Chemist Jobs in Glasgow, DE

AnalytiChem is a global company founded in 2021 that assists analytical testing laboratories in the industrial, environmental, and materials markets to collect actionable data to optimize their business. Our mission is to enable our customers' science by providing a solutions-oriented and integrated range of products that help them collect their best data. We are experiencing rapid growth, both organically and through acquisition, with 8 companies worldwide and counting. Our brands include SCP Science, Chem Service, Bernd Kraft, OREAS, Chem-Lab, Northeast Laboratories and BioTRADING and we support customers in a wide range of industries from Industrial to environmental and animal health. If you are looking for a dynamic work environment in a fast-growing organization where you can make a difference, AnalytiChem might be the challenge you are seeking. What will you do We are looking for a reliable Quality Control Chemist to ensure that all external and internal requirements for production of chemical reference materials are met before our high-quality product reaches our customers, while managing a team of two (2) quality control analysts. You will be responsible for developing and performing various tests on candidate reference materials, including techniques such as Gas Chromatography (GC-FID & GC-MS), HPLC, FT-IR, pH-testing, UV absorption testing and alike. An excellent Quality Control Supervisor is highly experienced in various instrumental and wet chemical testing methods and passionate about top quality products. The goal is to assure the high quality of our operations and services aiming to the long-term success of our business. Your main skills Plan and perform quality control inspections on candidate reference materials Define standard methods and their acceptance criteria for analysis of CRM Perform HPLC, GC, UV, FT-IR and similar instrumental QC tests Perform titrations, pH-tests and other wet-chemistry tests Document results in lab notebooks and ERP systems Perform Proficiency Tests to demonstrate the lab competence Writing standards operating procedures and method documentations. Handle all non-conformities and corrective actions Communicate with external quality assurance officers and assessors during on-site inspections What we are looking for Proven experience as a quality control analyst or similar relevant role Thorough knowledge (min 3 years) of methodologies of quality testing techniques and methods Experience handling Reference Materials according to ISO 17025 and/or ISO 17034. Good knowledge of MS Office Good communication skills Great attention to detail and a results driven approach Reliable and Trustworthy BSc/BA in Chemistry or another relevant field

Medical Solutions is seeking a travel Cath Lab Technologist for a travel job in Dover, Delaware. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel We're seeking talented healthcare professionals whose adventure game is as strong as their clinical game. Those that want flexibility and high pay, we have the positions for you! Some of the industry-leading benefits enjoyed by Medical Solutions travel nurses and travel allied healthcare professionals include: Day One Medical, Dental, and Vision with low premiums Day One 401(k) with Company Contribution Personalized Compensation Packages Loyalty Bonus Program and Referral Bonus Paid, Private, Fully Furnished, Pet-Friendly Housing Dedicated Recruiter and 24/7 Customer Care Line Per Diem Allowance and Paid Travel Licensure and Certification Reimbursement Free Liability Coverage Voluntary Benefits: Critical Illness, Hospital Indemnity, Accident, and Pet Insurance Equal Employment Opportunity And More! Estimated pay package based on bill rate at time job was posted. Bill rates can change frequently and without notice. Exact pay package may vary based on guaranteed hours, distance being traveled, and customizations available for travelers. Medical Solutions Job ID #841541. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cardiac Cath Lab About Medical Solutions At Medical Solutions, we're people who care, helping people who care. No matter how you look at it, there's a whole lot of care going on in our world and that's just the way we like it. What do we do? Medical Solutions is one of the nation's largest providers of total workforce solutions in the healthcare industry, connecting nurses and allied health clinicians with hospitals and healthcare systems across the country and around the corner. Through our family of brands, we also serve a segment of clients outside of the healthcare space. And we're the very best at what we do. You'll love our culture that's filled with heart and soul. As a company and employer, we're sincerely and unabashedly us. We lead as humans first and believe the unique qualities of each team member make us better together. We share a purpose for helping others and the drive to make a difference. And we offer endless opportunities for personal and professional growth, throughout your career. At Medical Solutions, you'll find a great place to work and a career home. We've received Best Places to Work awards, landed top industry awards, and received accolades for the impact we've made in business and within our community. But the only way to really get to know us, is to join us. We think you'll fit right in. Benefits Weekly pay Holiday Pay Guaranteed Hours Continuing Education 401k retirement plan Pet insurance Company provided housing options Cancelation protection Wellness and fitness programs Mileage reimbursement Referral bonus Employee assistance programs Medical benefits Dental benefits Vision benefits Benefits start day 1 License and certification reimbursement Life insurance Discount program

AMN Healthcare Allied is seeking a travel Cath Lab Technologist for a travel job in DOVER, Delaware. & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel Job Description & Requirements Cath Lab Technologist - (Cath Lab Tech) StartDate: ASAP Available Shifts: 10 D Pay Rate: $3092.21 - $3388.27 Dover, DE cath lab is seeking a DE licensed tech for assignment. 10 hour days, ARRT (R) EMR is EPIC. BLS from AHA. Cath, EP, and possibly structural if you have experience Required Qualifications Cath Lab Technologist, Cath Lab Licenses(At least one of the following): CLT-DE, RAD-DE Certifications(At least one of the following): RCIS-Cardiovascular Credentialing International, CERT-ARRT- R Facility Location The capital of the “First State,” Dover is a fascinating city known for its history, culture and best of all-tax-free shopping! Situated on the St. Jones River, the city offers panoramic views and dozens of historical attractions. Visit Biggs Museum of American Art where you can enjoy an extensive collection of art or spend time in downtown Dover where both architectural and culinary delights abound! Job Benefits Allied travel assignments are typically for 13 weeks and offer generous packages that include: Competitive pay rates Medical, Dental, Vision 401(k) and Flex Spending Life Insurance Accident and Short-term Disability Coverage Free Continuing Education Competitive Housing Deal Refer a friend and earn extra cash! About the Company At AMN Healthcare, we strive to be recognized as the most trusted, innovative, and influential force in helping healthcare organizations provide quality patient care that continually evolves to make healthcare more human, more effective, and more achievable. cath lab technologist, cardiac, invasive cardiac, diagnostic reports, cardiac cath lab, cath lab, allied, allied health, healthcare, health care, cath, catheterization, hospital, medical, patient care, RCVT, cath lab tech AMN Healthcare Allied Job ID #3229458. Pay package is based on 10 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Cath Lab Technologist - (Cath Lab Tech) About AMN Healthcare Allied AMN Healthcare is a leading force in the healthcare industry, committed to being the most trusted, innovative, and influential partner for healthcare organizations. With a focus on providing quality patient care, AMN Healthcare offers holistic solutions that reduce costs, streamline processes, and improve efficiencies. The company boasts over 30 years of experience and takes pride in staffing leading healthcare facilities with the nation's best travelers. As an industry leader, AMN Healthcare offers a diverse team dedicated to supporting healthcare workers and facilities, ensuring a personalized and supportive experience for both clients and candidates. Visit ****************************************************** for more information. Benefits Company provided housing options Medical benefits Dental benefits Continuing Education

This is a laboratory-based position that will aid in improving our various water analysis products as well as help design and implement new products. This position will report to the Director of R&D and has no direct reports. Job Responsibilities: Works safely Develops new and improved reagents and products. Develops formulations for tableted or powdered reagents Develops formulations for liquid and dried reagents Develops formulations for test strip reagents Ability to perform reagent calibrations on colorimeter/photometers Ability to use spread sheets and other data analysis applications Provides technical assistance to Customer Service and Marketing personnel. Resolves technical problems. Provides technical support to QC, QA, to resolve problems. Performs related laboratory duties as assigned. Conducts performance evaluations of our products versus competitor's products of similar specifications. Prepares calibration standards for checking performance of instruments. Provides technical input for quotations and product costs. Provides technical input for the preparation of SDS, instructions and labels. Maintains laboratory notebook and/or electronic notes and records. Prepares pre-production batches of reagents to establish specifications. Writes SOPs, TIs, operation instructions and manuals as needed. Participates in staff meetings as needed. Miscellaneous: Participates in lean activities, including but not limited to Lean training and lean events such as kaizen or a 5-day event. 5-S program in the various departments assigned. DMAICs. Continuously looks for ways to improve both departments' and own individual efficiencies and time management, as well ways to improve any aspect of the Company's operations and develops and implements DMAICs accordingly. Notifies Manager of any production, equipment, safety or personnel problems, etc. and cooperates in resolving such issues as well. For example, requests assistance when systems prevent the efficient performance of duties or when a system fails. Provides Manager with feedback to determine where additional training would benefit and obtains additional training as necessary. Complies with all Company policies (i.e. personnel, safety, etc.). Performs other duties as assigned. (Such duties may or may not be essential functions of the job. Travel will be required to our Chestertown facility of 10%-20%. Qualifications/Requirements: Requires a minimum of B.S. or B.A. degree in chemistry from an accredited institution, with 2 or more years of lab experience in chemistry or a related field (i.e. biochemistry), and/or an advanced degree in chemistry or pharmaceutical chemistry. Must have good laboratory skills to safely handle chemicals and instruments used in R&D laboratory, be familiar with computer-assisted instrumentation, possess good color perception and adequate manual dexterity, maintain accurate records, work according to established laboratory procedures, work independently without requiring day-to-day supervision and have proficient computer skills using Microsoft Office at a minimum, additional computer skills with data analysis applications an advantage. Environmental Factors/Physical/Mental Capabilities: Works indoors in temperature controlled environment.Handles various chemicals. Requires good problem solving, judgment, communication skills, math skills and color perception. Requires walking, standing, sitting, good manual dexterity and some transporting up to 30 lbs. LaMotte Company, a 100+ year-old global industry leader in developing and manufacturing premier water analysis solutions, operating in Newark, DE, Chestertown, MD and Warwick, UK. Our products are used around the world to accurately, quickly, and conveniently test water in a multitude of applications. LaMotte offers paid time off including vacation, sick leave, and paid holidays. Full-time employees, who regularly work at least 30 hours per week, are eligible for employer-provided insurance including health, dental, vision, disability, life insurance, and supplemental insurance. Full-time employees are eligible to contribute to our 401(k) plan with an employer match available. LaMotte is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, disability, military status, genetic information, sexual orientation, or any other legally recognized protected basis under federal, state, or local laws.

Provide expert technical and analytical support to the Quality Control (QC) function including instrumentation and methodology troubleshooting, non-routine analysis, and the evaluation of new technology. Individual should be qualified to Bachelor of Science level/or higher in a scientific field with a minimum of 3 years' experience in a GMP laboratory environment. Strong knowledge of analytical chemistry and laboratory instrumentation and GMP/GLP. Required skills: Individual should be qualified with a Bachelor of Science or graduate level degree in a scientific discipline with a minimum of 3 years' experience in GMP laboratory environment. Strong knowledge of analytical chemistry, laboratory instrumentation, and GMP/GLP. Mandatory Science Degrees/Experience/ Certifications: Bachelor of Science degree in a scientific discipline (i.e. chemistry, analytical chemistry, biochemistry, etc.) HPLC or HPIC experience 3 years minimum post-grad experience Semi-automatic dissolution bath experience Experience in a GMP environment and an understanding of those requirements Desirable skills: Validation Experience, Technical Transfer Methods, Experience with Lab Data Management Systems (LIMS or 1Lab) Preferred schedule 6am - 3pm or 10am - 7pm

The Research Chemist is responsible for conducting laboratory experiments, applying the principles of chemistry and processing towards new products while supporting current applications. They will assist with production scale-up in a manufacturing environment. The Chemist will interact with customers and within professional groups in support of the business. Responsibilities Support current chemistry applications within the business activities for the Highway group; Develop professional expertise in the company's core technologies and identify new opportunities for business growth and cost reductions Translate advances in materials chemistry, including paint formulations, into new product improvements and offerings Manage experiments for product improvement and new product development; Understands and optimizes water-based paint formulation Interface with customers in a support role to support technical initiatives; Coordinate process scale-up and production trial activities Maintain a high level of product knowledge of both legacy and new product offering; Investigate independently and collaborate with other groups on quality problems and recommend changes as needed Interface with sales and tech support to ensure customer requests are interpreted correctly into product advancements.; Interface with customers in a support role to support initiatives; Participate in professional trade meetings and conferences; Provide chemical and processing support to manufacturing plants to improve manufacturing efficiencies and capabilities Maintain a clean lab environment; Use established prudent practices in the laboratory while working; Follow manufacturing plant safety guidelines while on site Qualifications Bachelors Degree or higher in Chemistry, Chemical Engineering, or Materials Engineering 3 to 6 years of Chemist/Lab experience required 3 to 6 years of Manufacturing R&D Lab experience preferred Paint and Coatings experience preferred Glass chemistry, glass composition and optics experience are a plus Skills & Knowledge Microsoft Office - strong in Excel Laboratory Equipment Experience Ability to communicate clearly with manager and co-workers Good housekeeping and Lab cleanliness skills Strong attention to Detail and Organization Consistency and Accuracy for Lab Results

Compensation & Additional Details: Fully onsite in Malvern, PA 10 PTO Days + 6 Sick Days 12 month extending contract Compensation: $29-$32/hr exact rate is based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Minimum Qualifications: -Bachelor's degree in scientific field, preferably Biotech -Minimum 1 year of experience working in a lab environment, preferably GMP -Minimum 1-2 years of experience working within cell culture (not just academia) -Minimum 1 year of experience working with Aseptic techniques -cGPMP, GMP, GDP (Good documentation practice) -Strong attention to detail -Extremely motivated individual -Cell Banking experience (preferred) Day-to-Day: One of our large pharmaceutical clients is looking to hire an Associate Scientist of Cell Banking to perform Cell Banking for the Cell Culture processes and/or bio-analytical testing within the API Large Molecule Process Development group in Malvern PA. The candidate's primary responsibilities will include but are not limited to the production, testing, inventory, and supply of Master, Working, and development Cell Banks for clinical, and commercial production as well as analytical testing for J&J biopharmaceutical and cell therapy products. Responsibilities will include: -Support Cell banking organization by performing Cell banking for Cell Culture processes and analytical testing. -Execute production, testing, and release of Master, Working, development, and analytical cell Banks and ensures the timely supply to customers. -Work in a team environment as well as contributing individually to meet project timeline and objectives. -Participate in Cell culture and cryopreservation of cells using aseptic techniques under GMP Compliant conditions. -Execute all activities per established procedures and protocols -Interface with internal and external customers to ship cell banks and supply critical information as per their requirements. -Collaborate cross-functionally to represent Cell Banking department. -Author, review, and approve technical documents, SOPs, and batch records.

At RxSource, our passion drives us to be the bridge between pharma and patient. With offices in Canada, USA and Ireland we provide bespoke global clinical trial supply management services to pharma, biotech and CROs. Whether it's employing demand-led packaging, a local sourcing model or another flexible option, we guarantee on-time delivery without compromising quality. Our clients are our partners; success for them = success for us. We currently have an opening for a Quality Control Associate at our West Deptford, New Jersey facility. This role is a key position within our global Quality Assurance team and will be responsible for performing on-site quality activities. If you are a personable and proactive Quality professional with experience in clinical trial packaging and labelling, pharma manufacturing or pharma distribution, we would like to hear from you. What you will do: Release incoming goods Perform in-process and finished good quality inspections Initiate Quality Management System documentation (i.e. Deviation, CAPA, Change Control, etc.) Review batch records pre- and post-execution Perform periodic quality walkthrough inspections to verify compliance with SOPs Participate in process improvement initiatives Manage all controlled GMP documentation and document archives Assist with supplier and customer verification/qualification and approval Provide support for customer and regulatory inspections Review daily/weekly checks (e.g., temperature, sanitation, etc.) and facility maintenance reports Assist with facility qualification activities Your qualifications, skills and experience include: 2 or more years in a QA or QC role, clinical trial packaging or pharmaceutical manufacturing/distribution Working knowledge of Good Manufacturing Practices A degree or diploma from a recognized college or university Strong written and verbal communication skills Ability to prioritize Team player who works well with others A commitment to providing excellent internal and external customer service No matter your role at RxSource, successful team members are: Patient Champions, who put patients first and uphold strict ethical standards Achievers, who drive toward practical solutions Individuals Who Inspire Excellence in themselves and those around them High-quality and accountable executors, working towards goals and milestones with quality, precision, and speed

Title: Lab Instrument Coordinator Duration: 1 year The role involves managing and coordinating the onboarding, validation, and maintenance of laboratory instruments, including scheduling vendor services and overseeing routine repairs. The individual will work closely with internal and external teams to ensure lab operations are compliant and efficient. Responsibilities: Coordination and management of instrument onboarding and validation Scheduling vendor routine and repair service Escorting vendors in the lab space Facilitating instrument preventive maintenance, calibration, and repairs; may include some hands-on maintenance and calibration duties Qualifications: Minimum of an Associate's degree is required At least 1+ years of GxP experience is required Must have GMP record keeping experience Experience with chamber management, lab safety and housekeeping Software validation experience Must be proficient in MS Excel and PowerPoint Be able to coordinate activities with internal and external operations and service teams, service providers, IT, site quality, and analysts to ensure lab operation activities are completed and compliant.

Adesis Inc. is a subsidiary of Universal Display Corporation (Nasdaq: OLED), a global leader in organic light emitting diodes. Within our OLED Chemistry organization, we engage in research and development of new materials for use in the fabrication of OLED devices leading to the next generation of OLED displays. Our R&D footprint encompasses almost 100,000 square feet of state-of-the-art laboratory and manufacturing space in two U.S. locations - New Castle and Wilmington, DE, centrally located in the Mid-Atlantic biotech/pharmaceutical hub. We are an extraordinary company looking for extraordinary talent! If you would like to be a part of a multi-disciplinary team of scientists and engineers working on fast-paced and innovative OLED research programs that will impact the next generation of consumer electronics, then please come and join us! Position Summary: The manufacturing Process Chemist works both independently and as part of a team to assist in the development, optimization, and technology transfer of commercial manufacturing compounds. The position involves set-up, use, and cleaning of various laboratory equipment as well as running established protocols with the guidance of chemists and senior technical staff. Responsibilities: Develop robust processes for the target compounds to ensure safe and reproducible processes. Develop alternate synthetic routes to target molecules and modify reactants and/or equipment as required. Solve complex chemical problems which may arise during process development, optimization or scale up of processes. Understand the concepts of reaction kinetics, design of experiments, solubility and crystallization, mass transfer, heat transfer and process safety to ensure critical process parameters are identified. Accountable for documentation to ensure the consistent manufacture of products; including batch records, production instructions, and development / qualification reports. Performs other related duties as assigned by Management. Technical and Specialized Equipment: NMR (UP) LC/MS EasyMax, PolyBLOCK Jacketed reactors GC/MS Automated Chromatography Systems Hydrogenation equipment Qualifications: BS or MS in Chemistry or related field required. At least 2 - 5 years' experience in technical production, R&D, and/or new product development experience required. Ability to define problems, collect data, establish facts, and draw valid conclusions. Interpretation of technical instructions from disparate information sources, and deal with several abstract and concrete variables. Ability to work within a fast-paced, dynamic and team environment. Working knowledge of ISO-9001, cGMP, and/or ICH Q7 in pharma or chemical regulated environments preferred. Knowledge of Process Improvement methodology (ie., Lean Manufacturing, Six Sigma, and/or TOC) a plus. Experience with or ability to master the use of modern research tools such as EasyMax, PolyBlock, Continuous Flow Reactors, and in-situ process monitoring a plus. Strong computer skills in standard & scientific systems, such as Microsoft Word, Excel, PowerPoint, ChemDraw, Reaxys and Scifinder. Benefits Package: Our highly competitive employee package offers medical, dental and vision benefits. Also included are: 401K Plan Employee Stock Purchase Plan Life, Disability and AD&D Insurance A generous time-off policy that includes up to twelve weeks of maternity/parental leave Paid Volunteer Time Off Professional Development Program We want you to start with us and retire with us.

Wilmington PharmaTech (WPT) is seeking self-motivated Research Scientists to join our dynamic chemistry process department for active pharmaceutical ingredient (API) synthesis in clinical phase drug development. Key Responsibilities: Participates in the production of APIs in a kilolab or pilot plant setting by following batch records under cGMP environment. Records precisely all critical observations and documents all results during the production accurately. Diligently follows company SOPs to clean equipment for production and maintains appropriate cleaning records. Disassembles reactors for cleaning as necessary and reassembles them after the cleaning complete. Ensures and maintains kilolabs and related storage areas are in good condition. Performs routine qualifications for production equipment and maintains related records. Understands cGMP requirements of WPT and strictly follows all company policies, SOPs and best practices. Adheres to safety standards. Potential to conduct hands-on organic research with supervision for process optimization, and collect data to support the production of intermediates/APIs. Participates in the hazard operations (HAZOP) discussion and provide suggestions and solutions as necessary. Assists in trouble shootings and investigations of processes. Maintain good, clear laboratory records. Desired Qualifications: Academic or industrial research experience in organic chemistry. This position offers benefits, competitive salary and an opportunity to advance in a growing company.

It's an exciting time to be part of the IFF family. We are a global leader in taste, scent and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. IFF is seeking a highly motivated Scientist to work in the Advanced Analytical Biosciences group located at the Wilmington, Delaware site. The successful candidate will be part of the LC-MS group developing primarily HPLC and LC-MS based bioanalytical methods to support various business problems and research programs. In this role, close collaboration with scientists of multiple disciplines - chemists, biochemists, micro- and molecular biologists, and fermentation engineers is expected. The successful candidate should be adaptive, self-motivated, with a passion for science, and thriving in a team environment. The position will be located at the Experimental Station in Wilmington, Delaware, USA. Please note that this position is 100% laboratory based. Responsibilities: Performs sample preparations including organic solvent extractions, dilutions, and filtrations prior to instrument analysis. Troubleshoots instrument problems and performs general system maintenance, and prepares analytical standards for various projects Conducts research with guidance from experienced R&D leader or technical team leader. Use computer systems and software programs - Microsoft Office (Word, Excel, Access, Outlook), data acquisition programs - to acquire and document results Effectively collaborates with colleagues on laboratory techniques, sample preparation, instrumentation, data analysis, documentation, and safety Qualifications: Master's degree in a scientific discipline (chemistry, biochemistry, forensic chemistry) with a minimum of 3 to 5 years of experience, or a Bachelor's degree with 8-10 years experience. 3-5 years of demonstrated experience with HPLC sample preparation and analysis Familiarity with Thermo instrumentation and software (Chromeleon) is preferred Knowledge of laboratory safety precautions and protocols for safe handling and the disposal of hazardous agents/reagents, chemicals and materials Has intermediate knowledge of commonly used chemistry concepts, practices, procedures, and regulations Ability to understand and effectively communicate technical information, both oral and written to others, including co-workers, supervisors, and vendors Competence in Microsoft Word and Powerpoint, and Excel for data manipulation Excellent teamwork ability to contribute to multi-technique solutions to complex problems Ability to manage multiple concurrent projects and changing priorities We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Agilent Technologies is seeking a Production Chemist for its manufacturing facility in Newport, Delaware. The Newport site is part of Agilent's growing Consumables and Supplies Division (CSD), with a focus on liquid chromatography products. Agilent's product quality and technological innovation lead the market. As a leader, we are entering new phases of product transformation with increased emphasis on new product and process innovation, process standardization and production efficiency. This is a high-visibility and growing product line where you will have the opportunity to make a real difference to one of Agilent's key consumables businesses. Plus, we embrace 6-Sigma and Lean Manufacturing methodologies making for an engaging and rewarding mix of scientific discovery, process improvement, and employee growth and development. Key responsibilities include working individually or as part of multi-discipline, cross-functional teams to: Evolve existing chemistries and design new chemistries Provide support for and/or represent the site on new product introduction projects Scale existing chemistries in support for a rapidly growing line of liquid chromatography consumables Lead project teams to develop and deploy product and process improvements, which include capital projects and continuous improvement projects Support and actively pursue Lean, 6-Sigma, and Safety Improvement projects Provide daily support for the production of silica-based packing for high-performance liquid chromatography columns Resolve yield and scrap issues Execute and support the Management of Change control process, determine the disposition of nonconforming product, and create and execute corrective and preventive action plans to improve safety and quality Maintain SAP data accuracy (bills of materials, recipes) Qualifications Bachelors or Masters Degree in Chemistry, Material Science or equivalent 1+ years of experience in a chemistry based working environment Demonstrated technical and problem solving skills Demonstrated communication skills; written, oral and listening Demonstrated leadership skills Computer and digital skills Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least February 26, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $79,200.00 - $123,750.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing

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 Performs qualitative and quantitative chemical analysis of raw materials . Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non-conformances and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance. Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Qualifications The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Job Summary: We are seeking a dedicated and detail-oriented QC Chemist to join our team. The QC Chemist will be responsible for conducting routine and non-routine analyses of raw materials, in-process, and finished products to ensure they meet quality standards and safety regulations. The ideal candidate will have a strong analytical mindset, meticulous attention to detail, and extensive knowledge of laboratory procedures and equipment. Responsibilities * Conduct various chemical and instrumental analyses on raw materials, in-process samples, finished products, packaging, and composites. * Prepare and analyze samples using various procedures, including internal SOPs, specifications, analytical methods, compendial monographs, client procedures, research procedures, and protocols. * Utilize Wet Chemistry techniques (pH, Viscosity, and Titration) and Analytical Testing methods (GC, UV/Vis, and IR). * Maintain sophisticated analytical instruments, schedule preventative maintenance, and ensure trouble-free operation. * Ensure products meet quality standards and specifications, making critical pass/fail decisions. * Troubleshoot quality issues and identify root causes, preventive, and corrective actions. * Prepare and report results from timely preparation of monthly reports. * Maintain compliance with relevant regulations, standards, and guidelines. * Maintain accurate and complete records of all analytical activities. * Provide technical assistance to internal and external customers. * Make risk analysis and usage decisions of non-conformances. Essential Skills * Quality control * GMP * QC testing * Chemistry * Laboratory * Gas chromatography (GC) * Wet Chemistry techniques (pH, Viscosity, Titration) * UV/Vis * IR Additional Skills & Qualifications * Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field. * 1+ years of experience in a QC role within a cGMP facility. * Proficiency with Wet Chemistry techniques such as pH, Viscosity, and Titrations. * Familiarity with analytical techniques such as GC, UV/Vis, and IR. * Strong understanding of cGMP environment and regulatory standards. * Excellent attention to detail and problem-solving skills. * Ability to work independently and as part of a team. * Strong communication and documentation skills. Work Environment The QC Chemist will work in a cGMP-compliant laboratory setting, utilizing a range of sophisticated analytical instruments and equipment. The role requires adherence to safety protocols and regulatory guidelines. The work environment is collaborative, and you will have the opportunity to provide technical support to both internal and external customers. Flexibility and the ability to work independently and within a team are essential. Additional Information: This plant is a 24/7 operation and the QC department works a rotating shift (no set shifts, each employee must do the rotating shift). Ex: 4 12hr night shift followed by 7 days off then 5 8hr day shift followed by 3 days off then back to night. Pay and Benefits The pay range for this position is $30.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Newark,DE. Application Deadline This position is anticipated to close on Apr 8, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Title: Research & Development Chemist Department: R&D Reports To: Vice President of R&D _________________________________________________________________________________ This is a laboratory-based position that will aid in improving our various water analysis products as well as help design and implement new products. This position will be based in our Newark, DE location with some travel to our Chestertown, MD required. Job Responsibilities: · Works safely · Develops new and improved reagents and products. · Develops formulations for tableted or powdered reagents · Develops formulations for liquid and dried reagents · Develops formulations for test strip reagents · Ability to perform reagent calibrations on colorimeter/photometers · Ability to use spread sheets and other data analysis applications · Provides technical assistance to Customer Service and Marketing personnel. · Resolves technical problems. · Provides technical support to QC, QA, to resolve problems. · Performs related laboratory duties as assigned. · Conducts performance evaluations of our products versus competitor's products of similar specifications. · Prepares calibration standards for checking performance of instruments. · Provides technical input for quotations and product costs. · Provides technical input for the preparation of SDS, instructions and labels. · Maintains laboratory notebook and/or electronic notes and records. · Prepares pre-production batches of reagents to establish specifications. · Writes SOPs, TIs, operation instructions and manuals as needed. · Participates in staff meetings as needed. Miscellaneous: · Participates in lean activities, including but not limited to o Lean training and lean events such as kaizen or a 5-day event. o 5-S program in the various departments assigned. o DMAICs. Continuously looks for ways to improve both departments and own individual efficiencies and time management, as well ways to improve any aspect of the Company's operations and develops and implements DMAICs accordingly. · Notifies Manager of any production, equipment, safety or personnel problems, etc. and cooperates in resolving such issues as well. For example, requests assistance when systems prevent the efficient performance of duties or when a system fails. · Provides Manager with feedback to determine where additional training would benefit and obtains additional training as necessary. · Complies with all Company policies (i.e. personnel, safety, etc.). · Performs other duties as assigned. (Such duties may or may not be essential functions of the job. Requirements Qualifications/Requirements: Requires minimum of B.S. or B.A. degree in chemistry from an accredited institution, with 2 or more years of lab experience in chemistry or a related field (i.e. biochemistry), and/or an advanced degree in chemistry or pharmaceutical chemistry. Must have good laboratory skills to safely handle chemicals and instruments used in R&D laboratory, be familiar with computer assisted instrumentation, possess good color perception and adequate manual dexterity, maintain accurate records, work according to established laboratory procedures, work independently without requiring day-to-day supervision and have proficient computer skills using Microsoft Office at a minimum, additional computer skills with data analysis applications an advantage. Environmental Factors/Physical/Mental Capabilities: Works indoors in temperature-controlled environment. Handles various chemicals. Requires good problem solving, judgment, communication skills, math skills and color perception. Travels to both plants to interact with employees and managers and attend meetings. Travels to offsite training sessions/seminars, meetings, and other locations as needed. Travel will be required to our Chestertown facility of 10%-20% of the time. Requires walking, standing, sitting, good manual dexterity and some transporting up to 30 lbs. LaMotte Company, a 100+ year-old global industry leader in developing and manufacturing premier water analysis solutions, operating in Newark, DE, Chestertown, MD and Warwick, UK. Our products are used around the world to accurately, quickly, and conveniently test water in a multitude of applications. LaMotte offers paid time off including vacation, sick leave, and paid holidays. Full-time employees, who regularly work at least 30 hours per week, are eligible for employer-provided insurance including health, dental, vision, disability, life insurance, and supplemental insurance. Full-time employees are eligible to contribute to our 401(k) plan with an employer match available. LaMotte is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, disability, military status, genetic information, sexual orientation, or any other legally recognized protected basis under federal, state, or local laws.

div itemprop="description"section class="job-section" id="st-company Description"divp class="googlejobs-paragraph--empty"/ph2 class="title"Company Description/h2/divdiv class="wysiwyg"pArtech 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. /p/div/sectionsection class="job-section" id="st-"divp class="googlejobs-paragraph--empty"/ph2 class="title"Job Description/h2/divdiv class="wysiwyg" itemprop="responsibilities"p/pullibi Performs qualitative and quantitative chemical analysis of raw materials/i/b. Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. /lili Functions as a team member in the bi QA Chemical Laboratories/i/b to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. /lili Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non-conformances and recommends corrective actions. /lili Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. span Audits documentation, device history records, and test methods for compliance. /span/lili Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. /lili Assists in projects including the validation of test methods and transfer of new products/processes/test methods. /lilibi The candidate should be able to work 2nd or 3rd shifts. /i/b/lilibi Need to be flexible on working 2nd or 3rd. /i/b/li/ulpbr//pp/p/div/sectionsection class="job-section" id="st-qualifications"divp class="googlejobs-paragraph--empty"/ph2 class="title"Qualifications/h2/divdiv class="wysiwyg" itemprop="qualifications"p/pulli The candidate should be able to work 2nd or 3rd shifts. /lilispan Need to be flexible on working 2nd or 3rd. /spanbr//li/ulp/p/div/sectionsection class="job-section" id="st-additional Information"divp class="googlejobs-paragraph--empty"/ph2 class="title"Additional Information/h2/divdiv class="wysiwyg" itemprop="incentives"pb Sneha Shrivastava/b/ppb Technical Recruiter (Clinical/Scientific)/b/ppb /bb Artech Information Systems LLC/b/ppb360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 /b/ppb Office: 973. 967. 3348 | Fax: 973. 998. 2599/b/ppb Connect with us on - LinkedIn | Facebook | Twitter/bbr//ppbbr//b/ppbbr//b/pp/pp/pp/pp/pp/p/div/section/div

The Research Chemist is responsible for conducting laboratory experiments, applying the principles of chemistry and processing towards new products while supporting current applications. They will assist with production scale-up in a manufacturing environment. The Chemist will interact with customers and within professional groups in support of the business. Support current chemistry applications within the business activities for the Highway group; Develop professional expertise in the company's core technologies and identify new opportunities for business growth and cost reductions Translate advances in materials chemistry, including paint formulations, into new product improvements and offerings Manage experiments for product improvement and new product development; Understands and optimizes water-based paint formulation Interface with customers in a support role to support technical initiatives; Coordinate process scale-up and production trial activities Maintain a high level of product knowledge of both legacy and new product offering; Investigate independently and collaborate with other groups on quality problems and recommend changes as needed Interface with sales and tech support to ensure customer requests are interpreted correctly into product advancements.; Interface with customers in a support role to support initiatives; Participate in professional trade meetings and conferences; Provide chemical and processing support to manufacturing plants to improve manufacturing efficiencies and capabilities Maintain a clean lab environment; Use established prudent practices in the laboratory while working; Follow manufacturing plant safety guidelines while on site Minimum Requirements: Bachelor Degree or higher in Chemistry, Chemical Engineering, or Materials Engineering 3 to 6 years of Chemist/Lab experience required 3 to 6 years of Manufacturing R&D Lab experience preferred Paint and Coatings experience preferred Glass chemistry, glass composition and optics experience is a plus Skills & Knowledge: Microsoft Office - strong in Excel Laboratory Equipment Experience Ability to communicate clearly with manager and co-workers Good housekeeping and Lab cleanliness skills Strong attention to Detail and Organization Consistency and Accuracy for Lab Results

Job Summary: We are seeking a dedicated and detail-oriented QC Chemist to join our team. The QC Chemist will be responsible for conducting routine and non-routine analyses of raw materials, in-process, and finished products to ensure they meet quality standards and safety regulations. The ideal candidate will have a strong analytical mindset, meticulous attention to detail, and extensive knowledge of laboratory procedures and equipment. Responsibilities * Conduct various chemical and instrumental analyses on raw materials, in-process samples, finished products, packaging, and composites. * Prepare and analyze samples using various procedures, including internal SOPs, specifications, analytical methods, compendial monographs, client procedures, research procedures, and protocols. * Utilize Wet Chemistry techniques (pH, Viscosity, and Titration) and Analytical Testing methods (GC, UV/Vis, and IR). * Maintain sophisticated analytical instruments, schedule preventative maintenance, and ensure trouble-free operation. * Ensure products meet quality standards and specifications, making critical pass/fail decisions. * Troubleshoot quality issues and identify root causes, preventive, and corrective actions. * Prepare and report results from timely preparation of monthly reports. * Maintain compliance with relevant regulations, standards, and guidelines. * Maintain accurate and complete records of all analytical activities. * Provide technical assistance to internal and external customers. * Make risk analysis and usage decisions of non-conformances. Essential Skills * Quality control * GMP * QC testing * Chemistry * Laboratory * Gas chromatography (GC) * Wet Chemistry techniques (pH, Viscosity, Titration) * UV/Vis * IR Additional Skills & Qualifications * Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field. * 1+ years of experience in a QC role within a cGMP facility. * Proficiency with Wet Chemistry techniques such as pH, Viscosity, and Titrations. * Familiarity with analytical techniques such as GC, UV/Vis, and IR. * Strong understanding of cGMP environment and regulatory standards. * Excellent attention to detail and problem-solving skills. * Ability to work independently and as part of a team. * Strong communication and documentation skills. Work Environment The QC Chemist will work in a cGMP-compliant laboratory setting, utilizing a range of sophisticated analytical instruments and equipment. The role requires adherence to safety protocols and regulatory guidelines. The work environment is collaborative, and you will have the opportunity to provide technical support to both internal and external customers. Flexibility and the ability to work independently and within a team are essential. Additional Information: This plant is a 24/7 operation and the QC department works a rotating shift (no set shifts, each employee must do the rotating shift). Ex: 4 12hr night shift followed by 7 days off then 5 8hr day shift followed by 3 days off then back to night. Pay and Benefits The pay range for this position is $30.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Newark,DE. Application Deadline This position is anticipated to close on Apr 2, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.