Chemist Jobs in Gardena, CA

Our client, a Cosmetic Manufacturer that specializes in over the counter personal care products located in Southern California, a hub for the beauty industry, is actively looking to add a Sr. R&D Chemist to their team: Industry: Cosmetics Type: Direct Hire Shift: Monday-Friday: 8:00am-5:00pm KEY JOB RESPONSIBILITIES: Develop new formulas and reverse engineered formula based on customer's briefs and price target. Reformulate and improve existing formulas. Follow new trends closely with new products launches, ingredients and new concept such as “free from” claims. Be familiar with the formulation restrictions using these claims. Be familiar with cosmetic ingredient especially their function, delivery system, interaction depending of media/base. Meet with suppliers and keep product files (clinical and regulatory). Work on Innovation, create new textures, concepts, actives to keep our R&D with cutting edge formulation. Help creating marketing sheet to present to our customers in innovation seminars. Request raw material pricing and input in our pricing matrix. Evaluation/Selection/Advice regarding testing; Claims, Safety, Microbiology. Assist Regulatory department requesting all the necessary ingredient information. Be flexible with project priorities as they vary from time to time and manage a large workload under tight timeline. Be able to make decisions to troubleshoot production or compounding. Improve and/or revise manufacturing/filling process if needed. Work closely with our chemists to help on challenging projects or when needed. Work closely with our Quality department to improve knowledge about new formulas, establishing standards. Maintain the laboratory clean and organized, respecting GLP's. QUALIFICATIONS: Bachelor of Science or higher degree in chemistry or related field. Color formulation experience. Creative thinking, technical writing and organizational skills. At least 6 years and more of industry experience on the bench formulating. Knowledge of OTC cosmetic/personal care raw materials, functionality, and interactions. Understanding of emulsion and surfactant technology as well as general formulation techniques. Must be familiar with regulation for US market and other countries for globally approved formulas, especially for the natural and organic market (NSF, USDA/NOP, NPA). Estimated Min Rate: $90,000.00 Estimated Max Rate: $95000.00 #IND-SPG 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.

Who we are: 20bloc, Inc. (*************** is an early-stage biopharma company creating breakthrough protein-based drugs to save lives. We are developing a safe and effective hemoglobin-based oxygen carrier for first response, organ preservation and oxygen therapy. We value and encourage innovations through robust information exchange, hard work, and team interaction. We are collaborative. We are intellectual. We are hands-on. Job Title: Protein Scientist -Analytical Lead Position Overview: We are seeking a senior anlaytical protein-scientist with 10-15 years of biotech industrial experience to lead the analytical development of our hemoglobin based oxygen carrier, from the non-clinical /cGMP stage to beyond. This is a full-time position, on-site in Thousand Oaks, CA, for a self-driven professional. Key responsibilities: Lead and execute the development of robust analytical methods for protein-based products. Identify and prioritize assays both in-house and outsourced; establish vendors and contracts as needed. Qualify starting, in-process and final release of materials. Validate assays and protocols to measure purity, potency, and stability to GMP standards, including ELISA, gel electrophoresis and chromatographic-based assays. Set up lab and storage including samples for control and long-term stability programs. Design, write and help document SOPs, analytical protocols, CoA and reports to GMP standards. Requirements: Bachelor's degree or above in biological sciences and/or chemistry 10-15 years industrial experience in analytical method development and qualification activities. Track record in analytical method development for protein biologics, both compendial and non-compendial, such as HPLC (SEC, AEX/CEX, HIC, RP, etc.) and additional product-specific methods such as ELISAs, electrophoretic methods (SDS-PAGE, ic IEF), endotoxin, osmolality, pH, potency assays, PCR, Western Blot, LC-MS and other MS-based methods. Experience in transitioning to GMP, including SOP development, methods validation, and phase appropriate quality systems, including deviations, CAPA, change control, and document management systems. Strong problem Solving Skills (identify issues and root causes), communication skills (explain complex concepts and issues succinctly), interpersonal skills (seek buy-in and collaboration), and attention to details are essential in this role. This is an excellent opportunity for a motivated individual to grow and excel in a growing biopharma company and to help develop a groundbreaking drug that could have an impact on the life of many. 20bloc is an equal opportunity employer. We offer a comprehensive benefits package which includes: Medical, dental and vision plans 120 hours paid time off (PTO) 12 paid holidays annually 401(k) U.S. retirement savings plan Employee assistance program

I am hiring for a Senior Chemist for a market leading personal care contract manufacturer based in the Greater Los Angeles area. Key Responsibilities: Formulate and develop products for skin care and hair care categories. Optimise formulations based on market trends and customer requirements. Conduct stability, compatibility, and efficacy testing to ensure quality, performance, and safety. Mentor and train junior chemists and lab technicians. Requirements: Bachelor's degree in chemistry or related field. 5+ years of experience in formulation for personal care. Up-to-date with skin care and hair care market trends. Ability to collaborate cross-functionally with product development, marketing, sales, regulatory and quality teams. LOCAL APPLICANTS ONLY

Fully Onsite - Regular working hours. Job Details: Basic Qualifications: Master's degree or Bachelor's degree and 2-3 years of relevant scientific experience. Responsibilities include: 1) Follows established experimental design and protocols, as well as routine tasks and studies, to obtain reproducible and reliable results under supervision. 2) Plan, monitor or conduct experiments, analyze and record experiments and data, collaborate with group members, and communicate and present data to the team. 3) Effectively trouble-shoots equipment and experimental difficulties ? Contributes to internal/external reports, papers, presentations, regulatory documents, 4) Skilled and/or knowledgeable in the use of standard laboratory equipment 5) Participates in department-wide support efforts such as safety, data recording and centralizing by ELN Preferred Qualifications: • Skills: degree in Biology, Biochemistry; experience in a Biopharmaceutical working environment • Prior experience with biochemical, biophysical, molecular and cellular techniques including basic cell culturing, transient transfection and stable cell lines generation • Experience with small molecule drug screening campaigns • Excellent organizational, interpersonal and communication skills • Flexibility to work in teams to achieve changing project goals and meet timelines • Strong data analysis, interpret complex data sets and critical thinking skills Basic Qualifications Masters degree OR Bachelors degree and 2 years of experience OR Associate's degree and 4 years of experience OR High school diploma / GED and 6 years of experience Top 3 Must Have Skill Sets: Must have: Western Blots Cell culture Transient transfection Nice to have: Assay development experience, small molecule screening. Day to Day Responsibilities: 1) Follows established experimental design and protocols, as well as routine tasks and studies, to obtain reproducible and reliable results under supervision 2) Plan, monitor or conduct experiments, analyze and record experiments and data, collaborate with group members, and communicate and present data to the team. 3) Effectively trouble-shoots equipment and experimental difficulties 4) Contributes to internal/external reports, papers, presentations, regulatory documents, 5) Skilled and/or knowledgeable in the use of standard laboratory equipment 6) Participates in department-wide support efforts such as safety, data recording and centralizing by ELN

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

For over 50 years, SCIEX has been developing groundbreaking technologies and solutions in mass spectrometry and capillary electrophoresis. Our products enable our customers to quickly respond to environmental hazards, better understand biomarkers relevant to disease, improve patient care in the clinic, bring relevant drugs to market faster and keep food healthier and safer. At SCIEX, you'll find a rewarding role that amplifies your impact on the world and helps you realize life's potential. SCIEX is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the Danaher Business System which makes everything possible Are you ready for the next step in your mass spectrometry career? The Associate Hardware Research Scientist (Mass Spectrometry- Ion Traps) is responsible for driving innovation around ion traps and mass analyzers. This position is part of the Hardware Research Department and will be located in Concord, Ontario. In this role, you will have the opportunity to: Defines and tests novel ion trap hardware to enable improved performance for customer workflows Performs different methodologies to verify or validate different aspects of hardware/software under the mentorship of more senior scientists Drives innovation by generating novel ideas to advance scientific technology Identifies and implements opportunities for product improvement within a defined research area Contributes to on-time delivery of different research projects and translates development or scientific risks into a tangible research plan The essential requirements of the job include: Higher level Science degree in a related field such as Physics, Chemistry, or similar required (Ph.D. preferred) Broad background and knowledge of ion movement, mass analyzer technology, ion trap technology and ion trap theory Proven publication record within the field related to hardware design Experience with various sample introduction techniques It would be a plus if you also possess previous experience in: Understands the link between project goals and company strategy Ability to work independently Proven track record of innovation and patent generation preferred The salary range for this role is $90-$120K CAD. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. SCIEX, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.

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.

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.

3DEO is one of the few companies that operates at the intersection of machine development, R&D and engineering services, parts and assembly production, and strategic partnership sales. Our end-to-end approach enables us to unlock the true potential of additive manufacturing (AM) to optimize product performance and efficiency for our customers. We leverage our proprietary technology and multidisciplinary expertise to deliver low- to mid-volume complex metal components. With over 20 pending and awarded patents, we set the standard for what's possible in metal AM, transforming innovative designs into high-performing products. Our dedicated team collaborates with partners across the medical, industrial, aerospace, and semiconductor sectors, turning challenges into opportunities and pushing the boundaries of product development. At 3DEO, we don't just make parts; we create impactful solutions that redefine what's achievable with AM. Our Core Values: Accountability, Respect, and Teamwork (ART): Accountability: We own our actions and commitments, embracing continuous improvement and transparency. Respect: We value diversity, listen actively, and create an inclusive environment where everyone feels heard and empowered. Teamwork: We support one another, leverage each other's strengths, and celebrate shared successes. These values guide how we work and grow as a team. We manage to them and expect every team member to embody them daily. Job Summary: The R&D Technician II plays a key role in advancing new materials and technical processes within 3DEO's metal additive manufacturing (AM) R&D efforts. This position is responsible for setting up, operating, and maintaining R&D equipment, as well as executing and troubleshooting experiments that support the integration of new materials and process improvements into production. Working closely with the Lead R&D Technician and engineering teams, this role requires a strong technical background, problem-solving skills, and the ability to analyze and document results. The R&D Technician II also contributes to developing Standard Operating Procedures (SOPs), ensuring process validation, and optimizing workflows for manufacturing scalability. This position is fully on-site and requires hands-on technical expertise in industrial equipment, material processing, and process experimentation. Essential Functions: R&D Experimentation & Process Validation: Execute and support experiments focused on new materials, process development, and validation. Work with the Lead R&D Technician to troubleshoot and solve hardware, software, and materials-related issues in 3DEO's proprietary printing process. Assist in the development and refinement of new materials for metal additive manufacturing, ensuring smooth integration into production. Support data collection, analysis, and reporting to evaluate material and process performance. Equipment Operation & Maintenance: Set up, calibrate, and operate R&D and production support equipment, ensuring functionality and precision. Conduct preventive maintenance (PMs) and basic troubleshooting for printers, vacuum systems, powder handling equipment, and climate control systems. Maintain inventory of R&D consumables, ensuring sufficient materials for research projects. Ensure proper binder preparation and powder handling to support ongoing development efforts. Process Standardization & Documentation: Develop and refine Standard Operating Procedures (SOPs) for new materials and processes. Maintain detailed records and documentation, contributing to research reports and process development workflows. Work closely with Production, Quality, and Engineering teams to transition validated R&D processes into scalable manufacturing workflows. Continuous Improvement & Collaboration: Identify opportunities for workflow optimization, improving technician efficiency and process reliability. Assist in Lean 6 Sigma and process improvement initiatives within R&D. Participate in cross-functional team meetings, contributing technical insights and experimental findings to support R&D goals. Required Skills/Abilities: Technical expertise in industrial equipment operation, troubleshooting, and process development. Strong understanding of materials science, mechanical systems, or additive manufacturing processes. Ability to read mechanical drawings, schematics, and technical documentation. Hands-on experience with preventive maintenance, machine calibration, and process setup. High attention to detail for data collection, process control, and quality validation. Strong problem-solving skills, capable of analyzing experimental data and improving process workflows. Excellent written and verbal communication skills, with the ability to develop SOPs and process documentation. Ability to work in a fast-paced R&D environment, multitask effectively, and adapt to evolving priorities. Self-motivated with a collaborative, team-oriented mindset. Education and Experience: 2-4 years of hands-on experience in R&D, process development, or technical equipment maintenance. Technical training or accreditation from a technical school or skilled trades program is preferred. Experience in additive manufacturing, metal processing, or material science is a plus. Familiarity with 3DEO's proprietary technology, machines, and materials is preferred. Physical Requirements: Ability to work on the manufacturing floor, standing for extended periods. Capability to lift, carry, and move objects up to 50 lbs. regularly. Manual dexterity for assembling, adjusting, and troubleshooting mechanical components.

WHAT WE ARE LOOKING FOR: Simply Good Foods seeks a creative, curious, and passionate Food Scientist to join our collaborative and dynamic environment. The Food Scientist will be responsible for strategizing and optimizing our product line, developing new products across all brands, and ensuring raw materials meet specifications. This individual will work cross-functionally with internal teams and external partners and will create formulations and specifications for Contract Manufacturers, demonstrating expertise in Snack and/or Food science, recipe development, and scale-up. A successful Food scientist will have a growth mindset, be self-motivated, and is willing to learn and adapt within our R&D team. This hands-on role includes bench and analytical work, pilot plant management, and assisting with manufacturing scale-up and optimization, alongside troubleshooting day-to-day product issues. KEY RESPONSIBILITIES: Lead the development of new products across the Simply Good Foods line throughout all phases of product development - from initial bench development to commercial launch, while considering critical technical issues such as: food safety, food stability, shelf-life, scalability, processability, cost, nutritional and ingredient guidelines, etc. Understand and demonstrate the application of consumer product testing, sensory, analytical, etc. tools to deliver superior products in line with optimum product design. Conduct and document product development lab work, including the creation of benchtop prototypes, implementation and maintenance of stability testing and shelf-life, and support of sales samples and scale-ups for commercialization. Leverage formula documentation systems for development and implementation of product specification requirements. Partner internally (Marketing and Procurement) and externally to source ingredients, identify and leverage expertise in ingredient functionality Provide technical and business risk assessment /perspectives related to new product development and technical brand stewardship activities. Demonstrate ability to learn and leverage key internal processes and business applications. Work collaboratively between Quality, Contract Manufacturing, and Operations teams on new and renovated product development and introduction programs to assure that the product and its production-intent processes meet program objectives, manufacturability, timelines, and cost targets. Independently designs and analyzes results from multiple experiments, formulates conclusions, and designs future experiments. Work with cross-functional teams (marketing, insights, operations, food safety quality and regulatory) to delivery scalable products. Write technical and project status reports, protocols, finished product specifications, plant trial protocol/summary documents, shelf-life studies, etc. Work is highly diverse in scope. Utilize experience and problem-solving skills to solve complex technical challenges related to the development, manufacturing, and/or improvement of food products and processes and make appropriate technical recommendations. Understand and conduct basic analytical testing in support of product development. Work with external cross functional teams that include ingredient suppliers, equipment suppliers, technical sales and contract manufacturers. Prioritize and manage multiple projects with overlapping deadlines. Ensure the security and confidentiality of all information regarding product formulas and related data. Maintain GLP's, GMP's, and all required laboratory records, using electronic systems and written protocols, to ensure data integrity and compliance. Partner with the Coman team to lead the assessment and process capability studies when required, and provide on-site support to plant operations for existing products, productivity, and quality programs. KNOWLEDGE & SKILLS: Strong ability to work with R&D, Quality, Regulatory, Operations, and Marketing teams to support business objectives. Ability to manage multiple projects in a fast-paced environment while meeting deadlines and collaborating crossfunctionally. Ability to troubleshoot formulation, stability, and processing issues, ensuring quality and consistency. Familiarity with FDA, USDA, FSMA, and other food safety regulations, as well as labeling and nutritional requirements. Understanding of food chemistry, ingredient functionality, sensory evaluation and food microbiology. Strong communication skills, both written and verbal, to work effectively with internal customers and external partners. BASIC QUALIFICATIONS: Minimum of 3 years of experience in food product development, formulation, or food processing within the CPG industry, with a focus on nutrition bars (preferred); additional experience or knowledge in shakes, bakery products, and sweet or savory snacks is a plus Bachelor's degree in Food Science, Food Engineering, Chemistry, Nutrition or a related field. Experience developing new food and beverage products or improving existing formulations, including ingredient sourcing and functional testing. Exposure to pilot plant trials, production scale-ups, and manufacturing processes to ensure feasibility and commercialization. Experience with food formulation software (e.g., Genesis, ESHA), Microsoft Office and data analysis tools. Experience in successfully managing multiple projects and deadlines within a matrixed organization with strict attention to detail and prioritization. Travel: 25%, up to 40%, or as needed ** Work is performed in a fast-paced office environment and may be stressful at times. Work may require sitting for long periods of time; requires manual dexterity sufficient to operate a keyboard, calculator, telephone, copier and fax machine and scanner. ABOUT SIMPLY GOOD FOODS We're raising the bar on what food can be. We say no to the status quo, and we say yes to making better food. Food that offers robust nutrition, not hollow nutrition. Energy, not depletion. Enjoyment, not regret. Simply, we're on a mission to make food that works for you-that is radically nutritious and defyingly delicious. Better nutrition made easy so you can live well. We don't compromise, so you never have to. W H A T W E V A L U E : We are committed to attracting, developing and retaining a diverse workforce that infuses equity and belonging throughout our culture and business practices. We celebrate diversity and are dedicated to creating an inclusive environment for our employees. This commitment is driven by our core values: Simply Bold Simply Deliver Simply Learn & Grow Simply Together Simply Kind C O M PE N S A T I O N A N D BE N E F I T S : The health, satisfaction and well-being of our employees are important to us and an integral part of our organization's goals. In this spirit, we are excited to share the available compensation for this role, which includes a base salary range and an annual short-term incentive. We provide the base salary range, exclusive of benefits or additional incentives (highlighted here). Additionally, this position is eligible for a 5% annual short-term incentive. If you are hired at Simply Goods Foods, your final base salary compensation will be determined based upon such factors as: geographic locations, skills, training, education and/or experience. Please keep in mind that hiring at the compensation range maximum would not be typical to allow for future and continued salary growth. HQ / Office: CO salary range is: $80-100k with 5% annual bonus incentive We provide a comprehensive total rewards package featuring competitive compensation alongside top-tier health and wellness options. Our goal is to offer a benefits package that can be personalized to meet the diverse needs of each employee and their families. Full-time employees and their eligible dependents have access to a range of benefits including medical, dental, and vision insurance, a company-paid health reimbursement arrangement, life and disability coverage, and a 401(k)retirement plan, among others. Additionally, we prioritize time off benefits, offering vacation time, sick leave, flexible time off (for exempt positions), and paid parental leave. Simply Good Foods is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local laws.

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)

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.

A utility client is looking for a Environmental 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: Environmental 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!

1. Develop and execute plans to expand QC laboratory capabilities for microbiology, to include, but not limited to: a. identification and purchase of necessary equipment b. writing, coordinating and performance of equipment qualifications c. development and/or revision of new or improved microbiological methodologies d. writing, coordinating and performance of validation of microbiological methodologies e. development of standard operating procedures f. establishment of database for test results g. management of microbiology laboratory 2. Perform routine microbiological testing: a. product and water system bioburden b. biological indicator (BI) testing for sterility c. BI population verification d. product sterility e. material and product cytotoxicity f. endotoxin testing g. environment monitoring 3. Ensure that all the samples are tested according to specified methods and devise a system to ensure full traceability of the samples. 4. Review, analyze and interpret data from samples. 5. Subject Matter Expert for microbiology. 6. Lead and support research and development and method development efforts. 7. Develop or assist in developing experimental designs and test plans. 8. Perform regular site microbiological assessment which covers manufacturing processes, manufacturing environment, raw material receipt and handling systems, process water systems and hygienic practices. 9. Define and ensure the training of relevant personnel to required microbiological techniques. 10. Travel to other STAAR facilities, as required. 11. Perform additional duties as assigned EDUCATION & TRAINING • Minimum of a Bachelor of Science (BS) degree in Microbiology or equivalent combination of education/experience. • Master's Degree preferred. EXPERIENCE • Minimum eight years working experience as a Microbiologist in the medical device, pharmaceutical or biologics industry, with experience in the practical application of microbiology techniques, FDA Quality System Regulation and ISO 13485 or equivalent, required • Working experience with and understanding of industry best laboratory practices, techniques, equipment, materials and mathematical calculations, required. • Experience with development, writing and execution of equipment qualifications and method validations, required. • Experience in implementation and management of microbiology laboratory, required. SKILLS • Understanding and knowledge of current and emerging bioanalytical tools and techniques, required. • Excellent project management, organization, writing, communication and presentation skills required. • Ability to develop, write, execute qualification/validation protocols and reports. • Ability to compile, analyze, graph, and compare data using standard statistical techniques (i.e., t-tests, ANOVA, linear regression analysis, etc.). • Ability to work well independently and in a team-based environment. • A high level of initiative and leadership capabilities. • Demonstrated expert knowledge of Windows-based software, including Word, Excel, Access, Project, and Power Point. • Proficiency in written and spoken English required.

R&D Medical Device Assembly Technician - Join Our Cutting-Edge Team Pay: $35 per hour Schedule: Monday to Friday, 6:00 AM - 2:30 PM About the Role We're seeking a dedicated R&D Medical Device Assembly Technician to join our dynamic team. In this role, you will be working in the prototype phase of catheter assembly, utilizing soldering skills, binocular and digital microscopes, and precision hand tools to create devices that are at the forefront of medical innovation. Your work will directly contribute to life-saving products that improve the health and wellbeing of patients around the world. You will be an integral part of a team focused on process development, continuous improvement, and collaboration with engineering on testing and prototype refinement. Key Responsibilities Assemble catheters in the prototype phase with attention to detail, ensuring quality and precision. Soldering and performing tasks under microscopes (both binocular and digital) to create complex assemblies. Utilize hand tools to complete intricate assembly steps as part of the product development process. Maintain accurate documentation and note-taking in line with company and industry standards. Collaborate with engineering to provide feedback, develop processes, and contribute to ongoing improvements. Assist with testing and product evaluation to ensure adherence to product specifications. Why You'll Love Working With Us New Facility - Experience working in a brand-new, state-of-the-art workspace with upgraded amenities that make your workday comfortable and efficient. Growth Opportunities - This is more than just a job; it's a chance to build your career. We invest in your professional growth and offer room for advancement as part of a stable, long-term team. Culture of Innovation - Join a collaborative environment where your skills will be valued, and you'll have the opportunity to make a real impact in the field of medical devices. Commitment to Quality - Work alongside highly skilled professionals who are passionate about their work and committed to delivering excellence. Qualifications Hands-on soldering experience is essential. Comfortable working under microscopes and with fine detail work. Strong documentation skills and attention to detail. Ability to collaborate with cross-functional teams, especially engineering, to improve processes and troubleshoot. A passion for working in medical device development and a drive for continuous improvement. How to Apply If you're passionate about medical innovation, enjoy working in a team environment, and have the technical skills required to thrive in a fast-paced and rewarding setting, we want to hear from you. Apply today to become part of a team that's driving the future of healthcare.

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

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.

***Please Note: This is an onsite role in Santa Monica, CA - you must be either local to the area or plan to relocate on your own*** Our client, a leading Biotech company, is seeking a skilled Statistical Analyst who will work collaboratively with Process Engineers and Statisticians to meet project deliverables and timelines to author and approve Continued Process Verification (CPV) related reports, such as Process Monitoring Reports (PMR) and Annual Product Reviews (APR). See below for other details! Top Skills Needed: JMP Software Continued Process Verification (CPV) Statistical Analysis Duties: Performs Data Verification requirements per the companies Standard Operating Procedures (SOP), e.g., reproduces all CPV statistical output using JMP scripts, reviews documents for data and information accuracy, notifies author of errors and ensures corrections are made prior to approval and completes sign offs in QMS. Assists with report authoring by populating graphs, tables and attachments in Word templates and identifying deviations using QMS. Extracts and transforms data from excel or databases, as needed. Attends and participates in regular meetings to review and track report progress. Assists with the preparations for bi-monthly Process Monitoring Tier 4 meetings, attends meetings and takes meeting minutes. Must be able to effectively communicate and possess good problem solving as well as people/project leadership skills. Project Work: 1. Report Authoring: a. PMRs: pre-populate tables (including deviation tables) and graphs b. Control Limits: Manage and prepare data, compute and propose statistical limits and assist with report authoring 2. Report Verification: a. PMRs: raw data, figure and table formats, re-run all charts, check control limits, tables, statistics summaries and deviations against original data sources and metadata files. b. APRs: raw data, figure and table formats, re-run all charts, check control limits, tables, statistics summaries and deviations against original data sources and metadata files. c. Control limits: verify analytics approaches uses, re-run all analysis, verify updated limits. 3. Tier 4 Meetings: a. Take minutes b. Cross-site comparison prep: prepare data, generate outputs from JMP scripts and update the slide deck. Requirements and Preferred Qualifications: Bachelor's Degree and 2+ years of experience Proficient in SQL, SAS or equivalent for data extraction and transcription Proficient in JMP, SAS or equivalent for statistical analyses and familiar with Statistical Quality Control techniques, e.g., SPC and Process Capability. Knowledge of python code for report generation. Proficient in Microsoft Word and Excel

PropertyRate is a rapidly growing, venture capital backed Valuation Services Provider to the real estate and mortgage services industry, located in Orange, CA. We are currently seeking a Quality Control Analyst to join our team. We are passionate about making the often-complex process of home ownership, financing and appraisal process easier for borrowers, lenders and the professionals who help homeowners close their mortgage loans. We offer associates a supportive, casual, and energetic environment with significant opportunity for personal and professional growth and advancement. We provide associates with a meaningful opportunity to impact the culture while gaining exposure and mentorship from senior team members. This role is ideal for a driven problem solver with a high attention to detail and a strong interest in developing their professional expertise and knowledge as both an individual contributor and supportive team member. Compensation and Benefits The Quality Control Analyst (“Associate”) will receive a competitive base salary, participation in our quarterly performance bonus plan, health and retirement benefits, and company perks, including frequently catered meals and a great culture. $17.50 to $19.25 per hour depending on experience, location and remote status; Quarterly Bonus of 5 to 10% of base salary (bringing total potential compensation to $18.40 to $21.50 per hour); Participation in company 401(k) plan Medical and dental insurance; 10 holidays and 10 days paid time off Role Description The Associate will be responsible for efficiently and thoroughly reviewing appraisal reports to ensure completeness and compliance with company policies, customer-specific rules and industry standards; clearly communicating any required changes and the underlying reasons for such changes to our independent appraiser partners; accurately categorizing the nature of any errors; and communicating the status and nature of any corrections or changes to an appraisal report. All reviews involve responding to system generated prompts and the manual inspection of standard forms, written property descriptions, property photographs and floor plans. The Associate will also be expected to participate in periodic training (provided and paid for by the company) on mortgage and appraisal related regulations, industry standards and property valuation practices. Working hours and days will depend on shifts and location (with start times from 7am to 10am) and can vary, depending on the workload, with overtime often required during training or seasonal peaks. Depending on location and experience, this position may accommodate a fully remote Associate or a hybrid work schedule with two days per week onsite in our Orange, CA headquarters (schedules and onsite days are consistent from week to week). The company's primary office is located near the Honda Center, Angels Stadium, public transportation, and a wide array of food, retail and housing options. We also have regional offices in the Seattle, Phoenix/Mesa, Provo and Lexington metro areas. Key responsibilities include: Following system-generated prompts, written checklists and customer-specific instructions to competently and efficiently review appraisal reports, property inspections and related schedules (“Files”) to ensure that the Files conform with all relevant industry standards, state and federal regulations, and customer or company-specific rules; Identifying and accurately communicating the nature of missing information and/or errors in a File to clients, appraisers and team members; Efficiently and accurately entering data and written notes regarding a File in our system; Identifying when an error in, requested change to or other problem with a File requires input from a manager, operations executive or licensed appraiser to ensure the issue is resolved correctly and in compliance with appraisal and mortgage regulations and policies; Professionally communicating how industry standards, state and federal regulations, and order-specific rules may apply to the correct completion of a File; Promptly and professionally communicating the status of a File within our review process to clients, appraisers (and other professional services vendors) and team members via our proprietary workflow software, email or phone call. Qualifications The Associate should have a strong attention to detail, ability to consistently focus on reading and comparing large data sets for extended periods of time, and a passion for identifying patterns and solving problems. While the primary role of the QC Analyst will be to develop and employ technical knowledge in reviewing Files for compliance with our standards, all PropertyRate Associates are expected to carry on our relentless commitment to customer service. A successful Associate will also enjoy connecting with people, building expertise in new subjects and helping all our stakeholders (who include mortgage lenders, appraisers, borrowers, regulators and team members) achieve their goal of funding mortgage loans in support of home ownership and a stable home financing market. The Associate will be required to communicate mortgage and appraisal specific information in plain English, display patience under pressure, and exhibit insight and problem-solving skills for all client requests. As customer issues may vary widely and can be complex or urgent, a successful Associate will have attention to detail, be able to work independently in a fast-paced environment, make thoughtful decisions independently within set policies, and possess effective time management, prioritization, and multi-tasking skills. Qualified applicants should possess: Minimum of High School diploma or equivalent (post-secondary study/degree or industry-specific training strongly preferred); Minimum of two years' experience in either a role in the mortgage services industry (customer service, vendor management or quality control in mortgage lending, title insurance or valuation) or in a quality control role for another services industry; Familiarity with the mortgage, real estate, residential services or other consumer banking industries strongly preferred, but not required (industry specific training will be provided to all new Associates); Excellent phone etiquette and interpersonal/communication skills (written and verbal); Facility with basic computer skills including knowledge of Microsoft Office and/or Google Suite; Experience with customer relationship management or document processing and workflow software programs preferred, but not required; Minimum 45 WPM typing speed. PropertyRate is proud to be an Equal Opportunity Employer and provides equal employment opportunities to all associates and applicants without regard to race, color, religion, sex, age, national origin, disability, veteran status, pregnancy, sexual orientation, or any other characteristic protected by law.