Chemist jobs in New Britain, CT - 68 jobs

PPG Industries, Inc. has an S&T Product Development Chemist, Senior position at our Milford, OH Research and Development (R&D) Center, responsible for supporting PPG in the development of new coatings products for commercialization, including supporting current and next generation development of chemical coatings for PPG's Food Packaging business segment. Specific duties include: (i) supporting the continuous development of food packaging coatings and product launches for PPG's U.S. customers, including by leading all phases of several simultaneous coatings projects at different stages of completion, developing project goals, and recommending new projects in collaboration with the technical manager and other polymer chemists; (ii) applying knowledge of appropriate scientific, experimental, and statistical methods as well as detailed knowledge of PPG's chemical manufacturing processes and protocols while serving as a resource with respect to chemical interactions during PPG's proprietary packaging coatings new product development; (iii) developing new testing methods to accelerate coatings development processes, including testing production batches prior to customer trials, identifying root causes of problems, and ensuring that new products are developed in accordance with both PPG's EHS standards as well as customer specifications; (iv) driving new coatings products innovation by implementing new ideas, screening new chemical technologies, and submitting MOI's that PPG will convert into patent applications; and (v) participating in product robustness activities for current and new coating technologies, including by working with PPG's raw material suppliers, to improve product launch success. Must have a bachelor's degree (or foreign equivalent) in Chemistry or a directly related scientific field plus three (3) years of experience in a related position. Experience must include three (3) years with each of the following: (i) coating formulation techniques and testing procedures; (ii) new coatings development for food and beverage packaging, with an emphasis on sustainable materials and addressing materials of concern; and (iii) providing support to resolve customer and production-related issues in packaging coatings. Experience can be concurrent. Apply online at careers.ppg.com. PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply. Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverages and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents.

Challenge Yourself and Impact the Future! MacDermid Alpha Electronics Solutions, a business of Element Solutions Inc (NYSE: ESI), is renowned worldwide for its commitment to revolutionizing the electronics industry. With a legacy spanning over a century, we have continually set new benchmarks for excellence, reliability and sustainability in electronic materials. Our Expertise: Wafer Level Solutions - Revolutionizing wafer fabrication processes for enhanced efficiency and performance Semiconductor Assembly Solutions - Driving innovation in semiconductor assembly processes for unparallelled reliability Circuitry Solutions - Tailored solutions to meet the dynamic demands of modern circuitry Circuit Board Assembly Solutions - Elevating circuit board assembly processes for optimal performance Film & Smart Surface Solutions - Transforming electronics with cutting-edge materials and technologies for enhanced functionality and reliability Across diverse sectors including automotive, consumer electronics, mobile devices, telecom, data storage, and infrastructure, MacDermid Alpha Electronics Solutions has earned the trust of manufacturers worldwide. Our comprehensive range of high quality solutions and technical services covers the entire electronics supply chain, empowering businesses to thrive in today's competitive landscape. We strive to embody the five 'Elements of our Culture'- our '5C's'; Challenge, Commit, Collaborate, Choose, and Care. These core values are the foundation of our organization which our employees embrace in their interactions with customers, colleagues and other stakeholders, to drive financial performance and create a rewarding work environment. Who are we looking for? The purpose of this position is to drive the development of innovative, differentiated, and high-performance materials for the Circuitry Solutions product lines.The candidate will be responsible by developing new products, material testing strategies/protocols, formulations and modifying/optimizing existing products. In this role, the candidate will work closely with scientists, product managers, application, and marketing managers globally to execute product roadmaps and strategies in existing and adjacent markets that drive growth What will you be doing? * Hold self to the highest standards on safety. We are committed to building a strong safety culture in all laboratory and related activities. * Research, develop, and formulate new surface treatment products for the printed circuit board, molded interconnect, connector and IC substrate industries. * Have an in-depth understanding of the patent and literature for new resin systems, chemistry, and polymers across related technology areas. * Deliver presentations/reports that distill complex ideas into precise results and proposals; communicate appropriately to influence internal and external audiences. * Actively participate in workgroup team meetings to address safety, process improvement, problem-solving, and other workgroups, departments, and active topics. * Mentor junior level scientists and technologists. * Communicate and appropriately document work in the form of internal presentations and external publications/reports. Draft and submit patent disclosures as appropriate. * Leverage external networks for project success, establish relationships with customer/OEM, and regularly engage in appropriate scientific venues. * Understand and follow appropriate EH&S standards, policies, and procedures applicable to their job. * Carry out responsibilities under the organization's policies and applicable laws. Present a professional attitude and handle confidential information according to non-disclosure guidelines. * Ability to work in a high paced and multi-task environment. Self-motivated and able to work with minimal supervision Who are You? * PhD degree in inorganic or electrochemistry, Polymer/material science, or related field with 3+ years technical research experience. * Comfort working in a wet chemistry lab, including safe handling of chemicals, solvents, and lab equipment. * Strong organizational skills, attention to detail, and ability to follow procedures with high repeatability. * Ability to work effectively as part of a team, communicate clearly in English (written and verbal), and manage multiple tasks under guidance from senior staff * Internship or 1-3 years of industrial experience in metal electrodeposition, materials R&D, formulation, preferred * Additional hands-on experience with analytical techniques such as electrochemical analysis (CV, LSV, potentiostat) SEM/optical microscopy, or other materials characterization methods, preferred. * Prior exposure to semiconductor materials (photoresists, dielectrics, plating additives, etc.) or work in a cleanroom/fab environment (coating, lamination, lithography, metrology), preferred. * Experience with basic data analysis and statistical tools (e.g., Excel, JMP, Minitab) to interpret experimental results, preferred. We understand that not all candidates may meet the requirements listed above. If you believe you have the knowledge and experience necessary to excel in this role, we encourage you to apply. Competencies * Able to work independently as well as in groups. * Organized, self-motivated, and action-oriented, with the ability to adapt quickly to new challenges and opportunities. * Good oral, presentation, and written communication skills. An ability to communicate and interact successfully with a broad range of disciplines, whilst maintaining a strong professional image * Passion, high energy, self-motivation, and a focus on execution. Independent thinking and problem-solving skills necessary to succeed in an entrepreneurial culture, demonstrating significant initiative and effort. * An ability to follow clearly defined objectives to solve difficult technical challenges within specific timescales. Coordinating cross-functional and outside resources to resolve problems as appropriate We are Offering... Challenge Yourself and Impact the Future - You will be part of a highly collaborative culture that promotes continuous improvement through cross-functional partnerships to achieve our mission. We do this through a strong and unified culture and transparent management, which has empowered us to create high-performing global teams that achieve superior solutions for our customers. As part of the MAES Team, you will have ... Opportunities for career growth, competitive compensation (competitive base salary and performance-related bonus plan), and benefits packages (health, dental, and vision insurance, Wellness Program, PTO/Holidays, as well as a 401(k)-retirement plan with a company match). Innovative work environment where you will be a part of a dynamic and collaborative team. Perks and incentives include paid parental leave, tuition reimbursement, and opportunities for professional development. The typical base salary range for this position is between $92,402.00 and $138,604.00 #LI-SB1 Equal Opportunity Employer All qualified applications will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected category applicable under federal, state and local laws. Nearest Major Market: Bridgeport Nearest Secondary Market: Danbury

Are you looking for a new challenge? Passionate about innovation? Want to work for a global company that values integrity, teamwork, and loyalty? At LATICRETE International, we aim to be the leading construction brand trusted globally for high-performance tile and stone installation systems and building finishing solutions. We've been in business for over 65 years, family-owned for three generations, and can be found in over 100 countries. The Hartford Business Journal even named us one of Connecticut's top family-owned companies in 2017! We don't just make innovative, industry-leading products. Our purpose is to improve the built world and the lives of those who build it. We strive to connect with, engage with and improve the lives of our employees, our customers, our partners, and the global communities in which we operate. We are seeking passionate and ambitious employees who want to make a difference not just within our organization, but within their communities, our industry, and the world. If that sounds like you, then what are you waiting for? Join the family and expand your horizons! Just some of our benefits: Medical Dental Vision 401k Tuition reimbursement 13 paid holidays in addition to paid vacation and sick time Flexible spending Life Insurance, AD&D and Supplemental Insurance POSITION SUMMARY Under general supervision, the Chemist I is responsible for performing accurate formulation and analytical tests in accordance with Internal LATICRETE, ANSI, and ASTM procedures and/or other accepted methods. The Chemist I develops and conducts complex chemical studies and experiments on organic and/or inorganic formulations. With the supervisor's oversight, this role is expected to use independent judgment, while reporting and analyzing data. ESSENTIAL DUTIES AND RESPONSIBILITIES Additional duties and responsibilities may be assigned, as necessary. Design, Develop and Validate - (75%) Under general supervision, conduct experiments to solve increasingly complex problems. Review and perform competitive testing and analysis as required. Maintain a clean working laboratory environment as well as properly working equipment. Ensure that all instruments that require periodic calibration and validation requirements do so per laboratory calibration/validation procedures. Comply with all laboratory, company, State and Federal safety regulations. Provide Product Support - (15%) Support Technical Services requests to evaluate field complaints in specific area. With guidance, support Operations in evaluating product inconsistencies & providing disposition. Communicate results within R&D, cross-functional departments as required. Help organize and participate in field trials as required. Interact with end-use customers and contractors to understand product usage, limitations, and needs. Assist and guide the production scale-up of new products developed: Write batching formulas for the production department based upon completed and approved laboratory formulations. Follow process through to full commercialization. Assist in determining Quality Control parameters for product testing. Data Analysis and Documentation - (10%) Responsible for documenting all work via approved methods and sharing developments via occasional technical presentations. Independently process, analyze, and interpret results and data in specific area. Summarize ongoing work and findings to colleagues during department meetings. Document work continuously according to standard practice. Summarize all project work in a formal end report. REQUIRED SKILLS & QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and Experience: BA/BS in a Physical Science required, Chemistry is preferred. MS in Physical Science or Chemistry a plus. Experience in scientific lab is a plus. Specialized Skills and Experience: Some familiarity with the process of researching patents, writing invention disclosures, and other publications within the industry. Demonstrated analytical ability in a laboratory environment well organized, detail oriented, and systematic in documenting results. Demonstrated verbal and written communication skills in order to present and write reports. Ability to organize and present results in a clear concise manner. Able to analyze data independently and apply some specialized knowledge (e.g. DOE and statistical methods to solve problems). Must be a self-starter and able to multi-task. Computer skills: Intermediate to Advanced knowledge of Microsoft Office 365 (Word, Excel, PowerPoint, Outlook) and other specialty software systems as required. Physical Requirements: Lift: Must be able to lift and/or carry a minimum of 50 pounds. Push/Pull: Must be able to push/pull 50 pounds. Standing: Must be able to stand at least 50% of the day. Sitting: Must be able to sit at least 50% of the day. Travel: May require Domestic travel as needed

The purpose of this position is to grow our technical portfolio and sales in the areas of Polyurethane Dispersions (PUDs) and urethane coatings. Successful candidates will work with existing and prospective customers to understand market needs, apply our current product portfolio for material recommendations, and develop new formulations to expand our product offering and market presence. They will collaborate with sales, product development, marketing, to be able to lead technical projects, synthesize polyurethane dispersion's and prepolymers, and commercialize new products JOB RESPONSIBILITIES: Understand UBE product portfolio and apply product recommendations for existing markets. Meet with customers to discuss technical opportunities and grow sales in polyurethane dispersions and coatings. Hunt for new opportunities & develop relevant application data. Translate customer needs into relevant product chemistry and lead development efforts to solve unmet customer and market needs. Synthesize and formulate polyurethane dispersions, blocked isocyanates & prepolymers. Shepherd new product commercialization and scale up from lab to production. Prepare & characterize prototype formulations. Perform chemical and mechanical testing on formulations to generate relevant customer and application data. Develop new application testing methods as needed to grow business. Align with Sales, Product Mgmt, & colleagues globally to grow sales. Lead Cross-functional teams and opportunities to completion. Key Skills & Competencies: Independent thinker with strong problem-solving skills and ability to manage complex tasks while balancing multiple priorities. Demonstrates sound judgment and a disciplined approach to work. Highly self-motivated; takes initiative without requiring direction. Strong interpersonal skills; comfortable engaging with customers and driving new business opportunities. Advanced technical knowledge in organic chemistry, coating chemistry, polymer science, and urethane coatings. Ph.D. in organic chemistry, coating chemistry, or polymer science preferred. Proven ability to lead, organize, plan, execute, and communicate effectively within cross-functional teams. Skilled in interfacing with external customers, vendors, suppliers, and internal global colleagues across urethane functions. BASIC QUALIFICATIONS: BS or MS is required in organic chemistry, polymer science, or a related field with appropriate industrial experience. A Ph.D. in organic chemistry, coating chemistry or polymer chemistry is desirable. 5-10 years of Experience. PREFERRED QUALIFICATIONS: Synthesizing, formulating and characterizing urethane coating chemistry, i.e. polyurethane dispersions (PUD's), blocked isocyanates & prepolymers. Polyurethane coating and polyurethane dispersions formulation development and product commercialization. Developing & maintaining key customer relationships. Understanding of the coatings market related to polyurethane dispersions, blocked isocyanates and related prepolymers, applying to technology growth strategies. Equal Opportunity Employer Statement: UBE is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, age, status as a protected veteran, or status as a qualified individual with a disability.

Groton, CT, USA Full-time ** 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 agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 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 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** + Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product, throughout all phases of development. This may include excipient, packaging, and post packaging support + Analytical testing would include: compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methods + Set up and analysis of drug substance and drug product stability samples + Method development and validation of analytical methods for drug substance and drug product **Qualifications** + Strong computer, scientific, and organizational skills + Experience with eLN, LIMS and data trending are a plus + Excellent communication (oral and written) and attention to detail + Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude + Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies **Minimum Qualifications:** + Bachelor's degree in chemistry or other science related degree concentration, or equivalent directly related experience + Laboratory experience and some experience in GMP analytical chemistry, preferred **Additional Information** + Position is full-time, Monday - Friday 8am to 5 pm + Ability to work overtime as required. + Tasks require repetitive motion and standing for long periods of time. + May be required to respond to off-shift operational issues. + Candidates currently living within a commutable distance of **Groton, CT** are encouraged to apply. + Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays + **\#LI-EB1** + Authorization to work in the United States indefinitely without restriction or sponsorship **Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

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 agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 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 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 an associate scientist/scientist to join the SmartLab within Drug Product Design and Supply. The successful candidate will develop and deploy automation and technology processes for pharmaceutical drug candidates in a laboratory setting. Position Responsibilities: The successful candidate will help design, prototype and develop laboratory automation solutions for drug product development applications as part of a multi-disciplinary team. Assist with design and testing of modular hardware to facilitate data-rich experimentation. Enable use of digital tools for machine learning and self-optimization to enhance automation goals. Collaborate with internal and external stakeholders to implement automated equipment and develop novel solutions for execution of laboratory experimentation. Innovate with academic and industrial collaborators to identify unmet needs and develop novel solutions. Partner with research scientists and engineers on suitable experimentation to deliver DPDS workflows for solid dosage form development. Implement a robotic control system for orchestration of multiple workstreams using modular laboratory equipment. Enable data management systems to retrieve, process and store relevant lab data from both manual and automated experiments. Develop and implement data analytics tools for process optimization, process modeling, and visualization. Participation with departmental initiatives, continuous improvement teams, scientific presentations, and external collaborations to influence scientific and business impact of the group. Qualifications Basic Qualifications Master of Science Degree in Automation Engineering, Robotics, Electrical Engineering, Mechanical Engineering, Data Sciences or closely related discipline; OR a Bachelor's degree in these disciplines with 2-4 years of relevant experience in a laboratory setting. Strong coding with C/C++ or Python Experience working with Application Programming Interface (API) and Open Platform Communications (OPC) Data processing experience, including AI agents, machine learning, and Bayesian optimization Experience working with computer-aided vision systems for testing and analysis of product quality attributes Basic mechanical and electrical troubleshooting skills Preferred Requirements Experience with robotics, automation, data analytics, and machine vision systems used in laboratory automation Experience in pharmaceutical research and development Additional Information Position is Monday- Friday 8:00 AM- 5:00PM. Overtime as needed. Candidates currently living within a commutable distance of Groton, CT are encouraged to apply. Candidates currently living within a commutable distance of Indianapolis, IN are encouraged to apply Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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 agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 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 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 Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product, throughout all phases of development. This may include excipient, packaging, and post packaging support Analytical testing would include: compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methods Set up and analysis of drug substance and drug product stability samples Method development and validation of analytical methods for drug substance and drug product Qualifications Strong computer, scientific, and organizational skills Experience with eLN, LIMS and data trending are a plus Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Minimum Qualifications: Bachelor's degree in chemistry or other science related degree concentration, or equivalent directly related experience Laboratory experience and some experience in GMP analytical chemistry, preferred Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Groton, CT are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

The Associate Scientist will serve as the platform lead for Xenium spatial transcriptomics projects at Single Cell Biology Lab (SCBL) within The Jackson Laboratory for Genomic Medicine, ensuring the timely delivery of high-quality, robust data. The SCBL is a core facility supporting the scientific research community with cutting-edge single-cell technologies, including dissociative single-cell omics, spatial omics, and high-content screening. This role is central to the lab's spatial genomics capabilities, requiring deep expertise in the Xenium workflow, exceptional project coordination, and strong communication with scientific stakeholders. The ideal candidate will be the technical expert for all Xenium operations from sample handling and experimental execution to data quality control and workflow optimization. You will leverage your strong background in molecular biology, tissue handling, and single-cell technologies to enhance and expand the capabilities of the Single Cell Biology Lab. Key Responsibilities & Essential Functions Platform Leadership: Serve as the Xenium Platform Lead and Subject Matter Expert (SME), providing guidance and support to end-users and the broader scientific community. Project Management & Execution: Coordinate the full lifecycle of Xenium projects, including managing sample submission and receiving, providing service quotations, executing experiments, and ensuring final data quality control (QC). System Maintenance: Oversee instrument management, including maintaining the Xenium instrument, managing stock and inventory, and performing advanced troubleshooting of equipment and assays. Process Optimization & Development: Drive the continuous improvement of the platform by optimizing existing workflows and developing new spatial genomics capabilities and technologies. Scientific Awareness: Stay current with the newest developments in the spatial genomics field and effectively communicate technological updates to the team and research community. Meticulous Documentation: Maintain excellent documentation standards, including comprehensive lab notebooks, SOPs, error/work logs, metadata, and sample information. Stakeholder Communication: Ensure seamless communication with end-users, vendors, colleagues, and managers to coordinate and successfully complete all Xenium projects. Knowledge, Skills, and Abilities Required Education: Master's degree (M.S.) in Biology, Molecular Biology, or a related scientific field. Experience: 2-4 years of experience in a core facility or industry setting. Molecular & RNA Biology: Deep and comprehensive understanding of RNA and molecular biology principles, including associated assays. Imaging-Based Spatial Genomics Expertise: Hands-on experience with FISH-based platforms, including 10x Genomics Xenium, MERFISH, and seq FISH. Technical Breadth: Comprehensive knowledge of various spatial genomics technologies (e.g., Xenium, Visium, MERFISH, seq FISH). Sample Handling: Direct experience with tissue sectioning, handling, and immunohistochemistry (IHC) techniques. Documentation: Experience in writing Standard Operating Procedures (SOPs) and familiarity with Laboratory Information Management Systems (LIMS) and Electronic Lab Notebooks (ELN). Operational Skills: Proven project and lab management experience, including managing stock, inventory, and instrument uptime. Soft Skills: Exceptional communication, interpersonal, and presentation skills; proven ability to thrive as a team player within interdisciplinary groups. Preferred Education: Ph.D. preferred Single-Cell Experience: Hands-on experience with single-cell technologies (e.g., 10x Chromium, smart-seq, split-and-pool methods). Biopharma Industry Experience: Preferred experience working in an industrial setting, such as the biotechnology or pharmaceutical sector, demonstrating familiarity with industry-standard workflows and requirements. Histology Expertise: Experience in histopathology. Development: Proven track record in technology development or assay optimization. Pay Range: $69,711 - $90,624 #CA-NL6 About JAX: The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California), Japan and China. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health. Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visit *********** . EEO Statement: The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.

At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850. We are currently seeking a junior level quality focused QC Chemist with analytical or quality control laboratory experience in a Manufacturing environment. EDUCATION/EXPERIENCE: Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred. DUTIES: Under direction from the Laboratory Supervisor, performs quality control analysis on raw materials, in-process samples, finished/filled products, process validation/evaluation, and stability testing Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights, and measures Inspects production equipment for various Q.C. aspects Maintains proper documentation for Filling department quality control Assists in experiments relative to the discovery and development of new products Makes pilot batches of experimental products Creates processing batch sheets and batch records (PBR's), and checks artwork, crimp codes, log sheets, & shipping requirements Prepare artwork ingredient list General electronic and hard copy file, records, documents and database maintenance Maintain cleanliness and appearance of department, and assist in the disposal of hazardous (laboratory) waste Assist in laboratory instrument qualification and/or calibration Act as subject matter expert for laboratory instrumentation or analytical techniques Maintain proper liaison with all departments to contribute to the team philosophy Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.'

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 • Working with some supervision, applies established knowledge of laboratory techniques such as HPLC, dissolution, UV/VIS spectrophotometry, moisture by KF, and others to perform product stability testing. • Candidate will be responsible for understanding and performing routine analytical testing for stability samples, evaluating and documenting results in a timely manner. Understands and follows all SOPs and written test procedures. • Performs testing within established standard test times and maintains quality and productivity at acceptable levels as communicated by the supervisor. Candidate will execute troubleshooting of instrumentation and will be expected to maintain laboratory equipment in good working condition. • Candidate will perform laboratory investigation steps with appropriate approvals and with some guidance from supervisor. Keeps supervisor fully informed of all results and project status on a daily basis and reports critical information in a timely manner. Qualifications • Qualifications: Essential Skills- 1-3 years of experience in a related laboratory, HPLC, Dissolution, UV/VIS spectrometry, moisture by KF. Strong understanding of GMP concepts and requirements is desired. • Empower (CDAS) experience is desirable Additional Information For more information, please contact, Sneha Shrivastava **********

Analytical Chemist Lab Tech needs 4+ years of experience Analytical Lab Tech requires: Experience with common analytical techniques, instrumentation, and software Strong problem-solving skills and attention to detail Proficiency with Microsoft Office software Strong written and verbal communication skills Knowledge of safety protocols and proper laboratory practices Ability to work independently and as part of a team Analytical Lab Tech duties: Perform analytical chemistry tests and experiments per written procedures or compendial methods. Ensure accurate data is generated during laboratory testing. Report results according to standard operating procedures. Maintain laboratory notebook in accordance with standard operating procedures. Follow all safety protocols and maintain a clean and organized laboratory environment. Perform routine laboratory equipment maintenance and calibration tasks in accordance with standard operating procedures. Provide technical support to other team members as needed.

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. Qualifications These work hours are for 6:00 PM - 2:30 AM (primarily M-F, but some weekends might be possible) Associate Scientist with Associate's degree (A.A./A.S.) in a scientific discipline (preferred) Associate Scientist requires: possess effective verbal and written communication skills. Ability to work beyond normal work hours and various shift availability required. Ability to perform and record data entry via computer systems while conducting timed clinical procedures. Must possess skills necessary for sample processing and handling. Two years experience in a hospital based or clinical commercial lab, performing specimen processing. Associate Scientist duties: Specimen processing, verification of specimen compliance, and operation of centrifuges. Aliquoting specimens Delivering specimens to proper bench Preparing specimens for storage Retrieve samples from storage Arrange samples in proper order into specimen containers Properly pack specimen containers into shipping boxes and ship specimens•Receive shipments from outside lab Additional Information $21/hr 12 MONTHS

At Henkel, you can build on a strong legacy and leading positions in both industrial and consumer businesses to reimagine and improve life every day. If you love challenging the status quo, join our community of over 47.000 pioneers around the globe. Our teams at Henkel Adhesive Technologies help to transform entire industries and provide our customers with a competitive advantage through adhesives, sealants and functional coatings. With our trusted brands, our cutting-edge technologies and our disruptive solutions, you will have countless opportunities to explore new paths and develop your skills. Grow within our future-led businesses, our diverse and vibrant culture and find a place where you simply belong. All to leave your mark for more sustainable growth. Dare to make an impact? What you´ll do * Design, develop, execute, and support on-time commercialization of new adhesive formulations and products. * Prepare and deliver presentations on research projects for internal teams, management, customers, and technical conferences. * Understand state-of-art technology advancement and apply it to product development. Generate new intellectual properties. * Perform all laboratory work in a safe manner and comply with all regulations, safety precautions, PPE requirements, and 5Sprocesses. * Guide and mentor junior chemists as needed. What makes you a good fit * Master's or PhD degree in Chemistry, Chemical Engineering, Polymer Sciences, Materials Science, or in any other related scientific areas, is highly preferred. * Candidate with B.S. degree and a strong track record of >10 years of successful Product Development in the relevant area may be considered. * Proven track record of on-time product development delivery from idea generation to completion is required. * Minimum 5 years of experience in the areas of UV/Light stable Epoxy (1K & 2K) resin for outdoor applications. * Strong oral and written communication skills, and excellent interpersonal skills are essential. * The ability to work autonomously on multiple projects is needed. * Traveling of up to 10% will be required. Some perks of joining Henkel * Flexible or hybrid work model * Diverse national and international growth opportunities * Global wellbeing standards with health and preventive care programs * Gender-neutral parental leave for a minimum of 12 weeks * Employee Share Plan with voluntary investment and Henkel matching shares * Annual performance bonus * Comprehensive healthcare including mental health support and 401(k) plan matched by employer * Family benefits including fertility support, fully paid parental leave, caregiver services * Paid time off: Vacations days, sick leave, holidays, volunteer time off & more The salary for this role is $120,000.00- $145,000.00. This is the range that we in good faith anticipate relying on when setting wages for this position. We may ultimately pay more or less than the posted range and this range. This salary range may also be modified in the future. Henkel does not accept unsolicited resumes from search firms or employment agencies. Unsolicited referrals and resumes are considered Henkel property and therefore, Henkel will not pay a fee for any placement resulting from the receipt of an unsolicited referral. Henkel is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, genetic information, and other legally protected categories. JOB ID: 25074749 Job Locations: United States, CT, Rocky Hill, CT Contact information for application-related questions: ***************************** Please do not use this email address for sending your application or CV. To apply, please click on the "Apply for this role" button below. Applications sent via e-mail will not be accepted. Application Deadline: As long as the vacancy is listed on our Career Site, we are happy to receive your application Job-Center: If you have an application already, you can create or log in to your account here to check the status of your application. In case of new account creation, please use your email address that you applied with. Activate external content When clicking the button below external content will be loaded which involves transfer of personal data (e.g. IP address) to external servers. This may involve that cookies are set by the external content provider. Please see Data Protection Statement for further information. Accept for all YouTube content LOAD EXTERNAL CONTENT Deactivate loading external content from YouTube. How is work at Henkel About Henkel Building on a strong legacy of almost 150 years, we are leading the way to reimagine and improve life every day. Today and for generations to come. Through our innovative and sustainable brands and technologies, across our teams around the world. Henkel holds leading positions in both industrial and consumer businesses: Our portfolio includes well-known hair care products, laundry detergents, fabric softeners as well as adhesives, sealants, and functional coatings.

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 agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 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 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 Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product, throughout all phases of development. This may include excipient, packaging, and post packaging support Analytical testing would include: compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methods Set up and analysis of drug substance and drug product stability samples Method development and validation of analytical methods for drug substance and drug product Qualifications Strong computer, scientific, and organizational skills Experience with eLN, LIMS and data trending are a plus Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Minimum Qualifications: Bachelor's degree in chemistry or other science related degree concentration, or equivalent directly related experience Laboratory experience and some experience in GMP analytical chemistry, preferred Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Groton, CT are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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 agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 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 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 Responsible for utilizing analytical methodologies, systems, and processes to support GMP release and stability testing of clinical supplies for drug substance and drug product, throughout all phases of development. This may include excipient, packaging, and post packaging support Analytical testing would include: compendial testing (e.g., excipients/packaging release testing), disintegration, dissolution, HPLC/UPLC, SFC, generic testing (e.g., solvents, water, ash, titrations, heavy metals, ICP/MS, UV) and compound specific methods Set up and analysis of drug substance and drug product stability samples Method development and validation of analytical methods for drug substance and drug product Qualifications Strong computer, scientific, and organizational skills Experience with eLN, LIMS and data trending are a plus Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivated, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Minimum Qualifications: Bachelor's degree in chemistry or other science related degree concentration, or equivalent directly related experience Laboratory experience and some experience in GMP analytical chemistry, preferred Additional Information Position is full-time, Monday - Friday 8am to 5 pm Ability to work overtime as required. Tasks require repetitive motion and standing for long periods of time. May be required to respond to off-shift operational issues. Candidates currently living within a commutable distance of Groton, CT are encouraged to apply. Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Authorization to work in the United States indefinitely without restriction or sponsorship Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Are you looking for a new challenge? Passionate about innovation? Want to work for a global company that values integrity, teamwork, and loyalty? At LATICRETE International, we aim to be the leading construction brand trusted globally for high-performance tile and stone installation systems and building finishing solutions. We've been in business for over 65 years, family-owned for three generations, and can be found in over 100 countries. The Hartford Business Journal even named us one of Connecticut's top family-owned companies in 2017! We don't just make innovative, industry-leading products. Our purpose is to improve the built world and the lives of those who build it. We strive to connect with, engage with and improve the lives of our employees, our customers, our partners, and the global communities in which we operate. We are seeking passionate and ambitious employees who want to make a difference not just within our organization, but within their communities, our industry, and the world. If that sounds like you, then what are you waiting for? Join the family and expand your horizons! Just some of our benefits: Medical Dental Vision 401k Tuition reimbursement 13 paid holidays in addition to paid vacation and sick time Flexible spending Life Insurance, AD&D and Supplemental Insurance POSITION SUMMARY Under general supervision, the Senior Chemist is responsible for product development, while conducting analytical tests in accordance with International LATICRETE, ANSI, and ASTM procedures and/or other accepted methods. The Senior Chemist conducts complex chemical studies, experiments on organic and/or inorganic compounds and materials. A Senior Chemist must demonstrate strong technical knowledge and techniques in a specific area and an understanding of projects with respect to organization, research, production, and operations. With minimal supervisor oversight, they are expected to use independent judgment in designing experiments, determining appropriate approach to project work. Additionally, this role must identify new raw materials, suggest quality control tests for new products and may recommend improvements in analytical equipment, procedures, and techniques. Sr. Chemist is expected to train and devise experiments for team members as needed. ESSENTIAL DUTIES AND RESPONSIBILITIES Additional duties and responsibilities may be assigned, as necessary. Design, Develop and Validate - (50%) Under general supervision, formulate products to meet specified requirements. Devise and conduct experiments to solve increasingly complex problems. Evaluate and suggest new raw materials through increasing communication with raw material suppliers. Review and perform competitive testing and analysis as required. Maintain a clean working laboratory environment as well as properly working equipment. Ensure that all instruments that required periodic calibration and validation requirements do so per laboratory calibration/validation procedures. Comply with all laboratory, company, state and federal safety regulations. Provide Product Support - (20%) Maintain cooperative, professional attitude with all LATICRETE employees and customers. Support Technical Services requests to evaluate field complaints in specific area. Support Operations in evaluating product inconsistencies & providing disposition Participate in multi-disciplinary teams. Communicate results within R&D, cross-functional departments and Stage Gate Review meetings. Help organize and participate in field trials as required. Interact with end-use customers and contractors to understand product usage, limitations, and needs. Assist and guide the production scale-up of new products developed: Write batching formulas for the production department based upon completed and approved laboratory formulations. Follow process through to full commercialization. Determine Quality Control parameters for product testing. Data Analysis and Documentation - (15%) Responsible for documenting all work via approved methods and sharing developments via occasional technical presentations. Independently process, analyze, and interpret results and data in specific area. Summarize ongoing work and findings to colleagues during department meetings. Document work continuously according to standard practice. Summarize all project work in a formal end report. Mentor and Train New and Junior Team Members (10%) Write work instructions for R&D related test procedures. Help guide new and junior team members within the lab. Be a resource for escalations and problem solving. Impart Company knowledge of policies and procedures to help them orient to the organization. Consistently uphold Company culture through positive communications, managing conflict and fostering an open and constructive environment. REQUIRED SKILLS & QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and Experience: BA/BS in a physical science required, Chemistry highly preferred. MS a plus. 4+ years of relevant work experience in formulating construction materials, building products or related industry. Specialized Skills and Experience: Experience formulating products in a research and development lab environment in a specific area of the construction industry. Minimum 5+ years of hands-on experience in pigment chemistry, formulation, and color development within coatings, plastics, or related industries. Led end-to-end pigment formulation and color development projects, delivering custom solutions for coatings, plastics, and inks that met client specifications and industry standards. Applied advanced pigment chemistry and color science expertise to optimize formulations for durability, consistency, and reproducibility, resulting in improved product performance and reduced development time. Some experience with Production/Operations, Product Management, QC, ISO processes, Analytical Chemistry, Product Development, Finance, Accounting and Marketing departments. Some familiarity with the process of researching patents, writing invention disclosures, and other publications within the industry. Demonstrated analytical ability in specific area, well organized, detail oriented, and systematic in documenting results. Demonstrated verbal and written communication skills in order to present and write reports. Ability to organize and present results in a clear concise manner. With supervisor verification, able to analyze data independently and apply some specialized knowledge (e.g. DOE and statistical methods to solve problems). Must be a self-starter and able to multi-task. Computer skills: Intermediate to Advanced knowledge of Microsoft Office 365 (Word, Excel, PowerPoint), Outlook and other specialty software systems as required. Physical Requirements: Lift: Must be able to lift and/or carry a minimum of 50 pounds. Push/Pull: Must be able to push/pull 50 pounds. Standing: Must be able to stand at least 50% of the day. Sitting: Must be able to sit at least 50% of the day. Travel: May require Domestic travel as needed

The Associate Scientist will serve as the platform lead for Xenium spatial transcriptomics projects at Single Cell Biology Lab (SCBL) within The Jackson Laboratory for Genomic Medicine, ensuring the timely delivery of high-quality, robust data. The SCBL is a core facility supporting the scientific research community with cutting-edge single-cell technologies, including dissociative single-cell omics, spatial omics, and high-content screening. This role is central to the lab's spatial genomics capabilities, requiring deep expertise in the Xenium workflow, exceptional project coordination, and strong communication with scientific stakeholders. The ideal candidate will be the technical expert for all Xenium operations from sample handling and experimental execution to data quality control and workflow optimization. You will leverage your strong background in molecular biology, tissue handling, and single-cell technologies to enhance and expand the capabilities of the Single Cell Biology Lab. Key Responsibilities & Essential Functions * Platform Leadership: Serve as the Xenium Platform Lead and Subject Matter Expert (SME), providing guidance and support to end-users and the broader scientific community. * Project Management & Execution: Coordinate the full lifecycle of Xenium projects, including managing sample submission and receiving, providing service quotations, executing experiments, and ensuring final data quality control (QC). * System Maintenance: Oversee instrument management, including maintaining the Xenium instrument, managing stock and inventory, and performing advanced troubleshooting of equipment and assays. * Process Optimization & Development: Drive the continuous improvement of the platform by optimizing existing workflows and developing new spatial genomics capabilities and technologies. * Scientific Awareness: Stay current with the newest developments in the spatial genomics field and effectively communicate technological updates to the team and research community. * Meticulous Documentation: Maintain excellent documentation standards, including comprehensive lab notebooks, SOPs, error/work logs, metadata, and sample information. * Stakeholder Communication: Ensure seamless communication with end-users, vendors, colleagues, and managers to coordinate and successfully complete all Xenium projects. Knowledge, Skills, and Abilities Required * Education: Master's degree (M.S.) in Biology, Molecular Biology, or a related scientific field. * Experience: 2-4 years of experience in a core facility or industry setting. * Molecular & RNA Biology: Deep and comprehensive understanding of RNA and molecular biology principles, including associated assays. * Imaging-Based Spatial Genomics Expertise: Hands-on experience with FISH-based platforms, including 10x Genomics Xenium, MERFISH, and seq FISH. * Technical Breadth: Comprehensive knowledge of various spatial genomics technologies (e.g., Xenium, Visium, MERFISH, seq FISH). * Sample Handling: Direct experience with tissue sectioning, handling, and immunohistochemistry (IHC) techniques. * Documentation: Experience in writing Standard Operating Procedures (SOPs) and familiarity with Laboratory Information Management Systems (LIMS) and Electronic Lab Notebooks (ELN). * Operational Skills: Proven project and lab management experience, including managing stock, inventory, and instrument uptime. * Soft Skills: Exceptional communication, interpersonal, and presentation skills; proven ability to thrive as a team player within interdisciplinary groups. Preferred * Education: Ph.D. preferred * Single-Cell Experience: Hands-on experience with single-cell technologies (e.g., 10x Chromium, smart-seq, split-and-pool methods). * Biopharma Industry Experience: Preferred experience working in an industrial setting, such as the biotechnology or pharmaceutical sector, demonstrating familiarity with industry-standard workflows and requirements. * Histology Expertise: Experience in histopathology. * Development: Proven track record in technology development or assay optimization. Pay Range: $69,711 - $90,624 #CA-NL6 About JAX: The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California), Japan and China. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health. Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visit ************ EEO Statement: The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.

Job Description At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850. We are currently seeking a junior level quality focused QC Chemist with analytical or quality control laboratory experience in a Manufacturing environment. EDUCATION/EXPERIENCE: Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred. DUTIES: Under direction from the Laboratory Supervisor, performs quality control analysis on raw materials, in-process samples, finished/filled products, process validation/evaluation, and stability testing Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights, and measures Inspects production equipment for various Q.C. aspects Maintains proper documentation for Filling department quality control Assists in experiments relative to the discovery and development of new products Makes pilot batches of experimental products Creates processing batch sheets and batch records (PBR's), and checks artwork, crimp codes, log sheets, & shipping requirements Prepare artwork ingredient list General electronic and hard copy file, records, documents and database maintenance Maintain cleanliness and appearance of department, and assist in the disposal of hazardous (laboratory) waste Assist in laboratory instrument qualification and/or calibration Act as subject matter expert for laboratory instrumentation or analytical techniques Maintain proper liaison with all departments to contribute to the team philosophy Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.'

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. Qualifications These work hours are for 6:00 PM - 2:30 AM (primarily M-F, but some weekends might be possible) Associate Scientist with Associate's degree (A.A./A.S.) in a scientific discipline (preferred) Associate Scientist requires: possess effective verbal and written communication skills. Ability to work beyond normal work hours and various shift availability required. Ability to perform and record data entry via computer systems while conducting timed clinical procedures. Must possess skills necessary for sample processing and handling. Two years experience in a hospital based or clinical commercial lab, performing specimen processing. Associate Scientist duties: Specimen processing, verification of specimen compliance, and operation of centrifuges. Aliquoting specimens Delivering specimens to proper bench Preparing specimens for storage Retrieve samples from storage Arrange samples in proper order into specimen containers Properly pack specimen containers into shipping boxes and ship specimens•Receive shipments from outside lab Additional Information $21/hr 12 MONTHS