Chemist jobs in Lowell, MA

Prepare chemical solutions and maintain plating baths for electroplating operations. Operate and maintain electroplating equipment including tanks, rectifiers, and agitation systems. Calibrate and maintain laboratory instruments such as pH meters, spectrophotometers, and conductivity meters. Perform routine and specialized tests to monitor plating thickness, adhesion, and surface finish properties. Analyze chemical concentrations and adjust bath compositions to maintain optimal plating conditions. Document experimental procedures, results, and observations in lab notebooks and digital systems. Clearly and concisely communicate research to team lead and other team members. Collaborate with R&D teams to assist in research and development of new plating processes and surface treatments Collaborate with sales teams to troubleshoot customer plating issues. Ensure compliance with safety protocols, environmental regulations, and waste disposal procedures. Preferred: Experience with production-scale electroplating. Associate, Bachelor, or Master's degree in Chemistry, Chemical Engineering, Materials Science, or related field. 1+ years of experience in a chemical laboratory setting, with a focus on electroplating or surface finishing is a plus Strong understanding of electrochemical principles and electroplating chemistry (e.g., nickel, copper, silver, tin) is a plus Experience with a diverse range of analytical equipment, including UV-Vis, AA, SEM, XRF, XRD, wet chemical techniques, and surface analysis methods. Knowledge of ASTM and ISO standards and quality control procedures. Experience with corrosion science or surface science. Experience with Lean Six Sigma or certification. Qualifications: Strong bias for action and willing to go the extra mile Well-organized, detail-oriented, and results-driven team player. Methodical, proficient in data analysis, and excellent problem-solving skills. Ability to work both independently and as part of a multidisciplinary team. Familiarity with lab safety standards and chemical handling procedures

Title: QC Bioanalytical Scientist Employment Type: Contract (6 months) Status: Accepting Candidates About the role This role supports QC Bioanalytical activities focused on analytical method qualification, validation, and assay execution for biologic drug substances and process-related impurities. The scientist will work closely with QC and development teams to advance analytical methods into GMP testing environments. Key Responsibilities • Perform analytical method qualification and validation for biologics and process impurities. • Execute ELISA, qPCR, potency, and other immunochemical assays to support method lifecycle activities. • Support method development, transfer, and technology transfer into QC laboratories. • Prepare, review, and revise technical protocols, reports, and SOPs. • Collaborate with cross-functional teams to ensure assay readiness and compliance. • Provide training and technical guidance to QC staff as needed. Qualifications • Bachelor's degree with 8+ years, or Master's with 5+ years in Chemistry, Biology, or related field. • Hands-on experience with ELISA, qPCR, immunochemistry assays, and biologics analytical characterization. • Strong understanding of GMP, analytical method lifecycle, and QC environments. • Experience with SoftMax and plate-based analytical systems preferred. • Background working with biologics, monoclonal antibodies, and drug substances/products. • Strong technical documentation and communication skills. Compensation (MA Pay Transparency): • Estimated hourly range: $55-$65/hr (W-2). • Final rate within this range will be based on skills, experience, and interview results.

Vaxess is developing a pipeline of next-generation therapeutics on our novel micro-array patch platform. With only five minutes of wear-time on the skin, the Vaxess' patch combines room temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. Vaxess is a multi-disciplinary organization, integrating mechanical, industrial, biomedical, and chemical engineering with chemistry, biology, and human factors to address important unmet medical needs. We are seeking a skilled, collaborative, and highly motivated formulation technician with expertise in chemical, biotech, medical device or pharmaceutical manufacturing to join our growing team. The Formulation Technician will play a pivotal, hands-on role in meeting overall production goals by ensuring execution of formulation activities, while closely collaborating with cross-functional teams. Responsibilities Performs cGMP formulation operations according to documented procedures or batch records Operates formulation equipment such as fluid dispensers, mixers, pumps, and filtration systems Completes production batch records, logbooks, test records, and other documentation following Good Documentation Practices in a timely manner Performs in-process assays such as pH, density, filter integrity, and API concentration measurement Contributes to root cause analyses (RCA) and process development investigations Reviews and verifies documentation for completeness and compliance with regulatory standards Supports formulation related process development efforts as needed Adheres to all safety guidelines, including PPE usage, chemical handling, and emergency procedures. Performs other assigned duties related to manufacturing, facilities, and quality control as needed Qualifications 2 + years' relevant experience working in regulated environments in chemical, biotech, medical device or biopharmaceutical industries; experience working in a clean room is preferred High school diploma minimal, associate's degree or trade certifications preferred Strong laboratory techniques including pipetting, weighing, mixing solutions, aliquoting, and documentation Ability to work in a laboratory and clean room environment Good written and verbal communication skills, attention to detail, and a demonstrated ability to work independently as well as effectively within a team Entrepreneurial spirit and drive to positively impact global human health Vaxess is building a team of exceptional people to rapidly advance product development. We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you're interested in joining the Vaxess team, please submit your CV/resume to ******************.

A recognized pharma company is hiring a Senior Analyst I, Quality Control Chemistry on a one-year contract basis near Boston, MA. is for candidates who are able to work on a W2 basis.** Responsibilities: Execute analytical test methods to support product release and stability of AAV products using different analytical techniques (e.g. HPLC, LCMS, AUC, UV, CE-SDS, compendia methods like Osmolality, pH, Sub visible particulates and Appearance) Review and approval of cGMP analytical data for release and stability testing from chemistry analytical test methods Supports and leads QC Chemistry laboratory operations (ex. Instrument qualification and maintenance. Housekeeping, qualify critical reagents, etc). Author and support quality events; Change controls, Deviation, CAPA, OOS Investigation, as needed Write, prepare, and present technical data, technical reports, and standard operating procedures (SOPs), Method transfer/ validation protocol, Method transfer/ validation report for internal and external methods Perform other duties, as needed Qualifications: 5+ years of experience working in cGMP environment Bachelor's and/or Master's Degree in Analytical Chemistry, Biochemistry, Biophysics, or a related discipline Experience working in the cGMP QC lab of the Pharmaceutical or Biopharmaceutical industry Experience working with external contract labs (CMOs, CROs) Desired Skills: Experience analyzing Nucleic Acids, Virus Capsids, Antibodies, and/or other Biologics materials using HPLC/UPLC, LCMS, AUC, UV- Vis, CE-SDS

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at **************** . Astellas is announcing a **Computational Chemist Lead** opportunity at their Astellas Innovation Management (AIM) site in Cambridge, MA. **Purpose:** This role supports drug discovery efforts by applying advanced computational chemistry techniques to design and optimize small-molecule therapeutics. The position requires close collaboration with internal teams and external CROs to accelerate candidate selection and improve research productivity. The successful candidate will lead strategy across multiple programs and shapes the computational chemistry platform/standards in Innovation Lab, working closely with global teams. As Computational Chemist, you will be expected to contribute across multiple therapeutic areas and drug discovery efforts across various modalities including small molecules, proteins, bifunctional degraders, and biologics. **Essential Job Responsibilities:** + Computational Drug Design: Apply molecular modeling, docking, molecular dynamics, homology modeling, and structure-based design to guide compound optimization + Use cheminformatics and machine learning tools to analyze SAR, ADME/Tox profiles, and predict compound behavior. + Develop generative models, reinforcement learning pipelines, and predictive analytics for compound design and optimization + Curate chemical libraries, manage data pipelines, and support SAR/ADME analysis + Can make recommendations on compound progression, integrate new platforms and tools and can make Go/No-Go decisions on compound progression, setting project goals and defining plans + Drug Design & Synthesis: Design novel compounds based on ADME and SAR principles; optimize lead molecules for potency, selectivity, and pharmacokinetics. + Data Analysis & Reporting: Analyze large datasets from simulations and experimental data with scientific rigor; interpret computational results and prepare detailed research reports and present findings internally and externally to technical and non-technical audiences. + Cross-functional Collaboration: Work closely with medicinal chemistry, biology, pharmacology, protein science, and preclinical teams to ensure drug candidates meet efficacy and safety standards. Participate in program-related meetings and contribute strategic insight + Intellectual Property: Identify and protect IP through patent filings and strategic documentation. Ensure accurate documentation of compound synthesis and project data + Foster a collaborative, transparent, and creative team environment that drives innovation and invention. Close partnership with colleagues in Japan is expected. + Technology Integration: Explore and apply cutting-edge technologies and global scientific trends to enhance research capabilities + Stay current with scientific literature and emerging technologies + Manage team priorities and resources in alignment with the company's overall I-Lab strategy and objectives CRO Management + Oversee computational chemistry execution at CROs, including troubleshooting and performance enhancement + Evaluate and onboard new CROs to improve cost-efficiency and research quality + Maintain weekly communication and productivity tracking with CRO teams **Qualifications** **Required:** + Ph.D. in Computational Chemistry, Cheminformatics, Medicinal Chemistry, or related field; or M.S. with 5+ years of industry experience + Proven experience in computational support of small molecule drug discovery. + Familiarity with AI-driven drug design + Proficiency in software packages such as Schrodinger, MOE, OpenEye, Rosetta, and scientific programming (Python, Pipeline Pilot). + Strong understanding of organic and synthetic chemistry concepts. + Experience managing CRO relationships and external collaboration + Deep understanding of advancements in drug discovery, emerging technologies, and industry trends, and experience applying this knowledge to enhance research strategies. **Technical Expertise:** + Molecular Modeling & Simulation: Proficient in structure-based drug design (SBDD), including molecular docking, molecular dynamics (MD), and free energy perturbation (FEP). + Skilled in homology modeling, pharmacophore modeling, and quantum mechanics/molecular mechanics (QM/MM) methods. + Experienced in cryptic pocket identification and virtual screening for challenging targets + Chemoinformatics & Data Science: Applies cheminformatics tools to analyze structure-activity relationships (SAR), ADME/Tox profiles, and compound clustering. + Uses machine learning (ML) and AI-driven platforms for compound prioritization, generative design, and predictive modeling. + Familiar with scripting languages like Python and platforms such as Schrödinger, MOE, and KNIME + Drug Discovery Integration: Designs and optimizes small molecules for potency, selectivity, and pharmacokinetics. + Collaborates with medicinal chemists, biologists, and pharmacologists to guide compound progression from hit to lead **Skills:** + Strong collaboration and teamwork abilities. + Excellent oral and written communication in English. + Strategic thinking and problem-solving capabilities + Strong communication and influencing skills + Highly collaborative win-win mindset is essential **Working Environment:** + This position is based in Cambridge, MA and will require on-site work. **Salary Range** **:** $119,000 - $187,000 (Final compensation will be determined based on a variety of factors, including but not limited to skills, experience and organizational equity considerations) **Benefits** : + Medical, Dental and Vision Insurance + Generous Paid Time Off options, including Vacation and Sick time, plus national holidays including year-end shut down + 401(k) match and annual company contribution + Company paid life insurance + Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions + Long Term Incentive Plan for eligible positions + Company fleet vehicle for eligible positions + Referral bonus program \#LI-TR1 Category Innovation Incubation Lab US Astellas is committed to equality of opportunity in all aspects of employment. EOE including Disability/Protected Veterans

IRI believes in commitment, integrity and strategic workforce solutions. Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity. Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success. Job Description • A position is available for a highly skilled analytical chemist or engineer to join in Pharmacokinetics Dynamics and Metabolism New Biological Entities (PDM-NBE) ADME group with deep expertise in antibody ADME and inter-molecular binding • The lab based role entails training on the state-of-the-art technology for intermolecular interactions and quantification of binding affinity of Biotherapeutics drug to specific proteins in human biological matrices with unwanted immunogenicity • This position requires strong analytical expertise, with background in engineering, protein biochemistry, immunology or PK as a plus • The candidate will participate in all phases of laboratory operations including training on the technology, design of reagents, design of binding experiments, the development of sample preparation, assay execution, instrument maintenance, data analysis, summarization and reporting • We are looking for a scientist passionate about learning and able to quickly apply new skills to the project needs. Responsibilities- • Design of protein reagents to be used in binding studies • Run binding assays under minimal supervision; initiative in method development is expected • Independent daily operation, calibration, maintenance, and troubleshooting the binding instrument • Analysis of binding data and derive binding affinity using relevant software • Work with modeller to build computational immunogenicity model • Handling of biological samples, specifically human and preclinical serum and tissues • Summarize work and write reports Qualifications • BS/MS level education in Analytical Sciences, Biochemistry, Chemistry, Pharmacology or closely related fields required; advanced degree may be a plus • Industry experience in biopharma preferred • Attention to detail is critical, and be able to handle very delicate and complicated instrument to produce reproducible data • Strong analytical and biochemistry background is required. Good understanding of concepts of binding affinities is a plus • Fast learner and be able to master running/maintaining the instrument after a short period of training • Strong initiative for problem solving at a technical and intellectual level • Excellent communication skills, both written and oral • Works well both independently and as part of a team • Collaborative skills and effective partnering skills in a matrix-environment • Strong data organization and analysis skills Additional Information Thanks Regards Ricky

About Us Eat Well, Live Well. At Ajinomoto Cambrooke, we build careers grounded in helping improve people's health through nutritional therapies. Ajinomoto Cambrooke (ACI) was founded by parents looking to develop better solutions for their children with PKU. Over the subsequent 25 years, we have expanded into additional therapeutic areas with a focus on enjoyable nutrition as a core part of normalizing the life for people living with medical conditions. Joining ACI means becoming part of a diverse team of talented people who want to build their careers while contributing back to society in a positive way. We seek individuals who bring an entrepreneurial mindset with a bias for action and finding solutions. We provide an environment based in mutual respect and collaboration to support you and give you opportunities to learn and develop. Join us to find a rewarding work experience that lets you be at your best and have an impact on our patient communities. Why Join Us Our people are the key ingredient to our success. We offer a collaborative, innovative environment where you can grow your career and make an impact on global food and health solutions. We provide a comprehensive and competitive total rewards package, including: • Competitive Pay and Annual Bonus Opportunity • 401(k) with Company Contributions • Medical, Dental, and Vision - Effective Day 1 • Paid Time Off, Company Holidays, and Floating Holidays • Paid Parental Leave • Wellness Programs and Yearly Wellness Reimbursement • Work Flexibility • Company-Paid Life and Disability Insurance • Employee Assistance Program (EAP) • Tuition Reimbursement Opportunities • Career Growth and Development within a Global Organization • Company-Provided Mental Health and Caregiving support Overview The Product Development Team supports the medical nutrition business by developing new and revising existing product formulations to meet target characteristics that will deliver positive patient outcomes through therapeutic nutrition. Strong collaboration with the Directors of Medical Nutrition, Marketing, and Sales will be required to ensure desired nutritional levels are achieved throughout the product shelf-life, patient insights on flavor, texture, and palatability are incorporated. In this role, you will contribute to the ideation and exploration for uses of new to ACI ingredients and new to ACI business ventures in additional disease-states reliant on specialized medical nutrition. This position sits in our Corporate Office located in Ayer, MA. Qualifications EDUCATION, CERTIFICATIONS AND EXPERIENCE: • Minimum bachelor's in food science, nutrition, or related field; Master's degree preferred. PhD, PharmD a plus. • 5+ years of experience in product development, with ability to take concepts from bench top to commercialization for nutritional beverages and / or nutritional powder blends from concept to commercialization. • 5+ years in basic and applied research and development preferably in small/mid-sized nutrition, food and/or biotech company. Experience with food/beverage formulation and manufacture of nutritional products that meet stability, sensory and nutritional requirements. Direct experience with aseptic processing / Tetra Pak a plus. • Expert scientific knowledge in food science with emphasis on product development involving interaction amongst ingredients and impact of process techniques on use of micro-nutrients. • Experience with nutritional modeling software and familiarity with FDA regulations preferred, exposure to EU regulations a plus. • Able to design and monitor product shelf-life procedures both regular and accelerated for nutritional products. • Strong translational science background with experience in converting basic nutrition-science insights into consumable products. KNOWLEDGE, SKILLS AND ABILITIES: • Build relationships with vendors to source ingredients to meet product specifications. • Overall understanding of how business units interact to facilitate successful product development and commercialization. • Ability to define new product needs in terms of process needs and product characteristics including organoleptic needs / claims • Demonstrated Leadership capability with a focus on innovation to drive product development proactively and passionately. • Exhibit the understanding of use of standard operation procedures related to product development, process development and product shelf-life determination. • Well versed with food safety requirements and regulations. • An understanding of human nutrition and ability to review primary scientific literature. • A strong ability to communicate basic science and technical challenges to non-technical audiences. • A strong understanding of ingredient interactions in a food/beverage matrix throughout processing and shelf life. • Ability to design shelf-life evaluation matrices considering product composition, process impact and other critical factors when designing new products in medical nutrition arena. • An understanding of macro and micro-nutrient analytical procedures and their principles. • Ability to work in a fast paced, cross functional team environment. • Excellent analytical skills, strong attention to details, good communication and interpersonal skills. • Excellent organizational skills, the ability to balance multiple projects, set priorities, and drive results. Working Conditions / Physical Requirements WORKING CONDITIONS: This position works in a food manufacturing environment and requires the ability to adhere to all GMP, Food Safety, workplace safety and security policies including wearing required personal protective equipment, as well hair net, beard net, etc. as required PHYSICAL REQUIREMENTS: Position requires the ability to occasionally lift up to 50 pounds, stand, walk, bend, reach, push, and pull. Ability to use a computer, keyboard, telephone, and other office equipment. Ability to wear all required PPE. Responsibilities • Utilize your exemplary food science and ingredient know-how to co-create and execute medical formula products against ACI's strategic R&D roadmap to support the overall corporate strategy while meeting the internal quality expectations. • Support the Leadership and Management teams with scientific support in the areas of product development, clinical development, product manufacturing and new ingredient compound / product initiatives. • Research and help develop clinical evidence supporting existing and new products and ingredient compounds for use in commercial activities. • Participate in conferences, clinician meetings and other forums to present ACI's clinical evidence. • Ensure existing and new products, processes or ingredient compounds have strong Intellectual Property protection thus providing ACI a sustained competitive advantage. • Other duties as assigned. Salary Range $105,000 - $130,000 Annual with potential 12.5% Bonus EEO Statement Ajinomoto Cambrooke, Inc. is an Equal Opportunity Employer-Vets/Disabled, committed to a diverse workforce. If you need assistance with completion of an application for employment, please contact Human Resources Department at ************.

SES AI Corp. (NYSE: SES) is dedicated to accelerating the world's energy transition through groundbreaking material discovery and advanced battery management. We are at the forefront of revolutionizing battery creation, pioneering the integration of cutting-edge machine learning into our research and development. Our AI-enhanced, high-energy-density and high-power-density Li-Metal and Li-ion batteries are unique; they are the first in the world to utilize electrolyte materials discovered by AI. This powerful combination of "AI for science" and material engineering enables batteries that can be used across various applications, including transportation (land and air), energy storage, robotics, and drones. To learn more about us, please visit: ********** What We Offer: A highly competitive salary and robust benefits package, including comprehensive health coverage and an attractive equity/stock options program within our NYSE-listed company. The opportunity to contribute directly to a meaningful scientific project-accelerating the global energy transition-with a clear and broad public impact. Work in a dynamic, collaborative, and innovative environment at the intersection of AI and material science, driving the next generation of battery technology. Significant opportunities for professional growth and career development as you work alongside leading experts in AI, R&D, and engineering. Access to state-of-the-art facilities and proprietary technologies are used to discover and deploy AI-enhanced battery solutions. What we Need: The SES AI Prometheus team is seeking an exceptional Computational Materials & Molecular-Modeling Scientist to specialize in physics-based simulation, utilizing reactive force-field development and MD/DFT coupling. This role is critical for generating validated atomistic and mesoscale data that directly feeds our AI-driven materials discovery workflows. As a key scientist, you will bridge physics-based simulation with advanced AI methods, driving materials discovery through computational rigor. Essential Duties and Responsibilities: Advanced Simulation & Modeling Develop and apply advanced simulation techniques, specializing in Reactive Force Fields (ReaxFF) and MD/DFT coupling, to model complex materials phenomena. Conduct and analyze multi-scale computation projects, covering atomistic simulation up to mesoscale modeling. Utilize and maintain advanced simulation tools, including VASP, LAMMPS, GROMACS, and CP2K, for high-fidelity simulations. Perform rigorous physics-based validation on all simulation outputs to ensure accuracy and reliability. AI Data & Workflow Development Generate and validate high-quality atomistic and mesoscale datasets used for training ML potential and other scientific AI models. Develop advanced simulation workflows and contribute to the creation of ML potentials and AI-driven materials discovery tools. Coding & Collaboration Apply strong coding skills (e.g., Python, C++, FORTRAN) to automate complex simulation workflows and enhance computational efficiency. Maintain a solid understanding of battery chemistry modeling and collaborate effectively across computational and experimental teams. Education and/or Experience: Education: Ph.D. in Computational Chemistry of Energy Materials, Materials Science, or Computational Physics. Core Simulation Expertise: Deep, demonstrated expertise in advanced physics-based simulation, including proficiency with DFT, MD, and Quantum Mechanics (QM) simulation tools. Reactive Potentials: Proven experience with Reactive Force Fields (ReaxFF) and methods for MD/DFT coupling. Coding & Tools: Strong coding ability in languages such as Python, C++, or FORTRAN, and deep practical experience with simulation codes like VASP, LAMMPS, GROMACS, or CP2K. Domain Focus: Solid understanding of battery chemistry modeling and experience in generating and validating atomistic and mesoscale data. Preferred Qualifications: Machine Learning Integration: Experience with Neural Networks and Deep Learning, particularly in applying them to develop ML potential. Familiarity with geometric deep learning libraries like PyTorch Geometric is a plus. Multiscale Methods: Experience with specialized methods like the Materials-Point Method. Hybrid Literacy: Experience with experimental literacy, understanding characterization methods such as SEM, TEM, XPS, Raman, EIS, NMR, DSC, or TGA. Background: Previous experience at advanced simulation labs, battery multiscale modeling groups, or in the computational chemistry of energy materials.

Title: Analytical Chemist Contract Term: 12+ Months Shift/Hours: 1st Shift ( 8-9am to 4-5pm) / 40hrs Client: Medical Device Company Job Category: Research & Development Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) No H1B's Summary: The Analytical Chemist will work in a R&D laboratory to support chemical testing using chromatography and spectroscopy. Responsibilities • Conduct basic and complex analyses of raw material and or/stability samples chemical analytical techniques • Effectively document and communicate test results • Set up and operate laboratory equipment such UV, HPLC and Fluorometer including any computerized software required for the operation of the equipment or analysis of results. • Make recommendations with respect to the cause and resolution of equipment issues or malfunction • Co-ordinate and prioritize sample analysis in consultation with other laboratory personnel • Conduct investigations of laboratory incidents and the investigation of out-of-specification and out-of-trend results. • Document investigations in a clear, accurate and concise fashion. • Review the work for accuracy and completeness. • Perform routine maintenance activities in the laboratory and participates in the qualification and periodic calibration of equipment. • Participate in method transfer studies and in other laboratory testing to support compliance (e.g. testing of product validation samples). • Write protocols and execute analytical method validations. • Develop and execute testing protocols. • Support exploratory testing to define test equipment, test fixtures and test methods development. • Participate in training, test methods validation, and execution of testing as needed • Write engineering test reports and final test reports • Install and validate equipment and or test fixtures as needed, manage and maintain laboratory equipment and inventory • Support failure analysis Requirements: • Minimum of Bachelor's Degree in Chemistry • Industrial experience in the use of HPLC and/or UPLC. • Knowledge of Microsoft Office programs (Word, Excel, PowerPoint) is a must • Ability to understand and execute test procedures • Demonstrated attention to details and very organized

Job DescriptionSalary: The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. PRIMARY DUTIES AND RESPONSIBILITIES Prepares and analyzes products to determine chemical and physical properties. Will perform work under partial supervision and will provide over site to projects and assist other Chemists as needed. Works under partial supervision with chemists and other client personnel regarding research, procedures performed, related results and prepares reports. Is a subject matter expert in some techniques and will mentor others. Work to learn and improve on others techniques and tasks. Performs data generation, analysis and more complicated problem solving with a minimal rework. Reviews and assesses deviations; includes performing risk assessments, participating in root cause analysis investigations, tracking, follow-up and reporting. Works under partial supervision to ensure all work performed is performed in compliance with standard operating procedures, good manufacturing practices, and the regulations of the Food and Drug Administration. Ensures all work performed strictly adheres to Company, client and Pharmacopeial methodologies. Performs system maintenance and calibrations to ensure equipment is operating with specified requirements. Proper handling of hazardous waste in compliance with the Company and DES hazardous waste rules. Documents work in a clear and organized manner. Follows all safety rules and regulations and conducts periodic safety audits. Follows all cGMP rules and regulations. REQUIREMENTS & QUALIFICATIONS Qualifications include a Bachelors degree in Chemistry or a related discipline is required with 1+ years of related experience. Knowledge of cGMPs and related compliance regulations and guidances required. MINIMUM SKILLS REQUIREMENTS Must have the ability and skill to perform the detailed job requirements noted above competently, safely and proficiently. A self-starter, motivated person who possesses good interpersonal skills capable of effectively interacting with all departments and client personnel. Must have excellent organizational, verbal communication and technical documentation skills. Solid computer skills. Knowledge of safe laboratory practices, including the proper procedures in handling chemicals and samples. Must be a team player with integrity and concern for the quality of Company products, services and staff members.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description JobDescription: Skills: Must be detail-orientedand able to work with a high volume of documents in a fast-paced environment.Be highly organized and process-oriented. PreferredQualifications: Additional Information Best Regards, Sneha Shrivastava***********

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. We serve an extraordinary purpose. For more than 140 years, we have worked diligently to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world's greatest health challenges. At the Lilly Innovation Center in Boston, Massachusetts, we explore how next generation therapeutics, new technologies, data analytics and new care models can improve patient health and the healthcare system. Our Genetic Medicine team in Boston shares a passion for challenging conventional wisdom and creating an environment that embraces creative, break-through concepts. The Center offers a start-up environment with large company support. It is located in the heart of Massachusetts' exploding science and technology cluster and is within walking distance of some of the best academic and industry innovators in the world. The successful candidate will have a strong research track record in synthetic organic chemistry/chemical biology/biotechnology and be analytically minded, systematic, and embrace data-driven decision making. The scientist will collaborate with multidisciplinary teams across key Lilly therapeutic areas (e.g. neuroscience, diabetes, immunology) to perform synthesis and related experiments to aid development of RNA oligonucleotide drug candidates for the next generation of RNA therapies. Key responsibilities include: * Perform synthesis and chromatographic purification of innovative phosphoramidite monomers, and carry out conjugation of novel ligands-such as small molecules and peptides-to oligonucleotides for targeted delivery. * Design and execution of automated workflows for synthesizing, purifying, and analyzing ASOs, si RNAs, SSOs, and related oligonucleotides across various chemistries and scales using advanced instrumentation platforms. * Apply analytical techniques including UV-Vis spectroscopy, NMR, HPLC, and LC-MS to evaluate both crude and purified synthetic compounds. * Interpret and organize analytical data and research outcomes for presentation to project teams. * Support resolution of technical issues and contribute scientific and technical insights to ongoing projects. * Provide strategic input into experimental planning, integrated data analysis, and effective communication of results to scientific teams and leadership. * Maintain meticulous records of experimental procedures and key steps to ensure reproducibility, including accurate documentation in electronic lab notebooks in accordance with Lilly's quality standards. * Assist with general lab operations such as ordering supplies, preparing reagents, and maintaining equipment. * Collaborate closely with colleagues across multiple sub-teams within the Lilly LGM group. * Adhere strictly to all health and safety protocols. * Demonstrate a strong commitment to fostering a diverse and inclusive laboratory environment every day. Basic Qualifications: * Bachelor's or Master's Degree in chemistry, biochemistry, pharmacology, or related scientific field * 1+ years of work experience in an academic laboratory, or preferably in an industrial setting Additional Skills/Preferences: * Demonstrated expertise in organic synthesis and advanced chromatographic purification techniques is essential. Prior experience with the synthetic manipulation of nucleosides, nucleotides, phosphoramidites is highly desirable. * Hands-on experience in conjugation and bioconjugation chemistry; familiarity with solid-phase synthesis methods for oligonucleotides or peptides is a plus. * Proven laboratory proficiency with analytical instruments such as HPLC and LC-MS, including the ability to analyze, interpret, and effectively communicate data. * Adaptable and highly motivated to thrive in a dynamic, fast-paced research environment. * Strong communication skills and a collaborative mindset, with the ability to work efficiently across interdisciplinary teams. * Exceptional organizational abilities, attention to detail, and critical thinking skills; capable of multitasking and eager to learn new methodologies and contribute to innovation. * Skilled in processing, structuring, analyzing, and visualizing data from diverse sources, with the ability to derive meaningful insights. * Proficient in Microsoft Excel, Word, PowerPoint, and analytical software relevant to experimental methods. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $69,000 - $179,300 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

MST Process Engineer/Scientist III, Downstream - PLA JOB SUMMARY/OBJECTIVE: The primary responsibility is to participate in Manufacturing Sciences and Technology activities in support of downstream technology transfer, late stage clinical, PPQ and commercial manufacturing of viral vectors. The individual will serve as a process expert in downstream processing. This position requires close interaction with MS&T colleagues, Project Management, Manufacturing, Quality Assurance, Quality Control, Process Development, Engineering, Supply Chain, and other departments. This role will focus on aspects of implementing manufacturing processes to produce early- and late-phase human clinical trial and commercial gene therapy products. RESPONSIBILITIES: MST process lead for Downstream technology transfer activities involved in manufacturing viral vectors following cGMP guidelines. Collaborate with other sites or clients to ensure success of process transfer and scale up. Ensure effective information flow, risk assessment, timeline execution, issue resolution and documentation for multi-departmental teams (Process Development, Manufacturing, Quality, and Project Management). Includes authoring detailed process definition, facility fit, and raw material risk assessments. Author PPQ protocols and reports. Oversee execution of PPQ and PPQ related activities Develop sampling plans with clients and incorporate them into cGMP batch documentation. Monitor and trend process performance, including input and output parameters. Find opportunities to improve systems and practices KNOWLEDGE, SKILLS and QUALIFICATIONS: A degree in biochemical engineering, chemical engineering or related scientific field such as molecular biology, virology, biochemistry. Advanced degree preferred. B.S. with 8+ years, Master's degree with 6+ years, or PhD with 3+ years' professional history. Technical expertise in downstream biopharmaceutical manufacturing and/or process development. Experience with automated chromatography systems (AKTA) and automated tangential flow filtration (Repligen). Expertise in late stage/commercial technology transfer, process characterization and process validation biopharmaceutical/gene transfer vector manufacturing preferred. Knowledge of GMP and regulatory requirements of biopharmaceutical manufacturing, specifically cell and gene therapy vector production Ability to work both independently and as part of a team. Proficiency in operating effectively in a fast-paced dynamic environment while juggling multiple projects Project management skills desirable Ability to speak effectively before groups of customers. Excellent investigational skills and ability to solve technical issues. Ability to compile, analyze and interpret data; Ability to write routine reports and correspondence. Strong interpersonal skills to facilitate verbal and written communication. Excellent Benefits Benefits & Total Rewards | Thermo Fisher Scientific Medical, Dental, & Vision benefits-effective Day 1 Paid Time Off & Designated Paid Holidays Retirement Savings Plan Tuition Reimbursement OTHER Relocation assistance is not provided. Must be legally authorized to work in the United States now and in the future, without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening Compensation and Benefits The salary range estimated for this position based in Massachusetts is $83,300.00-$125,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Aktis Oncology is a biotechnology company pioneering the discovery and development of a new class of targeted alpha radiopharmaceuticals to treat a broad range of solid tumor cancers. Founded and incubated by MPM Capital, the company has developed proprietary platforms to generate tumor-targeting agents with ideal properties for alpha radiotherapy. Designed for high tumor penetration and long residence time, Aktis Oncology's molecules will quickly clear other areas of the body, thereby maximizing tumor elimination while minimizing side effects of treatment. This approach would enable clinicians to visualize and verify target engagement prior to exposure to therapeutic radioisotopes. The role will be responsible for all operations involved with routine manufacturing and quality control testing of radiopharmaceuticals produced in Aktis' GMP laboratory (Boston, MA), including but not limited to the list below: This role will report to the Director of Clinical Trial Manufacturing RESPONSIBILITIES This role will drive several areas of strategic importance to Aktis: * Manual and automated production of radiopharmaceuticals in a GMP facility * QC testing of radiopharmaceuticals * Execution and upkeep of the facilities' environmental monitoring program * Accurate and timely preparation and completion of manufacturing and Quality control records (Batch Records, Forms, Logbooks, etc.) * Process/analytical method validation for clinical manufacturing * Operation and maintenance of equipment in the GMP facility * Preparation of products for shipment to other sites * Drafting, reviewing and updating SOPs and other GMP documentation * Upkeep and maintenance of inventory in the GMP Facility * Maintenance of the GMP facility including assisting with radioactive waste stream management * Perform radiation and contamination surveys KNOWLEDGE, SKILLS, AND ABILITIES * Experience with aseptic operations and environmental monitoring * Experience with QC methodologies (HPLC, GC, MS, Gamma Spec, etc.) * Experience with assembly and interpretation of analytical data * Expertise with troubleshooting analytical and production equipment * High attention to detail and organizational skills to enable working in a fast-paced environment * Ability to work in an ISO7 environment with full gowning * Adhere to stringent cleanroom protocols and maintain a high level of hygiene * Perform precise aseptic manipulations in a restrictive environment * Awareness of FDA and EU GMP requirements * Ability to lift to 60lbs * Expertise with GMP radiopharmaceutical manufacturing and quality control is preferred QUALIFICATIONS * Minimum, undergraduate degree with 5+ years of experience in the pharma industry; preferred, M.Sc. with 3+ years of experience * Excellent verbal, written, and organizational skills * Strong desire to be part of a mission‐oriented company leading transformative change for patients * Proven demonstration of transparent communication and fostering open and diverse debate * Ability to work with agility and manage ambiguity * Personifies positive energy and exemplifies respect Aktis Oncology is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, disability, national origin, veteran status, or any other basis covered by appropriate law. Aktis Oncology is committed to promoting and maintaining a work environment in which all applicants, employees, and other individuals are treated with dignity and respect free from unlawful harassment, discrimination, or retaliation.

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. Job Description Perform a variety of analytical laboratory testing of raw materials and assure compliance with applicable laws, rules and regulations. Major Job Duties: Operate a variety of treatment test equipment, such as HPLC, spectrophotometer, pH meter, filtration devices, hot plates, TDS, Moisture Apparatus, Melting Point, balances, etc. Conduct a variety of analytical lab tests in compliance with standard testing methods, procedures and regulations; implement quality control specifications. Set up instruments and conduct sample tests; utilize a variety of methods to assure compliance to established standards and testing controls; interpret test results and prepare and submit reports related to test results. Perform, interpret, evaluate and record standard process control laboratory tests on ; perform calculations as needed and record results; notify appropriate personnel of abnormal or critical results and significant changes in lab results. Troubleshoot, clean and maintain instruments, glassware and equipment; conduct preliminary diagnostic test on equipment; assure materials meet standards of cleanliness to assure accurate test results; assure an adequate supply of test materials to perform daily testing; perform preventive maintenance on equipment. Qualifications WET CHEMISTRY GMP COMPENDIAL TESTING BS IN SCIENCES Additional Information $32/hr 9 MONTHS

HiFyve is hiring a Wet Chemistry Lab Technician for a Manufacturing company in Andover, MA!! Pay Rate- $22-$25/hr. Shift: Sun - Thur 12 am to 8 am Job Summary: This individual will work in the wet chemistry process lab to support all plating fabrication operations. The candidate will work with the wet chemistry lab team for day to day production analysis as well as special projects. Job Description Perform basic chemical analysis techniques. Utilize chemical analysis equipment to include Auto-Titration, CVS, ICP, and UV-VIS. Ability to input analysis results into TrueChem. Maintain lab safety policies and procedures. Education / Qualifications 1+ years of prior laboratory experience required. Experience with Titration analysis, ICP or AA, UV-VIS. Knowledge of operation and maintenance of lab equipment highly desired. Knowledge of Microsoft Word, Excel, and PowerPoint required. Must pay high attention to detail, possess self-motivating skills, and have the ability to self-inspect for quality and accuracy. Please apply or email your resume to: *********************

Do you want to take part in peptide drug discovery and thrive in a dynamic, high-throughput laboratory environment? If you are skilled in peptide synthesis and enjoy supporting innovation across disciplines, this role could be an excellent fit for you. At Gubra, you will see your efforts directly impact ongoing research projects, partnerships, and our growing drug discovery pipeline. And you will do so in a collaborative environment where colleagues are eager to help, share knowledge, and drive things forward. Help deliver high-quality peptides to drive our drug discovery projects forward As Laboratory Technician in our Chemistry department, your role will focus on supporting peptide synthesis and purification, operating automated workflows, and contributing to a well-run high-throughput laboratory. You will work closely with both Scientists and fellow Laboratory Technicians to ensure high-quality peptide production that enables rapid project progression. Gubra is looking for a Laboratory Technician to join our Chemistry department. You will be part of a strong team working with peptide chemistry and support our peptide drug discovery pipeline. If you are motivated by working in a multi-disciplinary environment, you should come and join us at Gubra. You will fill a new position in our growing Chemistry department. Your tasks as Laboratory Technician are diverse and include * Automated solid-phase peptide synthesis (SPPS). * Peptide purification by RP-HPLC. * Characterization and analysis of peptides by UPLC-MS and UPLC-CAD. * Liquid handling using automated liquid handlers (supporting task). * Data processing and documentation. * Instrument maintenance. * Contributing to the implementation of high-throughput laboratory processes to optimize workflows. * Supporting a wide range of parallel tasks in a fast-paced laboratory setting. Certified Laboratory Technician with hands-on peptide synthesis experience As part of an organization built on collaboration, knowledge sharing, and scientific rigor, you must enjoy teamwork and be comfortable juggling many tasks in an ever-evolving environment. You thrive in a high-throughput setup, where structure and prioritization are key, and where ongoing input from colleagues is part of everyday progress. Your resume ideally includes * A certified laboratory technician diploma or similar * Hands-on experience with peptide synthesis (required) * Knowledge of automated synthesis and solid-phase synthesis * Technical understanding of HPLC systems and peptide purification * Experience with data handling, documentation, and reporting * Good communication skills in both Danish and English * A collaborative mindset and motivation to contribute across shared workflows Chemistry at Gubra - your new Team You will join 5 Scientists and 5 Laboratory Technicians in the Chemistry department at Gubra HQ in Hørsholm, Greater Copenhagen. We work in a welcoming environment based on trust, helpfulness and a common desire to break new ground. We are experts in peptide chemistry, purification, and characterization, as well as peptide analytics by LC-MS and LC-CAD. Contact and application Please apply at our website using the "Apply" button and by uploading your motivated cover letter, resume and relevant diplomas. The deadline is December 31st, 2025. If you can recognize yourself in this description but still have a few questions, then please contact Department Manager Martin Kræmer (************). If necessary, we will set up an additional call to ensure your understanding of the job and your many opportunities. About Gubra Gubra is an ambitious contract research organisation (CRO) and biotech company striving for excellence at all levels. We insist on doing things efficiently - and often differently - to reach the results we aim for. Our vision is to become leaders in the fight for a more sustainable and healthier world. We do that by facilitating the discovery of new medicine, and by acting and inspiring others to fight the ongoing climate and biodiversity crises. Gubra's activities are focused on the early stages of drug development and are organised in two highly synergistic business areas: CRO Services and Discovery & Partnerships (D&P). We generate our revenue by performing research for life science companies as well as by partnering projects from our discovery and development pipeline. Our therapeutic focus is within metabolic and fibrotic diseases, and we specialize in in vivo pharmacology, ex vivo assays, drug profiling, histology, stereology and whole brain and organ imaging. In addition, we offer a full palette of advanced transcriptomics. Our ML/AI-driven peptide drug discovery platform strea MLine enables us to rapidly develop a peptide hit into a non-clinical candidate ready for development. Through a constant focus on high quality, scientific excellence, speed, and solid teamwork we have established ourselves as a highly professional and competent partner in the market. People are our greatest asset, and our team consists of +280 employees all located in Hørsholm, Denmark. The mix of people from different cultures and educational backgrounds combined with our entrepreneurial mindset have greatly impacted our working environment, which is characterized by entrepreneurial drive, scientific curiosity, and teamwork - we join forces!

& Purpose Allonnia's purpose is the pursuit of imaginative solutions to solve the world's toughest waste challenges through biology. Allonnia is leveraging the power of biotechnology and engineered systems to degrade or sequester pollutants and upcycle waste. Our ethos at Allonnia is to work in harmony with nature, combining biology and technology to fast forward time and bring Nature's future solutions to the present day. Through this collaboration we will unlock the potential in waste and enable a world where nothing is wasted. Allonnia is backed by Battelle, Ginkgo Bioworks, Viking Global, General Atlantic, EVOK and Cascade Investments. Mission of the Position The mission of the role is to 1) Advance the extraction and purification processes of mining ores through a multifaceted approach that includes use of biological and chemical solvents 2) perform lab experiments following SOPs and assisting with SOP optimization 3) operate and maintain laboratory instruments; record and manage data This is a full-time position that requires 100% time in the lab. This role is for Northeastern University students and will run from January-June 2026. Key Criteria/Requirements Preferred B.S or M.S. in chemistry, geology, chemical engineering or related field 0-2 years of Laboratory experience (college experience possible). Ability to follow standard operating procedures (SOPs) Strong analytical skills Excellent numerical skills Strong problem-solving skills Meticulous attention to detail and accuracy Experience with Microsoft Windows and Office tools Demonstrated ability to work independently as well as in team environment Excellent verbal and written communication skills Adaptable and able to work in a fast-paced environment Responsibilities & Measurable Accountabilities Perform a variety of laboratory experiments following SOPs and assist with SOP optimization Operate, maintain, and clean laboratory instruments and equipment Prepare buffers and media Knowledge of chemistry principles Comply with all safety standards Maintain a lab notebook; Record and manage data Communicate results, observations, and/or issues related to lab equipment, materials and experiments to supervisors Allonnia Core Values Purposeful Committing to work on the right things as individuals and as a company, making a difference every day Entrepreneurial Working with passion and curiosity to learn every day, creatively delivering results to the world Transparent Fostering a high trust environment that embraces constructive debate, achieving success together Key Competencies Analysis Skills Creativity Integrity Resourcefulness/Initiative Organization/Planning Listening Team Player Communications - Oral/Written Tenacity JOB CODE: 1000085

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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description Apply today for a rewarding career with opportunities for growth!! Must live a commutable distance to Derry, New Hampshire. We are looking for to fill full-time year round position. Mon-Fri 8:00am-4:30pm Compensation is $20-22/hour (DOE) plus benefits The Analyst I Organic Extractions prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins Quality Assurance programs and SOP's. Analyst I Organic Extractions responsibilities include, but are not limited to, the following: Demonstrates and promotes the company vision Regular attendance and punctuality Applies GMP/GLP in all areas of responsibility, as appropriate Performs routine lab tasks that provide experience and familiarization with methods, practices, and programs. These include: Preparation of samples using standard techniques Performing chemical analysis using standard techniques Calculating data Recording and reporting data and any unusual test occurrences to the supervisor Performing routine instrument maintenance Responsible for performing job functions in compliance with Eurofins EHS and QA standards Responsible for general housekeeping in his/her work area Ability to become trained and competent on complex instrumentation including but not limited to gas chromatography, gas chromatography/mass spectrometry, atomic absorption, ICP, and instrument specific data systems. Works under close supervision using routine and standard methods Aliquots and weighs samples Washes glassware Conducts all activities in a safe and efficient manner Performs other duties as assigned The ideal candidate would possess: Ability to use calculator/mathematical formulas and concepts Ability to complete work within time and quality constraints Can work independently following written or verbal instructions Cooperate and coordinate both orally and in writing Able to follow and learn appropriate protocols in one or more of the following disciplines: Organic preparation Metals preparation and analysis Gas Chromatography Gas Chromatography/Mass Spectrometry Wet Chemistry Qualifications Basic Minimum Qualifications: A minimum of an Associate of Science degree in Chemistry or equivalent experience Experience in an environmental lab is a plus At least 1-2 year's preparation, analytical experience, or combination, at company or equivalent experience elsewhere preferred Some previous PFAS experience preferred Experience with LC/MS-MS operation and general maintenance preferred Demonstrated effective communication skills and relate well to people in direct communication Consciousness of and a positive attitude toward quality, service and safety procedures Sound reasoning, good judgment and decision making Strong organization and problem solving skills Detail oriented, ability to handle multiple tasks simultaneously and able to coordinate multiple priorities Versatility, flexibility in dealing with people Ability to synthesize and retain information Computer skills, experience with LIMs software a plus Ability to perform basic math skills including multiplication, division and algebra Work independently Work within time constraints Must be able to lift up to 25 lbs frequently, and up to 50 lbs occasionally Willingness to put in overtime hours, as necessary to meet work needs Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Final candidate will be given pre-employment background check and drug screen Perform other duties as assigned Additional Information Please note - Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** 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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. We do not offer Visa Sponsorship for this role. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.