Chemist jobs in Greenburgh, NY - 72 jobs

Chemist needs 2 years Chemist requires: BS/MS in Chemistry, Chemical Engineering or related field plus 0-1 years of experience. Strong problem solving skills and positive attitude. Strong communication and analytical skills. Quick learner.nt Chemist duties: Prepare lab batches for hair color applications and conduct testing to verify release criteria under the supervision of Senior Chemist or Manager. Conduct stability and efficacy testing including detailing experiments, analysis and summary of results. Assist in the maintenance of laboratory raw materials, glassware, supplies and waste removal. Maintain documentation of lab results, conclusions and next steps. Understand, utilize and document within laboratory notebook and formulation software every batch made with details of reason for the batch, batching notes, batch specification results and other test results as applicable. Communicate effectively and routinely with supervisor and, as needed, colleagues on all projects. Communicate formulation stability and efficacy results and issues promptly and thoroughly. Maintain an organized, clean and tidy laboratory and cubicle workspace. Handle other projects and duties as assigned.

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

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.

Our client is a food/nutraceutical company. They are looking for an experienced Product Development Chemist (Oral Solid Dosage) to join their team. Salary/Hourly Rate: $85k - $90k DOE This Product Development Chemist (Oral Solid Dosage) position involves creating and improving formulations for dietary supplements in various dosage forms, including capsules, tablets, liquids, and oils. You will work closely with cross-functional teams to ensure successful product development and commercialization. Responsibilities for the Product Development Chemist (Oral Solid Dosage): * Develop formulations for capsules, powders, and granulations (or oils and liquids). * Collaborate with Purchasing and Quality teams to source raw materials and analyze costs. * Maintain accurate documentation for projects and formulations. * Perform QC analytical testing and ensure compliance with standards. * Use laboratory instruments such as GC, HPLC, and ICP-MS. * Assist with training lab personnel and monitoring lab needs. * Work with Sales, QA, and Operations teams to resolve technical issues. * Manage multiple projects and meet deadlines. * Conduct bench-top, pilot, and scale-up batches. * Maintain lab equipment and inventory. * Follow SOPs, cGMPs, and company policies. Required Experience/Skills for Product Development Chemist (Oral Solid Dosage): * Minimum of 3+ years in product development within the dietary supplement industry. * Strong knowledge of ingredient functionality and costing methods. Preferred Experience/Skills for the Product Development Chemist (Oral Solid Dosage): * Familiarity with natural product chemistry and nutritional products is preferred. * Excellent communication and organizational skills. * Ability to work collaboratively across teams. * Knowledge of GMPs and dietary supplements (DSHEA) regulations is preferred. Education Requirements: * Bachelor's degree in Food Science, Chemistry, Nutrition/Dietetics, or a related field is required. Benefits: * Health Insurance: medical, dental, and vision. * 401(K). * Paid time off: 15 days annually, accrued during the first.

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.

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

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.

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

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.

About Us Queens Carbon is pioneering breakthrough technology to efficiently produce carbon-neutral cementitious materials - without the green premium. Our patented manufacturing process, known as “The Instant Pot of Cement Manufacturing,” uses water to lower production temperatures, dramatically improving energy efficiency and cutting emissions. Backed by Breakthrough Energy Fellows, ARPA-E, world-class climate investors, and strategic partners, we're proving that sustainability can be both economically viable and globally competitive. Position Overview As a Lab Technician at Queens Carbon, you will operate testing machinery and lab testing equipment to characterize the physical properties and performance of materials that are used in cement manufacturing and the performance of products made using Queens Carbon's processes. The process includes following procedures for sample preparation according to either ASTM standards or Queens Carbon specific standard operating procedures. The technician is also tasked with maintaining the testing equipment to ensure it is operating according to either manufacturer's specifications or according to required standardized testing requirements. Lab Technicians have direct contact with Scientists and Engineers by reporting the results of testing or reporting observations of specimen performance. Roles and Responsibilities Manage material testing workflow from sample submission through testing completion. Accurately record testing results via database management. Follow SOPs to operate and maintain laboratory testing equipment and machinery. Import testing data to graphing programs for analysis by R&D team. Manage inventory of lab consumables. Work with the lab team to brainstorm improvements to our technology. Comply with all Health, Safety and Environmental policies and procedures. Requirements The job is performed in a hands-on work environment. The employee must have the ability to sit, stand, walk and lift 35 pounds unassisted or more than 35 pounds assisted. The employee must be able to communicate well in both verbal and written means and use fine motor skills to operate a computer, make measurements and control equipment/machinery. At least 1 year of research experience in an academic or industrial setting. Bachelor's Degree in Engineering or Applied Science disciplines Ability to work full time and in person at our lab in Pine Brook NJ. Strong problem-solving skills, the ability to learn quickly, and the propensity to tackle new problems. A great team-focused attitude, and a willingness to teach and learn from others. A desire to save the planet, and an interest in becoming a part of the growing group of climate change innovators. These requirements are not set in cement, so if you're passionate about this role and think you'd be a great fit, please reach out! Benefits and Salary A competitive salary Equity in the company Insurance options including health, dental, vision, life, and 401k. A friendly time-off policy that encourages a healthy work-life balance. Company-wide hiking retreat on Earth Day Cool company swag :) We're Committed to Diversity Queens Carbon is committed to building a diverse team and is home to an inclusive culture. We are an equal opportunity employer, and we strive to include a variety of voices in our team that can provide different perspectives. We do not discriminate based on race, religion, ethnicity, gender, sexuality, disability status, age, or veteran status.

Have you ever enjoyed Arnold, Brownberry or Oroweat bread? A Thomas' English muffin or bagel? Or perhaps snacked on a Sara Lee, Entenmann's or Marinela cake or donut? If the answer is yes, then you know Bimbo Bakeries USA! More than 20,000 associates in bakeries, sales centers, offices and on sales routes work to ensure our consumers have the freshest products at every meal. In addition to competitive pay and benefits, we provide a safe and inclusive work environment that appreciates diversity, promotes development and allows our associates to be their authentic selves. #LI-SO1 Come join the largest baking company in the world and our family of 20,000 associates nationwide! Top Reasons to Work at Bimbo Bakeries USA: Salary Range: $65,900 - $85,700 Comprehensive Benefits Package 401k & Company Match On the Job Training with Advancement Opportunities Annual Bonus Eligibility Position Summary: Conducts Research and product development activities throughout BBU for all BBU manufactured products and all co-manufactured, co-developed products. Brings key skills and knowledge in new product ideas/concepts and troubleshooting. Able to initiate product and /or processing concepts from idea to final production start-up. Spearhead new technology development and its application into all baked good areas. Develop and implement productivity project. Key Job Responsibilities: * Design and execute experimentation using established procedures, interpret results and translate results into possible solutions. * Contribute to key product improvement, cost reductions, new products, development, knowledge building or other technically based, business driven objective. * Describe/demonstrate research results or experimental protocols to colleagues in a professional manner. * Carry out those programs so laid out by designated supervisors under authority of the Director of Product Development, within the parameters of time and cost, etc. * To work both in a "hands-on" environment and /or direct as needed, ideas and concepts into product reality. * Utilizes practical and technical abilities both of his/her own and/or other team members, make changes, and is adaptive as required. * Utilizing services available - laboratory, accounting, packaging, technical services, marketing, engineering, etc. - ensure that product(s) are followed through to channels for final approval for sale. * To advise and guide, as requested, other R&D team members and other departments throughout BBU, on scientific/technical matters as necessary. * To prepare specifications and process operating guides for product developments and ensure flow of documentation is communicated to those who have a need to know. * To write reports/memos from time to time on status of developments * Interface with operations personnel in all facilities to implement product development objective effectively and efficiently to completion. * Deal effectively and professionally with outside ingredient supplier to meet R&D objectives (keeping Purchasing informed). * To ensure, always, communication with all R&D members of product development team throughout BBU and any other groups that may be added in the future. * To maintain a daily log outlining project status and activities in such detail that others may continue the test. * To lead in special projects concerning products, processes, equipment, and facility concepts and design. * Where approved to travel to all BBU technical facilities and co-packers to accomplish R&D objectives and interface professionally independently and effectively with representatives of the same. Education and Work History: * Strong commitment to and support of BBU's values, ethics, goals, and objectives. * B.S. degree in Food Sciences, Cereal Science, or in Chemical, or Food/Agricultural/Biological Sciences. * Minimum of 6 months of experience in Research and Development of foods, preferably in the bakery industry. Formulating and/or troubleshooting experience is desired. * Knowledge of the baking process and the function of ingredients. * Proven excellent work record with demonstrated high levels of initiative and self-direction. * Demonstrated strong problem-solving and critical-thinking skills. * Excellent organizational and communication (written and oral) skills. * Excellent verbal and written communication skills. * Excellent project management skills with ability to prioritize multiple activities simultaneously * Computer skills and proficiency with word processing, spreadsheet, database, and other software/applications. * Willing to travel as required * M.S. in Food Science or related field or significant experience and training beyond B.S. degree in the science of baking and a strong mechanical aptitude. Equivalent work experience in the bakery industry and specific experience within an R&D/Quality environment, developing or troubleshooting products may be considered. * Completion of the AIB Residence course preferred. * Knowledge of Statistical Process Control, statistical design of experiments, and data collection and analysis preferred. The physical and mental demands described in each job posting are representative of those that must be met by an associate to successfully perform the essential functions of each job. Reasonable accommodations may be requested to enable qualified individuals with disabilities to perform the essential functions of each job. Bimbo Bakeries USA is an equal opportunity employer with a policy that provides equal employment opportunity for applicants and employees regardless of race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, any other classification protected by law. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Join our team as a QC Scientist I working on the second shift from Sunday to Thursday. You will perform fit-for-purpose testing to support manufacturing, including in-line and finished product release testing using various analytical techniques. Your work will be essential in ensuring the quality of our products. Responsibilities + Perform fit-for-purpose testing following operating procedures. + Prepare standards and samples for analysis and run instrumentation with minimum supervision. + Document and report analytical testing data in LIMS Database and in a laboratory notebook following good documentation practices. + Assist in out-of-specification investigations by performing relevant testing and documenting appropriately. + Make recommendations regarding opportunities to optimize instrumentation methods and provide general feedback on non-instrumentation method opportunities. + Apply knowledge of Lean Six Sigma Processes focusing on supporting continuous improvement activities. + Maintain general lab housekeeping. + Engage in process improvement initiatives to identify cost savings to the business. + Perform additional tasks as assigned by the Supervisor. Essential Skills + Bachelor's degree in Analytical Chemistry, Organic Chemistry, Biochemistry, Biology, or related field from an accredited university. + Minimum of 1 year (2 years preferred) of industry or other relevant market experience, preferably in the chemistry or bio/pharmaceutical industry. + Hands-on experience with wet chemistry and basic analytical instruments. + Familiarity with Analytical test methods including ACS, USP/NF, EP/BP, JP, FCC. + Strong computer, scientific, and organizational skills. + Excellent communication skills (oral and written) with attention to detail, including problem-solving. + Familiarity with reviewing laboratory notebooks and understanding testing performed using various Analytical Chemistry Techniques and instrumentation. + Effective problem-solving abilities using Lean methods. Additional Skills & Qualifications + Familiarity with Lean Six Sigma Processes. + Ability to lift up to 40lbs. Work Environment + Work in a GMP Lab environment on a contingent basis, with responsibilities scheduled from Sunday to Thursday during the second shift. + The role involves active participation in process improvement activities to support continuous improvement and cost savings. Job Type & Location This is a Contract position based out of Fair Lawn, NJ. Pay and Benefits The pay range for this position is $36.00 - $36.00/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 Fair Lawn,NJ. Application Deadline This position is anticipated to close on Jan 29, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Quality Control Analytical ScientistAllendale, NJ Lynkx Staffing LLC specializes in placing talented professionals in the Biotechnology, Pharmaceutical and Medical Devices industries in New Jersey. The QC Analytical Scientist will be a member of the Quality Control Department. As a Senior Member of the team the QC Analytical Scientist will be involved in various QC projects and should have a deep understanding of general QC flow and the Product Cycle. Support internal and external customers to ensure that proper and timely execution of all aspects of the clinical analytical method life cycle across clients. Support routine GMP testing as assigned. Mentor and train team members Evaluate corporate and regulatory requirements along with coordination of activities for implementation of these requirements. Write the contents of Analytical Method Transfer and Validation life cycle documentation including master plans, protocols, test methods, and reports. Create validation project plan i.e., timelines and resources and provides status updates to management. Utilize statistical tools for evaluation of method validation and trending data. Identify, evaluate, and implement continuous business process improvements. Perform troubleshooting activities with respect to methods/assays, equipment malfunctions and investigations (Deviations and OOS). Provide support during laboratory investigations. Train QC personnel during method transfer and validation. Provide support during equipment qualification. Consistently produce elevated level of documentation accuracy and clarity according to cGMP documentation practices. Ability to set deadlines and prioritize work for self, group members, and support groups involved. Ability to review/approve work performed by coworkers for accuracy and alignment with procedures. Indirectly may supervise cross functional teams including product development, QA, PMP, and Manufacturing. REQUIREMENT B.S Analytical Chemistry or other scientific field or MS/Ph.D. in Analytical Chemistry or other scientific field with demonstrated experience in Quality Control laboratories for biotechnology products. 8-10 years of experience in the areas of method development, validation, and transfer. Direct GMP Experience. Proficiency in project management skills and tools. Strong background and in-depth knowledge in analytical chemistry e.g. Flow Cytometry, ELISA, HPLC, CE, PCR, etc. Extensive knowledge and experience of QC assay development, transfer and validation, along with cGMPs. Strong Quality orientation with attention to detail required. Analytical and problem-solving skills required. Excellent communication skills, both written and verbal, with all levels of the organization, including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution. Excellent presentation skills. Ability to communicate to upper management, across departments and within the immediate QC team. Ability to create and manage work plans and timelines and independently manage competing priorities with limited instruction. Highly motivated individual with good interpersonal skills that have proven effective in managing relationships and negotiating solutions while maintaining a level of approachability with colleagues both internal and external. Must be familiar with GMP lab environment and Aseptic techniques. Working EnvironmentMust have the ability to work in a team-oriented environment and with clients Must be able to work during the weekend, holidays, or overtime and as required by the company May be exposed to infectious diseases transmittable through human blood, tissues, or bodily fluids Must utilize proper personal protective equipment (PPE) when handling all human specimens, gases, corrosive chemicals, and liquid nitrogen Must have the ability to work with specialized equipment Must be able to handle the standard/moderate noise of the manufacturing facility May work with hazardous materials and chemicals Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

QUALITY CONTROL - WALDWICK NEW JERSEY START NOW !!!!!!!!!!!!!!!!!! ** We are looking for reliable and responsible candidate for warehouse associate in Waldwick. Pay rate: $13.50 (NEGOTIABLE DEPENDING ON EXPERIENCE) 2nd shift QA( Quality Assurance) Train for 2 weeks on 1st shift MONDAY - FRIDAY ( 7am-3:30pm) Regular hours MONDAY - FRIDAY 3pm-11:30pm OVERTIME AVAILABLE Must work weekends.( rotate) Requirements: Computer Knowledge, Inspecting Materials, Test Samples Able to stand all day performing this job. Bilingual is a plus Must have transportation Benefits offered - Health Care Sick Pay 401 k offered in 2021 MUST HAVE TRANSPORTATION!!!!!!!!!!!!!!!! Start now! Vaccinated

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.

Job ID 33235 **Technical Service Chemist** Regular Stamford - CT, United States of America (****************************************** - CT,United States of America) My candidate profile **Important EEO information related to openings in the US** 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.Click here (************************************************************************************** to access the Know Your Rights poster. 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 come. **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. \#LI-RC1 \#Onsite

Chemist/aerosol lab technician needs 1+ years fragrance development experience Chemist/aerosol lab technician requires: Chemistry degree Fragrance development, testing experience Previous experience with fragrance development and/or testing Chemist/aerosol lab technician duties: Hair fragrance coordination support, the role will involve all fragrance related tasks under the supervision of the fragrance coordinator. Support function will be responsible for collecting all required information for fragrance briefings and tracking to completion, request necessary paperwork and complete fragrance coding, maintain internal fragrance domain and local fragrance library, support fragrance evaluations, and liaise with core fragrance houses on new technologies and innovations Aerosol formulations of hair related products under a supervision and direction of experienced Scientist or Supervisor. Make batches in the lab, test finished products, document work and maintain a clean and organized laboratory environment. Collect raw material data from suppliers and update formulation system.

Our client is a consumer products company specializing in cosmetics and personal care products and operating in a very fast-paced environment. They are now seeking a Formulations Chemist to support formulation innovation and product development initiatives. Salary/Hourly Rate: $60k - $75k Position Overview: The Formulations Chemist will lead technical formulation efforts for powder-based cosmetic products, with occasional support for emulsion and anhydrous formulations. This role requires close cross-functional collaboration and the ability to thrive in a fast-paced, deadline-driven environment. Responsibilities of the Formulations Chemist: * Develop and improve powder cosmetic formulations, including new product development and reformulations. * Assist with emulsion and anhydrous product development as needed. * Evaluate and incorporate new raw materials and technologies to enhance performance while meeting cost and regulatory requirements. * Collaborate directly with clients to define formulation objectives, troubleshoot issues, and deliver solutions. * Provide technical support through clear documentation and communication. * Research emerging trends, ingredients, and technologies relevant to powder and cosmetic formulations. * Work cross-functionally with Marketing, Manufacturing, Quality, Regulatory, Packaging, and Research teams. * Monitor product stability and manage multiple formulation projects simultaneously. * Maintain accurate documentation of formulations and processes in compliance with internal and regulatory standards. * Support global standardization initiatives related to formulation and testing. Required Experience/Skills for the Formulations Chemist: * At least 6 months of hands-on powder formulation experience and 2+ years of cosmetic formulation experience. * Practical formulation experience in a fast-paced laboratory or R&D environment. * Strong understanding of powder technologies and basic emulsion and anhydrous formulation principles. * Knowledge of cosmetic raw materials, regulatory guidelines, and industry standards. * Ability to adapt quickly to changing priorities and manage multiple projects effectively. * Proficiency in Microsoft Word, Excel, SAP, DEVEX, or similar systems. * Strong communication, analytical, and problem-solving skills. * Highly organized, detail-oriented, and collaborative. Preferred Experience/Skills for the Formulations Chemist: * Prior experience working in a fast-paced product development environment. Education Requirements: * Bachelor's degree in Chemistry, Biology, Biochemistry, or a related scientific discipline required. Benefits: * Medical, dental, and vision coverage. * 401(k) plan. * Paid time off and paid holidays.