Scientist jobs in East Los Angeles, CA

Job Title:Associate Principal Data ScientistRequisition ID:R025545Job Description:Your Role Within Our KingdomWe are seeking an Associate Principal Data Scientist-a highly experienced and technically deep individual contributor who leads through influence, owns high-impact initiatives, and drives scientific excellence across experimentation and modeling.Responsibilities: Lead the design and execution of large-scale data science initiatives, shaping the roadmap for experimentation and modeling across teams. Apply advanced statistical, optimization, and machine learning techniques (e.g., time-series, regression/classification, recommendation engines, reinforcement learning, and gen AI) to drive system understanding and develop data-powered solutions across the organization. Own design and evaluation of experimentation for optimization systems. Provide technical direction, mentor senior data scientists, and set high standards for scientific rigor, communication, and reproducibility. Partner cross-functionally with Product, Engineering, and Game Studios to frame ambiguous problems, scope solutions, and influence strategy. Champion innovation by evaluating new methodologies and tools, and by raising the bar for scalable, interpretable, and actionable data science. Skills to Create ThrillsMinimum Qualifications: Master's degree or PhD in a quantitative field (e.g., Statistics, Mathematics, Computer Science, Economics, Engineering, Operations Research). 14+ years of industry experience (or equivalent post-graduate experience) in data science, experimentation, statistical modeling, and machine learning, including work with large-scale systems. Proficient in Python and SQL; familiarity with big data tools (e.g., Spark, Hive) and cloud computing platforms (e.g., GCP, AWS). Strong systems thinking-able to zoom out and define strategy while also diving deep into code and analysis. Excellent communication and collaboration skills, with demonstrated experience partnering across Product, Engineering and Businessteams. Demonstrated experience mentoring, influencing, and elevating the technical bar across a data science organization. Bonus Points Experience working with advertising data products or monetization systems. Prior work with mobile gaming studios or player behavior modeling. Experience in developing or maintaining experimentation platforms. Familiarity with modern data orchestration and versioning (e.g., Airflow, dbt, MLflow). We love hearing from anyone who is enthusiastic about changing the games industry. Not sure you meet all qualifications? Let us decide! Research shows that women, veterans, and members of other under-represented groups tend to not apply to jobs when they think they may not meet every qualification, when, in fact, they often do! We are committed to creating a diverse and inclusive environment and strongly encourage you to apply.We are committed to working with and providing reasonable assistance to individuals with physical and mental disabilities. If you are a disabled individual requiring an accommodation to apply for an open position, please email your request to accommodationrequests@activisionblizzard.com. General employment questions cannot be accepted or processed here. Thank you for your interest.We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, gender identity, age, marital status, veteran status, or disability status, among other characteristics. Rewards We provide a suite of benefits that promote physical, emotional and financial well-being for ‘Every World' - we've got our employees covered! Subject to eligibility requirements, the Company offers comprehensive benefits including: Medical, dental, vision, health savings account or health reimbursement account, healthcare spending accounts, dependent care spending accounts, life and AD&D insurance, disability insurance; 401(k) with Company match, tuition reimbursement, charitable donation matching; Paid holidays and vacation, paid sick time, floating holidays, compassion and bereavement leaves, parental leave; Mental health & wellbeing programs, fitness programs, free and discounted games, and a variety of other voluntary benefit programs like supplemental life & disability, legal service, ID protection, rental insurance, and others; If the Company requires that you move geographic locations for the job, then you may also be eligible for relocation assistance. Eligibility to participate in these benefits may vary for part time and temporary full-time employees and interns with the Company. You can learn more by visiting *************************************** In the U.S., the standard base pay range for this role is $143,060.00 - $264,846.00 Annual. These values reflect the expected base pay range of new hires across all U.S. locations. Ultimately, your specific range and offer will be based on several factors, including relevant experience, performance, and work location. Your Talent Professional can share this role's range details for your local geography during the hiring process. In addition to a competitive base pay, employees in this role may be eligible for incentive compensation. Incentive compensation is not guaranteed. While we strive to provide competitive offers to successful candidates, new hire compensation is negotiable. #J-18808-Ljbffr

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Kite is seeking a highly motivated Principal Scientist with a strong background in analytical method development to lead the Compendial and Impurities Team within Analytical Method Development. This role focuses on the development, validation, and life cycle management of compendial analytical methods, with a particular emphasis on process related impurities, host cell protein evaluations, method transfer, oversight of external partners (CMO/CTL), and PPQ readiness. The successful candidate will provide technical leadership, mentor team members, and drive strategic initiatives to ensure robust, phase-appropriate assays for gene-modified cell therapies, aligning with regulatory expectations and industry best practices. Key Responsibilities Lead and manage the Compendial and Impurities Team, providing mentorship, technical guidance, and strategic direction to ensure high-quality analytical method development and execution. Develop and implement host cell protein assays using ELISA, Ella, or mass spectrometry, ensuring comprehensive coverage assessments and alignment with regulatory expectations. Develop, validate, and oversee compendial and safety method development for mycoplasma, endotoxin, sterility, replication competent lentivector, and other critical quality attributes to ensure regulatory compliance and product safety. Lead analytical method transfers to external partners, including contract manufacturing organizations and contract testing laboratories. Ensure successful implementation, compliance with GxP guidelines, and alignment with quality and regulatory standards. Support process performance qualification activities by ensuring validated analytical methods are suitable for lot release and stability testing. Collaborate with Process Development and Quality teams to maintain assay consistency across manufacturing sites. Develop, optimize, validate, and manage the life cycle of compendial methods (e.g., USP, EP, JP) for the characterization and quality assessment of gene-modified cell therapies. Ensure compliance with evolving regulatory expectations for advanced therapy medicinal products. Oversee the continuous improvement and adaptation of analytical methods to ensure long-term suitability and robustness. Implement trend analysis and method performance monitoring to proactively address regulatory updates, industry advancements, and shifting product needs. Apply statistical analysis and data interpretation techniques to assess assay performance, method robustness, and long-term stability. Utilize risk-based approaches to troubleshoot technical challenges and optimize analytical procedures. Author and review technical documents, including validation protocols, regulatory submissions, and SOPs, ensuring clear alignment with global regulatory expectations and compendial method requirements. Work closely with Quality Control, Process Development, and Manufacturing teams to ensure analytical methods remain aligned with product and process requirements throughout their life cycle. Basic Qualifications PhD and 5+ years of relevant industry experience; OR Masters degree and 8+ years of relevant industry experience; OR Bachelors degree and 10+ years of relevant industry experience. Degree in Biological Sciences or related field. Industry experience in biotech, gene therapy, or pharmaceutical environments. Preferred Qualifications Proven experience in developing and validating HCP assays, including ELISA-based methods and orthogonal approaches for coverage assessments. Strong expertise in analytical method development, qualification, validation, and lifecycle management for biologics or cell/gene therapies. Familiarity with GxP guidelines and regulatory expectations for compendial methods, PPQ, and external laboratory oversight. Experience in team leadership and management, including mentoring scientists, driving strategic initiatives, and overseeing analytical operations. Method Transfer & Partner Oversight: Experience managing method transfers to external CMOs/CTLs, ensuring compliance and successful implementation. Proficiency in data analysis software (e.g., MS Excel, JMP, GraphPad Prism) and statistical evaluation for assay development and validation. Strong scientific writing skills with experience preparing validation reports, regulatory submissions, and SOPs. Excellent ability to diagnose assay performance challenges and implement effective solutions. Comfortable working in a dynamic, fast-paced environment with evolving priorities and cross-functional integration. People Leader Accountabilities Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose. Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem. We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description Kite is seeking a highly motivated Principal Scientist with a strong background in analytical method development to lead the Compendial and Impurities Team within Analytical Method Development. This role focuses on the development, validation, and life cycle management of compendial analytical methods, with a particular emphasis on process related impurities, host cell protein evaluations, method transfer, oversight of external partners (CMO/CTL), and PPQ readiness. The successful candidate will provide technical leadership, mentor team members, and drive strategic initiatives to ensure robust, phase-appropriate assays for gene-modified cell therapies, aligning with regulatory expectations and industry best practices. Key Responsibilities Lead and manage the Compendial and Impurities Team, providing mentorship, technical guidance, and strategic direction to ensure high-quality analytical method development and execution. Develop and implement host cell protein assays using ELISA, Ella, or mass spectrometry, ensuring comprehensive coverage assessments and alignment with regulatory expectations. Develop, validate, and oversee compendial and safety method development for mycoplasma, endotoxin, sterility, replication competent lentivector, and other critical quality attributes to ensure regulatory compliance and product safety. Lead analytical method transfers to external partners, including contract manufacturing organizations and contract testing laboratories. Ensure successful implementation, compliance with GxP guidelines, and alignment with quality and regulatory standards. Support process performance qualification activities by ensuring validated analytical methods are suitable for lot release and stability testing. Collaborate with Process Development and Quality teams to maintain assay consistency across manufacturing sites. Develop, optimize, validate, and manage the life cycle of compendial methods (e.g., USP, EP, JP) for the characterization and quality assessment of gene-modified cell therapies. Ensure compliance with evolving regulatory expectations for advanced therapy medicinal products. Oversee the continuous improvement and adaptation of analytical methods to ensure long-term suitability and robustness. Implement trend analysis and method performance monitoring to proactively address regulatory updates, industry advancements, and shifting product needs. Apply statistical analysis and data interpretation techniques to assess assay performance, method robustness, and long-term stability. Utilize risk-based approaches to troubleshoot technical challenges and optimize analytical procedures. Author and review technical documents, including validation protocols, regulatory submissions, and SOPs, ensuring clear alignment with global regulatory expectations and compendial method requirements. Work closely with Quality Control, Process Development, and Manufacturing teams to ensure analytical methods remain aligned with product and process requirements throughout their life cycle. Basic Qualifications PhD and 5+ years of relevant industry experience; OR Masters degree and 8+ years of relevant industry experience; OR Bachelors degree and 10+ years of relevant industry experience. Degree in Biological Sciences or related field. Industry experience in biotech, gene therapy, or pharmaceutical environments. Preferred Qualifications Proven experience in developing and validating HCP assays, including ELISA-based methods and orthogonal approaches for coverage assessments. Strong expertise in analytical method development, qualification, validation, and lifecycle management for biologics or cell/gene therapies. Familiarity with GxP guidelines and regulatory expectations for compendial methods, PPQ, and external laboratory oversight. Experience in team leadership and management, including mentoring scientists, driving strategic initiatives, and overseeing analytical operations. Method Transfer & Partner Oversight: Experience managing method transfers to external CMOs/CTLs, ensuring compliance and successful implementation. Proficiency in data analysis software (e.g., MS Excel, JMP, GraphPad Prism) and statistical evaluation for assay development and validation. Strong scientific writing skills with experience preparing validation reports, regulatory submissions, and SOPs. Excellent ability to diagnose assay performance challenges and implement effective solutions. Comfortable working in a dynamic, fast-paced environment with evolving priorities and cross-functional integration. People Leader Accountabilities Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose. Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem. The salary range for this position is: $177,905.00 - $230,230.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: ****************************************************************** * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit ****************** . Sign up to follow @KitePharma on Twitter at ************************** . For jobs in the United States: Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex , age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT PAY TRANSPARENCY NONDISCRIMINATION PROVISION Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday. Share: Job Requisition ID R0045750 Full Time/Part Time Full-Time Job Level Associate Director Click below to return to the Gilead Careers site Click below to see a list of upcoming events Click below to return to the Kite, a Gilead company Careers site #J-18808-Ljbffr

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Phenomenex, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and 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. The Senior Scientist NPD will innovate and advance separation sciences in the field of biologics and beyond. Working within a cross-functional team, the candidate will develop and commercialize differentiated separation solutions to meet the analytical needs in both industry and academia. This position reports to the R&D Manager - NPD and is part of the Research & Development department located in Torrance, CA, and will be an on-site role. In this role, you will have the opportunity to: • Develop and commercialize sample preparation consumables and liquid chromatography column products to address separation needs in the pharma/biopharma, environmental, and other industries. • Study and understand industrial separation challenges and propose technical solutions to initiate R&D efforts. • Develop methods, applications, and workflows for liquid chromatography column and sample preparation products. • Collaborate with Project Management, Product, Operations, and Marketing teams to ensure proper planning, resource allocation, execution, and on-time delivery of new products. Support Manufacturing and Quality Control by transferring SOPs and troubleshooting analytical issues. • Review literature, conduct experiments, present data, publish findings, and file patents as routine research responsibilities. The essential requirements of the job include: • Master's degree or equivalent in analytical chemistry, biochemistry, biology, chemistry, or a related field, with 3+ years of experience in liquid chromatography analysis and sample preparation techniques. A PhD is preferred. • Minimum 2 years of hands-on experience working with RNA-based therapeutics, including oligonucleotides, guide RNAs (gRNAs), and mRNA. Experience with other biotherapeutics like monoclonal antibodies (mAbs), AAVs, or antibody-drug conjugates (ADCs) is also valuable. • Proven skills in sample preparation workflows, such as extraction and liquid chromatography (LC)-based quantification. • Experience in purification, quantitative bioanalysis, and characterization of these molecules. • Ability to modify lab equipment or instrumentation to support R&D needs. • Demonstrated ability to effectively plan, execute, and manage multiple complex projects. • Creative problem-solving skills with the ability to apply scientific knowledge to real-world applications. It would be a plus if you also possess previous experience in: • 3 years of experience in the biopharmaceutical or biotechnology industry is preferred • Hands-on experience with mass spectrometry analysis is preferred. • Strong track record of scientific contributions through publications, patents, and conference presentations is preferred. Phenomenex, a Danaher operating 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 Danaher Benefits Info. The salary range for this role is $97,800 - $135,000. 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. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. 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. The EEO posters are available here . 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.

About the Company For over 125 years, our client has put customers first, delivering top-quality ingredients with great pricing and dependable lead times, all backed by outstanding service. While the company has grown, their commitment to small-town service hasn't changed. Whether supporting clients in baking, snack food, or beverage ensuring smooth operations is their top priority. From simple wheat flours to complex custom blends, every ingredient they deliver is marked by superior quality and exceptional value. Sourced globally from manufacturers who share a commitment to quality and sustainability, their products meet the highest standards - including precise customer specifications. Headquartered in Southern California, with manufacturing and distribution facilities across multiple U.S. regions, our client is positioned to serve customers nationwide with consistency and care. About the Role Reports to: R&D Manager Our client is seeking a Senior Food Scientist with strong leadership skills and hands-on bakery expertise to join their R&D team. This position will play a key role in developing and executing projects across bakery mixes, breadings, batters, and drink mixes. The ideal candidate will have experience formulating bakery products and leading small teams, with the ability to work cross-functionally to take projects from concept to commercialization. As the Senior Food Scientist, you'll be responsible for managing and mentoring two R&D Technicians while driving product innovation, experimentation, and technical documentation. You must be detail-oriented, self-motivated, and comfortable leading complex projects in both lab and plant environments. Responsibilities Lead new product development and process improvement initiatives, primarily in the bakery category. Mentor and oversee two R&D Technicians, providing direction, support, and training. Manage projects and individual tasks with minimal supervision. Design, execute, and analyze experiments with clear documentation of findings. Develop prototypes and technical proposals to support innovation and category expansion. Coordinate plant trials for new products or processes, ensuring smooth execution and scalability. Collaborate cross-functionally with Quality, Production, Purchasing, and Sales to ensure successful commercialization. Maintain thorough knowledge of industry trends, ingredients, processes, and regulatory requirements. Provide technical support to internal teams and external manufacturing partners. Review and validate documentation from junior staff using ESHA Genesis for nutritional labeling. Maintain a strong food safety mindset, incorporating GMP, HACCP, Organic standards, and other compliance frameworks. Test and evaluate ingredient and finished good expiration and when possible, advise on shelf-life extension. Update batch records and host preproduction scheduling meeting. Provide clear direction on what ingredients are allowed as substitutes or replacements. Required to approve and place product on hold. Required to provide instructions on how to rework product that have been placed on hold. Qualifications B.S. in Food Science or a related scientific discipline (M.S. preferred). 5+ years of food industry experience with a focus on R&D and manufacturing. Minimum 2 years of experience in bakery product development, including formulation. Prior experience leading or mentoring team members. Strong project management, communication, and organizational skills. Solid technical understanding of product formulation, sensory evaluation, and processing. Working knowledge of regulatory and quality systems including HACCP and GMP. Proficiency in Microsoft Office; ESHA Genesis software experience preferred. Bilingual English/Spanish is a plus. Must be able to taste products including those with allergens. Willingness to travel up to 15% to support plant trials and customer needs.

MUST RESIDE WITHIN DRIVING DISTANCE OF CARSON, CA. You may not know the Bakkavor name, but you may know our food. At Bakkavor, we produce a highly innovative array of private label, short-shelf life, fresh prepared products for the top grocery retailers. We provide healthy, convenient and delicious options for people who don't believe in compromising even when life is hectic. Here in the US we are in a period of exponential growth across our five facilities, demand for our products is high and improvements to our infrastructure are vast. 2021 performance has been excellent with even bigger expectations for 2022. Regulatory Technical Services Technologist SUMMARY This person is responsible for supporting Bakkavor's and Customer technical product information. Regulatory Guidelines (FDA/USDA) and Special Certifications (Kosher, Organic, Gluten Free, Non-GMO, etc.). This position is part of Bakkavor USA Central Technical Department and reports directly to the Corporate Technical Services Manager. Competencies 1. Technical Expertise (Quality, Food Safety and Regulatory) 2. Leadership (Vision, Organizational Savvy, Team Builder, Action-Results-Value Driven) 3. Customer Focus (Balanced Customer- Business/Science Oriented Decision-Making) RESPONSIBILITIES include the following, but are not limited to: I. Regulatory/Technical Expertise Finished Product/Materials Works with R&D to ensure at the time of management feasibility and future updates of products meet a regulatory requirement. Evaluate supplier ingredient information to verify product compliance against customer standards, labeling law, and regulations. Develops accurate nutrition facts panels and ingredient statements utilizing ESHA Genesis software. Responsible for the developing finished product nutrition labels and technical information such as, but not limited to statement of identity, nutrition facts, ingredient statement, allergen compliance, and validation of legal claims. Interact with customers and designers to ensure that all label development meet FDA/USDA requirements and are accurately incorporated in the final artwork. Conducts annual label review of product specifications for accuracy and compliance with regulations and customer requirements. Updates and maintains customer database. Also, creates technical datasheet specs for customers that have no databases. Supports USDA label submission and approval along with the maintenance of historical files for product labels. Uses the USDA/FSIS Label Submission Approval System (LSAS) Created and managed all unit labels, bag labels, and master case labels in the appropriate software (Bartender, Excel, CLARiSOFT, and Cryovac Hot Stamp). Able to work effectively with other team members within the department and cross-functionally to achieve projects/tasks on time and within budget. Quality and Food Safety Systems Updates and oversees the QA internal database. Works with the process team to collect analytical, CCP's, and QAS/line sheets. Supports Supplier and Materials approval process by retrieving and reviewing supplier records. Updates and maintains shelf life reference sheet, finished product reference sheet, and products quality testing log. Leadership A Driver who Promotes Safety and teamwork across all departments. Actively participates and carry out effective meetings to support team and company objectives to assure delivery of project within budget and planned timelines. II. Customer Focus Supports the resolution of customer feedback and identification of root causes and corrective/preventive actions as related to technical manners. Represent Bakkavor technical team in customer meetings and assure communication (written/verbal) between all parties professionally and assure proper confidentiality and conflict of interest. Maintain project lists and status up to date to assure delivery of goals within time and budget. Coordinates accurate technical information between parties to support input of information into customer's databases and development of internal materials such as, but not limited to, recipes, ingredient nutritional information, product/ingredients allergen profile, validation of product claims, product/ingredients specifications, serving size, boards /brochures. Participate in educational programs to do relevant trainings to keep abreast of the domestic and international regulations. Maintains all related customer information in a confidential and organized manner. Assures compliance to safety requirements when visiting suppliers and customers. Minimum Qualifications: EDUCATION and/or EXPERIENCE B.S. degree from a 4- year university In Food Science or related field is preferred. 5 - plus years food industry or equivalent experience required Experience using Genesis ESHA Software HACCP Certification Preferred Seafood HACCP Certification Preferred FDA/USDA Regulatory Labeling Training Preferred 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 regularly required to sit and talk or hear. The employee frequently is required to stand; walk; use hands to finger, handle, or feel; and reach with hands and arms. The employee is occasionally required to stoop, kneel, crouch, or crawl and taste or smell. The employee must occasionally lift and/or move up to 25 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 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. While performing the duties of this job, the employee is regularly required to work independently and with and around others. There is frequent verbal and face-to-face contact. The employee is frequently required to be available for extended hours. The noise level in the work environment is usually moderate.

Schedule: Full-Time | On-Site Salary: $100,000-$120,000/year DOE Industry: Personal Care / Cosmetics Manufacturing About the Role: We are a leading manufacturer of high-quality personal care and cosmetic products, dedicated to innovation, safety, and excellence. We are currently seeking a Senior Chemist to join our dynamic R&D team. The ideal candidate will have a strong background in product formulation within the personal care or cosmetics industry and a passion for developing effective, compliant, and market-ready products. Requirements: Bachelor's degree in Chemistry, Chemical Engineering, or related scientific field (required) Minimum of 5+ years of experience formulating products in personal care or cosmetics manufacturing (required) Strong understanding of raw materials, emulsions, surfactants, preservatives, and regulatory requirements (e.g., FDA, OTC, EU, etc.) Excellent laboratory skills and ability to manage multiple formulation projects simultaneously Bilingual in English and Spanish highly preferred Must pass background and drug Apply Today! If you are a hands-on chemist with a proven track record in personal care or cosmetics manufacturing and are looking to join a company that values innovation and quality, we encourage you to apply now.

Prepares specimens for analysis; performs and reports waived, moderate, or high complexity clinical laboratory procedures. Performs all procedures in compliance with written SOPs and FACT, AABB, ACHI, CAP, FDA and Joint Commission regulations. Assists in teaching students and staff. Works as authorized by the Laboratory Director under Clinical Laboratory Improvement Amendments of 1988, CFR Section 493.1445(a). Minimum Experience: 1+ years of relevant experience with experience in chemistry. MUST HAVE CCS License (clinical chemistry scientist) and CLS license strongly preferred. Minimum Education: Bachelor's Degree with a major in Chemical, Physical, Biological or Clinical Laboratory Sciences. CCS License in state of California. Essential Functions: Maintains knowledge of techniques for preparing and processing biological specimens for clinical analyses using universal precautions. Maintains knowledge and proficiency in manual, semi-automated and automated procedures. Performs a variety of complex laboratory tests and procedures according to prescribed protocols and assigned schedules. Completes procedures within established turnaround times. Reviews normal and critical results for accuracy and completeness before they are reported. Notifies supervisor of unusual results or discrepancies. Performs quality control procedures including preventive maintenance, calibrations, review of controls, and records data on appropriate forms. Supports and participates in the Quality Assurance efforts and Performance Improvement process. Utilizes standard laboratory equipment, and records and checks result for completeness and accuracy. Performs data entry of diagnostic information. Prepares and appropriately labels solutions, reagents, culture media, and stains according to standard formulas and procedures. Attends staff meetings and required institutional/safety training classes. Cross-trains (if applicable) through other sections within division/department. Develops and maintains skills to provide coverage as assigned by the supervisor.

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

Job Title: Chemist I Department: Quality Control Reports To: Laboratory Supervisor FLSA Status: Exempt This position is responsible for performing various laboratory tests to determine chemical and physical characteristics or composition of solid or liquid materials. Laboratory tests will primarily include wet chemistry and basic use of instrumentation such as Gas Chromatography and High Pressure Liquid Chromatography. The Chemist I will also be responsible for supporting the Quality Control laboratory through reagent compounding. This position will also be responsible for performing identification testing using wet chemistry or instrumentation analysis, physical property testing and general laboratory upkeep. The individual will also be responsible for maintaining a laboratory notebook in accordance with Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP). ESSENTIAL DUTIES AND RESPONSIBILITIES: Sets up, adjusts and operates basic laboratory equipment such as microscopes, centrifuges, viscometer, analytical balances, pH meter, and spectrophotometers. Basic operation of advanced instrumentation such as Gas Chromatography and High-Pressure Liquid Chromatography are also required. This position is responsible for performing tests on a wide variety of materials comprised of powders, granules, gases and liquids to confirm quality attributes such as purity, stability, viscosity, density, absorption, burning rate, and melting or flash point. Tests are conducted on such materials for the presence and content of elements or substances such as hydrocarbons, manganese, natural grease, tungsten, sulfur, cyanide, ash, or impurities. The individual will perform tests on a wide variety of samples of manufactured products to verify their conformity to defined specifications. Such products may be regulated under Good Manufacturing Practices and regulated by government regulatory agencies like FDA. As such the individual is required to have a basic knowledge of GMPs and other pertinent government regulations. Records test results on standardized forms and laboratory notebooks. Writes test reports describing procedures used and uses basic mathematical analysis following Good Documentation Practices. Prepares graphs and charts and understands basic statistical concepts that may be required to reach sound scientific conclusions. The individual will participate in Out of Specification investigation to resolve scientific issues in a timely manner. SUPERVISORY RESPONSIBILITIES: This position has no supervisory responsibilities. QUALIFICATIONS: To perform this job successfully, the individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and EXPERIENCE: A bachelor's degree from an accredited four-year college or University in chemistry, biochemistry or related scientific field with 2 - 4 years' experience working in a laboratory in an industrial or academic setting or, a master's degree from an accredited four-year college or university with 0-2 years' experience MATHEMATICAL SKILLS: The individual is required to have the ability to work with basic mathematical concepts such as probability and fundamentals of plane and solid geometry and trigonometry. The individual must also be able to apply basic mathematical skills such as fractions, percentages, ratios, and proportions to basic problem-solving techniques. Some knowledge of basic statistical techniques is required. CERTIFICATES, LICENSES, REGISTRATIONS: None required for this position. 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 regularly required to use hands to finger, handle, or feel and reach with hands and arms. The employee frequently is required to stand, walk, sit, talk or hear, and taste or smell. The employee is occasionally required to climb or balance and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Must pass respiratory fitness test, position requires employee to wear a respirator. 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. While performing the duties of this job, the employee is frequently exposed to fumes or airborne particles and toxic or caustic chemicals. The noise level in the work environment is usually quiet.

Air Technology Laboratories, Inc. has been providing high-quality air testing services since 1997. We specialize in air toxics analyses, processing samples from various sources such as underground plumes, indoor air, landfill gas, and ambient air monitoring sites. Utilizing custom-designed instrumentation, we meet the specialized requirements of environmental testing. Our experienced staff and management offer reliable technical assistance in compliance with both routine and non-routine site investigations and remediation. Based in City of Industry, CA, Air Technology Laboratories is a trusted resource in the air testing industry. Role Description This is an entry level full-time, on-site role based in City of Industry, CA for an Analytical Chemist. The Analytical Chemist will start training primarily in the sample control and project management department, with increasing training in the analytical procedures, eventually being responsible for conducting laboratory analyses, maintaining and operating laboratory equipment, and ensuring quality control. Daily tasks include sample preparation, data analysis, and compliance with laboratory protocols and safety standards. Qualifications Strong Laboratory Skills and proficiency with Laboratory Equipment Excellent Analytical Skills and attention to detail Bachelor's degree in Chemistry, Biochemistry, or a related field Ability to work independently and collaboratively in a team setting Effective written and verbal communication skills Familiarity with environmental testing is a plus

Clorox is the place that's committed to growth - for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact on consumers, communities, and teammates. Join our team. #CloroxIsThePlace Your role at Clorox: As a Scientist II in Product and Process Development, you will be part of a team responsible for the technical formulation development and scale-up of Glad products. You will collaborate with Packaging development counterparts, cross-functional colleagues domestically and internationally, and external supply partners to develop and recommend options to bring ideas to life. Glad is a fast-paced, exciting, innovative business. You will have a variety of assignments within the organization across new product innovation, formulation and claims improvements, optimization, cost savings, and sustainability. This position will be located in our Willowbrook, IL office, and the individual will be expected to be in the office 3 days a week. Relocation assistance will be offered. Travel expected around 20%. In this role, you will: * Lead the execution of Product Development for projects from concept through development, using technical leadership to fulfill charter needs. * Determine and create robust project plans for scaling up new and improved products and processes driven by consumer insights. * Collaborate in close partnership with R&D peers, as well as Marketing, Sales, Supply Chain, and Regulatory involved in development. * Leverage internal and external expertise, along with digital tools, as you tackle cutting-edge technical problems. You will need a flexible (agile) mindset as you drive ideas from concept to development, quickly readying technologies and bringing products to market that delight the consumer. * Proficiently identify, select, and apply formulation technology from inside and outside sources (suppliers, experts, etc.) to deliver against consumer and customer needs, create foundational understanding, and drive key business initiatives. * Lead the design and execute technical testing to converge on and validate product performance, including developing new test methods and demos with support as necessary. * Analyze and interpret data to drive technical understanding, meet project targets and objectives, problem solve, and make recommendations that drive efficiency, knowledge, and manage/elevate risk. * Closely track external industry technology development and trends to incorporate into business growth plans. * Collaborate with Supply Chain and engineering teams to ensure consistent communication, successful start-ups, define any new capital requirement, and influence future capabilities. * Work closely with domestic and international suppliers and manufacturers to provide innovative solutions and identify process improvements to meet objectives in projects. * Visit suppliers, Clorox plants, and external manufacturers (some being international) to work with them closely to enable new product launch. * Travel expected around 20%. What we look for: * Bachelor's degree from an accredited institution in Science or Engineering required. * Minimum 2 years of experience, preferably in consumer products or plastic film extrusion. * High energy, positive drive, and commitment in setting and meeting aggressive goals and seeking out new opportunities. * Strong technical curiosity and creative problem-solving skills with a record of implemented innovative technical solutions. * Proficiency in navigating IP and claims. * Critical thinking to adapt to formulation and manufacturing challenges and using innovative approaches to overcome those challenges. * Excellent verbal and written communication skills and interpersonal skills to work in a collaborative team environment, both internal and external to Clorox. * Ability to influence others, selling ideas to stakeholders and encouraging team direction. * Capability to work independently and implement multiple projects in a timely manner. * Effective leadership to work in a collaborative team environment, both internal and external to Clorox. #LI-Hybrid Workplace type: This position will be located in our Willowbrook, IL office, and the individual will be expected to be in the office 3 days a week. Relocation assistance will be offered. Travel expected around 20%. We seek out and celebrate diverse backgrounds and experiences. We're looking for fresh perspectives, a desire to bring your best, and a non-stop drive to keep growing and learning. At Clorox, we have a Culture of Inclusion. We believe our values-based culture connects to our purpose and helps our people be the best versions of themselves, professionally and personally. This means building a workplace where every person can feel respected, valued, and fully able to participate in our Clorox community. Learn more about our I&D program & initiatives here. [U.S.]Additional Information: At Clorox, we champion people to be well and thrive, starting with our own people. To help make this possible, we offer comprehensive, competitive benefits that prioritize all aspects of wellbeing and provide flexibility for our teammates' unique needs. This includes robust health plans, a market-leading 401(k) program with a company match, flexible time off benefits (including half-day summer Fridays depending on location), inclusive fertility/adoption benefits, and more. We are committed to fair and equitable pay and are transparent with current and future teammates about our full salary ranges. We use broad salary ranges that reflect the competitive market for similar jobs, provide sufficient opportunity for growth as you gain experience and expand responsibilities, while also allowing for differentiation based on performance. Based on the breadth of our ranges, most new hires will start at Clorox in the first half of the applicable range. Your starting pay will depend on job-related factors, including relevant skills, knowledge, experience and location. The applicable salary range for every role in the U.S. is based on your work location and is aligned to one of three zones according to the cost of labor in your area. -Zone A: $88,700 - $165,900 -Zone B: $81,300 - $152,100 -Zone C: $73,900 - $138,300 All ranges are subject to change in the future. Your recruiter can share more about the specific salary range for your location during the hiring process. This job is also eligible for participation in Clorox's incentive plans, subject to the terms of the applicable plan documents and policies. Please apply directly to our job postings and do not submit your resume to any person via text message. Clorox does not conduct text-based interviews and encourages you to be cautious of anyone posing as a Clorox recruiter via unsolicited texts during these uncertain times. To all recruitment agencies: Clorox (and its brand families) does not accept agency resumes. Please do not forward resumes to Clorox employees, including any members of our leadership team. Clorox is not responsible for any fees related to unsolicited resumes.

Join NELLSON and Become Part of a Winning Team of Professionals! We currently have an immediate opportunity for R&D Scientist to join the BAR DIVISION at our ONTARIO, CALIFORNIA location. Provide effective and functional technical support within the current R&D organization leadership. Responsible for the development of nutritional bar products for both new and existing Nellson customers. Provide data based technical leadership for innovation and product development from ideation to commercialization, utilizing standard best practices and procedures with hands on scale up and commercialization support. Collaborate with cross-functional disciplines to accomplish project goals. ESSENTIAL JOB DUTIES AND RESPONSIBILITIES: Support and lead the development of commercially successful and innovative new products for the bar business. Develop an effective relationship and work closely with the QA, Sales, Operations, and Nellson customers. Gain full command of internal formulation system for food product development and commercialization. Support and lead ideation and development of innovative products and platforms via formulation and/or process driven technologies using customer/marketing insights and existing/new technologies. Maintain awareness of market trends and comparative products Ability to clearly present and articulate product ideas and innovations to internal and external customers. Ability to identify and qualify new equipment and/or processes for new product commercialization (US only). Ability to run and monitor bench-top and manufacturing scale-up batches. Ability to conduct shelf-life testing protocols, including the preparation and/or review shelf-life testing protocols. Preparation and/or manufacture of shelf-life testing samples. Monitoring, evaluation, and summary of results for shelf-life test results. Support R&D team through the identification and sourcing of new, novel ingredients. Gain full command of process systems for effective and sustainable product commercialization and apply product development processes to ensure formulation robustness for commercialization. Support and lead product transfers from other processing locations for maximizing schedule flexibility, efficiency, and lowest cost production. Capture and analyze key process data to determine and communicate key process variables and execute corrective action steps. (US only) Assist R&D project Sr Scientist in completing development and commercialization of new products. Develop a network of outside contacts such as customers, vendors, consultants, and educators. Performs Technical Reports writing as required. Performs other related duties as assign. PERSONAL ATTRIBUTES: Strong problem solving and critical thinking skills for trouble shooting and expanding current equipment capital for developing new product forms and formats. Knowledge and practical experience with shelf stable water activity-controlled food products and/or functional foods product development, processing equipment and techniques and regulatory requirements. Advance communication skills, both written and verbal (French and English for Canadian positions). Ability to speak effectively in front of groups of customers or employees. Demonstrate attention to detail. Must work will in group problem solving and exhibit sound judgement. Ability to prioritize and use time effectively while managing competing demands. Contribute to building a positive team spirit and display a high amount of professionalism. Responds promptly to customer needs. A firm foundation in food engineering and food science is required. Strong product formulation skills. Firm understanding of ingredient functionality and nutrition. High level of professionalism and diplomacy. Experience conducting plant trials/ process validation testing. Demonstrates self-management by consistently at work and on-time, takes responsibility for own actions, takes initiative, generates suggestions for improving work, meets productivity standards, and monitors own work to ensure quality. QUALIFICATIONS AND EXPERIENCE: Requires a minimum of 3 years of experience in the food industry. Requires a four-year college or university degree or its equivalent in Food Engineering Sciences, Food Science, or other relevant science degree. Knowledge and Experience with Design of Experiment (DOE) techniques. At Nellson, we invest in highly talented individuals and provide them with opportunities to continuously learn and grow to realize their full potential. Our state-of-the-art facilities, warehouses, and corporate offices offer a knowledgeable and professional environment to employees. By joining our performance-oriented team, you will be able to put your expertise to use and positively impact many groups across our production process. Nellson offers competitive pay, career growth opportunities, and an outstanding benefits program that features: * Medical, Dental & Vision Coverage * Generous Paid Time Off * 401(k) with Company Match * Flexible schedules * Professional Development & Tuition Reimbursement * And Many More Employee-Friendly Programs!

Language Requirement: No Korean language skills required This role focuses on conducting sensory evaluations to ensure product quality within the New Product Development (NPD) process. The position also involves supporting R&D budget control and administrative tasks. Key Responsibilities: Conduct sensory evaluations to assess food product attributes for NPD and product excellence management. Organize, train, and maintain sensory panels for accurate data collection. Analyze sensory data and provide insights to guide product development. Collaborate with Marketing and other teams to align sensory insights with product strategies. Stay updated on industry trends and sensory evaluation techniques. Communicate sensory findings to food scientists and stakeholders. Support R&D budget monitoring and administrative tasks. Research industry trends and competitors to ensure market competitiveness. Qualifications: Bachelors degree in Food Science or a related field. 3+ years of experience in sensory evaluation within the food industry. Experience in food product development is a plus. Excellent communication and organizational skills. Proficiency in MS Office. Ability to manage tasks independently with minimal supervision. Strong attention to detail and ability to handle confidential information.

Permanent Pay Range Min. $114,000.00 Pay Range Max. $150,000.00 About Heraeus Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead. About Heraeus Precious Metals With more than 350 years of experience in precious metals processing, Heraeus Precious Metals is the world's leading provider of innovative products and services, such as precious metals trading and recycling. Our products are used in a wide range of industries, for example to reduce climate killers such as nitrous oxide and methane and in the form of pharmaceutical ingredients for the treatment of cancer. Our innovative strength is driven by our 3,000 employees in more than 15 countries, who work passionately with our partners to develop pioneering and sustainable solutions. We are aware of our responsibility towards people and the environment and have set ourselves ambitious CO₂ targets. Sustainability is at the heart of all our business activities. Heraeus, the German based technology group is a leading international family-owned company formed in 1851. We create high-quality solutions for our customers by combining material expertise with technological know-how. Our ideas are focused on themes such as environment, energy, health, mobility, and industrial applications. In 2015 Heraeus generated revenues without precious metals of €1.9 bn and a total revenue of €12.9 bn. in more than 100 subsidiaries in 38 countries we offer our worldwide 12,500 employees the freedom to develop and promote their own ideas. We call it: Open Space. For Open Minds. The primary responsibility of this position is the timely planning and execution of the physical and chemical experiments aimed at fulfilling the agreed H2CIRC project objectives, in conjunction with R&D management and, in accordance with Heraeus Holding management principles. Your role and responsibilities: * Conducts and oversees the design and development of new chemical processes or new applications for the Recycling Business Unit. * Collaborates with R&D management in the planning and coordination of projects for the development of new processes under special consideration of costs and future scale-up pathways. * Analyzes data and prepares technical reports to communicate findings and progress to stakeholders. * Maintains accurate and secure records of all experimental data, project spending and time spent on project. * Stays updated on industry trends and advancements to ensure cutting-edge research practices are employed. * Works with support staff to assure departments' adherence to quality, safety and environmental standards that exceed industry minimums. * Ensures with R&D management that new invented processes and products or improved processes and products are carried out in accordance with quality, safety and environmental standards of the industry and the authorities. * Is responsible for the reduction of accidents (occupational, reportable, recordable, and minor) in the department to zero. * Delivers data necessary for permit registration and authority compliance within CA and USA legislation. What is required for this role: * A Ph.D. degree in Chemistry or related field with a focus on chemical or material (especially inorganic, organometallic and/or ionomer) recycling required, with 0-2 years' related experience or; a B.S./M.S. in Chemistry or related field with 3-5 years' related experience. Experience should ideally include precious metals. * Experience with analytical chemistry methods and techniques (ICP, FTIR, IC, etc.) and spectra/data elucidation required. * Experience navigating chemical literature and use of search tools preferred. * Some experience in kilo-lab environment helpful, but not necessary. The expected base salary hiring range for this position is between $114k/annually and $150k/annually. This is a good faith estimate based on a full-time schedule. Base salaries are determined by various factors, including candidate qualifications, geographic location, market conditions, and internl equity. Additional compensation, including bonuses or benefits, may apply. Curious? Apply now! Heraeus is proud to be an Equal Opportunity Employer. We provide fair and equal consideration to all qualified applicants, regardless of sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other legally protected characteristic. Diversity is at the heart of our Vision, Mission, and Values. We are dedicated to cultivating an inclusive workforce that reflects a broad spectrum of cultures, backgrounds, and perspectives. Any further questions? If you need any assistance or have questions, please contact ***************************** or visit our website at jobs.heraeus.com. ReqID: 57615

Support the development of medical device products through R&D device design control phases. Tasks include designing new products; developing, performing, and documenting test methods and processes; identifying equipment and performing qualification; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job duties: Develop new product concepts and prototypes. Perform chemical reactions and utilize analytical techniques for characterization. Perform device feasibility and design verification testing. Perform process development and test method validations. Support product transfer from R&D to Manufacturing. Provide technical support for regulatory filings; perform testing required for various global product registrations. Provide technical support for marketing functions including competitive product testing and providing product related technical training to field staff. Provide technical support for physician preference testing. Provide technical support for product related complaints. Contribute to generating intellectual property and invention disclosures. May have oversight of junior staff members and train technicians and specialists as needed. Moderately self-directed, capable of meeting project goals with minimal supervision. Perform additional responsibilities as assigned. Bachelor's degree in Chemistry or related scientific field. Minimum of two (2) years of relevant work experience or Master's degree plus minimum one (1) year of relevant work experience. Strong written and verbal communication skills. Proficient computer skills including MS Office Suite and statistical software. Desired Qualifications Intermediate knowledge of design and development cycle of medical devices with focus on chemistry-based implants such as liquid embolics, hydrogels, microspheres, and coatings. Ability to draft technical documentation, reports, and design specifications. Intermediate knowledge of organic chemistry, synthesis, laboratory equipment and analytical techniques. Intermediate knowledge of medical device technical development. Intermediate knowledge of materials used in the medical device industry. Intermediate knowledge or experience in process development of chemistry based implantable devices.

Contract: 1 year **Responsibilities:** - Perform data and **document review to ensure data integrity** and compliance of laboratory reports including but not limited to Microbiology and Analytical data, method validation, stability and technical reports. - Draft technical documents including but not limited to OOS and non-conformance quarterly trend reports, equipment Out of Tolerance investigations, Standard Operating Procedures and Work Instructions. - Oversee critical laboratory instruments and equipment to ensure compliance with qualification, maintenance and calibration schedules. Initiate equipment change control and assist with coordination of set up and qualification activities for new assets. Assist with OOT investigations in the Asset Management System. Skills: - Experienced in GMP regulated drug development environment. - Knowledgeable of typical data, data types and documentation that are produced in CMC during clinical development of pharmaceutical and biological drugs (e.g manufacturing and QC of clinical trial material, stability testing, test method transfer). - Strong working knowledge of cGMP, FDA and EMA GMP regulation and ICH guidance documents. Familiarity with CDC compliance requirements for Select Agent Toxin program preferred. Experience: - Must possess a BS in molecular biology, biochemistry, or related field with at least three years of relevant experience. Knowledge of GMP, ISO, and FDA regulations a plus. Familiar with process and test method validations. Excellent communication skills. Ability to perform under pressure to meet project deadlines. **Top 5 skills/requirements this person is required** a. Required Skill 1: Strong working knowledge of data types and documentation produced in CMC during clinical development of pharmaceutical and biological drugs (e.g manufacturing and QC of clinical trial material, stability testing, test method transfer). b. Required Skill 2: Strong working knowledge of cGMP, FDA and EMA GMP regulation and ICH guidance documents. c. Required Skill 3: Experience in GMP regulated drug development environment. d. Required Skill 4: Experience with non-conformance investigations related to analytical testing and equipment out of tolerance results. e. Required Skill 5: Prior experience working in a biologics environment (regulated by CDC). + BS in molecular biology, biochemistry, or related field with 3+ years of relevant experience. + Familiarity with CDC regulations around Select Agents and Toxins. + Background check for the **SRA program for working in biologics laboratory** + Work environment: office, analytical, microbiology and biologic laboratories (toxins) About US Tech Solutions: US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************ US Tech Solutions 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. Recruiter Details: Name: Ravi Sharma Email: ********************************** Internal Id: **25-29624**

Support the development of medical device products through R&D device design control phases. Tasks include designing new products; developing, performing, and documenting test methods and processes; identifying equipment and performing qualification; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job duties: + Develop new product concepts and prototypes. + Perform chemical reactions and utilize analytical techniques for characterization. + Perform device feasibility and design verification testing. + Perform process development and test method validations. + Support product transfer from R&D to Manufacturing. + Provide technical support for regulatory filings; perform testing required for various global product registrations. + Provide technical support for marketing functions including competitive product testing and providing product related technical training to field staff. + Provide technical support for physician preference testing. + Provide technical support for product related complaints. + Contribute to generating intellectual property and invention disclosures. + May have oversight of junior staff members and train technicians and specialists as needed. + Moderately self-directed, capable of meeting project goals with minimal supervision. + Perform additional responsibilities as assigned. **Auto req ID:** 12420BR **Location:** Aliso Viejo, California, USA **Department Name:** 800-California Interventional Systems (CAIS) **Qualifications:** 1. Bachelor's degree in Chemistry or related scientific field. 2. Minimum of two (2) years of relevant work experience or Master's degree plus minimum one (1) year of relevant work experience. 3. Strong written and verbal communication skills. 4. Proficient computer skills including MS Office Suite and statistical software. **Desired Qualifications** 1. Intermediate knowledge of design and development cycle of medical devices with focus on chemistry-based implants such as liquid embolics, hydrogels, microspheres, and coatings. 2. Ability to draft technical documentation, reports, and design specifications. 3. Intermediate knowledge of organic chemistry, synthesis, laboratory equipment and analytical techniques. 4. Intermediate knowledge of medical device technical development. 5. Intermediate knowledge of materials used in the medical device industry. 6. Intermediate knowledge or experience in process development of chemistry based implantable devices. **External-Facing Title:** Scientist II, Product Development **Posting Country:** US - United States **Salary Range:** $76,000 - $100,000 (Compensation can vary based on education, experience and skill sets) We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, disability, religion, national origin, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law.

Rainmaker is pioneering a modern cloud seeding system to solve water scarcity and inclement weather problems. We develop and incorporate radar validation, weather-resistant UAS, numerical weather modeling, and sustainable cloud seeds into an effective precipitation enhancement solution. We're seeking a full-time, dedicated numerical weather prediction modeling specialist whose primary focus will be supporting our precipitation enhancement programs OR an experimentalist observationalist who will aid in experimental design of field campaigns and laboratory studies. This position will focus on convective cloud seeding research including aerosol invigoration of convection.What You'll Do Model Configuration and Development: Configure and maintain model setups in different domains. Simulate both convective processes in warm cloud systems, focusing on convective seeding to enhance precipitation through droplet growth and coalescence, examining ice nucleation and crystal growth dynamics to evaluate precipitation enhancement and cloud microphysics. Data Assimilation and Initialization: Design and implement data assimilation strategies using multiple data sources (surface observations, radiosondes, dropsondes, radar, satellite). Develop preprocessing workflows to ingest and quality-control observational data. Create automated procedures for model initialization and boundary condition updates. Model Analysis and Verification: Conduct comprehensive analysis of model output focusing on cloud properties, precipitation processes, atmospheric stability, and QPE. Perform systematic model verification against observational data, and inform future measurement principles to improve model accuracy and confidence. Precipitation Enhancement Applications: Validate and support precipitation enhancement operations by providing advanced forecasting models for convective storm systems at high spatial and temporal resolution. Experimental Design of Field Campaigns: Conceive of and aid in planning experimental field campaigns and laboratory studies to probe the effects of cloud seeding on convective systems and aerosol invigoration of convection. Process and analyze observational data and effectively communicate the findings to the greater scientific and engineering teams. Required Qualifications Master's degree or Ph.D. in meteorology, atmospheric science, physics, or a related field. Demonstrated success in modeling convective storm system development. Strong understanding of atmospheric kinematics, electro and thermodynamics, and computation principles and meteorological processes OR demonstrated success as an observationalist who has studied convective systems, aerosol-cloud interactions, or aerosol invigoration of convection. Experience with data acquisition, processing, and analysis of large datasets. This involves distributed computing methods, database management systems, data partitioning, vectorizing operations, and GPU acceleration. Experience with experimental design and data interpretation Experience with Amazon Web Services cloud computing for external data sources, and internal instance management. Proficiency in modeling, data analysis tools, and programming languages (e.g., Fortran, Python, MATLAB, R, C++). Knowledge of machine learning and deep learning techniques, for modeling applications. Previous experience working in both a research and operational environment. Preferred/Minimum Qualifications Preferred Education: PhD degree in atmospheric science, chemistry, physics or other relevant fields Preferred Experience: 5-10 years of research experience post PhD Preferred Field of Expertise: Convection, aerosol-cloud interactions, cloud microphysics, atmospheric science, aerosol invigoration of convection, ice nucleation $90,000 - $200,000 a year No recruiting agencies

Company & Culture: At GT's Living Foods, LLC, we've stayed true to the authentic brewing process for over 30 years. Our #1 selling Kombucha is raw, organic, naturally effervescent, and handcrafted in small batches - always cultured, never compromised. We're proud to remain a family owned & operated company. As our GT's family continues to grow, we are deeply humbled and sincerely grateful for every moment of this journey with you. Requirements: 1-2 years of experience in job related area Education: High School Diploma or Equivalent Bilingual: English/ Spanish (Preferred) Key Responsibilities: Assist with conducting lab tests, such as preparing samples of raw ingredients, juices, and finished products Data entry, manually recording product name, lot numbers, Ph, and Brix on tested product Assist in maintaining the cleanliness of laboratory equipment and inventory Accurately read and record the results of tests into internal database Assists in unloading, storage, and stocking supplies Organize R&D lab tidiness and ingredients samples. Coordinate and prepare sample requests for shipment. Work in a fast-paced, production lab environment with variable sample volume which requires flexibility in schedule to consistently meet turn-around time requirements. Assist in sample preparation for analytical tests in the lab as needed. Maintain organized records of test results, quality control data, and other relevant documentation. Perform routine maintenance and calibration of equipment to ensure accurate results. Troubleshoot and report any equipment malfunctions to the supervisor. Collaborate with other departments to ensure efficient workflow. Job Description: The R&D Associate is tasked with supporting various departmental needs, such as organizing documentation, preparing and collecting samples from different work sites, and returning samples to the R&D laboratory. They are responsible for ensuring proper storage and packaging of ingredients/samples during transport and within the lab. Additionally, the R&D Associate will carry out routine laboratory functions, including but not limited to: Qualification & Required Knowledge, Skills & Abilities: Strong attention to detail; passion for accuracy and granular details Proficient computer skills, including MS Outlook, Excel, and Word Communication: ability to convey information clearly and professionally both verbally and in writing Consistently meet deadlines; ensures time sensitive tests are completed as specified Works mainly under direct supervision. Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Capable of multi-tasking and being involved with many projects at the same time GT's Employee Experience (Benefits/Perks): Health Insurance: Medical, Dental, Vision 401K with Matching Discounts on the amazing GT's product line Others: Food trucks every weekday, and quarterly employee appreciation events Job Details: Work Attire: Smart/Business Casual Pay Range: $21.00-23.00 GT's Living Foods, LLC is an Equal Opportunity Employer committed to hiring a diverse workforce and maintaining an inclusive culture. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, disability or any other basis protected under federal, state or local laws.