Chemist Jobs in Pomona, CA

Clear Skies is incubating a stealth venture that uses an AI-powered platform to serve major stakeholders in private equity. We operate at the intersection of finance/AI to optimize deal flow, automate decisioning, and integrate networks into a seamless customer journey. Our team is composed of seasoned professionals from private equity, financial advisory, human capital, and AI engineering. We are seeking a Founding Head of AI Products to spearhead the development of AI-driven solutions that redefine how investments are sourced, evaluated, and executed. You will define the product and lead AI initiatives to solve real-world problems in a multi-billion-dollar industry. Key Responsibilities: Product Strategy Execute AI product strategies for market fit and business impact. Analyze customer needs and competitive landscape to uncover new product opportunities. Build business cases with market analysis, ROI projections, and scalability assessments. AI Product Development Define features and workflows to gather customer feedback and iterate on MVP development. Build AI-powered engines to transform large-scale unstructured data into actionable intelligence. Implement NLP techniques for semantic search and keyword matching from unstructured data. Utilize embedding models for vector-based search and context understanding. Workflow Automation Establish scalable AWS-based infrastructure and data pipelines. Develop automated communications, scheduling, and self-service AI tools. Implement best practices for AI model versioning, monitoring, and optimization. Leadership & Collaboration Lead and mentor AI and product teams, promoting innovation and learning. Collaborate with business leaders to align AI strategies with goals. Define and track KPIs to measure product success and guide development. Key Qualifications: 10+ years in product leadership with focus on AI/ML platforms and generative AI technologies. Expertise in AI/ML frameworks (TensorFlow, PyTorch, etc.) and cloud infrastructure. Experience in financial services or private equity is a plus. Application Process: Interested candidates are invited to submit their CV and cover letter detailing relevant experience and qualifications to ***************************. About Clear Skies: Clear Skies is a private equity investment firm that acquires middle-market businesses. We partner with management teams to drive growth and value through our global networks.

A utility client is looking for a Chemist who will work in the agency's air quality laboratory and may be called upon to assist in all laboratory departments or with the laboratory's field work. Position: Chemist Pay Rate: $30 - $35/hr., depending on experience Duration: Approximately 6 months (with a possibility to extend up to 12 months), working 40 hours per week. Schedule: Four 10-hour days, Tuesday - Friday, 7:00 a.m. to 5:30 p.m. however, on occasion, the schedule may switch to Monday through Thursday, or Wednesday through Saturday. Interested individuals must be willing to work these schedules within a Monday - Saturday timeframe. Flexibility is important for this assignment. MUST BE WILLING TO SUBMIT THEIR CURRENT COLLEGE TRANSCRIPTS/DIPLOMA BEFORE SUBMITTING OVERVIEW OF ASSIGNMENT This temporary Chemist will work in the agency's air quality laboratory and may be called upon to assist in all laboratory departments or with the laboratory's field work. May conduct qualitative and quantitative chemical and physical analyses of air samples, using a variety of techniques, procedures and instrumentation, including Ultra High Performance Liquid Chromatography (UHPLC), Gas Chromatography/Flame Ionization Detector (GC/FID), Gas Chromatography/Mass Spectrometry (GC/MS), Inductively Coupled Plasma Mass Spectrometry (ICP/MS), Ion Chromatography (IC), Proton Transfer Reaction Time-of-Flight Mass Spectrometry (PTR-MS), and spectroscopic methods to evaluate air quality samples for types and concentrations of contaminants present. May assist with other laboratory duties as needed. REQUIRED QUALIFICATIONS BS in Chemistry is required, from an accredited US college or university, preferably with an emphasis in analytical chemistry or instrumental analysis. Requires experience conducting qualitative and quantitative chemical and physical analyses using a variety of techniques, procedures and instrumentation. Knowledge of and experience with chromatographic, spectroscopic and/or mass spectrometric methods is highly desired. The ability to manage multiple tasks, while adhering to chain-of-custody and documentation requirements is critical. About our client: Our client is the air quality management agency for four local counties, responsible for regulating businesses so they don't pollute the air. “We clean the air we breathe.” About APR: Since 1980 APR Consulting, Inc. has provided professional recruiting and contingent workforce solutions to a diverse mix of clients, industries, and skill sets nationwide. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Don't miss out on this amazing opportunity! If you feel your experience is the match for this position, please apply today and join our team. We look forward to working with you!

Hi, My name is Gaurav and I am a recruiter with Net2Source Inc. I saw your profile on one of the job boards and our direct client is looking to hire a Chemist (0-3 years) in their growing team. Please find below the . Title: Chemist (0-3 years) Duration: 12 months Location: Pasadena, CA Job Description: • Work closely with senior scientists to accomplish team objectives and research milestones. • Design, validate and implement synthesis projects in organic synthesis, peptide synthesis, bioconjugation, purification, and characterization of compounds of interest. • Maintain accurate record keeping, perform independent data analyses, and report data in written and oral formats. Critically evaluate data and results and troubleshoot synthesis issues. • Perform work in compliance with Client Research Labs policies. Qualifications • Undergraduate degree in chemistry or a closely related field with laboratory research experience • At least 1 year of experience designing, validating, performing, and analyzing experiments to generate synthetic compounds of interest. • Demonstrable ability to function independently, work within a flexible, team-oriented lab environment, and work within cross-functional project teams. • Postgraduate training or equivalent experience in peptide synthesis, medicinal chemistry, protein engineering, and/or combinatorial chemistry • Strong communication skills and experience presenting data in a team environment. • Strong relationship-building and interaction skills with peers and supervisors. Thanks Gaurav Gupta Sr. Pharma Recruiter *************************** **************

Key Responsibilities: Conduct routine and non-routine chemical analysis using HPLC, GC, UV-Vis, FTIR, and other analytical techniques. Perform method development, validation, and transfer following USP, ICH, and FDA guidelines. Analyze raw materials, intermediates, and finished products to ensure compliance with specifications. Prepare and maintain detailed documentation, including test results, validation reports, and lab notebooks, in accordance with cGMP and GLP requirements. Troubleshoot and maintain analytical instruments, ensuring proper calibration and functionality. Assist in investigations of out-of-specification (OOS) results, deviations, and corrective actions. Work collaboratively with Quality Assurance, R&D, and Production teams to support manufacturing and product development. Stay updated with regulatory changes and industry best practices in pharmaceutical and cosmetic analytical testing. Qualifications: Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field. 2+ years of experience in a pharmaceutical, nutraceutical, or personal care laboratory performing HPLC and analytical testing. Strong knowledge of cGMP, USP, ICH, and FDA regulatory requirements. Experience with analytical instrument troubleshooting and maintenance. Excellent documentation, data interpretation, and problem-solving skills. Ability to work independently and in a team-oriented environment. Strong attention to detail and organizational skills.

About the Company PakLab is a leading contract manufacturer specializing in health & beauty and household products. With three decades of professional product development service experience, we are setting a new standard in contract manufacturing. With our innate understanding of product design, development and formulation, as well as manufacturing and packaging mechanics, we work with our clients as a fully integrated strategic partner, creating innovative products from the bottom up. We employ a world-class team of Engineers, Chemists, Microbiologists, Lab Technicians, Designers, and Packaging Specialists who oversee the process from conception to completion. Service is the cornerstone of our corporate culture, and we will devote whatever resources are necessary to ensure a complete understanding of our customers' needs in order to achieve their goals. About the Role The Chemist is responsible for the batching of PakLab and customer formulas. Requires an individual that keeps up-to-date with the latest applications of chemicals and is capable of transferring that knowledge into a functional product. Good Attendance. Able to work any shift and extended hours. Must be detailed oriented with strong clerical and time management skills. Able to follow procedures and instructions. Able to work in fast-paced environment with limited supervision. Must work well with others in a close environment. Typical Duties and Responsibilities Develop new personal care product formulations (e.g., cleansers, creams, lotions, serums, hair products) Modify and optimize existing formulas to improve stability, efficacy, or cost-effectiveness Ensure compatibility between active ingredients, emulsifiers, preservatives, and fragrance systems. Must conduct crash stability on all formulations. Ensure formulations comply with FDA, EU, and other regulatory bodies. Work closely with the process engineering team to scale formulations from lab to production. Collaborate with clients to develop formulations based on their briefs. Reformulate based on client feedback, cost targets and ingredient preferences Interact with vendors to obtain information on raw materials to troubleshoot formulas. Keep up with personal care industry trends, consumer demands, and competitor launches Attend trads shows and meet with suppliers for new technologies Follow GLP/GMP and notebook protocol. Maintain the laboratory in clean organized condition. Assist process engineers in first manufacture of production batches. Adjust simple parameters for manufacture of products (such as pH, viscosity, color, etc…). Performs other duties as assigned. Physical Requirements Ability to lift and pull a minimum of 25 lbs. Requires walking and standing for lengthy periods of time. Requires bending, twisting, pulling, pushing and climbing of ladders and stairs. Capable of climbing steps and retrieving material from shelves. Work Experience and Education Requirements Excellent English written and verbal communication skills. Bachelor's Degree in Chemistry, or related field, is required. Master's Degree or PhD preferred. 3 or more years' experience with cosmetics. Knowledge of computer applications. Pay range and compensation package - 75k-100k yearly salary. Equal Opportunity Statement - PakLab is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.

The Food Scientist plays a key role in developing best-in-class scratch-quality food products for Haliburton's food service, and industrial and retail customers. The ideal candidate is naturally passionate about food and food science understanding the balance between product design and profitability. The Food Scientist works actively with cross-functional teams collaborating on new product designs and providing technical support. The Food Scientist thrives working as a member of a team and prefers open communication and a fast-paced work environment. Essential Duties & Job Responsibilities Is capable of developing commercially viable, profitable product prototypes for a variety of product lines including kettle-cooked sauces, roasted vegetables, pickled vegetables, IQF grains and beans, salsas, hot and cold process condiments, dips, and spreads Relies on science to support assertions when troubleshooting or conducting root cause analysis. Strong working knowledge and proven track record of successful product “matching” Culinary-centric, food-savvy, and passionate about food, food science, and product development Stays current with respect to industry awareness, food trends, and product development innovation Ensures work tasks are documented according to company and regulatory standard Has a thorough understanding of food preservation methods, can execute a variety of sensory tests including preference and triangle Competent in physical chemistry testing including salt, pH, Brix, water activity, viscosity, and acid Supports continuous improvement initiatives working on cost optimization, process improvement, product design, ingredient sourcing, and cross-utilization projects Has a general understanding of microbiology Understands food safety consistent with the FDA food code Becomes a subject matter expert relative to Haliburton's processing and product capabilities Capable of developing solid working relationships with customer contacts through rapport building, earning trust, and being the customer's “go-to” R&D contact Leads customer R&D work sessions and attends customer meetings as assigned Collaborates and works with cross-functional teams in a productive, professional, and thoughtful way Maintains an exceptionally clean workspace, practicing “clean as you go” standard at all times including departmental appearance, behavior, and attitude standards. Executes product development projects in a manner consistent with Haliburton's quality and professionalism expectation Is able to translate customer “kitchen recipes” into working R&D formulas Adheres to and models good manufacturing practices (GMPS) whenever in the plant Minimum Qualification Requirements Education and Experience Bachelor's degree in food science required Associates degree or continuing education in culinary arts preferred 4 years of experience as a food scientist working in a related food manufacturing environment required 2 years of experience designing kettle-cooked shelf-stable, refrigerated, and frozen sauces required Demonstrates proficiency in knife handling and basic cooking techniques Strong knowledge of sensory testing Communication, Interpersonal and Professional Skills Exceptional business-level has written and verbal communication skills Must be an attentive listener Interacts well with customers including purchasing, development, and quality executives Is direct and to the point. Recognizes the value of time when communicating Is highly motivated and willing to “manage up” by providing leadership with honest feedback Organizational Skills Must demonstrate exemplary planning and time management skills Must be detail-oriented Can seamlessly manage multiple projects with tight deadlines Utilizes Outlook calendar for planning and scheduling Initiative & Creativity Possesses an acute sense of urgency in recognizing customer needs in a proactive way Is a highly motivated self-starter that is a solution-oriented problem-solver Demonstrates creativity through recommendations, input, and project results Computer Skills Must be well versed and demonstrate competency in Microsoft Word, Excel, PowerPoint, Access, Outlook, Adobe, and other computer applications as needed Prior experience and fluency with Genesis, ERP, and PLM systems preferred Mathematical Skills Proficient in addition, subtraction, division, multiplication, ratios, and percentages Physical Demands/work environment Able to sit and work at computer work station up to 30% of the time Able to stand and walk up to 70% of the time Able to work in a fast-paced environment Willing and able to participate in plant trials and runs as needed Withstand strong odors from the foods being processed

Atoco is a deep tech company tackling climate change by developing technologies in the fields of clean energies, carbon capture and atmospheric water harvesting. This position will join the materials synthesis and characterization team, collaborate with university research teams and will be in charge of materials synthesis, characterization and integration. This position will specifically be responsible for research and development efforts in the field of reticular materials optimization, scaling, integration, and characterization and supplying materials for prototype solid-state hydrogen storage systems. Roles and Responsibilities Synthesize various reticular materials at a variety of production scales and perform comprehensive characterization of the physical and chemical properties. Investigate and determine critical parameters to be addressed for commercialization. Operate instruments for the synthesis and characterization of materials. Analytical techniques may include gas isotherm measurements, physisorption surface area and pore size analysis, particle size analysis, thermal gravimetric analysis, electron microscopy, moisture content analysis, solid state NMR, etc. Develop synthetic process for larger-scale production of reticular materials of interest. Perform research activities to tune, and potentially innovate, reticular materials for higher performance of solid-state hydrogen storage. Investigate various additives and binders for enhancing thermal conductivity and reliability. Potentially mentor chemists and laboratory technicians to aid in research and development efforts and experiments. Maintain an electronic notebook detailing all data measured, observations, and steps performed Contribute to the intellectual property of the company by writing and participating in invention disclosures and/or peer-reviewed journals and conferences. Perform periodic reporting to management and participate in periodic joint brainstorming and technical meetings. Qualifications PhD in chemistry from a top-ranking institution 5-10 years of industry experience in synthetic chemistry Research experience in hydrogen storage materials characterization is a plus. Research experience in synthesis and characterization of MOF or COF materials is a plus. Strong research background, including peer-reviewed publications. A track record of successful scale-up prototypes or experimentation. Ability to meticulously record experimental processes and results and prepare detailed reports. Familiar with health and safety procedures in chemistry labs. Strong teamwork and collaboration skills. Effective written and verbal communication skills.

Yoh has an exciting, opportunity for a QC Chemist - Large Molecule (Contract) to join our rapidly growing life science manufacturing client based in Irvine, CA. This opportunity is ideal for candidates who have a BS in chemistry or related and 1+ years in a GMP/GLP setting with experience using various analytical chemistry methods. See below for complete job responsibilities and requirements. If after reviewing, you are interested in learning more about this, or other opportunities within the Biotech Industry, please apply with your updated resume ASAP. Title: QC Chemist - Large Molecule - Temp Compensation: $35/hr Location: Irvine, CA Type: Contract 2- 3 months Shift: M-F, 8:30 am - 5 pm Industry: Pharmaceutical Responsibilities: Perform analytical QC testing for various protein-based samples and maintain quality operations in GMP setting Must have experience with SDS-Page, HPLC, SEC, Dissolution, and UV-Vis techniques Requirements: BS in Chemistry or related degree 1+ years experience in GMP or GLP analytical environment #IND-SPG Estimated Min Rate: $33.00 Estimated Max Rate: $35.00 Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

B. Braun Medical, Inc. QC Microbiology Assoc I -EM Lab (Sun-Thurs 6:00am-6:00pm) US-CA-Irvine Type: Regular Full-Time # of Openings: 1 Irvine Facility About B. Braun B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap and CAPS . Globally, the B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise philosophy, B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about B. Braun Medical, visit ****************** Responsibilities Position Summary: Performs routine functions and analysis (dependent upon experience) as required by the specific laboratory requirement in compliance with B. Braun and cGMP specifications. Responsibilities: Essential Duties Responsible for microbiological sample receiving/labeling/preparation/sampling/test/ counting/checking and recording of data analysis on finished products, stability test samples and any other test requisitions as directed. Supports the department in ensuring laboratory equipment performance, i.e. scheduling and execution of equipment qualification (IQ/OQ/PQ), calibration, maintenance and trouble shooting. Responsible for the compilation and preparation of test results/reports related to laboratory testing. Supports the department in ensuring continuous test operation, good performance, maintenance and housekeeping of laboratory equipment and facilities. Checks on test results for compliance to the methods/specification/procedures, equipment operating instructions and guidelines for the superior. Supports the superior in the preparation of test methods/specification/procedures and equipment operating instructions. Participates in process and test methods/specification/procedures and equipment operating instructions. The job function listed is not exhaustive and shall also include any responsibilities as assigned by the Supervisor from time to time. Expertise: Knowledge & Skills Assignments are routine and repetitious in nature. Work performed within narrowly defined parameters. Follows established procedures and guidelines. Works under direct supervision and from detailed verbal and/or written instructions. Uses established procedures to accomplish assigned task. May require some limited judgement in resolving problems. Contacts are primarily with direct supervisor, peers and subordinates. The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate. #LI #AL Target Based Range $47,815 - $57,373 Qualifications Expertise: Qualifications - Experience/Training/Education/Etc Required: High school diploma/G.E.D or equivalent required, Associate's or technical degree preferred. 0-02 years related experience required. Desired: N/A While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk or bend and twist. The employee must occasionally lift and/or move up to 20 pounds. . Additional Information Responsibilities: Other Duties The preceding functions have been provided as examples of the types of work performed by employees assigned to this position. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed in this description are representative of the knowledge, skill, and/or ability required. Management reserves the right to add, modify, change or rescind the work assignments of different positions due to reasonable accommodation or other reasons. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is expected to: Light work - Exerting up to 20 lbs of force occasionally, and/or up to 10 pounds of force frequently, and/or a negligible amount of force constantly to move objects. Lifting, Carrying, Pushing, Pulling and Reaching: Occasionally:Reaching upward and downward, Push/pull Frequently: Stand, Sit Constantly: N/A Activities: Occasionally: Handling, Push/pull, Reaching upward and downward, Talking - ordinary, loud/quick, Walking Frequently: Sitting , Standing Constantly: N/A Environmental Conditions: Occasionally: N/A Frequently: N/A Constantly: N/A Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Noise Intensity: Moderate Occasionally: Production/manufacturing environment Frequently: N/A Constantly: Lab environment What We Offer B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at ****************** Through its “Sharing Expertise ” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services. Notices Equal Opportunity Employer Veterans/Disabled All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Compensation details: 57373 Yearly Salary PI03024793e1c8-26***********3

Are you excited by the potential of large-scale carbon removal? If so, Captura Corp. is seeking an R&D Lab Technician. Captura is an early-stage technology start-up with the mission to develop globally scalable carbon removal to support a sustainable future for the world's climate. Captura's unique technology was developed and proven in Caltech's laboratories and uses established electrochemical concepts to enable gigaton-scalable solutions for removing carbon dioxide (CO2) from the atmosphere via direct ocean capture. We capture carbon dioxide using only renewable electricity and seawater, creating no byproducts. CO2-depleted seawater is returned to the ocean to absorb CO2 that comes from the atmosphere. As well as building, testing, and deploying pilot systems, Captura also has a strong R&D effort to develop and scale proprietary ion exchange membranes for the electrodialysis component of our capture system. As an R&D technician in the electrodialysis and membrane team, you will be responsible for lab scale testing of our proprietary ion exchange membranes to support senior engineers in development and scale up of new membrane technologies. Key responsibilities: Follow standard procedures to conduct quality control measurements such as thickness, uniformity, defect analysis, haze, and swelling. Cut and punch membrane rolls and sheets to precise sizes using specialized tools to meet testing and processing requirements. Soak membranes in designated solutions for specific time periods to achieve the necessary chemical conditioning. Prepare chemical solutions following standard formulations and safety guidelines. Maintain an organized inventory of lab supplies, chemicals, and materials to ensure efficient operations. Keep workstations clean and properly maintained, including regular disposal of waste and adherence to safety protocols. Practice safe work habits, including complying with all safety, health, and environmental rules and regulations. Foster effective teamwork among R&D team members and complete expedited, high-value studies in a dynamic and fast-paced technical environment. Educational/Experience Requirements: Capability to execute precise measurements, follow step-by-step protocols, and document findings accurately. Ability to track and maintain detailed lab notes, inventory logs, and test results for quality control and compliance. Proficiency with Excel spreadsheets for logging and tracking data. Capacity to manage individual tasks efficiently while collaborating effectively with colleagues on larger projects. Ability to operate basic lab instruments such as balances, thickness gauges, and optical microscopes. Comfort working in a wet chemistry lab setting around dilute acids and bases and ability to follow safety procedures including use of proper PPE. Strong communication and collaboration skills, with a willingness to learn new tools and technologies as needed. Ability to complete tasks with little supervision. Strong time management skills, organization, attention to detail and ability to manage multiple projects at the same time. Ability to adapt quickly to shifting priorities in a dynamic, early stage startup environment while maintaining accuracy and attention to detail. High interest in climate tech and the CO₂ capture industry, with a passion for contributing to innovative environmental solutions. Preferred bachelor's degree in chemistry, materials science, chemical engineering, or equivalent discipline.

A contract manufacturing and formulation company in the Corona, California area is seeking a skilled and experienced Formulation Chemist to lead the development of innovative skincare and cosmetic products. This full-time, in-office position focuses on formulation and product development from concept to commercialization. Responsibilities: Develop and refine formulations for skincare, haircare, makeup, and other cosmetic products Research new ingredients, trends, and technologies to drive innovation Conduct stability and compatibility testing to ensure product integrity Optimize texture, fragrance, and performance characteristics to meet brand standards Ensure all formulations comply with regulatory and safety requirements (e.g., FDA, EU) Collaborate with marketing, packaging, and production teams to align on product objectives Maintain accurate records, formulation specs, and development documentation Qualifications: 3-5 years of hands-on formulation experience in the cosmetics or personal care industry Expertise in emulsions, surfactants, actives, polymers, and raw ingredient functionality Understanding of regulatory standards and product safety testing Detail-oriented with strong analytical, problem-solving, and communication skills Bachelor's or Master's degree in Chemistry, Cosmetic Science, or a related field preferred Preferred: Experience with clean, natural, or organic formulations Proven track record of bringing formulations from concept to final production Important: This role is focused on R&D and formulation. Candidates with experience solely in quality control or analytical testing are not a match. Hours: Full-time, in-office only Salary: $55,000 - $75,000 (depending on experience)

Kelly Science & Clinical is seeking a Senior R&D Chemist/Scientist III for a direct-hire position at a premier client in Irvine, CA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Salary/Pay Rate/Compensation: $78k Annually Overview This client is an industry-leading CDMO company focused on comprehensive API sourcing and drug product development solutions for the pharmaceutical, biotechnology, and compounding pharmacy industries. In this role, you'll be working with innovative leaders and colleagues to develop and enhance analytical methods for pharmaceuticals. This role will give you an opportunity to lead method development projects, conduct advanced analytical testing, and help bring new therapies to market, positively impacting patients and their families. Responsibilities: Perform HPLC, GC, ICP, UV, FTIR, Dissolution tester, and other analytical instrumentation in an analytical lab setup. Record work using MS Word, Excel, and chromatography data software like Empower, ChemStation. Validate and verify new and existing USP methods; draft, review, and approve method validation protocols, reports, and SOPs. Support and develop analytical methods for pharmaceuticals (solids, semi-solids, and liquid dosages) to ensure product strength and purity. Conduct method improvements, modifications, and USP method feasibility studies for pharmaceuticals. Troubleshoot analytical method issues for pharmaceuticals, including raw materials and finished products. Collaborate with the Lab Manager to establish documentation protocols for analytical methods. Analyze organic and inorganic compounds to determine chemical and physical properties. Coordinate with the Quality Control department to transfer validated methods to QC chemists. Qualifications: BS with 5+ years of related experience/MS with 3 years of experience/ PhD with 1 year of experience in relevant field Proficiency with MS Word, Excel, and chromatography data software such as Empower, ChemStation. Experience with cGMP principles and FDA regulations for pharmaceuticals. Ability to read and interpret scientific documents, FDA regulations, safety rules, and procedure manuals. Mastery in calculations and recording results according to SOPs and cGMP principles. Proficient in advanced mathematical concepts. Self-starter with the ability to work under limited supervision. Strong team player with professional communication skills. What happens next: Once you apply, you'll proceed to the next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless. Join us in making a difference by applying today!

Our client, a leading food and beverage manufacturer, is looking for a skilled Associate R&D Chemist to join their team in San Fernando area of California. Title: Associate R&D Chemist- Food Pay rate: $27- $30/ hr. Key Responsibilities: Assist in preparing flavor samples and prototypes for development. Perform basic laboratory tasks such as weighing, measuring, and mixing ingredients. Maintain accurate records of experiments, results, and observations. Clean, calibrate, and maintain laboratory equipment and workspaces to ensure a safe and efficient working environment. Assist in the sensory evaluation of samples, using established techniques. Follow safety protocols and laboratory procedures to ensure compliance with industry standards. Order and maintain inventory of laboratory supplies. Support senior scientists and flavorists in research and development projects as needed. Qualifications: Associate's or Bachelor's degree in Chemistry, Food Science, or a related field, or equivalent experience. Basic understanding of laboratory procedures and techniques. Strong attention to detail with excellent organizational skills. Ability to follow instructions and work independently. Excellent communication skills and the ability to work effectively in a team environment. A passion for food and flavor and a keen interest in flavor innovation.

R&D Chemist Responsibilities: Computer skills to manage formulations. Have basic technical knowledge of surfactant systems, emulsions, dispersion formulations. Have up to date knowledge on regulatory information. Correct lab notebook documentation including but not limited to formulation, procedure, specifications, stability data. Ability to operate laboratory pH meter and take and record readings Ability to operate laboratory viscometer and take and record readings Ability to operate moisture analyzer and take and record readings Communicate with raw material suppliers for information. Attend seminars and keep current with new technology. Supervise initial production batches. Write manufacturing procedures for production batches. Write finished product specifications for production batches Maintain and record stability data on formulations that are in the evaluation stages. Report stability issues and other relevant issues to supervisor in a timely manner. Communicate effectively with customers in regards to formulation. Position Requirements: Science-related college degree preferred. Computer skills to manage formula work and document all information. Must have at least 1-2 years' experience in formulation development in personal care Highly organized and can maintain diligent records. Communicate effectively with customers in regards to formulations Ability to ask questions and be honest about issues immediately. Highly motivated and interested in the Cosmetic industry. Pay: $25-$28/hr.

An Entry-level R&D Laboratory Technician position in Irvine, CA in the Biomedical Industry is available courtesy of Akkodis. Rate: $25.00 - $27.11 per hour; The rate may be negotiable based on experience, education, geographic location, and other factors. Duration: 8+ Months (possible extensions and conversion to Direct Hire) Location: Irvine, CA Duties: Performs various laboratory tasks to support R&D microbiology tests in preparation of substrates for Biological Indicators and Media Preparation Program. Daily work involves preparing metal and polymer substrates through deburring, washing, laying out under hood. Operate autoclave cycles to sterilize laboratory supplies, wash laboratory glassware, log and organize inventories and received lab supplies. Document work performed following the good documentation practice with attention to details. May assist in investigation and evaluation of problems with guidance. Assist other Scientists on microbial testing , reprocessing of endoscopes and medical devices, and operation of sterilizers to support project timeline, as needed. Compliance to trained environmental health and safety rules is required. Experience: Bachelor degree in science filed is required, preferred in Microbiology, Biology or Biochemistry. Entry level, science. Past use with laboratory equipment. GxP experience not required, but it is a plus. Good organization skills and laboratory course experience is needed. Be able to function independently per instructions provided and work as a team member with others in the lab as well as other functions such as Engineering, Chemistry and Quality. Should be able to handle about 25 lbs of load throughout the day. If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at ****************************. We are open to working with professionals who are authorized to work in the US without sponsorship. No C2C Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit ****************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: · The California Fair Chance Act · Los Angeles City Fair Chance Ordinance · Los Angeles County Fair Chance Ordinance for Employers · San Francisco Fair Chance Ordinance

Pharmaceuticals company is hiring a Quality Control Research Associate II for a 6-month contract. You will conduct non-routine analysis of raw materials, intermediates, and finished product samples. Responsibilities Evaluates equipment for purchase and performs installations and qualifications of the new instruments. Perform reviews of assays and maintain laboratory in a state of compliance. Troubleshoot instrumentation and test methods. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory. Writes and executes protocols and SOPs. Assists in the training of QC staff as needed. Qualifications Bachelor's degree in scientific discipline. 2+ years of Quality Control Analytical Testing experience (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. Working knowledge and proficiency with Microsoft Office software. Pay $29.80-$37.26/hr Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: Medical insurance - PPO, HMO & HSA Dental & Vision insurance 401k plan Employee Assistance Program Long-term disability Weekly payroll Expense reimbursement Online timecard approval R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer.

All of previous level plus: Conduct non-routine analysis of raw materials, intermediates, and finished product samples. Troubleshoot instrumentation and test methods. Assists in the training of QC staff as needed. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. Writes and executes protocols and reports. Evaluates equipment for purchase and performs installations and qualifications of the new instruments. Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. Perform reviews of assays and maintain laboratory in a state of compliance. Troubleshoot instrumentation and test methods. Assists in the training of QC staff as needed. Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. Writes and executes protocols and SOPs. MOST IMPORTANT PART: Conduct Quality Control Analtyical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. Perform reviews of assays and maintain laboratory in a state of compliance.

Born from the will of LVMH Group, world leader in luxury, to establish itself in the eyewear sector, Thélios designs, produces and distributes sunglasses and optical frames for some of its most prestigious Maisons: Dior, Fendi, Celine, Givenchy, Loewe, Stella McCartney, Kenzo, Berluti, Bulgari, Tag Heuer and Fred! In addition, Thélios owns two proprietary brands, Barton Perreira and Vuarnet. QUALITY CONTROL ASSOCIATE POSITION SUMMARY: Based out of our Irvine, California warehouse, we are looking for a detail-oriented Quality Control Associate to ensure the highest standards of craftsmanship and precision in our products. This role is responsible for performing visual inspections, identifying quality issues, and supporting corrective actions to maintain our brand's commitment to excellence. KEY RESPONSIBILITIES Conduct visual inspections of the product to ensure compliance with company quality standards. Identify and document any product defects or deviations, ensuring accurate reporting. Communicate quality concerns to management promptly and provide recommendations for corrective actions. Work closely with production teams to ensure continuous improvement in quality and manufacturing processes. Assist in the implementation of corrective and preventive actions to resolve quality issues. Support incoming product inspections and verify adherence to product specifications. Perform other duties as assigned. PROFILE High School Diploma or equivalent Minimum of 2+ years of Quality Control experience, preferably within the eyewear, fashion, or luxury goods industry. Strong ability to detect defects, inconsistencies, and deviations from quality standards. Familiarity with inspection tools and measurement equipment used in quality control. Strong interpersonal skills and excellent communication skills both verbal and written; possess a friendly and positive attitude Ability to work in a fast-paced production environment while upholding the brand's dedication to quality and craftsmanship. Genuine passion and advocate of diversity and inclusion and integrates this mentality when making all business decisions (both internal & external). The hiring range for this position ranges from $18-21/hour. The rate of pay offered will be dependent upon candidates' relevant skills and experience. What are the employee benefits at Barton Perreira? We offer a generous benefits package including medical insurance, paid time off, holiday pay, 401k, and more. Thank you in advance for your interest in this opening. Thélios is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, religious creed, national origin, ancestry, citizenship, sex, gender (including gender identity and expression), pregnancy, age, sexual orientation, physical or mental disability, medical condition, genetic information, marital status, familial status, veteran status, or any other legally protected status under applicable federal, state or local laws. At this time, only qualified candidates will be contacted. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Direct applicants only, no third-party staffing inquiries, please.

Gather and analyze pH buffering data across a variety of ingredients and formulations to understand pH behavior and its impact on product stability. Build and refine predictive models for pH behavior based on data collected from ingredient and formulation testing. Validate the accuracy and reliability of the predictive models through testing and comparison with experimental results. Provide data-driven insights and recommendations to support the commercialization of new products, ensuring the models align with product specifications and regulatory requirements. Work closely with R&D Services, R&D Developers, Quality Assurance, and other departments to ensure that the pH data and models contribute effectively to product development and scale-up activities. Responsibilities * Gather and analyze pH buffering data across various ingredients and formulations. * Build and refine predictive models for pH behavior based on collected data. * Validate the accuracy and reliability of predictive models through testing. * Provide data-driven insights and recommendations to support product commercialization. * Work closely with R&D Services, Developers, and Quality Assurance to ensure effective data and model contribution to product development. * Strategize ingredient testing and data analysis. * Input data into the ingredient library and improve the formatting of Excel sheets. * Follow priority task lists and perform necessary calculations. Essential Skills * Bachelor's or advanced degree in Chemistry, Food Science, or a related field. * Understanding of pH systems. * Experience with statistical analysis tools and software for data modeling and validation. * Experience with titration methods. * Strong math and statistical background. * Experience with pH titrations in a food manufacturing setting. * Understanding of basic Chemistry principles. Additional Skills & Qualifications * Bachelor of Science degree in Chemistry. * 1+ years of Chemistry experience in a food manufacturing company. * Experience in model validation and data analysis. Work Environment Shift: Monday - Friday with a flexible start time around 8am. Work in an office setting with an R&D prep kitchen. Collaborate with a team including a Microbiologist and another experienced team member. Pay and Benefits The pay range for this position is $24.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Brea,CA. Application Deadline This position is anticipated to close on Apr 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.