analytical chemist

Compunnel Inc.

<div>
 
 Analytical Chemist
 
 
 12-18 Months
 
 
 Location : Boulder, CO
 
 
 
 
 
 
 
 
 Client is looking to add a Research Associate to their analytical services team in the Development department at their contract Active Pharmaceutical Ingredient manufacturing facility that specializes in oligonucleotide chemistries located in Boulder, Colorado. The Research Associate will perform all duties on-site at the Boulder location.
 
 
 As a Research Associate on the Analytical Services team, the candidate will be responsible for executing analytical techniques for sample analyses used to support process development studies and Active Pharmaceutical Ingredient (API) manufacturing.
 
 <ul>
 <li>
 Design and conduct laboratory scale experiments using analytical instrumentation such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, Karl Fischer
 </li>
 <li>
 Perform analyses with adherence to ICH guidelines and internal standard operating procedures (SOPs)
 </li>
 <li>
 Design and safely conduct laboratory scale experiments using current best practices for API testing
 </li>
 <li>
 Properly record and summarize experiments in notebooks and reports, and construct analysis summaries to present to internal and external teams
 </li>
 <li>
 Maintain process compliance integrity by adhering to SOPs and current good manufacturing practices (cGMP) as appropriate
 </li>
 <li>
 Operate laboratory equipment by following operating instructions, troubleshooting instrumentation and method issues, and performing routine preventative maintenance
 </li>
 </ul>
 
 
 
 
 Job Posting Qualifications
 
 <ul>
 <li>
 Bachelor&rsquo;s Degree or equivalent
 </li>
 <li>
 Post-graduate, certification, and/or license may be required
 </li>
 <li>
 3+ years relevant experience and/or training; or equivalent combination of education and experience
 </li>
 <li>
 Experience in following SOPs and methods for analytical techniques, such as HPLC/UPLC, HPLC-MS, ICP-MS, IC, GC, GC-MS, UV, and Karl Fischer, is highly desired
 </li>
 <li>
 Knowledge of analytical test methods used in the testing of oligonucleotide API or related molecules is highly desired
 </li>
 <li>
 Ability to work with interdisciplinary project teams, understand project requirements, and follow project timelines
 </li>
 </ul>
 
 
</div>

Analytical Chemist

Hemlock Semiconductor

<div>
 At Hemlock Semiconductor (HSC), we transform people&rsquo;s lives by energizing and connecting our world through silicon technology. Since 1961, HSC has been a leading global provider of hyper-pure polysilicon, and is the only polysilicon manufacturer headquartered in the United States. HSC plays an essential role in the semiconductor and solar industries, with the vision of becoming the preferred supplier of silicon-enabled technologies to the low-carbon, digital world.
 
 
 Our polysilicon is used to make computer chips &ndash; the &ldquo;brains&rdquo; behind the electronic devices we rely on to make our lives easier, safer and more enjoyable. HSC is just one of six major manufacturers in the world that makes polysilicon used to create semiconductor wafers. In fact, nearly all electronic devices in the world contain HSC polysilicon.
 
 
 We&rsquo;re also moving the world toward a greener future by supplying the rapidly growing solar power industry. HSC is committed to doing good for our local Michigan and global communities, relentlessly improving our operations to remove supply chain carbon emissions. The low embodied greenhouse gas emissions in our polysilicon materials facilitates the production of ultra low-carbon solar panels. These panels allow solar project developers and owners to lower the embodied carbon of their projects by up to 50 percent.
 
 
 To achieve our goals, we draw on the talents of more than 1,350 employees and contractors. Our employees thrive in a culture that values teamwork, excellence, responsibility and customer focus. We recognize and value the diverse backgrounds and experiences of all of our people working together as One Team. At HSC, you belong to a team that is transforming our world.
 
 
 
 Summary
 
 
 
 We are seeking a motivated
 
 Analytical Chemist
 
 with at least three years of hands-on experience in materials characterization techniques such as Scanning Electron Microscopy (SEM), Inductively Coupled Plasma Mass Spectrometry (ICP-MS), or general spectroscopic methods of analysis. The successful candidate will be part of the Metrology Team and support product quality and process development by applying advanced analytical techniques to investigate materials, contaminants, and process-related phenomena. This role involves close collaboration with cross-functional teams including Technology, Quality, and Manufacturing.
 
 
 
 Essential Functions
 
 
 
 <ul>
 <li>
 Technical Expertise
 </li>
 <li>
 Perform routine and non-routine chemical and materials analyses using techniques such as:
 </li>
 <li>
 ICP-MS / ICP-OES for trace metals detection.
 </li>
 <li>
 SEM for surface morphology and elemental analysis.
 </li>
 <li>
 Photoluminescence for semiconductor and optical material characterization.
 </li>
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 Support method development and validation for new analytical protocols.
 </li>
 <li>
 Interpret complex data sets and provide actionable insights to improve product quality and yield.
 </li>
 <li>
 Instrument Operation &amp; Maintenance
 </li>
 <li>
 Operate and maintain analytical instruments to ensure optimal performance.
 </li>
 <li>
 Troubleshoot equipment issues and coordinate with vendors for service and calibration.
 </li>
 <li>
 Ensure compliance with internal standards and external regulatory requirements.
 
 
 </li>
 </ul>
 
 Essential Functions Con't
 
 
 
 <ul>
 <li>
 Data Analysis &amp; Reporting
 </li>
 <li>
 Apply statistical tools to analyze measurement data and assess process stability.
 </li>
 <li>
 Document findings in technical reports and communicate results effectively to stakeholders.
 </li>
 <li>
 Maintain accurate records of experiments, procedures, and results.
 </li>
 <li>
 Collaboration &amp; Support
 </li>
 <li>
 Work closely with Metrology, Quality, and Process Engineering teams to support material investigations.
 </li>
 <li>
 Participate in cross-functional projects aimed at process improvement and innovation.
 </li>
 <li>
 Instrument Stewardship
 </li>
 <li>
 Develop and validate robust, state-of-the-art measurement methods.
 </li>
 <li>
 Evaluate and optimize measurement systems for accuracy and reliability.
 </li>
 <li>
 Diagnose and resolve issues related to measurement tools and protocols.
 </li>
 <li>
 Knowledge Documentation
 </li>
 <li>
 Document technical expertise, challenges encountered, and innovative solutions.
 </li>
 <li>
 Serve as a long-term, reliable source of institutional knowledge.
 
 
 </li>
 </ul>
 
 Skills &amp; Competencies
 
 
 
 <ul>
 <li>
 Strong foundation in analytical chemistry and materials science.
 </li>
 <li>
 Hands-on experience with one or more of the following: SEM, ICP-MS, Photoluminescence, UV-Vis, FTIR.
 </li>
 <li>
 Familiarity with cleanroom protocols and contamination control.
 </li>
 <li>
 Proficiency in data analysis and statistical process control (SPC).
 </li>
 <li>
 Effective communication and documentation skills.
 </li>
 <li>
 Ability to work independently and in team settings.
 </li>
 <li>
 Proactive and action-oriented mindset. Ability to manage complexity.
 
 
 </li>
 </ul>
 
 Education Requirements
 
 
 
 <ul>
 <li>
 B.S. or M.S. in Analytical Chemistry, Materials Science, or related field.
 </li>
 <li>
 Minimum 3 years of relevant laboratory experience.
 
 
 </li>
 </ul>
 
 Preferred Experience
 
 
 
 <ul>
 <li>
 Experience in semiconductor or high-purity materials industry.
 </li>
 <li>
 Hands-on experience with microscopy and trace metals analysis.
 </li>
 <li>
 Familiarity with cleanroom protocols and contamination control procedures.
 </li>
 <li>
 Knowledge of spectroscopy techniques such as photoluminescence or FTIR.
 </li>
 <li>
 Exposure to separation science (e.g., GC, GC-MS) is a plus.
 
 
 </li>
 </ul>
 
 Required Work Experience
 
 
 
 <ul>
 <li>
 General Analytical Chemistry Laboratory.
 </li>
 <li>
 Metals Testing: Proficiency in ICP-MS and ICP-OES techniques.
 </li>
 <li>
 Applied Silicon Spectroscopy is a plus.
 
 
 </li>
 </ul>
 The range for this position is $92,000 - $140,000 assuming full time status. Starting pay for the successful applicant is dependent on a variety of job-related factors, including but not limited to market demands, experience, training, and education. The benefits available for this position are dependent on hours worked and may include medical, dental, vision, 401(k) plan, variable bonus, life insurance coverage, disability benefits, and PTO.
 
 
 HSC is an equal employment opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, status as a qualified individual with a disability, marital status, pregnancy, sexual orientation, ancestry, genetic information, or any other characteristic protected by law.
 
 
 If You Are An Individual With a Disability And You Need An Accommodation Or Other Assistance During The Application Process, Please Call Our Human Resources Department At
 
 
 989.301.5333
 
 
 or email your request to
 
 
 G1HSC-HR@hscpoly.com
 
 
 All qualified applicants are encouraged to apply.
 
 
 Req No. 1062
</div>

PuEr Lab

Job Summary We&rsquo;re seeking an Analytical Chemist to join our ISO-accredited cannabis testing laboratory. The successful candidate will take a lead role in operating and troubleshooting advanced instrumentation (HPLC, LC-MS/MS, GC-MS, ICP-MS) and will provide technical guidance to laboratory technicians while maintaining our high quality and safety standards. This position may occasionally require weekend or off-hour coverage as part of a rotating schedule to ensure timely client service.Duties and Responsibilities<ul><li>Operate, troubleshoot, and maintain LC-MS/MS, GC-MS, ICP-MS, and HPLC systems.</li><li>Review analytical results for accuracy and compliance with ISO and state regulations; initiate corrective actions when necessary.</li><li>Provide day-to-day technical guidance and training to laboratory technicians and assistants (no formal HR supervisory duties).</li><li>Ensure sample preparation, chain of custody, and data integrity meet regulatory and internal quality standards.</li><li>Participate in a rotating schedule that may include weekend or off-hour coverage to support laboratory throughput.</li><li>Adhere to safety protocols and maintain accurate records and inventories.</li><li>Participate in method improvements and quality initiatives.</li></ul>Required Qualifications<ul><li>Bachelor&rsquo;s degree in Chemistry, Biochemistry, or related field.</li><li>2+ years of experience in a regulated laboratory environment (ISO/IEC, NELAP, EPA, FDA, etc.).</li><li>Hands-on experience with LC-MS/MS, GC-MS, or ICP-MS instrumentation.</li><li>Proficiency with Microsoft Office and electronic data systems.</li></ul>Preferred Skills/Experience.<ul><li>Experience in cannabis testing laboratories.</li><li>Demonstrated ability to train or mentor junior staff.</li></ul>Working Conditions<ul><li>Expected to wear proper PPE in accordance with SDS and SOP.</li><li>Exposed to moderate noise.</li><li>Expected to work with/near hazardous chemicals, cryogenic liquids, compressed gasses, cannabis, and cannabis-related products.</li></ul>Physical Requirements<ul><li>Ability to climb stairs and ladders.</li><li>Ability to lift 35lbs.</li><li>Visual and auditory acuity.</li><li>Ability to walk and bend down.</li><li>Ability to sit or stand for extended periods of time.</li><li>Good eye/hand coordination and dexterity.</li></ul>Management This position does not supervise or manage personnel.This position reports directly to the Laboratory Manager. Day-to-day mentoring, positive and negative feedback, and performance reviews will be provided by the direct supervisor in consultation with indirect management.Job Type: Full-timePay: From $55,000.00 per yearBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Application Question(s):<ul><li>Why are you interested in working in the cannabis industry?</li></ul>Experience:<ul><li>cannabis/&quot;startup&quot; industry: 1 year (Required)</li><li>regulated laboratory: 2 years (Required)</li><li>Analytical chemistry: 2 years (Preferred)</li></ul>Work Location: In person

Eurofins

<div>Company Description 
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.
In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. 
Job Description 
We are seeking a Formulation Analytical Chemist to support a dynamic client team focused on formulation research and development for cutting-edge drug modalities. This role is ideal for a scientist with strong LC-MS experience and a background in analytical chemistry, who thrives in a fast-paced, collaborative environment.
Key Responsibilities<ul><li>
Develop, optimize, and execute LCMS-based analytical assays to support formulation and process development of lipid nanoparticles, mRNA, and protein therapeutics.</li><li>
Perform advanced characterization using LC-MS, LC-MS/MS, UPLC, SEC-MALS, and related techniques.</li><li>
Author test methods, SOPs, and technical reports to document assay development and results.</li><li>
Collaborate cross-functionally with formulation, genetic medicine, and analytical development teams to ensure timely and accurate data delivery.</li><li>
Troubleshoot instrumentation and assay performance, interpret complex data sets, and present findings in multidisciplinary team meetings.</li><li>
Maintain meticulous records in electronic lab notebooks and sample tracking systems.</li><li>
Take initiative in expanding responsibilities and contributing to team success.</li></ul> 

Qualifications 
Minimum Qualifications<ul><li>
B.S. in Chemistry, Biochemistry, or related field with 3&ndash;4 years of industry experience, or M.S. with 1&ndash;2 years of experience.</li><li>
Hands-on experience with LCMS, including method development and troubleshooting.</li><li>
Proficiency with QExactive or Orbitrap mass spectrometry platforms.</li><li>
Experience analyzing lipids, RNA, and proteins using LC-MS workflows.</li><li>
Ability to work independently after initial training and manage multiple priorities effectively.</li><li>
Strong communication skills and a collaborative mindset.</li></ul>
Preferred Qualifications<ul><li>
Familiarity with ICH guidelines for assay qualification.</li><li>
Experience in a regulated environment supporting drug development.</li><li>
Authorization to work in the U.S. without restriction or sponsorship.</li></ul> 

Additional Information 
What to Expect in the Hiring Process:<ul><li>
10-15 Minute Phone Interview with Region Recruiter</li><li>
45-60 Minute Virtual Interview with Manager and/or Group Leader</li><li>
45-60 Minute In-Person Meeting over Coffee for a Casual Discussion of the Role with the Team</li></ul>
The position is Full Time, Monday-Friday, 8 am-5 pm. Candidates currently living within a commutable distance of Boston, MA, are encouraged to apply.<ul><li>
Excellent full-time benefits<ul><li>
comprehensive medical coverage, dental, and vision options</li></ul></li><li>
Life and disability insurance</li><li>
401(k) with company match</li><li>
Paid vacation and holidays</li><li>
Hourly rate is between $36 - $39, depending on education and experience<ul><li>
Annual: $74,880&ndash;$81,120</li></ul></li></ul>
Eurofins Lancaster Laboratories Professional Scientific Services&reg; (PSS) is a global, award-winning insourcing solution that places our people at our clients&rsquo; sites, dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client&rsquo;s quality systems and equipment.
To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.<div></div>
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.</div>

Formulation Analytical Chemist

Kerry

<div>
 Requisition ID: 59972
 
 
 Position Type: FT Permanent
 
 
 
 
 About Kerry
 
 
 
 
 Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
 
 
 
 About The Role
 
 
 
 We are seeking a Senior Analytical Chemist with a passion for innovation and a proven track record in food flavour analysis, rheology, and ingredient functionality. We are looking for a strategic thinker and hands-on expert who can build and lead a cutting-edge analytical lab and help translate complex analytical data into actionable insights for our R&amp;D and product development teams.
 
 
 
 
 Key responsibilities
 
 
 
 
 <ul>
 <li>
 Manage a state-of-the-art analytical laboratory tailored to food and flavour innovation.
 </li>
 <li>
 Select and validate analytical instruments and methodologies aligned with Kerry&rsquo;s innovation goals.
 </li>
 <li>
 Operate and carry out analysis for Flavour (GC, GC-MS, LC, SPME, etc.), Food rheology and Ingredient functionality
 </li>
 <li>
 Develop SOPs, quality systems, and safety protocols in accordance with regulatory compliance.
 </li>
 <li>
 Interpret complex data to support formulation, shelf-life, and sensory performance.
 </li>
 <li>
 Partner with R&amp;D, sensory, and application teams to translate analytical results into practical insights for product development.
 </li>
 <li>
 Provide technical leadership in troubleshooting formulation challenges using analytical insights.
 </li>
 <li>
 Stay ahead of emerging technologies and trends in food analysis.
 </li>
 <li>
 Train other team members and foster a culture of scientific excellence and curiosity.
 
 
 </li>
 </ul>
 
 Qualifications And Skills
 
 
 
 <ul>
 <li>
 MSc or PhD in Analytical Chemistry, Food Science, or related field.
 </li>
 <li>
 Minimum 8 years of experience in food and flavor analysis, experience working in flavour house is desirable
 </li>
 <li>
 Strong hands-on experience with analytical instrumentation and method development.
 </li>
 <li>
 Proven ability to interpret data and influence product development.
 </li>
 <li>
 Strong stakeholder management and workload prioritization skills.
 </li>
 <li>
 Proven ability to manage multiple projects at various stages of development in a fast-paced environment.
 </li>
 <li>
 Excellent communication and problem-solving skills.
 
 
 </li>
 </ul>
 Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a &ldquo;starter kit,&rdquo; investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
 
 
 
 Recruiter
 
 
 
 
 Posting Type:
 
 LI
 
 
</div>

RD&A Senior Analytical Chemist

Tedor Pharma Services

<div>
 
 The Pharma Method Development and Validation Chemist will perform studies for the development of immediate release and controlled release tablet and capsules dosage formulations, topical formulations (creams and gels) and liquid formulations.
 
 
 Develop methods per ICH/USP requirements for excipient, API and final formulations of solid oral dosages form.
 
 
 Writes method protocols for full validation and verifications to USP methods.
 
 
 Does forced degradation studies.
 
 
 Can make a method from scratch and or improves such by fine tuning the method parameters to meet USP or vendor specifications.
 
 
 Works with QC to due testing . However, main job is taking a tech pack and making method validation protocols for submitting into ANDA .
 
 
 Perform testing on raw materials and in-process and finished dosage forms.
 
 
 Write technical documents including laboratory notebooks, batch records, project summaries, development reports, sampling and testing protocols, planned deviation reports, incident reports, and change control forms.
 
 
 Maintain technical documents in the formulation development department.
 
 
 Calibrate in-process testing equipment, interpret and analyze experimental data, identify the next steps to be taken and perform scale-up and technology transfers of formulations from research and development to the submission/clinical to production/commercial scale batches.
 
 
 Direct the work of scientists and technicians in the formulation department, reviewing their laboratory notebooks, batch records, project summaries, product development reports and standard operating procedures.
 
 
 Attend project meetings.
 
 
 Manage R&amp;D projects and report project progress to the project manager.
 
 
 Communicate the status of various batches to the production, QA, RA and QC departments and to clients, as needed.
 
 
 Assist in FDA filings.
 
 
 Review project contracts.
 
 
 Assist IT in development and implementation of the database system.
 
 
 Bachelor's Degree in Chemistry required.
 
 
 Proficiency in computer usage and Microsoft Office required.
 
 
 Job Type: Full-time
 
 
 Required experience:&nbsp;Chemistry: 4 years
 
</div>

Analytical Development Chemist

Barrington James

<div>
 
 I am partnered with an outstanding client who are adding to their team. They are looking to bring on multiple Analytical Development Scientists to support process development and clinical manufacturing activities. This role focuses on developing and improving analytical methods, supporting technology transfer, and ensuring high-quality data for regulatory and manufacturing needs.
 
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Perform analytical R&amp;D to support process design, optimization, and clinical trial material production.
 </li>
 <li>
 Develop, validate, and transfer analytical methods using techniques such as HPLC, UPLC, LC/MS, LC/MS/MS, GC/MS, and process chromatography.
 </li>
 <li>
 Author and review analytical procedures, reports, and documentation for regulatory and manufacturing support.
 </li>
 <li>
 Provide analytical expertise to cross-functional R&amp;D teams and assist in troubleshooting laboratory and manufacturing challenges.
 </li>
 <li>
 Participate in batch analysis and release of drug substances and intermediates for clinical and registration programs.
 </li>
 </ul>
 
 
 
 Qualifications
 
 
 
 <ul>
 <li>
 PhD or MS in Chemistry with 2+ years of relevant experience, or BS with 6+ years.
 </li>
 <li>
 Hands-on experience with MS, LC/MS, GC/MS, and related analytical technologies.
 </li>
 <li>
 Background in method development, validation, and technology transfer.
 </li>
 <li>
 CDMO/ GMP experience needed
 </li>
 </ul>
 
 
</div>

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