ANALYTICAL CHEMIST JOB DESCRIPTION

An analytical chemist in pharma turns raw samples into release decisions. The work spans bioanalytical method validation under GLP, GMP release testing of in process materials, and impurity profiling tied to ICH and FDA submission standards. Some labs require BSL2 clearance for sterile product handling, while others center on liquid chromatography purity assays for biologics like nucleic acids and proteins. The job sits at the point where a compound stops being a hypothesis and becomes a documented, defensible result.

As the Analytical Chemist, you own method development, validation, and routine testing that determines whether a batch meets release criteria under GMP and GLP frameworks. The role reports into quality or analytical development, working alongside QC technicians and regulatory teams to keep submissions and disposition decisions on schedule.

Career Impact: Hands-on validation work under ICH and FDA regulated frameworks builds a qualification record that travels across pharma and biotech employers.

Business Impact: Accurate impurity and purity assay results directly determine whether a batch of drug product can be released to patients.

Growth Opportunity: Experience with bioanalytical extraction from biological fluids opens a path toward senior method development or regulatory affairs roles.

• Develop liquid chromatography methods for purity and impurity analysis across biological and drug product matrices.
• Validate analytical and bioanalytical test methods to support GMP release of raw materials and finished products.
• Document experimental methods and conclusions in laboratory notebooks to preserve data integrity.
• Review analytical data for product stability and release, flagging out of specification results.
• Investigate non-conformances and out of trend results, escalating to quality teams as needed.
• Author and revise SOPs, validation protocols, and certificates of analysis for regulatory readiness.
• Coordinate daily testing priorities with department timelines to support submission deadlines.

• Bachelor's degree in Chemistry, Biochemistry, or a related discipline, or equivalent work experience.
• 1 or more years of pharmaceutical analytical development experience, with hands-on chromatography exposure.
• Direct experience with liquid chromatography techniques such as RP-HPLC, SEC, or IEX for purity testing.
• Working knowledge of cGMP and GLP documentation practices in a regulated lab.
• Strong critical thinking applied to recognizing and resolving analytical problems.
• Effective oral and written communication for technical reports and presentations.
• Ability to coordinate daily lab activities against department priorities and timelines.

• Experience with mass spectrometry techniques applied to impurity or structural characterization.
• Bioanalytical method development experience involving extraction from biological fluids or tissues.
• Familiarity with ICH, FDA, and EU regulatory guidelines for pharmaceutical testing.
• Experience handling sterile products or working in a BSL2 laboratory setting.

• Method validation cycle time, measuring days from protocol draft to approved validation report.
• Percentage of batches released without OOS investigation, reflecting testing accuracy.
• Number of non-conformances documented per quarter, tracking data integrity discipline.
• SOP and validation protocol turnaround time, measuring documentation throughput.
• Audit observations tied to analytical records, reflecting regulatory readiness of lab documentation.

• Base Salary Range: 60,000 to 85,000 USD annually for entry to mid level.
• Bonus: Annual performance bonus of 3 to 8 percent of base salary.
• Equity: Rarely offered outside larger biotech employers.
• Health Benefits: Medical, dental, and vision coverage typically employer subsidized.
• PTO: 15 to 20 days annually, plus standard holidays.
• Common Perks: Tuition assistance and lab certification reimbursement.

Figures are estimates based on general US market benchmarks and may be outdated. Adjust based on location, company size, and seniority level.

Employment with this organization is contingent upon successful completion of a background check. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or veteran status, in accordance with applicable federal, state, and local law. Reasonable accommodations are available upon request for qualified individuals with disabilities throughout the application process. Candidates must be authorized to work in the United States without employer sponsorship.

The Analytical Chemist owns research efforts in gas chromatography techniques such as GC/MS, headspace analysis, and pyrolysis to support new product development and competitive analysis for Lubrizol Additives technology groups. Partnering with internal and external customers and technical staff, the Analytical Chemist drives projects from inception through completion while mentoring junior staff and maintaining safety standards.

Key Responsibilities

• Apply knowledge of and lead research efforts in gas chromatography techniques including GC, GC/MS, headspace analysis, GCxGC, and pyrolysis to support new product development.
• Generate, organize, interpret, and report data in support of technical projects and service requests.
• Perform hands-on research and direct and prioritize the work of technical staff.
• Proactively seek understanding of customer needs.
• Convey technical information across departments and divisions.
• Drive projects from inception through completion.
• Maintain familiarity with current literature and advances in relevant analytical techniques.
• Integrate new technology for new applications and product support.
• Troubleshoot and maintain test equipment and procedures.
• Participate in the recruitment, training, and mentoring of technical staff.

Required Qualifications

• PhD in Chemistry with 2 or more years of relevant industrial experience, or M.S. in Chemistry with 5 or more years of relevant industrial experience.
• PhD in Analytical Chemistry with a focus in separation sciences preferred.
• Experience writing technical reports of publication quality.
• Demonstrated project management experience including managing multiple projects simultaneously.
• Experience with odor analysis.
• Strong interpersonal skills with demonstrated ability to build relationships across organizational levels.
• Self-motivated with ability to organize and prioritize multiple tasks under pressure to meet deadlines.

Embedded within the GMP quality team, the Analytical Chemist delivers development, validation, and method transfer of analytical and bioanalytical test methods to support release of raw materials and finished radiopharmaceutical products. Working closely with QC technicians and regulatory stakeholders, the Analytical Chemist ensures sterile and compliant test methods across HPLC, GC, and TLC platforms.

Core Functions

• Conduct quality control testing of raw materials and finished radiopharmaceutical products using HPLC, GC, TLC, pH, IRF, ELISA, bacterial endotoxin testing, sterility testing, and bioburden testing.
• Calibrate and maintain lab equipment including refrigerators, freezers, incubators, HPLCs, and GCs.
• Manage inventory of QC materials and maintain eukaryotic cell lines.
• Develop, transfer, troubleshoot, and validate analytical methods.
• Investigate out-of-specification or out-of-trend results and document non-conformances.
• Write, revise, and review technical documents including SOPs, test methods, validation protocols, and reports.

Qualifications & Experience

• Degree in Biology, Biological Chemistry, Biotechnology, or related discipline, M.Sc. or Ph.D preferred.
• 5 or more years of hands-on experience in a pharmaceutical GMP environment with HPLC, GC, and TLC.
• Experience in QC testing, method development, and validation, including documentation of assay methods.
• Experience working with sterile products and in a BSL2 laboratory is an asset.
• Knowledge of UV, IR, mass spectrometry, and NMR is an asset.
• Knowledge of microbiological testing including bioburden, sterility, and bacterial endotoxins is an asset.
• Proficiency with spreadsheets such as Excel and Google Sheets.
• Good writing skills with ability to produce technical documents, reports, and presentations.
• Excellent communication skills in English with ability to work independently and cooperatively in a team.

Reporting to the Regulatory and Quality team, the Analytical Chemist owns the investigation of small molecules, flavors, and compounds of novel proteins and fermentation products using HPLC, IC, MS, GCMS, and FTIR. Partnering with Product Development, Manufacturing, and R&D, the Analytical Chemist investigates root causes of organoleptic properties to ensure product quality at the Chicago, IL facility.

Primary Duties

• Investigate novel food ingredients, flavors, and compounds.
• Develop, validate, and verify qualitative and quantitative methodology.
• Work cross-functionally with Product Development, Manufacturing, R&D, and Quality teams to investigate root causes of organoleptic properties.
• Identify and manage analytical testing instrumentation.
• Provide accurate documentation of lab and testing activities.
• Prepare and present clear communications detailing research and testing results.

Skills & Qualifications

• 7 or more years of experience working in food ingredients, flavorings, or sensory testing.
• Experience developing, validating, and implementing quantitative and qualitative analytical methods for food testing.
• Experience working with LC, IC, GC, MS, and other analytical instrumentation.
• Demonstrated ability to prioritize and manage complexity.
• Ability to accurately plan, define, and manage project tasks.
• Excellent written and verbal communication skills.
• Ability to work effectively in a team and influence technical direction.
• Detail-oriented, organized, and able to meet deadlines.
• Demonstrated history of laboratory safety culture.

Sitting at the intersection of analytical chemistry and silicone product commercialization, the Analytical Chemist builds analytical methods for immediate application across global business units. Operating across R&D teams and extended global analytical stakeholders, the Analytical Chemist trains new staff while fostering a culture of safety and continuous scientific engagement.

Functions

• Provide timely analytical support to multiple business units in the silicone business.
• Develop analytical methods for immediate application and adaptation by other laboratories.
• Communicate analytical ideas, data, and results to key stakeholders verbally and through detailed reports.
• Influence and positively engage with the extended global analytical team and other stakeholders.
• Interact with R&D scientists to develop innovative analytical solutions.
• Foster a safety culture through active participation in safety initiatives.
• Train and supervise new employees and technicians.
• Participate in scientific organizations to enhance career and company brand.

Requirements

• Ph.D. in Analytical Chemistry or related discipline.
• More than 3 years of industrial or postdoctoral experience preferred.
• Expert level skills troubleshooting and maintaining analytical instrumentation.
• Experience in chromatography, spectroscopy, and thermal analyses.
• Self-motivated with ability to work independently and collaboratively.
• Excellent problem-solving and communication skills with willingness to take initiative.

A key member of the R&D method development team, the Analytical Chemist builds and validates analytical test methods for HPLC and GC in a contract capacity. Collaborating across a highly regulated R&D setting, the Analytical Chemist executes method transfer and validation protocols while maintaining detailed records.

Accountabilities

• Develop, validate, and transfer analytical test methods for HPLC and GC in an R&D setting.
• Operate and perform basic maintenance of lab equipment.
• Create test methods for analytical instruments.
• Maintain detailed records in a highly regulated R&D setting.
• Execute method transfer and validation protocols.
• Prepare necessary reporting.

Experience & Qualifications

• Bachelors or Masters in Chemistry or Analytical Chemistry, industry experience more important than education.
• 2 or more years of method development experience in a regulated industry such as pharma, cosmetics, or consumer goods.
• Industry experience focusing on HPLC and GC instruments.
• Experience in a fast-paced GMP and FDA environment.
• Good communication skills and ability to collaborate with others.
• A hands-on approach to solving problems.
• Ability to work in a contract role in the US for any employer.

Quality compliance across raw materials, packaging components, and finished products depends on the Analytical Chemist, who carries out testing according to USP/NF, FCC, and JSCI Pharmacopoeia standards. Based within the quality lab, the Analytical Chemist escalates events impacting product quality and supports validation activities under cGMP and ISO frameworks.

Activities

• Carry out the testing and analysis of raw materials, packaging components, intermediate batches, packaging, and finished products in a timely manner.
• Support routine raw material, packaging material, bulk, and finished product disposition decisions.
• Follow reduced testing programs and annual full testing using USP/NF, FCC, JSCI Pharmacopoeia, and other methodology.
• Check relevant documentation as part of raw material analysis and communicate with the responsible person regarding missing documentation.
• Enter test results in laboratory notebooks and internal data systems such as SLIMS and SAP.
• Escalate events with potential impact on product quality, safety, compliance, EHS, or laboratory cycle time to senior personnel.
• Support troubleshooting and investigation of out of specification results.
• Support method and product transfer, NPI activities, and execution of test method validation protocols.
• Prepare and document test solutions and standards and ensure proper storage.
• Clean, maintain, calibrate, and support validation of laboratory equipment.
• Order chemicals and consumables from appropriate suppliers.
• Participate in cross-functional teams and support Operational Excellence initiatives.
• Lead by example in EHS and Quality culture initiatives.

Technical Qualifications

• Associate of Science Degree required, Bachelor of Science Degree preferred, in an applicable scientific discipline.
• Working laboratory experience, preferably with FMCG experience.
• Experience implementing Quality Systems in regulated environments.
• Experience writing, reviewing, and revising SOPs.
• Working knowledge of Quality standards, GLP and GMP requirements, validations, calibration systems, and instrumentation.
• Problem solving and continuous improvement skills.
• High computer literacy with Microsoft Word, Excel, and Laboratory Information Systems such as SLIMS.
• Familiarity with statistical software such as Statistica.
• Developed coaching, interpersonal communication, team building, and training facilitation skills.
• Excellent written and oral communication and ability to interact with all levels of the organization.
• Ability to set priorities and work on multiple projects simultaneously in a team-based environment.

As the Analytical Chemist at ESS, this role measures chemical compositions and material properties of samples while supporting raw material testing, quality checks, and long-term stability studies. The Engineering and Manufacturing teams rely on this work to monitor chemical processes and resolve failure analysis issues across the facility.

Operational Focus

• Help R&D scientists and engineers in researching, developing, and producing chemical products and processes.
• Provide analytical testing support to R&D, Engineering, and Manufacturing.
• Monitor chemical processes and utilize analytical techniques to support manufacturing, quality, defects, and failure analysis.
• Conduct chemical experiments including measuring chemical compositions, pH, and titrations, and prepare chemical solutions.
• Test chemical products to ensure they meet specifications and check for impurities.
• Clean, calibrate, maintain, install, troubleshoot, repair, and operate laboratory equipment such as TGA, FTIR, chromatography, and UV-Vis.
• Conduct physical experiments, tests, and analyses.
• Train technicians on technique, analytical methods, and best practices.
• Build and revise LIMS and maintain accurate records.
• Expand analytical capability, develop new test methods, and review sample load and resources.
• Determine testing needs for unique samples, coordinate with outsource test labs, and communicate results to meet R&D needs.
• Review and report on material degradation and communicate test results across departments.
• Write and revise reports, SOPs, specifications, and experimentation documents.
• Manage multiple projects and prioritize tasks.

Position Requirements

• BS in Chemistry, Chemical Engineering, Environmental Chemistry, Biology, or similar discipline, BS or MS in Analytical Chemistry preferred.
• 2 or more years of professional experience in an analytical or quality control environment.
• Experience testing chemicals and materials with wet chemistry techniques and comfort working with acids and bases.
• Experience managing projects or teams, and in method and product development.
• Knowledge of material science or electrochemistry.
• Experience with root cause analysis, contamination analysis, and long term stability testing and vendor validation.
• Strong attention to detail and ability to work from standard operating procedures.
• Proficient with MS Office programs including Word, Excel, Outlook, PowerPoint, and SharePoint.
• Experience with Oracle and Vault applications.
• Good interpersonal and communication skills to work effectively with a small, dynamic team.
• Ability to recognize trends outside of expected results.

Analytical Chemist guides product quality investigations by comparing analytical results to specifications across Brewing, Batching, and Packaging operations, escalating concerns to operating and senior management. Success in the position means resolving customer complaints and ensuring co-packer operations remain within desired parameters through sensory evaluation and stability testing.

Day-to-Day Responsibilities

• Learn and understand processes throughout the facility to assist with troubleshooting and determining root cause.
• Evaluate finished goods quality and audit production processes to ensure specifications are met.
• Troubleshoot and resolve product quality issues, including initiating and monitoring corrective actions.
• Manage non-conforming products to ensure they are not released without further analysis and approval.
• Contribute to developing quality specifications and clearly display data.
• Operate and maintain lab equipment including Alcolyzer, DMA, pH meters, GC, HPLC, and spectrophotometer.
• Manage laboratory inventory and sample retains.
• Participate in sensory evaluation and taste panels.
• Support primary and secondary packaging material development and improvement initiatives.
• Conduct product integrity and stability testing.

Background & Experience

• Bachelor's Degree in Chemistry, Chemical Engineering, or Biochemistry required.
• TTB certified chemist preferred.
• 3 to 5 years of QA experience, with 1 to 3 years in food, carbonated beverage, or alcohol highly preferred.
• Experience managing and performing micro and sensory analysis preferred.
• Working knowledge of current regulatory policy relative to raw materials, ingredients, products, and processes.
• Proficiency in good lab practices including sample prep, handling, and record keeping.
• Strong experience with instrument calibration, maintenance, and control charts.
• Statistical process control skills and use of statistical analysis software preferred.
• Proficiency with Excel, Microsoft Office, and Word.
• Strong analytical skills with attention to detail and accuracy.
• Ability to prioritize and multitask in a fast-paced environment.

Reporting to the chemistry development team, the Analytical Chemist produces analytical data using HPLC, UPLC, GC, NMR, and LC/MS techniques to support structural elucidation work. Partnering with chemistry teams across functional areas, the Analytical Chemist trains new staff and authors SOPs to advance development projects.

Key Deliverables

• Prepare and analyze samples using HPLC, UPLC, Chiral LC, IC, GPC, prep-LC, LC/MS, GC, headspace GC, and GC/MS techniques.
• Prepare and analyze samples using NMR and spectroscopic, potentiometric, thermal, X-ray, and laser diffraction techniques.
• Prepare solvent mixtures for LC and perform instrument maintenance, repair, and calibration.
• Document analytical work and process and compile analytical data packages.
• Review analytical data packages to determine data matches proposed structure and report findings.
• Work closely with chemistry teams to develop innovative approaches to sample analysis and structural elucidation.
• Author and review SOPs, test methods, protocols, and reports.
• Store and archive analytical data according to company procedures.
• Coordinate with other functional areas to advance development projects.
• Train new chemists on the use of analytical equipment.
• Evaluate and purchase new instruments.

Professional Experience

• BS in Organic Chemistry, Analytical Chemistry, or related discipline.
• 2 to 5 years of industrial experience, with pharmaceutical API QC experience preferred.
• Strong experience operating HPLC, UPLC, GC, FTIR, and KF instruments with data interpretation.
• Strong understanding of chromatographic and spectrophotometric techniques and instrument hardware and software.
• Experience with sample preparation for qualitative and quantitative analysis.
• Experience with LCMS, GCMS, headspace GC for residual solvents, chiral LC, and GPC techniques.
• Experience with CAD, ELSD, and RI detectors, NMR spectroscopy, XRPD, DSC, and TGA techniques.
• Experience with wet chemistry and potentiometry techniques and instrument calibrations.
• Understanding of GLPs and good documentation practices.
• Independently motivated, detail oriented, and possess strong problem-solving ability.
• Strong organizational and communication skills with ability to multitask in a fast-paced environment.
• Ability to collaborate with and mentor peers across all levels of the organization.

The Analytical Chemist shapes routine analyses supporting chemistry, formulation, and biological research studies while ensuring data integrity and proper documentation in laboratory notebooks. Reporting to the analytical development department, the Analytical Chemist partners with cross-functional teams to identify technical and process improvement opportunities.

Areas of Ownership

• Perform routine analyses in support of chemistry, formulation, and biological research studies.
• Provide testing support for method development and method validation.
• Ensure data integrity including proper documentation of experimental methods, results, and conclusions in laboratory notebooks.
• Perform analytical data review for product stability and release.
• Follow SOPs related to safety, documentation, analytical methods, and corporate policies.
• Maintain assigned laboratory equipment in a clean and safe manner including routine operation and calibration.
• Generate and review SOPs, certificates of analysis, analytical reports, and other documents.
• Identify technical or process improvement opportunities.
• Follow safe laboratory practices according to corporate policies.

Education & Experience

• Bachelor's Degree or M.S in Chemistry, Biochemistry, or related discipline relevant to pharmaceutical analytical development, with 1 or more years of industry experience.
• Hands-on experience in analytical chromatography or oligonucleotide characterization.
• Direct experience in liquid chromatography such as RP-HPLC, SEC, or IEX for purity and impurity analysis, HPLC experience essential.
• Mass spectrometry experience is a plus.
• Experience in bioanalytical method development including analyte extractions from biological fluids.
• Experience working with nucleic acids, proteins, or nanoparticles is a plus.
• Familiarity with cGMPs, GLPs, and relevant regulations including ICH, FDA, and EU is a plus.
• Strong preference for experience in routine cleaning, maintenance, and performance verification for HPLC systems.
• Strong ability to apply scientific principles and critical thinking to solving problems.
• Effective oral, written, and presentation communication skills.
• Proficient in basic software applications including Microsoft Office, with demonstrated experience in scientific software applications.
• Ability to plan and coordinate daily activities to align with department priorities and timelines.

The Analytical Chemist owns NMR analysis conditions for various materials, applying advanced techniques and processing spectra using Mnova to interpret chemical structures. Reporting to the NMR technical team, the Analytical Chemist partners with R&D scientists and manufacturing engineers in Korea and globally to deliver integrated analytical solutions.

Role Responsibilities

• Set up effective NMR analysis conditions for various materials and apply advanced NMR techniques as well as routine analysis.
• Process NMR spectra using Mnova and interpret results into chemical structures.
• Document results and technical interpretation in analytical reports for internal customers.
• Engage in technical discussions with NMR experts, analytical technology experts, and internal business customers.
• Communicate with R&D scientists and manufacturing engineers to understand technical challenges and analytical requests.
• Prioritize work based on project status and business impact and deliver reliable results in a timely manner.
• Document experimental details and results accurately in technical reports and presentations.
• Participate in technical communication with global analytical scientists to leverage technologies and deliver integrated solutions.
• Develop technical competence by proactively learning advanced NMR techniques.
• Expand technical capability to other analytical technologies as needed.

Knowledge Skills & Abilities

• MS in Analytical or Organic Chemistry with up to 5 years of work experience.
• Excellent knowledge of NMR technology with a proven track record of NMR technical skills.
• Chromatography experience is a plus.
• Effective verbal and written communication in Korean and English.
• Demonstrated problem-solving skills with ability to quickly become competent in unfamiliar technologies or assignments.
• Highly motivated self-starter with ability to handle multiple tasks and prioritize workload under pressure.
• Ability to work independently with limited supervision and in a team environment with good interpersonal skills.

Embedded within the Analytical Technology group, the Analytical Chemist builds and validates analytical methods for trace metallic impurities in organosilicon and organometallic precursors used in semiconductor fabrication. Working closely with R&D, production, quality, and commercial teams in Carlsbad, CA, the Analytical Chemist ensures rapid delivery of new products to customers.

What You'll Do

• Develop and validate analytical methods for trace metals analysis and transfer operating procedures to production QC laboratories.
• Partner closely and quickly with client groups across different business sectors.
• Align team resources to S&OP while supporting product sustaining efforts, new product development, and manufacturing site efficiency projects.
• Work closely with R&D, production, quality, and commercial teams to ensure rapid delivery of new products to customers.
• Perform routine and non-routine sample analysis.
• Provide analytical and troubleshooting support for product quality issues.
• Conduct hands-on laboratory work.
• Work with ICPMS and other analytical instrumentation such as GC, GC-MS, NMR, IC, FTIR, RAMAN, and TGA.

Background & Experience

• Ph.D. in Physics, Chemistry, or related scientific discipline with 5 or more years of hands-on experience in method development using ICPMS, or Master's degree with 10 or more years of equivalent experience.
• Experience with chromatographic and spectroscopic methods with an emphasis in trace metals analysis.
• Analytical method development experience.
• Advanced statistical techniques and data mining experience.
• Strong fundamentals and practical experience in the use of statistics.
• Ability to work independently and in a team environment.
• Strong written and verbal communication skills with excellent interpersonal skills supporting a diverse team environment.
• Creativity and strong problem-solving skills.

Sitting at the intersection of trace element analysis and environmental sample preparation, the Analytical Chemist owns digestion, dilution, and purification of actinides for analysis by MC-ICP-MS and Q-ICP-MS. Operating across collaborative research projects with group members and the principal investigator, the Analytical Chemist maintains detailed laboratory records and clean labware supplies.

Duties

• Perform sample preparation of many types of sample matrices for trace element analysis by Q-ICP-MS and SF-ICP-MS, including digestions and dilutions.
• Purify uranium, plutonium, and other actinides from environmental matrices for analysis by MC-ICP-MS.
• Optimize instrument performance and set up analytical runs on a Q-ICP-MS.
• Maintain an accurate and detailed laboratory notebook to ensure results are properly annotated and organized for reports.
• Maintain a stock of clean labware to support sample preparation, including re-ordering general lab supplies.
• Manage sample disposal to the appropriate waste stream.
• Collaborate with group members and the principal investigator on multiple projects.
• Perform other duties as assigned.

Minimum Qualifications

• Bachelor's degree in Geochemistry, Chemistry, or related discipline.
• Experience with sample digestion techniques using concentrated acids.
• Experience with clean room environments.
• Experience with critical data record-keeping in a laboratory environment.
• Experience using Microsoft Excel.
• Effective communication and interpersonal skills to work in a collaborative research environment and document and present research results.

A key member of the QC laboratory team, the Analytical Chemist validates and verifies physical, physicochemical, and chemical methods including potentiometric titration and Karl Fischer water determination at Novo Nordisk. Collaborating across multiple Novo Nordisk sites, the Analytical Chemist leads timely implementation of pharmacopoeia changes and equipment upgrades.

Job Functions

• Validate and verify physical, physicochemical, and chemical methods including potentiometric titration, Karl Fischer water determination, pH, gravimetric analyses, viscosity, density, and optical rotation.
• Lead projects for timely implementation of pharmacopoeia changes.
• Provide QC support for deviations, out-of-specification results, and laboratory investigations.
• Qualify and implement new equipment to support the upgrade of the QC laboratory.
• Transfer physical, physicochemical, and chemical methods to other Novo Nordisk sites.

Position Requirements

• Master's Degree in Chemistry, Pharmacy, Engineering, or another relevant natural science field.
• Strong practical and theoretical background within analytical chemistry.
• Experience with pharmacopoeia compliance.
• Strong proficiency in both written and spoken English.
• High GMP and compliance mindset.
• Knowledge of systematic problem solving and a good eye for process optimization is an advantage.

Reporting to the lab manager, the QC Analytical Chemist owns analytical testing of raw materials, in-process samples, and final products following Vantage SOPs, AOCS, and USP/NF standards. Partnering with QC technicians and operations staff in Linden, the QC Analytical Chemist supervises training and ensures instruments remain validated under cGMP and FDA requirements.

Scope of Work

• Conduct analytical testing safely following SOPs, AOCS, USP/NF, and other official methods, including physical, chemical, and organoleptic testing reported accurately in LIMS.
• Supervise and train QC technicians in safe lab practices, equipment use, LIMS, and other systems.
• Inspect materials in repack staging areas and the warehouse to review, release, and investigate discrepancies.
• Operate GC instruments and Empower software for quantitation and calibration of volatile chemicals, and maintain and troubleshoot lab instruments.
• Maintain instrument calibration records and validate new instruments to meet cGMP and FDA requirements.
• Investigate Out of Specification results and customer complaints, following FDA OOS procedures as required.
• Order supplies, maintain chemical inventory, prepare stock lab solutions, and maintain COA documentation.
• Maintain good safe housekeeping including cleaning, glassware washing, and retain storage.
• Coordinate QC lab activities under direction from the lab manager, covering safe practices, staff training, testing, and LIMS use within ISO 9000 and cGMP frameworks.

Requirements

• Associate degree in science or bachelor's in chemistry with a minimum of three years of lab experience.
• Two or more years of experience using analytical instruments such as HPLC and GC, as well as wet chemistry techniques.
• Ability to distinguish colors and olfactory results to a given standard.
• Computer competence including email, MS Office, internal databases, Epicor, and LIMS.
• Clear written and verbal communication with the quality and operations team.
• Good organizational and record keeping skills with ability to make decisions and prioritize lab needs.
• Flexibility to work other shifts and overtime as needed.

Reporting to the technical project lead, the Analytical Chemist II owns development and validation of methods to quantify small molecules in biological matrices supporting exploratory and GLP studies using LC-MS/MS and GC-MSD. Partnering with scientists, technical support staff, and clients, the Analytical Chemist II oversees proposal efforts and mentors junior staff while ensuring compliance with laboratory data quality objectives.

Leadership Responsibilities

• Develop and validate methods to quantify small molecules in biological matrices supporting exploratory and GLP studies.
• Conduct experiments using mass spectrometry techniques including LC-MS/MS and GC-MSD, determine acceptance criteria, review data, and write technical reports.
• Troubleshoot complex laboratory problems and develop innovative testing methods to improve results and efficiency.
• Lead small research and technical projects, providing technical direction to scientists and support staff within time and budget constraints.
• Identify new technologies, assays, and techniques to drive business.
• Prepare and deliver technical presentations to clients and conferences.
• Oversee, train, and mentor junior staff.
• Assist with proposal efforts including technical sections, cost, and schedule estimates.
• Troubleshoot creatively and correctly interpret results to resolve technical challenges.
• Perform complex analysis to check accuracy and reasonableness of project work against quality objectives.
• Ensure compliance with in-house specifications, standards, and GLP.
• Maintain, calibrate, and clean equipment to specifications.
• Follow safety guidelines while working with hazardous materials.

Professional Experience

• Bachelor's degree with 2 years of experience, or Master's or PhD with post-degree experience, in analytical chemistry in an industrial or post-doc environment.
• Demonstrated experience using GC or LC systems coupled with MS, including tandem MS/MS systems.
• Proven experience with operation, calibration, and maintenance of MS instruments and data interpretation.
• Proficient in standard wet chemistry sample extraction and cleanup techniques.
• Demonstrated experience with quantitative chemical analysis.
• Must be a US person for export purposes and able to pass medical screening including PPE use and random drug screening.
• Excellent oral and written communication skills.
• Willing to work with biological sample matrices and hazardous materials.

Associate Analytical Chemist creates solution-based and solid sample preparations for ICP-MS, ICP-OES, and XRF analyses across organic and inorganic matrices at Chemours. The work directly supports analytical method development for compositionally complex commercial materials, with full training provided for ICP-OES instrumentation.

Engineering Responsibilities

• Carry out solution-based sample preparation for ICP analysis including ashing, digestion, extraction, separation, filtration, and dilutions.
• Carry out solid sample preparation for XRF analysis including grinding, pressed pellets, and fused beads.
• Carry out analyses with minimal supervision in a safe, timely, efficient, and effective manner.
• Perform elemental analyses on organic and inorganic matrices using ICP-OES instruments.
• Develop, validate, and document new analytical methods for compositionally complex commercial materials.
• Ensure analytical results are accurate, properly documented, and effectively communicated.
• Take part in training and development opportunities to meet changing company needs.

Education & Experience

• BS or MS in Chemistry or related field, equivalent experience considered.
• Minimum of 2 years of experience in an analytical laboratory environment.
• Direct experience with one or more techniques such as ICP-OES, ICP-MS, WD-XRF, AAS, or HPLC.
• Experience in sample preparation for trace metals analysis in complex organic and inorganic matrices, including microwave digestions.
• Demonstrable experience in analytical measurements, record keeping, and report writing.
• Experience developing and validating new analytical methods in a commercial or research laboratory.
• Strong awareness of chemical hazards and safe laboratory operation, with willingness to handle hazardous materials including strong acids, bases, and solvents.
• Strong spoken and written communication skills.

Embedded within the supply chain and pilot plant teams at Syngenta, the Analytical Chemist refines analytical data supporting residual impurity determinations across manufacturing operations and the Greensboro pilot plant. Working closely with sourcing, regulatory, and supply chain stakeholders, the Analytical Chemist develops and validates methods for active ingredient assay and stability testing.

Strategic Responsibilities

• Provide analytical data supporting residual impurity determinations across manufacturing operations and pilot plant sites.
• Provide timely analytical support to the supply chain through accurate data and effective problem solving.
• Develop and validate analytical methods for active ingredient and impurity assay, stability testing, and chemical property determinations.
• Support analytical investigations associated with active ingredient sourcing.
• Prepare reports and technical documents for regulatory submissions.
• Conduct product chemistry characterization studies and GLP regulated work supporting the Crop Protection portfolio and supply chain.
• Prepare standard operating procedures as required.
• Collaborate by building cross-functional networks and relationships.
• Propose suggestions to improve operational effectiveness of the team.

Requirements

• BS degree in Chemistry or related scientific field.
• Authorized to work in the U.S.
• Background or hands-on experience in separation science techniques including HPLC and GC.
• Excellent organizational, communication, and time management skills.
• Demonstrated critical thinking, problem solving, and innovation capabilities.
• Flexibility to adjust to business needs.
• Strong interpersonal relationship building with customers and colleagues.
• Continuous technical growth that drives innovation.

As the Analytical Chemist, this role supports new product development and field analysis for print hardware materials, using instrumentation including GC/MS, LC/MS, FTIR, and SEM to determine root cause of field issues. The materials analysis team relies on this work to develop new test methods and communicate findings to management, coworkers, and suppliers.

Technical Responsibilities

• Support new product development and current product field analysis in a team environment.
• Use analytical tools and develop new methods for effective materials analysis.
• Determine root cause for issues seen during development and in the field.
• Develop proficiency in instrumentation including GC/MS, LC/MS, ICP, UV/VIS, FTIR, TGA, DSC, TMA, SEM, EDS, and rheometry.
• Conduct analytical analysis of samples, collect and analyze data, document results, and resolve technical challenges with partners.
• Design and execute experiments and tests.
• Develop and optimize new methods to meet new demands.
• Share chemistry expertise and provide guidance to non-scientists across the company.
• Create clear written documentation of findings and recommendations.
• Communicate effectively with management, coworkers, partners, and suppliers.
• Ensure all work conforms with EHS requirements.

Background & Experience

• BS degree in Chemistry, Analytical Chemistry, or Materials Science.
• Experience in an industrial research environment working with adhesives, polymers, and contaminants.
• Experience assessing outgassing, VOC, and semi-VOC analysis.
• Experience in manufacturing processes, quality control, reliability, and risk assessment.
• Familiarity with print mechanisms and materials unique to printer hardware.
• Knowledge of Agilent ChemStation and Thermo Fisher Chromeleon.
• Ability to connect general chemistry, physics, and material science principles to practice.
• Self-motivated, curious, and growth-minded with a persistent problem-solving approach.
• Effective communicator with strong verbal and written reporting skills, and a collaborative team mindset.

Coatings product launch success depends on the Senior Analytical Chemist, who plans and conducts accelerated aging tests aligned with customer specifications and global product platform needs. Serving as the technical liaison between regional labs and R&D, the Senior Analytical Chemist develops new test methods to simulate customer line conditions and accelerate coating assessments.

Strategic Initiatives

• Plan and conduct accelerated aging tests on paint products in agreement with customer specifications.
• Analyze and interpret experimental results.
• Work closely with regional labs to understand needs and incorporate them into new product platforms.
• Collaborate with R&D and other functions globally on new product platform development.
• Maintain and grow understanding of methods of analysis.
• Develop new test methods to accelerate assessment of new coatings and simulate customer line conditions.
• Build and maintain networks with commercial and technical teams across regions.
• Communicate results through written and verbal summaries, test reports, and gate review updates.

Knowledge Skills & Abilities

• PhD in Chemistry with 3 or more years of experience, or MS/BS in Analytical Chemistry, Chemical Engineering, Chemistry, Polymer Science, Materials Science.
• Proficient knowledge of design of experiments and statistical analysis.
• Proficient English with outstanding cross-cultural communication skills.
• Strong desire to develop leadership skills in a dynamic global environment.
• Ability to successfully balance and progress multiple projects.
• Proven expertise in structured problem-solving methods preferred.
• History of detailing observations, analyzing results, and applying know-how to future work.

Reporting to the QC laboratory manager, the Analytical Chemist guides routine quality control analytical testing using fully validated and specified methods and procedures. Partnering with auditing and EHS teams, the Analytical Chemist writes and reviews laboratory procedures supporting analytical testing, instrumentation use, and continuous improvement initiatives.

Core Responsibilities

• Perform routine Quality Control analytical testing using fully validated and specified methods and procedures.
• Submit analytical data into LIMS with high regard for accuracy and precision.
• Review and authorize sample release following required analytical testing to ensure compliance and confidence.
• Write and review laboratory procedures to support analytical testing, instrumentation use, and QA processes.
• Write reports to support laboratory investigations, improvements, or modifications.
• Comply with EHS and GLP standards and assist in continuous improvement through auditing and housekeeping.

Required Qualifications

• Degree or higher diploma in Chemistry or a scientific subject with a major analytical chemistry component, or equivalent experience.
• Experience working in a high-pressure, high-volume laboratory environment and managing sample priorities.
• Theoretical knowledge and competence in inorganic analysis techniques, both classical and instrumented.
• Knowledge of key factors influencing analytical data quality and sources of measurement uncertainty.
• Ability to plan and organize work to meet data reporting deadlines.
• Awareness of risk, COSHH assessments, and other safety frameworks.

Embedded within an accredited environmental testing laboratory, the LCMS Analyst executes trace organic analysis on a wide range of samples using single and triple quadrupole LC-MS instrumentation. Working closely with extraction staff, the LCMS Analyst ensures samples are prepared and analytical results processed accurately onto LIMS.

Operational Focus

• Perform trace organic analysis on a wide range of samples and matrices following established procedures.
• Operate single and triple quadrupole LC-MS instrumentation and other laboratory equipment.
• Coordinate with extraction staff to ensure samples are prepared according to customer requirements.
• Perform routine maintenance and troubleshooting of LC-MS and other analytical equipment.
• Prepare samples, solutions, and reagents following standard laboratory formulas and procedures.
• Process and interpret analytical results for entry onto LIMS.

Qualifications & Experience

• Experience working within an accredited analytical testing laboratory, ideally in the environmental sector.
• Experience with single and triple quadrupole LC-MS systems operating in EI and CI ionisation modes.
• Use of Agilent Chemstation and Masshunter software.
• Experience with sample preparation techniques such as liquid-liquid extraction and solid phase extraction.
• Experience conducting routine maintenance and troubleshooting of LC based systems.

Sitting at the intersection of polymer chemistry and mechanical materials testing, the Analytical Chemist coordinates laboratory analysis of roll cover products using FTIR, DSC, TGA, and SEM at ANDRITZ. Operating across scientist and non-scientist audiences, the Analytical Chemist serves as subject matter expert in instrumental analysis and failure root cause investigations.

Delivery Expectations

• Perform laboratory analysis of roll cover products using instruments such as FTIR, DSC, TGA, and SEM.
• Perform mechanical testing of rubber, polyurethane, or epoxy-based composites using DMTA, TMA, and UTM equipment.
• Perform analysis related to QC non-compliance and failure root cause analysis.
• Maintain laboratory instruments and equipment.
• Prepare and write testing reports for scientist and non-scientist audiences.
• Follow laboratory safety protocols.
• Serve as subject matter expert in instrumental analysis and laboratory testing.
• Perform other duties and projects as assigned by management.

Skills & Qualifications

• BS in Materials Science, Analytical Chemistry, Polymer Chemistry, or Chemical Engineering, Master's or advanced degree preferred.
• Background in polymer chemistry or paper manufacturing with strong understanding of structure-property relationships preferred.
• Experience operating analytical equipment such as DSC, TGA, FTIR, DMA, SEM, and rheology instruments.
• Fluent in Excel, Word, Outlook, PowerPoint, and Teams.
• Ability to communicate effectively in English, other languages a plus.

A key member of the laboratory testing team, the Analytical Chemist maintains proficiency on SOPs, safety, and quality training while independently performing routine and sophisticated testing across ICP-OES, HPLC, and LCMS platforms. Collaborating across customer and management stakeholders, the Analytical Chemist compiles and presents technical information in a high-efficiency environment.

Performance Expectations

• Maintain proficiency on applicable SOPs, safety, security, and annual quality-related training.
• Adhere strictly to all safety and emergency procedures.
• Independently perform routine and sophisticated testing applying established SOPs.
• Analyze data and report results using job-specific software applications.
• Solve sophisticated technical problems and manage projects.
• Compile and present technical information to customers and management.
• Perform other duties as requested by laboratory management.

Position Requirements

• Experience with ICP-OES and/or ICP-MS, ion chromatography, HPLC, and/or LCMS.
• Experience with molecular spectroscopy techniques including FTIR, UV/Vis/NIR, RAMAN, PL, and ellipsometry.
• Experience with GC and GCMS and particle size distribution techniques.
• Familiarity with surface analysis techniques such as XPS, XRD, or SIMS is a plus.
• Data science background or advanced skills with Power BI or Excel VBA is a plus.
• Familiarity with LIMS systems.
• Strong written and verbal communication skills with experience in a team environment.
• Excellent customer service skills and ability to learn new software packages.
• Comfortable performing in a high-efficiency environment with minimal supervision, willing to work any shift.

Reporting to the laboratory quality team, the Analytical Chemist creates characterization data for products through experiments while interpreting and reporting results according to applicable documentation procedures. Partnering with suppliers and compliance teams, the Analytical Chemist documents packaging needs and special handling conditions.

Core Functions

• Conduct experiments to characterize products while ensuring effective use of resources.
• Interpret and report analysis results according to applicable procedures, adhering to documentation and reporting guidelines.
• Order chemicals and laboratory supplies as required.
• Dispose of waste solvents appropriately and maintain compliance with health and safety standards.
• Document and verify packaging needs, additional requirements, supplier information, and special handling conditions.

Minimum Qualifications

• Bachelor's or Master's degree in synthetic organic chemistry, bioorganic chemistry, or similar program with an emphasis on analytical chemistry.
• Good theoretical and practical knowledge of NMR, MS, and separation techniques.
• Strong knowledge of gas chromatography, MS, liquid chromatography, or inductively coupled plasma.
• Solid knowledge and experience using analytical techniques and instrumentation.
• Willingness to work weekends as required.