Chemist Jobs in Irvine, CA

Job Purpose Support product development projects from concept through commercialization, with limited supervision. As part of a team, assist with developing and testing formulas and processes for new products, quality improvements, and cost reductions. Essential Functions Plan and execute experiments using established laboratory/pilot plant/operations methods, ensuring all experiments meet FDA food manufacturing guidelines; keep accurate and detailed records on lab work and data analysis Interpret experiment results and translate them into possible solutions Execute pilot lab runs, consumer tests, plant trials, and validation trials Lead small and medium projects, demonstrating good teamwork, effectively managing time, and delivering projects on time and in full Maintain ingredient inventory and lot code tracking Work with internal resources to quickly communicate needed information for recalls Safely operate, clean, and maintain labware and equipment used for testing, adhering to sanitation requirements in the handling and preparation of food products Write product, ingredient, and process specifications Develop strong cross-functional relationships within the R&D team as well as with Marketing, Insights, Quality, Operations, Engineering, Regulatory, etc. Bring innovative ideas to support strategic plans and enable R&D to apply this knowledge to assigned projects Collaborate with R&D Supervisor/Manager to develop contingency plans Support food safety program, quality standards, and legality of products manufactured in the facility Perform other job-related duties as assigned Qualifications (Education, Experience, Competencies) Bachelor's degree in food science or related field 2-4 years of R&D product development experience in the food and/or beverage industry Knowledge of food ingredient functionality, product formulations, and modification techniques Knowledge of all stages of the product development life cycle and product development methodologies Understanding of manufacturing equipment, their processes, and capabilities Strong passion for science, creative thinking, and product development Good cross-functional and peer relationship building skills Proficient computer skills including Microsoft Office programs: Outlook, Word, Excel, PowerPoint Strong written, verbal, and interpersonal communication skills Detail oriented with strong problem-solving and analytical skills Self-motivated with the ability to work independently, organize and prioritize, show flexibility, and multi-task to execute simultaneous projects and activities to meet objectives and deadlines Ability to thrive in a fast-moving and constantly evolving high-growth environment California, Colorado, Connecticut, Hawaii, Illinois, Maryland, Massachusetts, Minnesota, Nevada, New Jersey, New York, Rhode Island, Vermont, Washington, Washington, D.C. Residents Only: The salary range for this role is $58,839 to $73,549 annually. Pay is based upon several factors including but not limited to local labor markets, education, work experience, certifications, etc. Rise Baking Company complies with all minimum wage laws as applicable. In addition to your annual salary, Rise Baking Company offers benefits such as a comprehensive benefits package, annual bonus eligibility, incentive and recognition programs and 401k contributions (all benefits are subject to eligibility requirements). At Rise Baking Company, our people are our finest ingredient. MON123 RISE123 Compensation details: 68640-80000 Yearly Salary PIfc15c1674164-26***********6

B. Braun Medical, Inc. Company: B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine, California, United States Functional Area: Quality Working Model: Onsite Days of Work: Thursday, Wednesday, Tuesday, Monday, Sunday Shift: 5X8 Requisition ID: 3884 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 ***************** 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 $47,815 - $57,373 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. 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 Equal Opportunity Employer Veterans/Disabled 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. 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. We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here. 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: 47815-57373 Yearly Salary PI280c2363eafa-26***********7

Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements. We are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry-level candidates that are interested in working for a great company with opportunities to grow, competitive pay and benefits. Summary Develop and validate/verify HPLC, UPLC_MS/MS, ICP_MS, GC_MSMS methods for raw, in-process and finished products. Perform routine and non-routine physical and chemical testing of raw, in-process and finished products using various analytical methodology (chromatography, spectroscopy, physical and chemical separation techniques). Process, interpret, trend and report testing results in a timely and professional manner. Assist with development, validation, and periodic review of lab testing methodologies. Lead investigations of Out-of-Trend (OOT) and Out-of-Specs (OOS) results. Comply with all applicable regulations and policies. Essential Duties & Responsibilities Develop and validate/verify HPLC, UPLC_MS/MS, ICP_MS, GC_MSMS methods for raw, in-process and finished products. Performs routine and non-routine analytical testing of raw materials, in-process, and final products in support of production and R&D. Conduct analytical (HPLC_UV, UPLC_MS/MS, ICP_MS, GC_MSMS) analysis per established lab SOPs and /or per external methods (vendor or customer methods, monographs, contract lab methods). Perform testing with accuracy and precision; maintain accurate and detailed records. Prepare sample, standard and reagent solutions as required by the test methods Handle and store all chemicals according to safely guidelines. Ensure that chemicals are within their respective shelf life. Operate and maintain laboratory equipment (pipettes, pH meters, analytical balances…) and instruments (IR, HTLC, UV, HPLC, UPLC_MSMS, ICP_MS, GC_MSMS). Manage complex OOS investigations and review routine OOS reports from chemists. Make recommendations with respect to root cause and corrective action to prevent recurrence (i.e. CAPA), inclusive of changes to methods and procedures. Demonstrate an understanding of the factors impacting analytical test results. Compile, analyze, trend and interpret results of tests; determine acceptability and identify areas of improvement with rejection and deviation of data. Review peer data and reports and resolve complex testing issues using internal and external resources. Monitor and evaluate stability studies data to establish stability trends. Evaluate the suitability of the reference standards used in the quantitative assays. Troubleshoot instrument errors as needed. Ensure that adequate documentation is kept in the appropriate equipment logbook. Promptly report incident to senior chemist and/or supervisor. Communicate testing status in a timely and effective manner to management and to the lab coordinators. Recommend opportunities for continuous lab improvement including new or revised analytical technologies. Assist with training junior staff in the usage and maintenance of analytical instruments (HPLC, ICP_MS, GC_MSMS, UPLC_MSMS) and on testing methodologies. Revise SOPs for compliance with cGMP and cGLP and creates original SOPs Comply with cGMP, cGLP and other applicable government regulations; as well as company compliance guidelines, standards and objectives. Coordinate lab activities and give final approval for QC sample release in the absence of the Lab Manager and /or Chemistry Supervisor. Perform other duties and special projects as assigned and directed by management. Qualifications BS or MS degree in Chemistry, Biochemistry, Chemical Engineering or related science degree. Minimum 5 years hands-on experience in an analytical lab, preferably in the dietary supplement or a related industry HPLC / UPLC experience required along two or more other analytical instruments (such as GC, ICP, FTIR/FTNIR, HPTLC, UV/VIS). MS highly desirable (such as ICP/MS, HPLC/MS, GC/MS/MS or UPLC/MS/MS). Botanicals identity and potency testing knowledge desired Excellent computer skills with knowledge of Microsoft Word and Excel required. Knowledge of Access and PowerPoint a plus. In depth understanding of scientific principles associated with method development, method transfer and method validation and hands-on experience with conducting such tasks. Ability to think critically and creatively to identify and solve scientific problems using internal and external resources. Ability to achieve and maintain high analytical standards with meticulous attention to detail. Ability to work independently and manage multiple projects simultaneously in a fast-paced, deadline driven environment. Exemplify accountability, high attention to detail, and organizational skills Strong interpersonal skills and excellent oral and written communication skills. Ability to communicate effectively in a credible and confident manner in a cross functional team environment. Physical Demands Able to work with and around hazardous materials, chemicals, and equipment The employee is regularly required to communicate with others (talk and hear) The employee is frequently required to sit and use hands to finger, handle or feel objects, tools or controls The employee is regularly required to stand, walk, and reach with hands and arms The employee must occasionally lift and/or move up to 50 pounds Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus Work Environment Computer workstation and climate-controlled office environment. QC Lab with various analytical instruments and various lab equipment, chemicals and solvents where PPE is required (lab coats, gloves, protective glasses, and any additional PPE as necessary). May occasionally enter production areas where personal protective equipment might be required to prevent or lessens exposure to airborne-borne powdered nutritional supplement substances. NAI is an Affirmative Action/Equal Opportunity Employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, physical or mental disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

Job title: Chemist duration: 12 months Pay rate: $33/hours 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. Responsibilities: • 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.

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.

This is what you'll do: Support receiving and shipping of packages. Manage material inventories and kit parts for assembly and/or rework. Perform PCBA modifications such as component rework, soldering/de-soldering of electronic components, blue wire modifications per IPC-610 class 3. Build wire harnesses per IPC/WHMA A-620C standard. Build and/or setup custom test equipment per engineering diagrams/specifications. Conduct functional testing of electronic circuit assemblies and engineering prototypes. Perform unit assembly of ECU modules per engineering diagrams/specifications. Maintain accurate records of test results and update of procedures as needed. Troubleshoot to identify root cause of failures. Qualifications 2+ years of technician work experience in electronics/engineering labs Technology/Technician degree or equivalent experience Electric vehicle experience a plus Basic electrical understanding Excellent soldering and harnessing skills Familiar with test equipment such as multimeters, oscilloscopes, eloads, etc. Strong technical ability Ability to solder fine pitch ICs and 0402 components. Experience with MS office tools (Outlook/Excel/Word/PowerPoint/Project) Familiarity with Jira tools is a plus Python Scripting is a plus IPC-610, IPC-620, IPC-7711, IPC-7721 or J-STD-001 certifications are a plus

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.

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.

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!

The Associate Process Group Chemist, in accordance with forecasted requirements and assignment, participates in the Chemistry Manufacturing department via: Manufacture products within QSR and ISO regulations Review/reconcile documents and work orders Support assigned projects with supervision Support departmental troubleshooting and process improvement teams Participate in product transfers May write/revise documentation with supervision May train lab technicians Display improving working knowledge of business processes as they relate to manufacturing Maintain daily adherence to Production goals relating to MUV/LUV, labor utilization, work order closure, and schedule adherence ESSENTIAL FUNCTIONS: Manufactures (ie. Formulates bulks, and Quality Controls) products (ie. Lateral flow devices, controls/calibrators and microtitre systems) while adhering to regulatory requirements and business polices /procedures and schedules. Support departmental troubleshooting and process improvement teams. Support cross-functional projects and training. Reviews completed Device History Records and performs financial review of work orders. Reports on variances to supervisor. Carries out all duties in a professional manner and in compliance with established business practices. INTERACTIONS: Associate Process Group Chemist may have interaction with the following groups/systems. Typically with supervision: Inventory control - obtain/return materials, resolve material variances related to work order usage LN - reconcile work orders, enter/check labor hours, check material availability, BOMs, general manufacturing queries, and close work orders. Prepare work order variance reports. Management - on a day to day basis as it relates to the tasks at hand, personnel issues Process engineering - technical troubleshooting, product transfers Production - coordinate optimization/matrix assembly Planning - report on schedule adherence Quality/Documentation - ECO's, NCMR's, deviations, validations, QTP's Facilities - request repairs/changes to facilities IT - request repairs Safety - training, compliance, may participate in safety committee, recommends safety and housekeeping improvements. Identify and articulate moderately complex problems. Make decisions related to tasks at hand. Work almost entirely self-directed within the scope of their job description. EDUCATION, SKILLS & EXPERIENCE (indicate if required or preferred): Education and Experience B.S./B.A. Life/Applied Sciences or equivalent experience and a preferred minimum of 6 months related work experience in a GMP environment. Knowledge/Skills Basic algebraic, statistical and mathematical skills General computer knowledge Good organizational skills Laboratory skills, such as protein purification, antibody conjugation, solution preparation ELISA experience, assay development skills, etc. Good verbal and written communication skills Good interpersonal skills Knowledge of QSR's and ISO 9001 Knowledge of experimental design Basic Chemistry or Biochemistry

About the Role: Seeking a Quality Assurance Associate III to support quality operations within the CMI business unit. This position is responsible for executing quality processes related to batch record review, change control, incoming inspection, and labeling, ensuring compliance with applicable regulations and internal procedures. The role involves cross-functional collaboration and independent problem-solving in a fast-paced medical device manufacturing environment. Key Responsibilities: Perform and review batch records, Certificates of Analysis/Conformance, and labeling documentation. Facilitate and guide change control processes using electronic systems. Review Quality records (SOPs, logs, forms) for compliance and completeness. Work cross-functionally to resolve documentation issues and support continuous improvement. Ensure compliance with QSR, ISO 13485, and other regulatory requirements. Coach junior staff and contribute to quality system improvements. Qualifications: Required: High School Diploma or GED with 3-5 years of related QA experience; proficiency in MS Office; strong communication and organizational skills. Preferred: Bachelor's degree; QA experience in medical device or in-vitro diagnostics; working knowledge of QSRs and ISO standards.

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)

An Entry-level R&D Laboratory Technician position in Irvine, CA in the Biomedical Industry is available courtesy of Akkodis. Rate: $25.00 - $28.00 per hour; The rate may be negotiable based on experience, education, geographic location, and other factors. Duration: 8+ Months (possible extensions) Location: Irvine, CA Shift: 12:30 p.m. to 8:00 p.m. (Occassional OT) 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

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.

Established in 1971, GEOCON is a dynamic Geotechnical Engineering, Environmental Services, Engineering Geology, and Construction Inspection firm with 9 offices throughout Northern and Southern California. GEOCON is ranked on ENR's TOP 500 Design Firms year after year. We work on a wide variety of projects ranging from new and innovative school campuses to major transportation projects which help maintain infrastructure and alleviate traffic congestion in California. Experience/Requirements: 3-5 years of experience in a soils/materials laboratory Basic computer skills using Excel and Microsoft word Excellent written and verbal communication skills Role Description: Senior Lab Technician in the Irvine Soils/Material Lab. Work Level requires responsible self management for soil lab testing including compaction curves Expansion index and corrosion testing along with logging striping storing and compression testing of concrete cylinders. Physical Demands: This job requires ability to lift 50 pound samples. Expected Hours of Work: Generally Monday through Friday 7am to 4pm in office hours Compensation Range: Competitive salary and benefits commensurate with experience, pay range $25-$30/hr. Contact: For immediate consideration please email resume to Phillip Stephens, Regional Laboratory Manager, ********************** Benefits: Competitive compensation, expense/mileage reimbursement, 401(k) with company match, medical, dental, and vision insurance coverage options, company-provided life and disability insurance coverage, paid time off, paid holidays, training and development opportunities, company picnics, holiday parties, and a friendly working environment.

The Lab Support Operator I is responsible for a wide range of tasks within the manufacturing process, including preparing work orders, packing chromatography columns, assembling products, managing stock levels, and supplying necessary solvents and hardware. Additionally, the role involves manufacturing security guard cartridges in various sizes and types, as well as recycling failed columns. You will be cross trained to rotate through different departments as needed, gaining experience in: Sorbent Room: Weigh and label sorbents; select appropriate empty column assemblies and order components when required. Product Assembly: Assemble column hardware, including end fittings, frits, and tubing. Security Guard: Pack various sorbents into security guard hardware. Recycling: Unpack and recycle columns, following the proper procedures. Manufacturing Support: Prepare work orders and ensure all tasks are completed to specification. Maintain accurate inventory levels and assist with the supply of necessary materials. Key Requirements: Education: High School diploma (or equivalent). Experience: Minimum of 1 year of relevant experience (preferred). Skills: Strong analytical thinking and problem-solving abilities. High attention to detail and the ability to focus on tasks with precision. Ability to follow standard operating procedures (SOP)

One of our top clients in Higher Education is seeking a Lab Technician to join their team in Santa Monica, CA! In this role, you will play a crucial part in supporting clinical research trials by processing and managing biological samples. We offer a benefits package, which includes enrollable medical, dental, and vision coverage, as well as flexible spending accounts, 401(k) Savings Plans, and employee assistance programs. This is a 6-month contract with potential for extensions. Required Skills & Experience 1+ years of lab processing experience Experience reading lab manuals Experience using a centrifuge and piperidone Ability to work independently Strong lab processing terminology Key Responsibilities: Operate within a laboratory environment, adhering to all safety and procedural protocols. Receive and handle clinical samples delivered to the lab, ensuring proper identification and documentation. Follow detailed instructions outlined in the lab manual to ensure accurate processing of samples. Maintain the integrity of samples by storing them at specified temperatures. Utilize a centrifuge for the separation and preparation of samples. Employ piperidine in various lab processing tasks. Efficiently process between 30 to 50 samples daily, maintaining high standards of accuracy and efficiency.

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.