Chemist jobs in Yonkers, NY

The ERP Analyst will play a critical role in supporting, maintaining, and optimizing the Infor Lawson ERP platform. This role requires a strong blend of technical expertise, business acumen, and interpersonal skills. The analyst will act as a liaison between business and technical teams, ensuring that ERP solutions align with organizational goals while improving efficiency and data integrity. Experience, Skills, and Qualifications:Education: Bachelor's degree in Finance, Accounting, Information Technology, or a related field. Experience: Minimum 3+ years as an ERP or Financial Analyst. Hands-on experience in Infor Lawson ERP preferred. Strong knowledge of GAAP, budgeting principles, and financial controls. Proficiency with Microsoft Excel and other Microsoft Office applications.

Primary Duties & Responsibilities Member of prototype fabrication team: Project planning, execution, tracking and reporting Develop and improve processing methods for inorganic composite materials (preform fabrication, metal casting, mold production and assembly, programming and operation of advanced furnaces, programming and operation of CNC machining centers, precision finishing/lapping of hard materials, and other associated activities) Characterization of materials properties Measurement of dimensions, both manually and via computer controlled CMMs Interface with outside entities (raw materials suppliers, equipment vendors, toll manufacturers, machine shops, and test labs) Transfer successful products to manufacturing, including documentation and training Education & Experience New AAS in Engineering or Science fields (or equivalent training and experience) Relevant certifications a strong plus, such as CAM, CAD, ISO, Lean, CMM, others Skills Familiarity with manufacturing and/or lab environment Experience with advanced equipment (materials processing, furnaces, CNC machining centers, CMMs, etc.) Knowledge of assembly operations Strong mechanical aptitude Strong computer aptitude (data summaries, programmable furnaces and machining centers, etc.) Working Conditions Position requires on-site activities for prototype fabrication. Work schedule is 5 days, 40 hrs per week, first shift. Working in lab, production and office Physical Requirements Hands-on, lab-based job environment: Required to frequently lift/push/pull a minimum of 35 lbs Must be able to sit, bend, squat and walk about facility Depending on project assignment, may be required to walk/stand for entire 8 hour day Safety Requirements All employees are required to attend scheduled training, follow the site EHS procedures and Corporate EHS standards. This includes the use of proper protective equipment (PPE) as required by the job responsibilities. Managers will ensure that all safety and environmental procedures are followed consistently. They will ensure that risk assessments are performed, proper training, work instructions, required PPE is available, and will monitor compliance. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

Who We Are iLABS is an innovation-focused, full service, global beauty company with proven track record for award winning formulas and product development. The art and science of innovation is in our DNA. Through our worldwide network of talented chemists, scientists and creatives, we bring authentic innovation and cutting-edge technology to every product we design. The Way We Work Whether you're an established brand or an indie start-up, our team of beauty industry professionals nurture your project through each phase of development, from concept to finished goods. We take the time to understand your goals through access to cutting-edge technologies, raw materials, sustainable materials and the latest marketing analysis. Our dedicated team guides your vision, ensuring your product takes center stage in a crowded market. Job Summary We are seeking a Chemist II to join our R&D team, focused on creating personal care, skincare, hair care, and color cosmetics. They would develop and test new products, solve technical issues, and ensure they meet industry standards. They will lead and mentor junior chemists, help scale products for manufacturing, manage lab documentation, and support project management. Additionally, they will contribute to improving lab processes and managing raw material data. Responsibilities Formulate personal care, skin care, hair care and/or color products Perform necessary research, test products and troubleshoot Supervise and mentor junior level chemists Adhere to a cGMP environment, document and follow lab procedures with attention to detail Attend cosmetic seminars and meetings Attend relevant internal meetings and provide reports Attend scale-up and manufacturing Assist R&D leaders with various tasks, including the following: Project management support Customer calls support Lab procedure and specifications Raw material data management Efficiency improvement task force Requirements 6+ years of previous makeup, OTC and/or skincare formulation experience Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering or related field Master's degree in Cosmetic Science or related field, preferred Ability to supervise and mentor chemists Extensive knowledge of formulation science Strong time and project management skills Knowledge of rules and regulations (FDA, CTFA, PCPC) for formulation Knowledge of current Good Manufacturing Practices (cGMP) Knowledge of and ability to assist in scale-up and manufacturing process Strong problem-solving skills Strong communication skills, both written and verbal Strong computer skills Benefits Comprehensive Health Benefits package (Medical, Dental, Vision, Life, AD&D) Competitive 401(k) match with immediate vesting Paid time off (Vacation, Sick, Holiday, Summer Fridays) Monthly birthday celebrations + other fun activities! Daily subsidized meals iLABS (Innovation Labs) Inc. is an equal opportunity employer. We do not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other characteristic protected by federal, state or local laws. All employment is decided on the basis of qualifications, merit, and business need.

What Nuclear Manufacturing contributes to Cardinal Health Manufacturing is responsible for cost of production and maintenance activities including process improvement, supply chain management, quality assurance, employee safety and engagement, and environmental commitment. Nuclear Manufacturing is responsible for the manufacturing of time sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (i.e. FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Schedule * Monday - Friday * Overnights/Early mornings * Schedule can vary but you must be willing to work what is needed based off of business needs. * Candidate must be flexible to work different shifts, schedules, holidays, weekends and overtime as needed. Responsibilities * Manufactures radioactive isotopes (includes synthesis set up, hot cell manipulations, distribution) * Conducts quality control testing of each batch (utilizing gas chromatograph, dose calibrator, multi-channel analyzer, TLC plate scanner, high pressure liquid chromatograph, analytical balance, PTS, laminar flow hood and fume hood) * Performs environmental and personnel monitoring in ISO 5, ISO 7, and ISO 8 environments * Works in ISO 7 cleanroom to make product vials and customer vials for use in drug production * Coordinates daily production run schedule based on customer and pharmacy needs * Demonstrates strong documentation practices, oral communication, and writing skills. Performs clerical and administrative tasks, including maintenance of daily production records, report preparation and maintenance records * Manages SAP Inventory (includes receiving materials, properly inspecting materials for use, and maintaining proper cycle counts) * Performs daily radiation safety tasks, along with general lab cleaning * Ability to troubleshoot equipment issues * Advanced chromatography skills * Provide feedback on method development around time of Tech Transfer * Communication with external innovator/sponsor * Ability to lead; judgement to prioritize quickly Qualifications * Bachelor's degree in related field, or equivalent work experience preferred. Sciences preferred * 0-2 years of experience preferred * Lab experience highly preferred * Prior experience working with HPLC and GC, including maintenance and peak analysis preferred * Experience and understanding of radiation and radioactive materials preferred * Ability to follow instructions accurately and work as a member of a team * Must be able to work overnight shift/different shifts based on business needs * Ability to travel (~10%) within the region and network to support other facilities if needed by the business * Prior experience in manufacturing, preferably in a controlled environment and/or regulated industry preferred * Effective written and verbal English communication skills * Ability to manage weight up to 75 pounds What is expected of you and others at this level * Applies basic concepts, principles and technical capabilities to perform routine tasks * Works on projects of limited scope and complexity * Follows established procedures to resolve readily identifiable technical problems * Works under direct supervision and receives detailed instructions * Develops competence by performing structured work assignments Anticipated hourly range: $33.60 per hour - $47.90 per hour Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. * Medical, dental and vision coverage * Paid time off plan * Health savings account (HSA) * 401k savings plan * Access to wages before pay day with my FlexPay * Flexible spending accounts (FSAs) * Short- and long-term disability coverage * Work-Life resources * Paid parental leave * Healthy lifestyle programs Application window anticipated to close: 02/01/2026 *if interested in opportunity, please submit application as soon as possible. The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

Who are we? Since Day 1, KIND has had a vision for a kinder and healthier world. A world in which people never have to choose between what tastes good, feels good, and does good when it comes to their snacking. Our iconic KIND bars - made with real, recognizable ingredients - sparked the growth of an entirely new healthy snacking category back in 2004. Now, KIND has a family of more than 80 snacks that offer solutions for a variety of occasions. All of KIND's products lead with a nutrient-dense first ingredient - like nuts or whole grains - and do not contain genetically engineered ingredients, sugar alcohols or artificial sweeteners. We're looking for passionate collaborators to help us become the foremost leader in health & wellness and positively impact society along the way. If you're looking to be a part of an inspiring, energetic and entrepreneurial environment, you've found the right place. What you'll do Reporting within KIND's Product Development team, the Food Scientist role is responsible for executing Product Development initiatives to further enhance KIND's portfolio of healthy snacks. This role will be responsible for leading the development and launch of innovations, renovations, productivity, and quality improvements for KIND North America. You will have a visible impact to the Product Development Organization and help bring fresh thinking to evolve our processes and Ways of Working. Responsible for prototyping, formulation, pilot production and scale-up to plant implementation of innovation & renovation projects. Technical lead responsible for product development and product optimization, working in collaboration with project managers & the cross functional teams (following stage gate methodology). Provide technical support to manufacturing and quality for commissioning of innovation and renovation projects. Conduct trials, data collection and interpret results to drive program/project and technical knowledge forward, develop robust action plans, risk assessment and contingency planning. Possess strong product development skills in ingredient functionality, material selection and formulation to understand effects on finished product performance. Ensure compliance to internal and external policies, quality standards and legal requirements. Provides support in building technical expertise and maintain community of best practice to technical colleagues. Possess technical leadership to execute time sensitive programs, including new product line trials, alternate line qualifications and supplier/ingredient qualifications. What you'll bring to KIND You are entrepreneurial and pursue our mission with tireless passion and constant innovation. Sense of urgency and can-do attitude A partnership and relationship-based approach in working with internal and external business A willingness to challenge our “way of work” to maximize our resources and enhance our success Genuine in your desire to help the make the world a kinder place, committing to always spreading and celebrating kindness. You have... A BS or MS degree in Food Science or Chemical Engineering At least 4-6 years of relevant concept to launch experience in a Corporate R&D setting including experience in formulation, start-up & continuous improvement projects. Ability to build strong trusted working relationships and rapport at all levels & demonstrated ability to work collaboratively. Strong problem-solving and analytical skills. Are familiar with the activities in Marketing, Market Research, Legal/Regulatory, QA and Manufacturing. Be able to travel up to 35%. Certain states and localities require employers to post a reasonable estimate of salary range. A reasonable estimate of the current base salary range for this position is $83,000.00 - $109,000.00. Actual salary will be based on a variety of factors, including location, experience, skill set, performance, licensure and certification, and business needs. The range for this position in other geographic locations may differ. What KIND offers 401(K) or RRSP's with generous company match Flexible Paid Time Off. Choose what works best for you, including summer hours. Paid parental leave. Excellent health, dental & vision insurance, with options to fit you & your family's needs Company paid disability and life insurance to provide income protection Your health is important! Our wellness strategy focuses on mental and physical wellbeing via programs like Employee Assistance Program, a wellness subsidy, healthy food options and gym facility in HQ. Casual office dress code- feel free to wear your KIND gear Stock up on your favorite KIND bars to share with your family & friends, through a quarterly voucher Training & tuition reimbursement program, because continuing to learn matters and we support your development A dynamic, ambitious, fun and KIND work environment Charitable Donation Matching: KIND matches your charitable donations up to $1000 annually through our donation matching portal. EEO At KIND, we are committed to an inclusive workplace where diversity in all its forms is championed. KIND is proud to be an equal opportunity workplace, and we are an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants with criminal histories, consistent with legal requirements. If you require special accommodation, please let us know. Privacy Policy Mars and its family of brands is committed to transparency and responsibility in how we handle the personal data entrusted to us by our customers and consumers. To learn more about our privacy policy please follow this link.

Analytical Chemist Duration : 12 Months Total Hours/week : 40.00 1 st Shift Client: Medical Device Company Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only) Job Description: Conduct material and/or chemical characterizations to support Specimen Management projects Prepare samples/prototypes for internal or external analysis Develop and execute test protocols and document results in a timely fashion Review documentation for accuracy Maintenance of equipment and laboratory facilities Minimum qualifications: B.S. + degree in Materials Science, Chemistry, or related disciplines Good understanding of material structure-property relationships Hands-on experience with analytical or material characterization instrumentation such as INSTRON, DSC/TGA, DMA and FTIR, UV-VIS Hands-on experience with wet laboratory equipment and skills. Strong inter-personal and communication skills Preferred qualifications M.S. or Ph.D. degree in Material Science, chemistry, or related discipline Experience and knowledge in blood biology and clinical assays Proficient with Minitab Experience in design of experiments Excellent written and verbal communication skills as well as ability to communicate effectively with scientists and engineers from a wide range of technical backgrounds.

AIRCO is a world leader in carbon conversion technology, paving the way to global energy security by transforming CO₂ into a valuable resource. Its proprietary AIRMADE™ Technology is an adaptable platform that allows any industry to efficiently produce high-demand, fully-formulated synthetic fuels from waste CO₂ and hydrogen. The company has commercial partnerships with airlines including JetBlue and Virgin Atlantic, amongst others, and has been awarded multiple government contracts, including with NASA and the United States Department of Defense's Defense Innovation Unit. The company has received industry recognition through awards such as Time Best Inventions, Inc. Best in Business, Fast Company World Changing Ideas, and the XPrize for Carbon Removal. AIRCO's many accolades include winning the prestigious Green Chemistry Challenge Award from the Environmental Protection Agency in October 2023, an award given to organizations that reinvent processes to reduce the generation of hazardous substances and byproducts. AIRCO was also declared a winner for the World Economic Forum UpLink Sustainable Aviation Challenge, which accelerates the development of promising technology pathways that enable widespread uptake of SAF. The Position We are seeking an Analytical Chemist to join our team. This role will report to our Senior Analytical Chemist. This position will play a key role in our analytical chemistry laboratory, supporting research and development efforts, conducting quantitative analysis, and ensuring high-quality control of analytical data. The candidate should have experience with Chemstation and Chromeleon, and ideal industry experience in chemical, pharmaceutical, or environmental sectors. This role will be based in New Britain, PA with initial 3 month training in Brooklyn, PA. What you get to do Operate, maintain, and troubleshoot GC, GCMS, and LC instruments. Perform routine and non-routine sample analysis using GC, GCMS, and LC techniques, interpret data, and prepare analytical reports with high attention to detail and accuracy. Develop and validate analytical methods for the quantitative analysis of samples using GC, GCMS, and LC techniques, following established protocols and industry standards. Conduct sample preparation techniques, including extraction, derivatization, and purification, as necessary for analysis. Collaborate with other team members to ensure timely delivery of analytical results, and effectively communicate any deviations or issues encountered during analysis. Assist in the maintenance of laboratory equipment, including calibration, troubleshooting, and documentation of instrument performance. Follow all safety protocols and maintain a clean and organized laboratory environment. Other duties as needed. What you bring to AIRCO Bachelor's in Analytical Chemistry or related field and 2+ years of experience in operating and maintaining GC, GCMS, and LC instruments, and developing analytical methods using these techniques. In-depth knowledge of Chemstation and Chromeleon software, ensuring optimal performance and reliability. Strong understanding of the principles of analytical chemistry, quantitative analysis, and quality control. Proficiency in interpreting and analyzing complex analytical data, and preparing detailed analytical reports. Familiarity with relevant industry standards, regulations, and guidelines. Ideal industry experience in chemical, pharmaceutical, or environmental sectors. Excellent problem-solving skills, with the ability to troubleshoot and resolve instrument issues. Ability to work independently and in a team-oriented environment. Strong communication skills, both written and verbal. Ability to prioritize and manage multiple tasks effectively. Attention to detail and accuracy in all aspects of work. Salary Range: $80-85K The approximate annual base compensation range and benefits listed above may vary based on the applicant's experience, skills, abilities, and relevant industry expertise. Working at AIRCO - In addition to standard medical and dental benefits, that kick in Day 1, we provide: Comprehensive Health Benefits Full coverage for employee base premiums on health, dental, and vision insurance. 70% coverage for spouse and dependent base premiums. Choose between base plans or enhanced options to fit your needs. Health Savings & Flexibility Access company-sponsored HSA and FSA accounts to save on healthcare and dependent care expenses. Income Protection & Insurance Company-paid Short-Term Disability insurance. Optional Long-Term Disability and Life Insurance plans. Time Off & Leave Flexible and generous paid time off, including national holidays and sick leave. Paid family leave to support you during important life moments. Retirement Savings Tax-deferred 401(k) plan with a 3% company match to help you invest in your future. Commuter Benefits Pre-tax savings on transit and parking, plus monthly company contributions. Additional Perks Ancillary benefits through Sequoia, including pet insurance and financial wellness programs. Employee wellness program to support your well-being.Inclusive of Wellhub & One Medical. Company-sponsored events and programs that promote an inclusive and values-driven workplace. In person weekly catered lunch every Wednesday. At AIRCO we value employees for their unique perspectives. We are an inclusive affirmative action Equal Employment Opportunity employer. We consider applicants without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, present or past history of intellectual, learning, mental, or physical disability (including but not limited to blindness) unless AIRCO determines that such disability prevents performance of the work involved, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. Don't meet every single requirement? Studies have shown that women, marginalized genders and people of color are less likely to apply to jobs unless they meet every single qualification. At AIRCO we are dedicated to building a diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the , we encourage you to apply anyways. You may be just the right candidate for this or other roles This position requires access to technology, software and other information that is subject to governmental access control restrictions, due to export controls, security classification and/or designation as Controlled Unclassified Information. Employment in this position is conditioned on the candidate's ability to obtain and maintain appropriate government authorization to access technology or information, to the extent required, including without limitation a security clearance, export license, or other documentation required to establish authorization to receive access to such items technology or information. We may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to Company facilities and information systems, as we deem appropriate, in order to ensure compliance with applicable government access control restrictions. At AIRCO we value employees for their unique perspectives. We are an inclusive affirmative action Equal Employment Opportunity employer. We consider applicants without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, present or past history of intellectual, learning, mental, or physical disability (including but not limited to blindness) unless AIRCO determines that such disability prevents performance of the work involved, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. Don't meet every single requirement? Studies have shown that women, marginalized genders and people of color are less likely to apply to jobs unless they meet every single qualification. At AIRCO we are dedicated to building a diverse, inclusive and authentic workplace, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description, we encourage you to apply anyways. You may be just the right candidate for this or other roles This position requires access to technology, software and other information that is subject to governmental access control restrictions, due to export controls, security classification and/or designation as Controlled Unclassified Information. Employment in this position is conditioned on the candidate's ability to obtain and maintain appropriate government authorization to access technology or information, to the extent required, including without limitation a security clearance, export license, or other documentation required to establish authorization to receive access to such items technology or information. We may delay commencement of employment, rescind an offer of employment, terminate employment, and/or modify job responsibilities, compensation, benefits, and/or access to Company facilities and information systems, as we deem appropriate, in order to ensure compliance with applicable government access control restrictions. I consent to transfer my data to Air Company in the U.S. and to its use in accordance with the Air Company , and I opt in to receiving information from Air Company. Air Company does not sell or share personal information to third parties within the meanings given under applicable laws.

As the first full-time scientist on the team, you will perform hands-on formulation, drive product improvements, help establish the new lab, and influence the company's technical direction. You'll Want to Explore this Opportunity Because: You will contribute immediately in the lab while also helping to build and shape a new product development function from the ground up in a company with an aggressive growth plan. (More chemists to be hired soon). You'll work directly with a passionate, visionary CEO who values collaboration, scientific insight, and real innovation. He's demonstrated an open mindset and is driven by continuous learning and improvement. Join an entrepreneurial team of people who are driven, curious, and deeply committed to building a brand that's changing the way things are done in their industry. What You'll Be Doing: This is a hand-on lab position with a build in progressing from formulation chemist to synthesis and project ownership. Lead the development of innovative chemical formulations and new product forms. This may also involve reverse engineering of 3rd party chemicals currently marketed and sold. Develop improvements to existing products to boost performance and address supply chain challenges. Participate with the R&D Consultant/Advisor in opening the new R&D lab. Translate market insights and company priorities into actionable product concepts. Oversee efficacy, user experience, safety, shelf life, and regulatory testing to ensure product excellence. Manage pilot studies and field trials to confirm real-world performance. Act as the scientific expert on water treatment chemistry, particularly in customer service and education. Collaborate with Operations and Marketing teams to take products from concept to commercialization. What You'll Bring to the Job: Ph.D. or M.S. in Chemistry or related field. 5+ years of hands-on experience in chemical product development, ideally in the specialty chemical or water treatment chemicals space Proven success in formulating products and bringing them to market. Strong analytical skills with expertise in experimental design and statistical analysis. Familiarity with regulatory frameworks (such as EPA, NSF etc.) and safety testing protocols. Experience with water treatment technologies is highly preferred. Must be authorized to work for any U.S. employer without sponsorship now or in the future. Our client is an Equal Opportunity Employer with fantastic benefits as described below: 20 days PTO Medical Insurance: 3 plan levels ($300-$6,350 deductibles; 80-100% coverage) Dental Insurance: PPO plan with $1,500 annual max; 100% preventive, 90% basic, 60% major; orthodontia up to $1,500 Vision Insurance: $10 copays; $150 frame or contact allowance every 12 months Life Insurance: 2× salary up to $500,000, company-paid Voluntary Life & AD&D: Employee up to $300K; spouse/child up to 50% of employee coverage Long-Term Disability: 60% of monthly earnings, up to $12,000, company-paid Continuing Education & Tuition Assistance Employee Assistance Program and Wellness Benefits If you're passionate about product development, eager to lead innovation in a fast-paced environment, and ready to make an impact, this opportunity is for you! Apply now!

Voyant Beauty believes our people are more than just employees; they're the driving force behind everything we achieve. Our culture fosters teamwork, respect, and camaraderie, ensuring that every individual's contribution is valued and celebrated. We invest in their growth, providing opportunities for development and advancement within our dynamic team. Voyant Beauty is a company that specializes in the development and manufacturing, of beauty, personal and home care products. We work with various brands, retailers, and businesses to create customer formulations and products tailored to their needs. This can include skincare, haircare, bath and body products, fragrances, and more. Essentially, Voyant Beauty serves as a one-stop-shop for companies looking to bring their beauty and personal care product ideas to life. Safety is a core value at Voyant Beauty. We prioritize the well-being of our team members, ensuring a safe and secure environment where everyone can thrive and excel. If you're seeking to be part of a team where your talents are valued, your safety is paramount, and your efforts contribute to meaningful change, then Voyant Beauty is the place for you. Come join us and be a part of our journey. A Brief Overview Ensures accuracy and reliability in laboratory testing and analysis. The QC Analytical Chemist is responsible for conducting quantitative and qualitative analysis of raw materials and products, developing analytical methods, and ensuring compliance with industry standards. What you will do * Conduct quantitative and qualitative analysis of raw materials and products. * Collaborate with production teams to troubleshoot production issues. * Ensure compliance with industry standards and regulations. * Prepare technical documents and reports. * Develop and validate analytical methods. * Calibrate and maintain analytical instrumentation. * Manage standard chemical inventory and safety protocols. * Some duties may vary slightly by location. Education Qualifications * Bachelor's Degree in Chemistry or related scientific discipline (Preferred) Experience Qualifications * 1-3 years Analytical chemistry in a manufacturing environment (Preferred) * 1-3 years Method development and validation (Preferred) Skills and Abilities * Analytical Chemistry (High proficiency) * Quality Control (Medium proficiency) * Laboratory Safety (Medium proficiency) * Technical Documentation (Medium proficiency) * Regulatory Compliance (Medium proficiency) * Data Analysis (Low proficiency) * Instrumentation Calibration (Low proficiency) * Method Validation (Low proficiency) * Chemical Handling (Low proficiency) * Collaboration (Low proficiency) To Staffing and Recruiting Agencies: Our company does not accept unsolicited curriculum vitae's or applications from agencies. We are not responsible for any fees related to unsolicited curriculum vitae's or applications and explicitly reserve its right to contact candidates presented in such unsolicited curriculum vitae's or application. Our company provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, color, national origin, sexual orientation, age, disability or veteran status. Voyant Beauty will consider requests for accommodations due to a disability impacting a qualified employee's ability to perform the essential functions of their position consistent with applicable laws. In addition to federal law requirements, Voyant Beauty complies with applicable provincial and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Category Labs (formerly known as Monad Labs) is a team of systems engineers and researchers on a mission to design and build at the frontier of decentralized technology. We strive to design and build step-function improvements over existing blockchain solutions. After recently raising $225M in series A funding, led by Paradigm, we are growing our team. The Role We are looking for systems researchers with a strong interest in databases and operating systems. Candidates with research experience in systems verification, operating systems, multi-core algorithms, or systems architecture, are an ideal match. You will be part of a small, deeply technical team, working on high-impact problems in a fast-paced environment. Although we are building a new blockchain, previous experience with crypto is not expected. What You Will Do Designing performant algorithms and architectures related to storage or recovery, in single-node or distributed environments. Researching new architectures Tech stack: C++, clang, LLVM, gdb, perf, unix, git Who You Are PhD in Computer Science or equivalent Significant research experience into databases or operating systems Experience writing performant algorithms Experience writing production-grade code Resourceful and self-motivated Collaborative Adaptive; able to make meaningful contributions in a fast-paced environment Curious about lower-level system details Interested in building high-value, performant and distributed systems Why Work with Us Challenging problems. You'll work on extremely challenging problems with massive impact. See our Blogs and Papers & Talks for a flavor of the problems we are solving in the real world. Huge opportunity. The Ethereum Virtual Machine (EVM) standard is ubiquitous, but existing EVM-compatible chains are very slow. Monad's core innovations offer developers the best of both worlds (portability and performance) and are a game-changer for mass user adoption in crypto. The right team. You'll be part of a small, exceptional team (engineers and researchers make up 90% of the team). Culture. We're a lean team working together to achieve very ambitious goals. We are united in our culture of collaboration, low ego, and high-quality output. As an early member of our team, you'll help to shape our culture. Compensation. You'll receive a competitive salary and equity package. Resources and growth. We're well-capitalized, with backing from leading venture funds like Paradigm, Electric Capital, Greenoaks, Dragonfly, and Coinbase Ventures. We keep a lean team, and this is a rare opportunity to join. You'll learn a lot and grow as our company scales. Salary and Benefits Target full-time salary of $250,000. (**This is not a guarantee of compensation or salary; a final offer amount may vary based on factors including but not limited to experience, domain expertise, and geographic location.) Benefits for US employees include: World class benefits package (medical/dental/vision) Unlimited paid time off 401(k) retirement plan + company match Lunch and dinner stipend (in-office NYC) Monthly wellness benefit Paid parental leave

Syensqo is all about chemistry. We're not just referring to chemical reactions here, but also to the magic that occurs when the brightest minds get to work together. This is where our true strength lies. In you. In your future colleagues and in all your differences. And of course, in your ideas to improve lives while preserving our planet's beauty for the generations to co We are looking for: We are seeking a motivated and detail-oriented Technical Service Chemist/Engineer to join our Polymer Additives team. This role is responsible for providing technical support to customers and internal teams, with a strong emphasis on hands-on polymer processing. The ideal candidate will have experience with polymer additives, laboratory testing, and polymer processing equipment such as extrusion, injection molding, and compression molding. We count on you for: * Prepare resin/additive formulations and produce test specimens using injection and compression molding to support both existing product testing for customer projects and new product development (NPI projects). * Perform hands-on laboratory operations, including polymer processing, color and gloss measurement, physical property testing, and data analysis. * Prepare presentations and project updates for customer-related and NPI projects. * Document and update laboratory procedures in accordance with Standard Operating Procedures (SOPs). * Maintain calibration and maintenance schedules for laboratory equipment. * Troubleshoot and resolve operational issues with laboratory equipment. * Coordinate and execute Joint Customer Technical Service Work Requests (TSRs) in a timely manner. * Collaborate with field Technical Service and Sales teams to provide monthly data summaries and project updates. * Maintain a regional database of all completed and active projects, including documentation of commercial outcomes. * Stay current with technological developments in core market segments. * Coordinate with third-party laboratories and Stamford Analytical to complete required analyses. You can count on us for: * We offer the opportunity to join an exciting growth company * A full range of benefits as expected of a successful company * Opportunities for growth and learning * Encouraging a diverse and inclusive workplace culture that values and respects individual differences and backgrounds * Long-lasting excellent customer relations, self-dependent working, and a variety of tasks in one of the world's leading chemical companies. You will bring: * Associate degree with 3+ years of relevant experience, or Bachelor's degree (B.S.) with 0+ years of experience in Plastics Engineering, Chemical Engineering, Chemistry, Polymer & Material Science, or a related field. * Hands-on experience with polymer processing equipment (extrusion, compounding, injection molding, compression molding) preferred. * Demonstrated troubleshooting and problem-solving skills in polymer processing environments. * Proficient in operating polymer processing and testing equipment: injection molding, polymer extruder, colorimeter, gloss meter, Instron, thermal oven, melt-flow tester, heated press, UV-Vis, FT-IR, etc. * Strong analytical skills with attention to detail and the ability to interpret complex data. * Customer-focused with a commercial and marketing mindset. * Proactive, flexible, and able to take initiative. * Creative and open to new ideas. * Excellent presentation and communication skills. * Effective team player with the ability to manage multiple projects and meet deadlines. * Committed to understanding and meeting customer needs. You will get: * Competitive salary and benefits * The U.S. base salary range reasonably expected to be paid for this position is $78,500.00 to $103,000.00 per year. Since actual compensation packages are based on a variety of factors unique to each candidate we may ultimately pay more or less than the posted base salary range. Total compensation for this role also includes bonus and/or other incentives. * 16, or more, weeks of maternity/paternity and co-parenting leave, according to local regulations * Training platform for all employees * Free well-being sessions (physical and psychological) About us * Syensqo is a science company developing groundbreaking solutions that enhance the way we live, work, travel and play. Inspired by the scientific councils which Ernest Solvay initiated in 1911, we bring great minds together to push the limits of science and innovation for the benefit of our customers, with a diverse, global team of more than 13,000 associates. Our solutions contribute to safer, cleaner, and more sustainable products found in homes, food and consumer goods, planes, cars, batteries, smart devices and health care applications. Our innovation power enables us to deliver on the ambition of a circular economy and explore breakthrough technologies that advance humanity. * At Syensqo, we seek to promote unity and not uniformity. We value the diversity that individuals bring and we invite you to consider a future with us, regardless of background, age, gender, national origin, ethnicity, religion, sexual orientation, ability or identity. We encourage individuals who may require any assistance or accommodations to let us know to ensure a seamless application experience. We are here to support you throughout the application journey and want to ensure all candidates are treated equally. If you are unsure whether you meet all the criteria or qualifications listed in the job description, we still encourage you to apply. * Syensqo is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristics. Nearest Major Market: Bridgeport Nearest Secondary Market: Danbury

Driven by a commitment to research, quality, and service, PDI provides innovative products, educational resources, training, and support to prevent infection transmission and promote health and wellness. Encompassing three areas, our Healthcare, Sani Professional and Contract manufacturing divisions, we develop, manufacture, and distribute leading edge products for North America and the world. We have several locations across the US and are looking for new Associates to join our team! POSITION PURPOSE *This position is for 3rd Shift (Sun-Thurs, 11:00 pm-7:30 am)* Responsible for the accurate analysis of incoming raw materials utilizing current USP, Standard Operating Procedures (SOPs), Work Instructions (WIs), Nice Pak's / PDI Test Methods (NPTM), Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMPs). Assures tested raw materials have met the required specification criteria prior to release. Maintain accurate, complete, and traceable documentation related to analysis and disposition. ESSENTIAL FUNCTIONS AND BASIC DUTIES Testing Requirements: Performance of diversified chemical testing as needed by using current USP, Standard Operating Procedures (SOPs), Work Instructions (WIs), Nice Pak's / PDI Test Methods (NPTM), and or customer supply method on raw materials, the testing may include but not limited to: pH determination, viscosity, refractive index, specific gravity, etc. Conduct wet chemical titration to determine the percentage of activity on various solutions and raw materials Determine the active percentage of various components as required by specifications using of instruments (IR, UV, Auto-titrator, etc.) Perform identification of various chemicals or formulations as per methodology and requirements Perform daily calibration, reading, and recording of instruments within the Analytical Lab Test incoming raw chemicals, components and assure that all the required certification required is accurate and within specification. Assist in the sampling, testing and release of raw materials when needed REPORTING & ANALYSIS: Ensure that all results are accurately recorded in appropriate laboratory logs, designated forms and/or LIMS system. Lab Maintenance: Update management or designee with analytical supplies issue Clean laboratory at specified intervals by following appropriate SOP and/or WI Prepare and maintain laboratory test solutions and titrants Additional Requirements: Determine products' QC disposition from the lab Complete necessary forms, as needed PERFORMANCE MEASUREMENTS Test Raw Materials and release it in a timely manner Ensure sampling, testing, and release of raw materials is done efficiently. Maintain lab cleanliness in a timely manner. QUALIFICATIONS EDUCATION/CERTIFICATION: Bachelor's degree in Chemistry, Analytical Chemistry, other related science REQUIRED KNOWLEDGE: Must know Microsoft Office Suite (Outlook, Word, Excel) Be able to read, write and speak English Read and comprehend Company policies and procedures, including safety rules and regulations EXPERIENCE REQUIRED: A minimum of 0 - 3 years' work experience in a laboratory environment (Analytical Chemistry Lab preferred) or an equivalent combination of training and experience. SKILLS/ABILITIES: Ability to multi-task and have good time management skills. Must have good communication and customer service skills. WORKING CONDITIONS Incumbents in this class are subject to extended periods of sitting, standing, walking, lifting materials weighing up to 30 pounds, vision to monitor and moderate to loud noise levels. Incumbents may be exposed to or work with toxic materials, toxic gases, electrical hazards, dangerous tools and equipment. Work is performed in laboratory environment. Incumbents must be able to use personal protective equipment (e.g. respirators, gloves, etc.) SALARY RANGE $55,000 - $60,000 annually, plus bonus PDI is pleased to offer a comprehensive and affordable benefits program to our associates, which includes: Medical & prescription drug coverage Dental / Vision plan 401(k) savings plan with company match Basic and supplemental life insurance Flexible Spending Accounts (FSAs) Short- and long-term disability benefits Health Advocacy Program / Employee Assistance Program (EAP) Many other voluntary benefit plans such as: Legal assistance, critical illness, hospital indemnity and accident coverage, discounted home/auto/rental insurance, employee discounts and pet insurance At PDI, we are also committed to helping our associates maintain a healthy and sustainable work/life balance and are proud to provide: Sick leave, generous vacation and holiday time, paid parental leave, summer hours, flex place/flex time options

Formulation chemist needs Bachelor of Science or Master of Science in Chemistry, Biology, Engineering or related field Formulation chemist requires: Minimum 0-1 years of industry experience (Bachelor degree) Bachelor of Science or Master of Science in Chemistry, Biology, Engineering or related field Minimum 0-1 years of industry experience (Master degree) Great Computer skills Strong communication skills Travel to pilot facility in Trumbull, CT and manufacturing facility in Geneva New York Formulation chemist duties: Formulate hair related products under supervision of Senior Chemist or Manager. Understand, utilize and document within laboratory notebook and Enginuity every batch made with details of reason for the batch, batching notes, batch specification results and other test results as applicable. Understand, follow and adhere to project cost objectives and timelines for each project and develop cost estimates with supervisor. Follow requirements of the new product development process and follow through with action plans to meet the goals and timeline of the project. Conduct stability as required by department policy, i.e., track stability, update results charts and summarize data for review at each test period. Design and develop, as well as conduct efficacy testing, as required for projects and requested by supervisor - Co-ordinate Salon Testing; Design & conduct laboratory efficacy, field and claims tests and write reports detailing experiments, and analysis and summary of results. Co-ordinate Microbiological and Safety Testing. Communicate formulation stability and efficacy results and issues promptly and thoroughly as well as make recommendations for change/improvements when stability or efficacy testing fails. Interact with raw material vendors and other industry representatives to further expand on the understanding of their products, technologies and services.

Chronosphere Chronosphere is the observability platform built for control in the modern, containerized world. Chronosphere empowers customers to focus on the data and insights that matter by reducing data complexity, optimizing costs, and remediating issues faster. The observability platform reduces data volumes and associated costs by 60% on average while saving developers thousands of hours. Chronosphere's Fluent Bit-based Telemetry Pipeline optimizes and simplifies observability and security log data. The product transforms logs at the source and routes them to any destination without lock-in. Recognized as a leader by major analyst firms, Chronosphere is trusted by the world's most innovative brands, including Snap, Robinhood, DoorDash, and Zillow. Learn more at Chronosphere.io. Follow at LinkedIn and X. About the role Responsible for owning the vision, strategy and execution plan to bring new innovative products to market, starting with Chronosphere's log data management product. Responsible for bridging Chronosphere's customers and the Engineering team, building feedback loops and testing hypotheses to develop a deeply technical product that will serve a deeply technical Audience. You Will Own the vision, strategy roadmap and execution of new SaaS software products, specifically data driven products starting with Chronosphere's log data management product; Perform primary research and interview end-users and buyers to design these software products; Uncover innovative approaches to solve end-user needs through the use of Artificial Intelligence (AI), Machine Learning (ML) and/or data science techniques; Bring the new products to market from inception to significant revenue; Develop a deep understanding of Chronosphere's competition and their businesses; Set priorities and shape the roadmap for building and developing the new product; Communicate priorities and the roadmap, and align the team around them; Convert product concepts for the new product into projects buildable by software engineering teams; Serve as a product owner for a Scrum team working on observability features for the new log management product; Manage the backlog, groom stories, and breakdown tasks for the design, development, and building of the new product in an Agile framework; Develop a feedback system with a select group of customers to get feedback on new products to drive iterative product improvements; Drive new product requirements down onto our Data stores and SaaS infrastructure teams; Coordinate with product marketing and sales teams on positioning and messaging for the new product; Hire and manage a team of product managers; and Own the revenue target and incubate the business. You have Bachelor's degree or foreign equivalent in Computer Science, Computer Engineering, Management Science, or a related field followed by 7 years of post-baccalaureate experience as a Product Manager. Experience must include the following, which may have been gained concurrently: 5 years of experience managing SaaS (software as a service) products on cloud technologies such as Amazon Web Services (AWS), Google Cloud Platform (GCP) or Microsoft Azure; 5 Years of experience in a SCRUM or Agile software development processes; 5 years of experience overseeing entire product lifecycle including product vision, strategy, and design; 3 years of experience using, running, developing and building solutions on modern data storage technologies such as Data Platforms or No-SQL databases; 3 years of experience using, running, developing and building solutions on traditional Relational Database Management Systems (RDMBS) and using Structured Query Language (SQL); 3 years of experience developing applications using object-oriented languages including C#; 3 years of experience building end-user solutions leveraging Artificial Intelligence models, Machine Learning models, and data science techniques; 3 years of experience managing a team of 2 or more product managers. May telecommute from anywhere in the U.S. 15% Travel required across the United States. Location 33 Irving Place, Suite 8109, New York, NY 10004. Salary: $256,000 to $300,000 per year. Full-time employment. Please apply online at ********************************* This position is part of Chronosphere Inc.'s employee referral program and is eligible for an employee referral incentive. #LI-DNI Our benefits Health Insurance Coverage Flexible Time Off Competitive Salary Stock Options And More Chronosphere is an equal opportunity employer. You're encouraged to apply even if your experience doesn't line up exactly with the job description. Your skills, passion, and desire to make a difference will stand out. At Chronosphere, we welcome diverse perspectives and people who think rigorously and aren't afraid to challenge the standard. If you need additional accommodations to feel comfortable during your interview process, please email us at ********************** Before clicking “Submit Application”. To support our Diversity, Equity, and Inclusion (DEI) initiatives, we urge applicants to omit personal identifiers, including names, and any details that explicitly indicate gender or ethnicity from their applications to reduce bias. However, applying through our Applicant Tracking System (ATS) will include identifiable contact information. Although this step is optional, Chronosphere is deeply committed to DEI. We recognize that achieving DEI is an ongoing journey for us as a company, and we believe it begins with our approach to hiring. Identifying information includes your name, photos, LinkedIn URL, email address, and more.

Job DescriptionDescription: RK Pharma Inc, a vertically integrated pharmaceutical company with our main manufacturing site in Pearl River, NY, is seeking a Quality Control Chemist to work with our growing Quality Teams as we scale towards commercial manufacturing in the next upcoming months. As a company focused on the development, manufacturing and sale of high quality and affordable generic pharmaceutical products worldwide we are looking for sharp, driven, self-directed individuals to help us grow our mid-stage start-up team. Requirements: If this sounds interesting to you, it's probably because up to this point you have: Bachelor of Science of higher 0-3 years of quality Control experience, preferably in a pharmaceutical, manufacturing, or regulated environment. Familiarity with cGMP, GDP, and standards. Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint) and experience with ERP or document management systems (e.g., SAP, Master Control). Excellent organization, time management, and communication skills. The main responsibilities for this position are: Perform daily verification /performance check of the QC analytical instruments such as Analytical balance, Microbalance, KF titrator, KF coulometer, Auto titrator etc., Perform calibrations of all the QC analytical instruments/equipment's as per the calibration calendar schedule or when required. Perform Instrument/ equipment performance qualification as and when required. Maintain inventories of chemicals, Standards, samples etc., Operation, calibration, maintenance and qualification of all analytical instruments such as HPLC, GC, TOC, UV, IR, automatic titrator, dissolution equipment, etc. Follow the procedures as per the SOP's/ guidelines. Perform Sampling of raw materials, drug substance, packaging components, stability samples, cleaning samples, In-process samples and finished products. Perform analytical tests and wet chemistry tests on raw materials, drug substance, packaging components, stability samples, cleaning samples, In- process samples and finished products in compliance with the STP and SOP's. Follow and document all test results under GLP, GDP, GMP and Lab Safety guidelines. Document test results, problems and other issues, perform troubleshooting of issues that arise during analysis. Logging various samples received to QC as per the SOP into their respective log books. Monitors Stability chambers, Photostability chamber, freezers, refrigerators etc. Performs Stability samples loading/charging and pull-out according to the stability calendar. Record the results and prepares CoA to be released in a timely manner. Perform analysis using various software's such as Empower, Tiamo, Spectrum two, Flex etc. Write and perform investigation of out of specification results. Train other QC chemists in a timely manner on all the general Laboratory SOPs and test methods. Preparation and review of Standard Operating Procedures, specifications and STP's for Raw materials, Packaging components, drug substances and finished products (based on ICH/Pharmacopeial reference). Preparation and execution of protocols for Method Validations, Method Transfers, Cleaning Validation, Raw material qualifications, Stability studies and any other studies. Maintains lab, instruments, logbooks and notebooks at all times. Maintains lab instruments and performs calibration/preventive maintenance to ensure proper working order and troubleshoot when necessary. Perform additional duties and responsibilities designated by the supervisor on the need basis after receiving the required training. RK Pharma Inc is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

Our client is seeking Full -Time Clinical Lab Technologists for their Chemistry Lab! Full time - Alternate Weekends 11:30 pm - 8:00 am 10% night shift differential!! Perform routine and emergency tests on blood and other body fluids using a variety of automated and manual instrumentation promptly. Maintain equipment and records according to department procedures and regulatory agencies guidelines in the areas of QA and QC. Use independent judgment to solve technical and procedural problems. In some instances, the ability to stand or sit for extended periods of time is necessary. Pay Range based on experience: $82,979.96 - $103,286.06 Requirements Must have an active New York license At least 2 years of work experience preferred Bachelor's Degree in physical science, medical technology preferred. Benefits 1199 Members Medical & Dental 403B matching up to 8% of salary Room for Growth Great leadership and support, utilizing the latest advances in computer technology.

Medical Laboratory Technician to work in the Chemistry/Core Laboratory under the direct supervision of supervisor. Will be responsible for performing a variety of complex and routine test within the Core Laboratory complying with all safety and regulatory requirement. Rotate weekends and scheduled holidays base on the needs of the department; participate in interdepartmental collaboration within the institution, to provide the highest quality patient care.

Our client, a leader in the semiconductor industry, is looking for a “Chemical Technician” based out of Totowa, NJ. Duration: Long Term Contract(Possibility Of Further Extension) Pay Rate: $28/hr The Chemical Technician is responsible for managing manufacturing (MFG) chemical requests, ensuring proper inventory control, handling chemical waste disposal, and maintaining compliance with safety protocols. This role involves monitoring chemical processes, managing inbound/outbound chemical shipments, preparing orders, and operating laboratory equipment. Key Responsibilities Maintain chemical inventory, log received and outbound chemicals. Prepare and fulfill chemical orders for MFG, R&D, and engineering teams. Conduct chemical testing to ensure compliance with quality standards. Set up, operate, and troubleshoot laboratory equipment and instruments. Manage chemical waste disposal and adhere to environmental regulations. Ensure proper SDS documentation, hazard labeling, and safety compliance. Collaborate with cross-functional teams and participate in safety programs/audits. Perform quarterly planning and ordering of chemicals for manufacturing. Key Skills Chemical Inventory Management Chemical Handling & Disposal (SDS, Hazardous Materials) Laboratory Equipment Operation & Maintenance Chemical Process Monitoring & Testing Safety & Compliance (OSHA, Environmental Regulations) Attention to Detail & Documentation Cross-functional Collaboration & Teamwork Education & Experience Bachelor's degree in Chemistry (No experience required) Associate's degree in Chemistry (2+ years of experience) Experience in chemical storage, ordering, and waste management preferred. Company Benefits include: Healthcare, Paid Sick leave & 401k (with 4% employer match) If interested, kindly send us your update resume at hr@dawarconsulting.com/************************

The primary role of a Chemical Technician is to perform chemical and physical laboratory tests, aiding scientists in qualitative and quantitative analyses of solids, liquids, and gaseous materials. The position may be in an experimental lab as a research technician or in a manufacturing setting as a process control technician. Responsibilities * Monitor product quality to ensure compliance with standards and specifications. * Set up and conduct chemical experiments, tests, and analyses using techniques such as chromatography, spectroscopy, physical and chemical separation techniques, and microscopy. * Conduct chemical and physical laboratory tests to assist scientists in qualitative and quantitative analyses. * Compile and interpret results of tests and analyses. * Provide technical support and assistance to chemists and engineers. * Prepare chemical solutions for products and processes following standardized formulas or create experimental formulas. * Maintain, clean, and sterilize laboratory instruments and equipment. * Write technical reports or prepare graphs and charts to document experimental results. * Order and inventory materials to maintain supplies. * Communicate daily with customers in person to address requests and weekly with a simple PSR. Essential Skills * Mechanical aptitude, including simple pump repair. * Effective communication skills to work with customers. * Basic understanding of chemistry, which can be taught. Additional Skills & Qualifications * Any experience in the paper industry. * Experience in lab analysis. * Mechanical experience, such as motor or pump repair. * Associate's degree in applied science or related field required; Bachelor's degree in chemistry or biology preferred. * 0-2 years of experience. Work Environment The work schedule is Monday to Friday from 8 am to 4 pm. The first 30 days involve shadowing a current full-time representative and on-the-job training. The dress code includes jeans or khakis with a polo or button-up shirt. Personal protective equipment such as steel-toe shoes, a high-visibility safety vest, hard hat, and eye and ear protection will be provided. Job Type & Location This is a Contract to Hire position based out of Elmwood Park, NJ. Pay and Benefits The pay range for this position is $21.00 - $22.00/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 Elmwood Park,NJ. Application Deadline This position is anticipated to close on Dec 22, 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.