Chemist jobs in Mahwah, NJ - 96 jobs

Provide product formulation support by accurately preparing laboratory beverages and concentrates. Maintain laboratory and sample inventory of ingredients and supplies. Maintain laboratory equipment. Implement and maintain storage studies. Submission of samples for analytical and sensory evaluation. Support Product Developers in conducting production runs, managing ingredient orders, handling, ensuring product meets specifications. Required Job Skills & Years of Experience for Each: Ability to flawlessly execute bench work, plan ahead for tech center runs, ability to communicate with several plant coordinators to ensure ingredient supply. Ability to proactively and positively interface with various analytical functions in order to assure timely execution of testing. Must be well organized, capture work details and learning and highlight any unexpected learning. Good communication skills (verbal and written), manage expectations of group support. Must be proactive, reliable and self-motivated. Essential Job Requirements: AS/BS in a scientific field with bench work experience. Outstanding team working skills, strong initiative. Ability to analyze and communicate implications of experimental results. Computer Skills Word, Excel, PowerPoint. Prior Beverage/Food experiences a real plus. Able to lift packages with ingredients and cases with products-up to 50 lbs

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 ****************************** .

**Now Hiring! Analytical Associate Chemist (ECT-Chemetall)** **Come create chemistry with us!** BASF/Chemetall, is the Surface Treatment global business unit of BASF's Coatings division, operating under the Chemetall brand, and a leading supplier of applied surface treatments worldwide. At BASF/Chemetall, we develop and manufacture tailor-made technology and system solutions for applied surface technology. Our products protect metals from corrosion, facilitate forming and treatment, prepare parts optimally for the painting process and ensure excellent coating adhesion. Our technologies and products are used in a variety of industries and end markets such as automotive, aerospace, aluminum finishing and metal forming. The chemical treatment of metal surfaces is BASF/Chemetall core competence. The focus of our worldwide activities is on the development and implementation of customized technology and system solutions for surface treatment. **We are looking for a Analytical Associate Chemist to join our Technical Service team in New Providence, NJ.** This position will perform routine testing and provide analytical support for the Corporation. The ideal candidate will complete any special projects as requested by the Analytical Specialist. **As a Analytical Associate Chemist (ECT-Chemetall), you create chemistry by...** + Performs required analytical tests on customer's samples from the field and on samples submitted by team leaders. + Writes clear, concise lab reports on work completed, making appropriate recommendations with the assistance of the Analytical Specialist and other technical resources. + Learns operation and maintenance of all analytical instrumentation; assists in troubleshooting problems. + Maintains supplies for all analytical requirements in accordance with Chemetalls quality system. + Maintains calibration and validation equipment log for lab instrumentation. + Works with Technical Service and support manager to log in solution analysis projects daily and maintaining these logs for the New Providence Lab. + Prepares and presents seminars/lectures to the department on analytical topics. + Works with analytical team members to develop new test procedures as required. + Continuously upgrade technical skills by working in the laboratories with other technical personnel, staying abreast of technical developments, reading journals, and learning new methods of analysis. + Attend industry seminars and in-house seminars to keep current with new technologies. + Polish written and verbal communication with technical and business stakeholders; continue to improve computer skills and learn new digitalization tools. + Works in the analytical laboratory in a safe and clean manner. + Maintain laboratory equipment in accordance with Chemetall/BASF's quality system; maintain appropriate inventory levels of analytical supplies. **If you have...** + Bachelor's Degree in Chemistry or Chemical Engineering is required + 3-5 years' industrial experience. + Prior lab experience is required (understanding of lab procedures, use of chemicals, importance of safety) + Prior lab testing experience is required. + Prior experience with analytical equiptment. + Experience is data science is preferred. + Strong analytical/computer skills required. + Excellent communication skills, both verbal and written. + Ability to maintain lab supplies, manage inventory, and order lab supplies. + Travel: 10% as needed. **Create your own chemistry with you@BASF** At BASF, you will have the chance to do meaningful work towards building a more sustainable future. In addition to competitive compensation and benefits, BASF provides you with access to a wide range of elements to help you be your best. It's what we call **you@BASF** . We are committed to providing benefits, programs, and opportunities that support our employees' overall well-being, personal growth, and a safe, collaborative, and inclusive work environment. Just some of the many benefits we offer include: + Flexible work arrangements whenever possible + Highly competitive retirement savings plan with company match and investment options + Well-being programs that include comprehensive mental health support for you and your household family members + Family forming benefits (fertility, adoption and surrogacy reimbursement, maternity/parental leave, and more) + Back-up child and elder care with discount programs for families of all ages and stages + Mentoring and career development opportunities that allow you to share, learn, and thrive + Matching gifts program that allows you to deepen the impact of your contributions to qualified charities. + Employee crisis support for when the unexpected happens + Access to our BASF wine cellar, employee discounts, and much more! **About us** As one of the largest chemical companies in North America we have been finding solutions for your everyday needs and addressing the most complex economic, environmental, and sustainability challenges for more than 150 years! At BASF we empower our employees with the tools, guidance and opportunities they need to advance and succeed in work and life. Giving you the support you need to be your best and fulfill your personal ambitions is what helps us create chemistry. After all, our success is linked to yours. Whatever path you envision, BASF is a great place to build a rewarding, successful career. Belong to Something Bigger. #belongat BASF **Privacy statement** BASF takes security & data privacy very seriously. We will never request financial information of any kind via email, private text message or direct message on any social medial platform or job board. Furthermore, we will never send a candidate a check for equipment or request any type of payment during the job application process. If you have experienced any of the above, please contact ***************************** to report fraud. **Pay transparency** BASF is committed to pay transparency practices. The competitive Pay Range for this role is $65,000-$70,000. Actual pay will be determined based on education, certifications, experience, and other job-related factors permitted by law. **Equal employment opportunities** We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, age, citizenship, color, religion, sex, marital status, national origin, disability status, gender identity or expression, protected veteran status, or any other characteristic protected by law. Applicants must be currently authorized to work in the United States on a full-time basis.

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 Responsible for assuring the accurate analysis of incoming raw materials, bulk liquids, and finished products utilizing Standard Operating Procedures (SOPs), Work Instructions (WIs), Nice Pak's Test Methods (NPTM) Good Laboratory Practices (GLPs), and Good Manufacturing Practices (GMPs). Assures tested raw materials, bulk liquids, and finished products have met the required specification criteria prior to release. Investigate out of specification results to determine final disposition. Maintain accurate, complete and traceable documentation related to analysis and disposition. Ensure the effective and efficient functioning of the Analytical Laboratory. Designate appropriate and trained personnel to perform required tasks. Review documentation to ensure adherence to internal and external requirements 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), (NPTM on raw materials, bulk liquids, and finished products. The testing may include but is 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, bulk liquids, and finished products. By the use of instruments (GC, HPLC, IR, UV, Auto-titrator, etc.) determine the percentage of various components as required by specifications. Perform identification of various chemicals or formulations as per methodology USP/NF and other test requirements Coordinate release of liquid batches including designation of reassay/expiration date. Assist in the sampling, testing and release of raw materials when needed Determine the toxicity and pH of waste tanks at designated intervals REPORTING & ANALYSIS: Ensure that all results are accurately recorded in appropriate laboratory logs or other designated forms Review all data generated by the laboratory associated with the manufacturing of Drug and OTC products Perform investigations into laboratory Out of Specification Results (OOS). Lab Maintenance: Ensure that all instruments that perform analysis are validated and calibrated. Ensure that all Analytical Methods utilized for analysis of Drug and OTC products, at the least, are validated according to International Standards Purchase analytical supplies Prepare solutions and titrants when required Clean laboratory at specified intervals Perform calibration, reading, and recording of instruments within the Analytical Chemistry Lab Prepare and maintain laboratory test solutions Additional Requirements: Determine products' disposition Complete necessary forms Lead, Direct and Train lower level Chemists ( I, II) in the use of instruments, methodology, SOPs, WIs, GLP, GMPs, etc. Furnish report to QC Lab Manager on a continuous basis. Assign workflow in the laboratory in conjunction with Analytical Chemist Senior Level. SPECIAL PROJECTS: Handles special projects and assignments as delegated (method transfer, method validation). PERFORMANCE MEASUREMENTS Test raw materials, batches, and finished products in a timely manner. Ensure release of raw materials, batches, and finished products are done efficiently. Maintain Lab cleanliness in a timely manner. Ensure proper new / refresher training of Analytical I Chemists. QUALIFICATIONS EDUCATION/CERTIFICATION: Bachelor's degree in Chemistry, Analytical Chemistry, or other related science REQUIRED KNOWLEDGE: Knowledge of Analytical techniques and able to incorporate them into daily tasks. Computer literate. Demonstrate ability to perform work accurately and be able to follow test methodology. Ability to perform well under pressure and work with minimum supervision. Some supervisor skills required. Able to delegate the required testing to competent and trained chemists EXPERIENCE REQUIRED: A minimum of 5 - 7 years' experience in a laboratory environment (Analytical Chemistry Lab preferred) At least three years in a regulated laboratory setting. WORKING CONDITIONS No hazardous or significantly unpleasant conditions. SALARY RANGE $80,000 - $90,000 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

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 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.

Analytical Chemist-Florham Park, NJ Arxada is a global leader in innovative solutions that protect our world. Our groundbreaking technologies, in-depth regulatory know-how, manufacturing and process development help our customers to safeguard nutrition, health and infrastructure efficiently through chemistry and biotechnology that enhance sustainability. We offer a broad portfolio of ingredients and services for multiple end-markets that include Human Health & Nutrition, Home & Personal Care, Professional Hygiene, Paints & Coatings and Wood Protection. With customers in more than 100 countries, the company achieved sales of CHF 2 billion in 2024. Headquartered in Basel (Switzerland), Arxada employs 3,200 associates across 24 production sites and 14 R&D centers, all committed to our customers' success. As a member of the Analytical Chemistry team, the candidate has an important role to play in support of a wide range of tasks including the analysis of R&D and customer samples, as well as troubleshooting issues related to manufacturing and customer complaints. The incumbent will utilize a variety of analytical techniques to deliver accurate and timely results in a dynamic, fast-paced environment Essential Job Functions: Perform analytical testing on R&D, customer and production samples using chromatographic, spectroscopic, wet chemistry, and other techniques. Develop, validate, and optimize analytical methods for both new and existing products and raw materials as needed. Ensure analytical results are accurate, reliable, and delivered within required timelines, following proper documentation protocols. Prepare technical reports and data summaries for internal use and customer reporting. Collaborate with R&D, manufacturing, and quality teams to support product development, resolve manufacturing issues etc. Adhere strictly to company policies, health and safety guidelines, and ISO Quality Management procedures. Perform additional duties and special projects as assigned. Qualifications & Experience: Bachelor's or master's degree require in preferred areas of study: General or Analytical Chemistry 5 years analytical professional experience with bachelor's degree or 2 years' experience with Masters degree Proficient in HPLC (UPLC), GC, spectroscopy ( UV-Vis, FT-IR), wet chemistry, and other modern techniques as well as sample preparation techniques Proficient with common software, including MS Office Effective written and verbal communication skills The expected salary range for this role is 75-92k annually, but specific employee compensation may vary depending on factors including experience, education, training, licensure, certification, location and other job-related, non-discriminatory factors permitted by law. This role is also eligible to earn a short-term incentive bonus and the following benefits: 401(k) plan, medical, dental, vision, life, and disability insurance, paid time off, paid holidays and paid sick leave. Arxada has world class offering in two distinct areas: Microbial Control Solutions (MCS) focuses on threats posed by microorganisms to people and planet through five distinct business lines including Professional Hygiene, Home & Personal Care, Wood Protection, Paints & Coatings and Material Protection. Nutrition, Care & Environmental (NCE), meanwhile, provides materials used to manufacture composites for electronics, aerospace and other markets, as well as vitamins and nutritional ingredients, chemicals and performance intermediates, and raw materials for a wide range of high-performance applications. Arxada is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. #LI-BR1 US41

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.

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.

About Us: Shamrock Technologies is a family-owned business which prides itself on its enterprising spirit. This atmosphere inspires associates to pursue their ambitions without the boundaries of classic organizational structure. Headquartered in Newark, New Jersey, Shamrock Technologies is one of the world's largest processors of micronized polytetrafluoroethylene (PTFE), as well as a leading worldwide manufacturer and supplier of a broad line of specialty products. Our materials are found in Inks and Coatings, Lubricants, Grease, Thermoplastics, and more. Using advanced technology and sophisticated production equipment, combined with our state-of-the-art Application and R&D laboratory facilities, Shamrock creates products to help customers meet their challenging formulation needs. Shamrock differentiates itself by hiring associates with an approach to thinking that actively seeks change rather than waiting to adapt to it. Our business embraces originality, curiosity, critical questioning, service, and continuous improvement, while creating a work culture that values cooperation. Summary: We are seeking a hands-on, innovative Research Chemist to support product development and applications research within the Wax Additives business. This role focuses on designing and conducting laboratory experiments, characterizing materials, and generating data that help bring new wax powders, dispersions, emulsions, and surface-modified products to market. The Research Chemist will work closely with the Technical Director and cross-functional teams to translate customer needs into technical solutions. Primary Responsibilities Plan, execute, and document lab experiments to develop new wax additives and improve existing products. Formulate and test emulsions, dispersions, blends, and surface-modified waxes for coatings, inks, and plastic applications. Operate and maintain laboratory equipment such as mills, mixers, particle size analyzers, DSC, FTIR, and rheometers. Collect, interpret, and summarize experimental data to guide decision-making. Prepare technical reports and communicate findings to the technical teams. Screen new raw materials and evaluate competitive technologies. Support scale-up trials by providing lab-to-pilot correlations and data. Assist in preparing technical presentations and samples for customer trials. Follow established safety protocols and maintain a clean, organized lab environment. Ensure accurate documentation and compliance with internal and external standards. Qualifications Education and Experience Bachelor's degree in Chemistry, Polymer Science, Materials Science, or Chemical Engineering. 0-5 years of experience in a chemical, polymer, or coatings laboratory (industrial or academic research). Hands-on experience with emulsions, dispersions, or polymer/wax formulations is highly preferred. Experience with polyamide chemistry or related polymer modification techniques is a plus. Professional Skills Strong experimental design and data analysis skills. Proficiency with common lab instrumentation (particle size, DSC, FTIR, rheology). Creative problem-solver with curiosity and initiative. Effective communicator with ability to work cross-functionally. Comfortable with multitasking in a fast-paced environment. Work Environment & Physical Requirements: Laboratory-based position with occasional pilot plant and production floor exposure. Required to wear PPE and complete safety training. Able to stand/sit for extended periods of time, may include bending/stooping. Prepared for prolonged periods sitting at a desk and working on a computer. Compensation package We offer a competitive salary complemented by an annual performance-based bonus. Our comprehensive benefits package includes generous paid time off hours, a 401(k) plan with employer matching, comprehensive healthcare coverage, employer-sponsored life insurance, and additional benefits designed to support your well-being and financial security. Equal Opportunity Statement Shamrock Technologies provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 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. Request for Assistance If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to access job openings or apply for a job on this site as a result of your disability. You can request reasonable accommodations by contacting Human Resources via email at ***************************. Reasonable Accommodation Applicants with disabilities may contact Shamrock Technologies via telephone, e-mail, and other means to request and arrange accommodation. If you need assistance to accommodate the disability, you may request accommodation at any time. Please contact the Shamrock Technologies Human Resources department at ***************************.

Background and Purpose of the Job Pepsi Lipton is a joint venture between Unilever and PepsiCo operating in the ready-to-drink Tea segment globally with three well-established brands Lipton, Brisk and Pure Leaf and Yachak. Our global business is worth 3.0 billion USD today, growing volume and with a double digit increase in net revenues. We operate across complex and diverse regions spanning Western Europe to Australia and New Zealand to the United States and Latin America with markets at different stages of development, with different consumer habits and different routes to market via a matrix of franchise, company-owned and third-party manufacturing operating models in which innovation delivery is key enable to accelerate growth. We have an established global R&D function based in two centres: Colworth UK, and Valhalla US. The centre at Valhalla is the primary `hub' from where the R&D team is focused on the North America and Latin America markets, whilst also supporting global programes and some international markets. Our other R&D Site, Colworth, is our lead centre for tea expertise, bringing this to our product and process development to deliver products across our platforms to meet a wide range of consumer benefits and needs. A role in Pepsi Lipton is a unique experience in which to develop and add value to your career. Pepsi Lipton, although a Joint Venture between Unilever and PepsiCo, operates independently and has its own Board of Directors. Whilst we have the full backing and support of our two parent companies, our entrepreneurial set up gives us real autonomy. Our roles are broad, our responsibilities big and our experiences even bigger. We have high visibility and great exposure - to senior leadership and to talented colleagues all over the world. It means we need to be impactful, smart influencers. In order to support our ambitious growth agenda, we are looking for a Product Development Associate Scientist to join our team in Valhalla, NY. To learn more, visit ********************** Who You Are & What You'll Do: The job holder will be a member of cross functional project teams providing product development capability across the Ready to Drink brand portfolio. This role will focus on product development for Brisk and Pure Leaf, which are North American brands. In this role they will be responsible for owning and delivering product development activities within agreed projects with an onus on practical based activities in our food laboratory or pilot plant facility including: * Design and execute practical and lab-based work programs linked to assigned projects, including initiating and maintaining formal lab notes, trial reports, experimental write-ups, and handover documents. * Contribute to project timelines, risk analysis, and resource loading for assigned projects, ensuring compliance with safety, regulatory aspects, and company policies. * Source ingredients and manage supplier interactions, including documentation, samples, ordering, and specification builds, while integrating quality into parent company systems and processes. * Generate prototypes to meet project requirements, liaising with the pilot plant for larger-scale production, managing non-standard ingredient ordering, and providing key documentation. * Lead the creation and delivery of product-related documentation, including consumer testing materials, registration, certification, and local BU-specific requests. * Own functional specification delivery and utilize digital tools to ensure technical outputs for artwork and labeling, coordinating with specification experts, concentrate teams, and QA for alignment. * Manage scale-up trials to confirm viability, including trial briefing and acting as point of contact with SC, Technical Contact Managers, Quality teams, and suppliers. * Coordinate with Consumer Technical Insights, Sensory, and Brand Insights to support prototypes, panels, and consumer tastings, and manage prototype sample shipments to test locations and stakeholders. * Ensure regulatory compliance for prototype development and ingredient selection, liaising with local deploy partners and cascading outputs to relevant stakeholders. * Support broader technical activities and R&D requirements, maintain awareness of competitor landscape, supply chain models, and liaise with parent company groups for knowledge building. What You'll Need To Succeed: * Able to work in Valhalla, NY * Degree (or equivalent) in Food Science, Chemical Science or Engineering and/or relevant experience in FMCG in fields related to product or process development/manufacturing in foods or beverages * Experience of working cross-functionally and with external suppliers * Experience of delivery of innovations from brief to market deployment * Foundation training/qualification in food hygiene * Passion to work in a practical & lab- based setting * Proven track record of product development * Creativity & flair with ability to innovate and translate product brief into winning launches * Strong communication skills * Attention to detail especially with experimentation, data recording, analysis & reporting * Strong organizational skills * Good time management and priority setting skills * An ability to flex and multitask. Pay: The pay range for this position is $86,080 to $129,120. Unilever takes into consideration a wide range of factors that are utilized in making compensation decisions including, but not limited to, skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. Bonus: This position is bonus eligible. Long-Term Incentive (LTI): This position is LTI eligible. Benefits: Unilever employees are eligible to participate in our benefits plan. Should the employee choose to participate, they can choose from a range of benefits to include, but is not limited to, health insurance (including prescription drug, dental, and vision coverage), retirement savings benefits, life insurance and disability benefits, parental leave, sick leave, paid vacation and holidays, as well as access to numerous voluntary benefits. Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. * ----------------------------------- At Unilever, inclusion is at the heart of everything we do. We welcome applicants from all walks of life and are committed to creating an environment where everyone can thrive/succeed. All applicants will receive fair and respectful consideration, and we actively support the growth and development of every employee. Unilever is an Equal Opportunity Employer/Protected Veterans/Persons with Disabilities. For more information on your federal rights, please see Know Your Rights: Workplace Discrimination is Illegal Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check. If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment.

The Analytical Chemist will support the Quality Control Analytical Laboratory by performing raw material qualification, identification testing, and requalification activities to ensure compliance with internal specifications, GMP requirements, and regulatory standards. This role is critical to supporting manufacturing operations for cosmetic and OTC products by ensuring raw materials and active ingredients are tested, released, and maintained in a compliant state prior to use in production. Key Responsibilities * Perform raw material identification (ID) testing using FTIR and comparison to approved standards * Conduct visual inspections (color, appearance, condition) of incoming raw materials and active ingredients * Support requalification of raw materials, including review of specifications, expiration extensions, and release decisions * Identify and define critical testing requirements based on material specifications and regulatory needs * Perform in-house analytical testing when applicable and coordinate external laboratory testing for analyses not performed internal * Review raw material specifications and ensure all testing aligns with approved methods and requirements * Maintain accurate and compliant documentation, submissions, and records for all testing activities * Ensure all results are reviewed, verified, and compliant prior to material release for manufacturing use * Archive documentation and maintain organized records in accordance with GMP and internal quality systems * Coordinate with external laboratories regarding testing scope, timelines, and results Required Qualifications * Bachelor's degree in Chemistry or related scientific discipline * 3-5+ years of analytical or QC laboratory experience, preferably within cosmetics, OTC, or contract manufacturing * Hands-on experience with raw material testing, qualification, and requalification * Strong understanding of GMP practices, documentation, and compliance requirements * Ability to review specifications and determine appropriate testing strategies * High attention to detail and strong organizational skills * Effective written and verbal communication skills * Team-oriented mindset with the flexibility to support broader lab operations as needed Job Type & Location This is a Contract to Hire position based out of Wharton, NJ. Pay and Benefits The pay range for this position is $31.00 - $32.00/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 Wharton,NJ. Application Deadline This position is anticipated to close on Jan 16, 2026. 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.

Join a Fortune 500 leader in the personal care industry, dedicated to delivering innovative, high-quality products that inspire confidence and wellness. We are seeking a Formulation Chemist to contribute to the development of cutting-edge consumer health and personal care solutions. Position Summary The Formulation Chemist will play a key role in designing, optimizing, and testing formulations for personal care products. This role requires hands-on laboratory experience, scientific curiosity, and a strong commitment to product quality and compliance. Key Responsibilities Formulate prototypes to support formula optimization and innovation initiatives Assess physical and clinical properties of formulations in alignment with project requirements Design and optimize formulas for performance, stability, and consumer appeal Select and evaluate raw materials and ingredients for efficacy and safety Conduct laboratory stability testing and monitor product performance over time Perform lab aesthetics assessments to ensure consumer-preferred sensory attributes Prepare formulas for internal and external testing, including clinical evaluations Ensure compliance with Good Manufacturing Practices (GMP) during formulation activities Qualifications Bachelor s degree in Chemistry or a related scientific discipline (required) 1 5 years of laboratory and formulation experience within consumer health, hair care, skin care or personal care industries Strong knowledge of formulation principles, raw material functionality, and product development processes Experience with stability testing, sensory evaluation, and GMP practices Excellent problem-solving skills and ability to work collaboratively in cross-functional teams Strong communication and documentation skills Preferred Attributes Experience in hair care formulation strongly preferred Familiarity with regulatory and safety requirements for consumer health products Ability to balance technical rigor with creativity in product design What We Offer Competitive compensation and benefits package Opportunity to work with a Fortune 100 organization at the forefront of consumer health innovation Collaborative, science-driven environment with career growth potential Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws. By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.

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.

Introduction Werfen Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Position Summary: Performs formulations of Clinical Chemistry, Co-Oximeter, and/or Coagulation controls and reagents using various automated and manual techniques. Formulations are to be performed in accordance with established Quality Standards and GMP requirements Responsibilities Key Accountabilities: Must be capable of performing all duties required of a Formulation Tech I. Assists in the formulation of products with senior team personnel. Must demonstrate good understanding of all team Standard Operation Procedures. Maintains equipment in compliance with Good Manufacturing Practices and written Standards of Procedures. Assists in all areas of team as needed. Maintains manufacturing documentation and records, i.e., Standard Production. Methods, enzyme use logs, sterilization charts, etc. Initiates purchase requisitions for team supplies as needed. All other duties as assigned by manager Budget Managed (if applicable) N/A Internal Networking/Key Relationships To be determined based on department needs Skills & Capabilities: Oral and written communication skills Qualifications Min Knowledge & Experience Required for the Position: B.S. in a Science field or equivalent plus 2 years of experience Physical Requirements This position requires the ability to lift and move materials per current OSHA standards. International Mobility Required: No Travel Requirements: No The hourly wage range Werfen reasonably expects to pay for the position is $25 to $28. Compensation is reasonably based upon multiple factors including education, relevant experience, skillset, knowledge, and specific needs of the business. Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact ****************************** for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. **************

Introduction Werfen Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Position Summary: Performs formulations of Clinical Chemistry, Co-Oximeter, and/or Coagulation controls and reagents using various automated and manual techniques. Formulations are to be performed in accordance with established Quality Standards and GMP requirements Responsibilities Key Accountabilities: Must be capable of performing all duties required of a Formulation Tech I. Assists in the formulation of products with senior team personnel. Must demonstrate good understanding of all team Standard Operation Procedures. Maintains equipment in compliance with Good Manufacturing Practices and written Standards of Procedures. Assists in all areas of team as needed. Maintains manufacturing documentation and records, i.e., Standard Production. Methods, enzyme use logs, sterilization charts, etc. Initiates purchase requisitions for team supplies as needed. All other duties as assigned by manager Budget Managed (if applicable) N/A Internal Networking/Key Relationships To be determined based on department needs Skills & Capabilities: Oral and written communication skills Qualifications Min Knowledge & Experience Required for the Position: B.S. in a Science field or equivalent plus 2 years of experience Physical Requirements This position requires the ability to lift and move materials per current OSHA standards. International Mobility Required: No Travel Requirements: No The hourly wage range Werfen reasonably expects to pay for the position is $25 to $28. Compensation is reasonably based upon multiple factors including education, relevant experience, skillset, knowledge, and specific needs of the business. Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact ****************************** for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. **************

We help Procurement and Recruiting departments faced with the challenge of filling multiple IT-related openings for either long-term employment, or short-term projects. They need to find reliable candidates, with the right expertise, quickly and at the right cost to enable their company to remain competitive, and to increase profit and efficiency. Stefanini provides the IT contract resources you need to implement crucial projects, handle short-term assignments, or fulfill long-term placements. Our IT staffing services free you from the challenges of finding, recruiting, training and retaining high-quality professional staff, and allow you to focus on managing your business growth. We provide the ongoing skill development to ensure that professionals placed at your site are trained in leading technologies to support your information technology hardware, software, and network infrastructure. Augment your staff for short or long-term engagements, or for specialized expertise on specific projects. We have more than 25 years of staffing industry knowledge and can provide you with superior candidates to match your technical and professional needs. Job Description The role requires the job holder to work under a moderate degree of autonomy to plan and conduct independent projects as a fully engaged cross-functional partner interacting with senior leaders as required aligning on research deliverables. The job holder develops project objectives and strategies independently in response to business needs, executing against same and recommending action plans to implement key findings. The job holder is able to solve complex problems and get things done through both formal and informal channels. The job holder significantly impacts the directions/quality of work done by other technical people and delivers expert technical knowledge representing the function. The job holder interacts regularly with key stakeholders and may direct activities of junior professionals and/or temporary staff while completing assignments. Qualifications • BS in Food Science and/or Technology or a related discipline (e.g. psychology, statistics, consumer science) with min. 6years relevant training/work experience with sensory evaluation and consumer research as a core element of the role, including statistical analysis of data (especially design of experiments and multivariate techniques). • Proven track record of experience in the application of sensory (descriptive, discrimination), consumer research (CLT, HUT, focus groups) and other related technical fields, such as physiology, psychology and statistics in a FMCG client-side commercial environment. • Ability to integrate sensory and consumer methods into research plans, integrate data and draw conclusions. • Proven experience of partnering with client/stakeholders as individuals and teams, ability to influence is essential, as a strong element of this role will be the ability to build and maintain relationships. • Proven experience in line-management and the ability to lead coach and mentor others. • Must have excellent communication skills (verbal and written). • Strong organizational, planning and interpersonal skills and be able to work with flexibility. • Computer literate, inquisitive, self-starter. • Knowledge of biscuit products is a plus. • Partner with clients to deliver excellent sensory and consumer guidance and contribute to decision making. • Lead and conduct Consumer Science projects to produce high-quality, value-added, actionable research delivered to agreed timelines. • Develop and maintain knowledge of category. • Contribute to Category and Global Consumer Science Objectives. • A motivated self-starter and team player. • Good written and verbal communication skills. • Committed to maintaining a safe working environment for both self and others Additional Information Contract for 3 - 4 Months

Pay rate: $44/hr Title: Product Development Scientist Duration: 12 months ABOUT FOOD SOLUTIONS Act like a founder, be part of a Winning team, accelerate your growth, stay ahead of the curve, enjoy the journey: Client is the the 2nd largest Business Unit of client, is one of the 3 Power brands of the Foods Business Group, and a global market leader in Food Service. We are an independent Global Business Unit that operates in over 76 countries, generating ~€3 Billion in Turnover, and employing ~4000 employees. We have a unique B2B business model focused on serving chefs and our purpose is to free them to love what they do. We at Client have a bold and clear ambition and strategy in place to reach €5bn by 2030 with accretive profitability, by being the best solution provider to our 5 million operators. We plan to do this via a product first focus on superiority, by becoming the leader in AI powered Customer experience and by nurturing a Winning culture. We have had a history of delivering with excellence and resilient performance in the past few years. We also strive to stay 3 steps ahead in the industry. For example, our Future Menus Report identifies emerging culinary trends, making us a trendsetter for inspiring innovative solutions for chefs worldwide. We have a culture of caring deeply not just for our business but also for our people. We foster an entrepreneurial culture built on speed, simplicity, trust, and a deep hunger to grow. Our people thrive on their roles being empowered and end to end - across all functions. We also invest heavily in building future skills and leaders. Our People agenda of Accelerate-Grow-Thrive consistently helps us lead in employee engagement, with Univoice scores exceeding *** scores across all dimensions and being one of the most engaged teams at ***. Here, you will continuously learn, unlearn, and relearn, challenging yourself to accelerate your development in an end-to-end business and in end-to-end roles. If you're dreaming of contributing to ***'s 2 nd largest Business unit, a fast-growing business, where you're empowered so you can play to win and thrive as part of One Team with One Goal, then come and join us! WHO YOU ARE & WHAT YOU'LL DO: As a member of Client R&D Cooking Aids team you will be working to develop relevant products under Knorr Brand for menus to local guests, whether that is meeting the need for healthy, delicious, guilt-free dining experiences, localizing a global offering, or bringing the world's most exciting cuisines to our North America market. Partnership with Marketing, Culinary, Quality, Procurement and Supply Chain teams supporting business objectives. Support technical development (recipe development, specifications, risk management) for North America Cooking Aids products. Support R&D initiatives of quality, nutrition, cost savings, complexity reduction and sustainability by design. Works as a member of a cross functional project team to deliver projects on time and in full. You're a born leader: Works independently at times and completes assigned tasks with some initiative and follow-through, contributing to results as needed. You're a dot connector: Ability to manage complex relationships and propose solutions for complex problems. You love to win, and have fun doing it: Passion for product development and strong customer/consumer focus. You're a changemaker: Ability to identify and address emerging issues as well as set and manage priorities and continuously propose improvements on processes and practices. You're a culture & change champion: Comfort with multi-tasking and operating in a fast paced, multi-faceted, and multi-cultural environment. WHAT WILL YOUR MAIN RESPONSIBILITIES BE? Support the R&D activities to deliver the brand's program, ranging from innovation, renovation, quality and nutrition improvement and cost savings initiatives. Support the technical discussions in cross functional meetings and represent the R&D view for the project team to technical and non-technical audiences. Support the technical risk assessments and provide recommendations on risk mitigation plans. Demonstrate flexibility to manage multiple priorities by adapting to daily challenges and priority changes within business environment. Support the project team on the definition of the technical project brief and targets against which products can be designed (performance and attributes), developed and measured. Translate the brand philosophy, culinary and operator insights into superior new products. Demonstrate strong formulation expertise in Cooking Aids to lead new product design and renovations with speed. Design and execute test protocols for the various technical aspects of projects as required (e.G., prototype development and scale-up, shelf-life testing, analytical testing, performance testing, etc.). Support and drive the process of specification/label creation in SAP PLM from initial request through approved status including lower order specifications/new ingredient specifications and artwork brief generation. Organize and participate in trials, providing onsite monitoring and technical assistance, while providing formulation adjustment recommendations as needed. Analyze and interpret data with guidance on final conclusions incl the ability to prepare comprehensive trial/lab reports and presentations, including recommendations and next steps. Support cost savings (5S) initiatives and supply chain efficiency projects to support quality, cost savings, and complexity reduction initiatives. Assess feasibility of new ideas and troubleshoot activities where formulation knowledge is essential. Support technical investigations using root-cause analysis and problem-solving techniques as required for existing and new products. Provide product expertise and insights into innovation and activation strategies. Be a product ambassador internally and externally, demonstrate awareness of operator insights and needs/behavior. Develop and maintain strong working relationships and communicate effectively across R&D and non-R&D functions (with key business and strategic vendor partners) to support business initiatives KEY REQUIREMENTS Education: Bachelors of Science in Food Science or equivalent degree. Relevant Experience: 3-5 years of experience in the food industry, preferably in product development, processing, and/or project management. Experience with SAP PLM/Minerva, specification creation and approval process, demonstrated knowledge/experience in Cooking Aids technology, and good understanding of Supply Chain. Food Service business preferred.

About Atrium: What you do matters. As a people-centric organization, we foster an environment of collaboration, high performance, and innovation where your talents are valued, and your achievements are celebrated. Join us and become part of an inclusive team. Client Overview: Our client is an established consumer goods company and is looking to add a Chemistry Lab Technician to their team Salary/Hourly Rate: $20/hr Position Overview: The Chemistry Lab Technician will work in the lab formulating products and assisting with testing samples. The ideal candidate should have strong attention to detail and organization skills, and the ability to work well individually as well as in a team environment. Responsibilities of the Chemistry Lab Technician: * Formulate and perform testing on products using established formulas and protocols. * Conduct testing on samples, including pH, viscosity, and color. * Calibrate and maintain lab equipment and instrumentation. * The Chemistry Lab Technician will maintain accurate test results and lab data. * Follow all SOPs and company rules and regulations. Required Experience/Skills for the Chemistry Lab Technician: * Knowledge of basic lab equipment. * Familiarity with Microsoft Office Suite. * Work well in a fast-paced environment. * Good written and oral communication skills. Education Requirements: * Associate's or Bachelor's degree in Chemistry, Biochemistry, Biology, or a related science is preferred. Benefits: * Atrium Care Package available, upon eligibility (including healthcare plans, discount programs, and paid time off).