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<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><p>Agilent is a global leader in laboratory and clinical technologies; we are passionate about bringing great science to life. &nbsp;Our commitment to quality and innovation supports cutting-edge life science research, patient diagnostics, and ensures the safety of water, food, and pharmaceuticals. As scientists and clinicians pursue small, everyday advances and life-changing discoveries, we provide trusted answers to their most critical questions and challenges. We can’t wait for you to join us as we continue our mission to improve the world around us</p><h3><strong>Gas Phase Application Engineer</strong></h3><h4><strong>Job Description</strong></h4><ul><li>Assists sales account managers and product specialists to meet or exceed sales quota by providing sales and customers with technical/scientific expertise, primarily in the areas of application and technical support.</li><li>May be client or product oriented.</li><li>Contributes to sales account planning.</li><li>Participates actively in the sales process from deal qualification to deal closure.</li><li>Owns the deal’s technical closure.</li><li>Responsible for meeting sales targets and for supporting sales organizations to meet targets.</li><li>Is knowledgeable of competition and able to identify lockout specifications (identify Agilent's competitive advantage over competition).</li><li>Analyzes customer requirements and recommends appropriate solutions.</li><li>Collaborates with the sales team in the development of technical sales strategies.</li><li>Evaluates and supports management on ramp to volume strategies for new products prior to release.</li><li>Is responsible for demos and for enhancing customers’ experience and satisfaction.</li><li>Provides training to the sales force.</li><li>Acts as the customer voice to influence future product/application design that meets customer needs, including writing application briefs to highlight product capabilities.</li><li>Prepares and delivers technical seminars to customers or potential customers and contributes to recognized scientific forums, including written, oral and poster presentations.</li><li>May also contribute to post-sales activities.</li></ul><h4><strong>Qualifications</strong></h4><ul><li>Bachelor's or Master's Degree in Chemistry or equivalent.</li><li>Minimum 8 years operational experience of GC/GCMS.</li><li>Method development/optimization skills involving GC/GCMS.</li><li>Excellent verbal and written communication skills.</li><li>Great presentation skills.</li></ul><p>Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity 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.</p><ul><li><strong>Travel Required:</strong> Yes</li><li><strong>Schedule:</strong> 50% of the Time</li><li><strong>Shift:</strong> Day</li><li><strong>Duration:</strong> No End Date</li><li><strong>Job Function:</strong> Sales</li></ul>

Gas Phase Application 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>Senior QC Chemist</strong></h3><div><div><div><section><div><div><div><div><div><p>As a Senior Chemist, you will play a vital role in delivering world-class analytical solutions through outstanding expertise in biologic chemistry. Your work will significantly impact our ambitious projects, ensuring flawless quality control operations that meet regulatory compliance and data integrity principles. You will collaborate closely with other functions, promoting a proactive business partnership to successfully implement method qualifications and validation strategies.</p><h3><strong>Responsibilities</strong></h3><ul><li>Support new equipment qualification, lab computerized systems, and chemistry lab setup.</li><li>Perform transfer, verification, and validation of laboratory procedures.</li><li>Prepare technical documentation, including protocols, analytical write-ups, standard operating procedures, specifications, investigations, and reports.</li><li>Analyze incoming goods, intermediates, and finished products under cGMP conditions for QC release and stability studies.</li><li>Lead the testing process from sampling to the release of raw materials, drug substances, process aids, and packaging materials.</li><li>Ensure timely and compliant testing of all chemistry-related analyses, including HPLC, GC, and stability analysis.</li><li>Manage daily laboratory operations, ensuring compliance with GMP standards.</li><li>Identify and address compliance gaps with updated pharmacopoeia and regulations.</li><li>Lead laboratory investigations, deviations, and ensure timely closure in line with quality management systems.</li><li>Review analytical and laboratory data for accuracy and compliance.</li><li>Perform maintenance and calibrations on laboratory equipment.</li><li>Troubleshoot technical issues related to analytical equipment and methods.</li><li>Manage QC chemical, reference standard, and consumable stock levels.</li><li>Train fellow chemists, serving as a mentor and expert.</li><li>Maintain a detailed understanding of international regulatory requirements.</li><li>Communicate effectively with cross-functional teams and participate in problem-solving activities.</li><li>Act as a Subject Matter Expert during audits and inspections.</li><li>Undertake internal audits and support continuous improvement initiatives.</li><li>Promote a culture of quality and adherence to cGMP, EHS, and 5S standards.</li><li>Be prepared to support shift work if needed.</li></ul><h3><strong>Minimum Requirements/Qualifications</strong></h3><h4><strong>Education:</strong></h4><ul><li>University degree or equivalent experience in chemistry, biochemistry, or life sciences.</li></ul><h4><strong>Experience:</strong></h4><ul><li>At least 7 years of proven experience in the pharmaceutical or medical devices industry, with a focus on Quality Control.</li><li>Extensive knowledge of regulatory expectations including PICS, ICH, Singapore HSA, EMA, and US FDA.</li></ul><h4><strong>Proficiencies:</strong></h4><ul><li>Knowledge and exposure to cGMP environment.</li><li>Sound technical knowledge of QC chemistry techniques (HPLC, UPLC, CE, etc.).</li><li>Strong interpersonal and communication skills in English.</li><li>Ability to work cross-functionally and meet timelines and objectives.</li><li>Experience with Health Agency/internal audits.</li></ul></div></div></div></div></div></section></div></div></div><h4><strong>Work Schedule</strong></h4><ul><li>Standard (Mon-Fri)</li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li><span>Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials</span></li></ul>

Senior QC Chemist

<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>Mass Spectrometry R&amp;D Manager</strong></h3><h4><strong>Job Description</strong></h4><div><p>We are looking for an R&amp;D Project manager to join the fast-paced Agilent Mass Spectrometry R&amp;D Team. As an R&amp;D Project Manager in the Agilent Mass Spec Division, you will lead one or more project teams involved in the investigation, development, productizing, and support of existing and new Mass Spectrometry technologies, processes, and products. The ideal candidate will have experience with Mass Spectrometry design and/or manufacturing as well as team management and personnel development.</p><h4><strong>Responsibilities include:</strong></h4><ul><li>Partner with cross-functional leaders within Agilent including marketing, engineering, application development, manufacturing, quality, product support, and sales to achieve business objectives.</li><li>Work closely with the Mass Spectrometry Marketing team to effectively meet new product introduction goals.</li><li>Establishing and maintaining close coordination with other business units within Agilent.</li><li>Participating as part of the Agilent Mass Spectrometry leadership team to handle the project and product portfolio, set direction, and promote a culture that supports calculated risk-taking, and interdisciplinary problem-solving and emphasizes changes that “make a difference” for the company and the industry.</li><li>Lead, motivate and develop a cross-disciplinary team of 5-8 scientists and engineers. Coaching and developing team members to expand the team’s capabilities and professional satisfaction.</li><li>Balancing a technology development focus with future market or business needs and manufacturing capabilities.</li><li>Coordinating both near-term and long-term development programs.</li></ul><h4><strong>Qualifications</strong></h4><ul><li>Bachelor Degree in Engineering, Chemistry, Physics, or equivalent with over 10 years of experience.</li><li>Experience working in multidisciplinary teams, spanning physics, mechanical design, electronics, firmware development, manufacturing, and process development.</li><li>Excellent people management and interpersonal skills. Ability to be a mentor and an advocate for the members of your team. A proven track record of setting measurable and achievable goals and managing to achieve them.</li><li>Strong interpersonal skills. Be able to demonstrate the ability to set priorities based on alignment with business goals and strategic direction, define timelines and deliver to commitments.</li><li>Demonstrated ability to make practical tradeoffs of resources, design, and testing to meet time-critical objectives.</li><li>Must exhibit critical thinking, teamwork, creativity, planning, and execution skills backed by strong analytical and decision making.</li></ul><h5><strong>Desired:</strong></h5><ul><li>Prior experience leading a team of technical specialists (Ph.D., MS. and BS. level <span style="text-decoration:inherit;">Engineers/Scientists)</span> engaged in technology or product development</li><li>Experience with some type of analytical instrumentation development and in at least one aspect of mass spectrometer system design.</li><li>Involvement in at least one project that led to a successful commercial product introduction, preferably in a leadership role.</li><li>Good verbal, written, and presentation communication skills.</li></ul><h4><strong>Additional Details</strong></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: <span style="text-decoration:inherit;">https://careers.agilent.com/locations</span></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>25% of the Time</p><p><strong>Shift: </strong>Day</p><p><strong>Duration: </strong>No End Date</p><p><strong>Job Function: </strong>R&amp;D</p></div><p><a target="_blank" rel="noopener noreferrer" href="https://agilent.wd5.myworkdayjobs.com/en-US/Agilent_Careers/job/Singapore-Yishun/Mass-Spectrometry-R-D-Manager_4034780/apply"><strong>Apply</strong></a></p>

Mass Spectrometry R&D Manager

<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>Chemist I</strong></h3><p>Reporting to the QC Manager Chemistry, the role is responsible for writing laboratory procedures, transfer/verification/validation of methodology, and project work within the department to support manufacture and release of pharmaceutical raw materials, intermediates and products. The role contributes to building and maintaining QC lab cGMP system, delivers analytical solution to clients through specific method qualification and validation strategies while ensuring timely delivery for projects. The role will include performing testing for incoming materials, in-process products and DS testing, etc.</p><h4><strong>Responsibilities:</strong></h4><ul><li>To support new equipment qualification, lab computerized system and chemistry lab set up</li><li>To perform transfer/verification/validation of laboratory procedures within the team where required</li><li>To prepare technical documentation including but not limited to protocols, analytical write-ups, standard operating procedures, specifications, investigations and reports.</li><li>To perform analysis of incoming goods, intermediates and/or finished products (including HPLC and GC) under cGMP conditions for QC release or as part of stability studies.</li><li>To review analytical and laboratory data within the department for accuracy, completeness and compliance with documented procedures.</li><li>To perform planned preventative maintenance and performance calibrations on equipment.</li><li>Management of QC chemical, reference standard and consumable stock levels</li><li>To maintain own training records</li><li>To communicate optimally with others on site</li><li>Participate/contribute in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab</li><li>Support and encourage a “Quality Culture” and company 4i values throughout QC</li><li>Ensure cGMP is applied in their area of work and align with cGMP in all areas of the business.</li><li>To work with HSE, cGMP and 5S in mind at all times.</li><li>Undertake ad-hoc activities that may be required by the business</li><li>To support shift work (if necessary) in future</li></ul><h4><strong>Minimum Requirements/Qualifications:</strong></h4><ul><li>Degree in Chemistry or strongly related scientific field</li><li>At least 2 years relevant industrial experience</li><li>Ability to apply GMP regulations and other international guidelines to all aspects of the position.</li><li>Ability to work independently and adhere to critical timelines</li><li>Excellent attention to detail</li></ul>

Chemist I

<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>Chemist I (12 hours rotating shift)</strong></h3><p>Be part of our Quality Control team at Thermo Fisher Scientific, where you'll contribute by ensuring the quality and reliability of products that help make the world healthier, cleaner and safer. You'll perform testing and analysis to support the development of innovative therapeutic products. You'll conduct quality control testing of raw materials, in-process samples, and finished products using various analytical techniques. You'll document and analyze test results, participate in investigations, and contribute to continuous improvement initiatives. This role offers opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.</p><h4><strong>Laboratory Testing &amp; cGMP Compliance</strong></h4><ul><li>Perform accurate and precise QC testing on a variety of samples including raw materials, incoming goods, in-process intermediates, and finished products in strict compliance with current Good Manufacturing Practices (cGMP).</li><li>Execute analytical methods primarily using techniques such as HPLC, GC, UV-Vis, FTIR, titration, and dissolution testing as per approved pharmacopoeial (e.g., USP, EP) or internal specifications.</li></ul><h4><strong>Documentation &amp; Quality Systems</strong></h4><ul><li>&nbsp;Author, review, and lead the preparation of high-quality technical documents including Standard Operating Procedures (SOPs), test methods, protocols, risk assessments (e.g., FMEA), and technical position papers.</li><li>Conduct thorough laboratory investigations for out-of-specification (OOS), out-of-trend (OOT), and aberrant results. Write detailed investigation reports, identify root causes, and implement effective corrective and preventive actions (CAPA) to prevent recurrence.</li><li>Manage deviations and non-conformances within the Quality Management System (QMS), ensuring they are documented, investigated, and closed in a timely manner.</li><li>Perform periodic reviews of laboratory documents (e.g., SOPs, test methods) to ensure they remain current, accurate, and reflective of actual practices.</li></ul><h4><strong>Methodology &amp; New Product Introduction</strong></h4><ul><li>Provide active support for method transfer, verification, and validation activities for new product introductions. This includes executing validation protocols, analyzing data, and co-authoring validation reports to ensure methods are suitable for their intended use.</li><li>Assist in troubleshooting method-related issues and contribute to method improvement and optimization initiatives.</li></ul><h4><strong>Laboratory Operations &amp; Continuous Improvement</strong></h4><ul><li>Manage the inventory of QC laboratory chemicals, reference standards, and critical consumables. Conduct regular stock checks, place orders, and ensure materials are received and stored correctly with proper documentation.</li><li>Maintain the laboratory in an audit-ready state, adhering to 5S principles and all Health, Safety, and Environmental regulations.</li><li>Actively participate in and contribute to continuous improvement initiatives, such as Practical Process Improvement projects, to enhance laboratory efficiency, quality, and safety.</li><li>Maintain personal training records to ensure full compliance with all required procedural and technical training.</li></ul><h4><strong>REQUIREMENTS:</strong></h4><ul><li>Bachelor's degree, no prior experience required. Experience in quality control laboratory environment, preferably in pharmaceutical/biotech industry preferred</li><li>Minimum of 2 years of relevant industrial experience within a cGMP-regulated environment, preferably in pharmaceuticals, biotechnology, or medical devices.</li><li>Strong knowledge of cGMP, GLP, and quality management systems</li><li>Proficiency in analytical techniques such as HPLC, ICP-MS, UV-Vis spectroscopy, and dissolution testing</li><li>Ability to follow SOPs and maintain detailed documentation per GDP requirements</li><li>Strong computer skills including LIMS, Microsoft Office, and analytical software</li><li>Excellent attention to detail and organizational skills</li><li>Strong analytical and problem-solving capabilities</li><li>Ability to work both independently and collaboratively in a team environment</li><li>Clear written and verbal communication skills</li><li>Experience with laboratory equipment maintenance and calibration</li><li>Knowledge of relevant pharmacopeia standards and regulatory requirements</li><li>Ability to manage multiple priorities effectively</li><li>Flexible scheduling may be required</li></ul><h4><strong>Work Schedule</strong></h4><ul><li><strong>12 hr shift/days</strong></li></ul><h4><strong>Environmental Conditions</strong></h4><ul><li>Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials</li></ul>

Chemist I 

Lab technician

Liquid chromatography-mass spectrometry

Scientific and Research Fellow

Sales Representative

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)

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