></p><h4><strong>Experience</strong></h4><ul><li>15+ years</li></ul><h4><strong>Reporting To</strong></h4><ul><li>Team Lead</li></ul><h4><strong>Skills required</strong></h4><ul><li>15+ years of previous experience as a C++ product developer for frontend and backend as per object-oriented programming (OOPS) concepts.</li><li>5+ Years’ experience in developing complex Software/Firmware architecture for frontend and backend.</li><li>Strong experience working with design patterns and following SOLID principles.</li><li>Extensive hands-on experience in documenting Software/Firmware architecture and communicating the same using UML.</li><li>Expertise in creating solution architecture for GUI-based application (for e.g., QT QML-driven HMI SW architecture)</li><li>Strong experience in multithread-based software application architecture and design on different operating systems.</li><li>Deep understanding of quality aspects such as Static, Dynamic code review, unit, integration, and system testing.</li><li>Working experience with test frameworks and automation projects.</li></ul><h4><strong>Responsibilities</strong></h4><ul><li>Translate business needs and requirements into technical requirements for software applications.</li><li>Prepare and document application architecture and design (Flexible for new changes or modifications).</li><li>Responsible for ensuring code quality as per Coding standards, and best coding practices for the entire software team.</li><li>Coaching and mentoring software engineers to increase their technical skills.</li><li>Also working on the development of source code as per the architecture, code review, Unit, Integration, and system-level test implementation.</li><li>Serve as a technical liaison among project leads/managers, developers, and stakeholders.</li><li>Diagnose and resolve highly complex issues of the application.</li></ul><h4><strong>Secondary skills</strong></h4><ul><li>Experience with RDBMS like SQLite, MySQL.</li><li>Experience in QT application software Design and Development (familiar with QT Core, QT GUI, QT Widgets, QT QML, QT Creator IDE).</li><li>Experience in programming for microprocessor/microcontroller-based embedded devices.</li><li>Experience with agile software development process during product development.</li><li>Experience in Linux programming concepts (Process, Threads, Semaphore, Mutex, IPC, signal handling, exception handling, networking protocols).</li></ul><h4><strong>Behaviours &amp; Aptitude</strong></h4><ul><li>Excellent interpersonal and written communication skills in English.</li><li>Good time-management skills.</li></ul><h4><strong>We are Looking for You with</strong></h4><ul><li>Qualification - B.E. / M.E (Computer Science/ IT /Electronics) or equivalent higher-level degree.</li><li>Technical Certifications - A Certified software architecture course will be an added advantage</li></ul>

Software Architect- C++

<p><strong>Waters Corporation is a global leader in analytical instruments, separations technologies, and software, serving the life, materials, food, and environmental sciences for over 65 years. Our Company helps ensure the efficacy of medicines, the safety of food and the purity of water, and the quality and sustainability of products used every day. In over 100 countries, our 7,600+ passionate employees collaborate with customers in laboratories, manufacturing sites, and hospitals to accelerate the benefits of groundbreaking science.&nbsp;</strong></p><h3><strong>Design Quality Assurance Engineer</strong></h3><h4><strong>Overview</strong></h4><p>Waters, the world's leading speciality measurement company that cares about inclusion and diversity, is recruiting for a <strong>Design Quality Assurance Engineer</strong> to be positioned in Wilmslow, Cheshire, UK. This position will have a <strong>hybrid work schedule</strong> (three days per week on-site).</p><p>Clinical Design Quality supports the development of all new IVD products in compliance with applicable regulatory standards/systems, including ISO 13485, ISO 9001, IVDR 2017/746 &amp; 21CFR 820. The role provides support and enables the delivery of the product roadmap by evaluation and monitoring of product design and development activities, including Risk Management, for Waters Clinical Business Unit [IVD devices, RUO products and non-IVD products] to ensure conformity to Waters and regulatory requirements, plus input into continual improvement of processes and working practices.</p><p>Also supports post-market activities (e.g. product release, design changes, non-conformances, CAPA, complaints, post-market surveillance), regulatory documentation creation and maintenance, supplier management, auditing and general Quality Management System (QMS) activities.</p><h4><strong>Responsibilities</strong></h4><ul><li>Act as Quality specialist in relation to design and development ensuring conformance and up-to-date information on applicable regulatory requirements including as appropriate: ISO 9001; ISO 13485; 21 CFR parts 11 and 820, IEC 62304, IEC 62366, ISO 14971.</li><li>Collaborate with Design Quality Engineers, Clinical on design control requirements and approach</li><li>Provide mentorship on industry methods for implementing process changes to improve quality system compliance.</li><li>Evaluate the acceptability of products for release, ensuring customer requirements /specifications and internal Waters policies and procedures are met.</li><li>Offer mentorship and direction on all quality tasks crucial for improving quality standards to ensure consistency in advancing work, especially work related to product safety, usability, risk management, alignment, product performance, and registration.</li><li>Participate in developing, reviewing, and approving requirements for product development, risk management, maintenance, and problem resolution.</li></ul><h4><strong>Qualifications</strong></h4><h5><strong>Education:</strong></h5><ul><li>A Bachelor's Degree or equivalent experience required, in Chemistry, Medical, or Science, is preferred.&nbsp;</li></ul><h5><strong>Experience:</strong></h5><ul><li>Proven experience in quality assurance activities - ISO 13485, ISO 14971, IEC 62304, IEC 62366 and applicable good manufacturing practice regulations, including 21 CFR part 820.</li><li>Demonstrated expertise in the application of design controls and risk management, including design transfer, process validation and process control plans.</li><li>Desired – product development in a medical device environment</li></ul><h5>Proficiencies:</h5><ul><li>A practical approach towards problem-solving</li><li>Be capable of working independently and as part of a multi-functional team, balancing multiple tasks and prioritizing to meet high demands and tight deadlines.</li><li>Strong organization/prioritization skills</li><li>Strong interpersonal skills in verbal and written communication required for clear report writing and effective interaction with colleagues and peers.</li><li>Computer literate, preferably with knowledge of software packages such as Microsoft 365, Atlassian, and SAP.</li></ul><p>In addition to salary, we work flexibly and provide 25 days' holidays, excellent family-friendly benefits such as attractive employer pension contribution, life assurance, income protection and private medical. With Waters, there are plenty of opportunities for you to grow, develop and contribute.</p>

Design Quality Assurance Engineer

<p><strong>Waters Corporation is a global leader in analytical instruments, separations technologies, and software, serving the life, materials, food, and environmental sciences for over 65 years. Our Company helps ensure the efficacy of medicines, the safety of food and the purity of water, and the quality and sustainability of products used every day. In over 100 countries, our 7,600+ passionate employees collaborate with customers in laboratories, manufacturing sites, and hospitals to accelerate the benefits of pioneering science.</strong></p><h3><strong>Senior Software Engineer, Clinical</strong></h3><h4><strong>Overview</strong></h4><p>Waters’ Clinical Systems Development Software team is seeking <strong>skilled and collaborative Senior Software Engineers</strong> who enjoy solving complex problems, exploring innovative solutions, and building impactful products. Based in our modern Wilmslow facility, this role focuses on developing software for the clinical market segment, ideally with experience in:</p><ul><li>C#/.NET</li><li>Python</li><li>Angular</li><li>Database technologies</li></ul><h5><strong>About the Team</strong></h5><p>Clinical Systems Development is responsible for creating Waters’ Clinical and In-Vitro Diagnostics (IVD) systems — both hardware and software. Our mission is to deliver meaningful customer benefits through the evaluation, development, and deployment of innovative clinical system capabilities.</p><p>As part of this team, you’ll help build software used globally by scientists and clinical professionals for advanced scientific analysis. You’ll work alongside a multidisciplinary group of software engineers, R&amp;D scientists, evaluators, and hardware developers — we thrive on collaboration and shared learning.</p><p>Whether or not you come from a scientific background or have experience with every technology listed, if you're enthusiastic about software engineering and eager to grow, we’d love to hear from you.</p><h5><strong>What We Offer</strong></h5><ul><li>A personalised development plan supported by your manager, including access to training and learning opportunities.</li><li>Flexible working hours and a hybrid model</li><li>Competitive salary.</li><li>32 days paid annual leave (including UK bank holidays) with opportunity for holiday buy back.</li><li>Private health and dental insurance.</li><li>Contributory pension scheme.</li><li>Subsidised on-site gym, restaurant, and social/cultural activities.</li><li>Employee Assistance Program (EAP).</li><li>On-Site electric vehicle charging.</li></ul><h4><strong>Responsibilities</strong></h4><ul><li>Develop clean, maintainable, scalable, and secure code using C#/.NET, Angular, JavaScript, TypeScript, and Python.</li><li>Apply SOLID principles, TDD, and CI/CD practices.</li><li>Collaborate with QA engineers and evaluators to ensure high-quality outputs.</li><li>Take ownership of technical challenges and contribute to effective solutions.</li><li>Communicate clearly with technical and non-technical stakeholders.</li><li>Support continuous integration and delivery frameworks.</li><li>Contribute to team growth and continuous improvement in Agile/Kanban environments.</li></ul><h4><strong>Qualifications</strong></h4><p>We’d love to hear from you if you have:</p><ul><li>Proven experience in software development with technologies such as C#, .NET, Angular (or similar), TypeScript, and Python.</li><li>Practical knowledge of software engineering best practices, including <strong>TDD (required)</strong>, Unit Testing, CI/CD, and SOLID principles.</li><li>A degree in a relevant field or equivalent industry experience.</li></ul><h5><strong>Our Commitment to Inclusion</strong></h5><p>We’re actively building diverse teams and fostering an inclusive environment where everyone can thrive. We celebrate our differences and believe our teams should reflect the communities we serve.&nbsp;</p><p>We’re happy to make reasonable adjustments to our interview process to support your needs.&nbsp;</p><p>Please feel free to ask about hybrid working and flexibility during the recruitment process — we’ll do our best to accommodate.&nbsp;</p>

Senior Software Engineer, Clinical

Lab technician

Liquid chromatography-mass spectrometry

Scientific and Research Fellow

Sales Representative

Academic staff

Laboratory services

Service engineer

Manager

Software

Molecular biology

Product Specialist

Application Specialist

Molecular spectroscopy UV-Vis, RAMAN, FTIR

Marketing

Analytical chemist

Technologist/Engineer

Laboratory instruments

Spectroscopy

Chemist

Quality Control (QC)

Microbiology

Liquid chromatography

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