Quality control analyst jobs in Chico, CA

RESPONSIBILITIES: Maintain accurate and up‐to‐date acceptance and rejection records and/or certifications systems as required by the applicable specifications. Determine acceptance or rejection after inspection and/or calibration of parts, tools, instruments or x‐ray film. Identify defective conditions and test failures and prepare all appropriate documentation and/or calibration history. INSPECTION: Perform inspection on complex parts using a wide variety of measuring and test equipment. Adapt and develop complex inspection set‐ups to check sample parts, forgings and castings. Check tool and jig layouts. Perform first article and envelope inspections, source inspections, and/or complex surface plate set‐ups. Interpret specifications, charts, manuals and other data to arrive at acceptance or rejection. Recommend changes to supervision. Use mathematics to convert blueprint dimension and tolerances. Work within the guidelines of drawings, schematics, blueprints, route sheets, travelers, quality directives, technical engineering specifications, customer's requirements and military standards. Layout all component part characteristics onto rough or semi‐machined castings, forgings and machine parts to maintain control of machining cycle during manufacturing. CALIBRATION: Perform calibration on complex multi‐function electronic measuring and test equipment. Set‐up calibration test conditions having various circuit requirements interpreting calibration procedures, specifications, manufacturer's instructions, or related documents. Ability to interpret drawings and electronic schematics. Document and evaluate historical data to determine calibration intervals. Diagnose and calibrate newly acquired complex electronic equipment. NONDESTRUCTIVE TEST: Perform daily, weekly and monthly equipment and material checks. Perform pre‐inspection and post‐inspection cleaning. Set‐up equipment and conduct tests. Interpret, evaluate and document inspection results in accordance with approved procedures. Perform complete inspections in accordance with applicable specifications, standards and other contractual documents. Operate X‐ray equipment and film processor. Select the method and technique to be used for a specific inspection. Prepare and verify the adequacy of inspection procedures. Job Requirements: Five years related inspection experience or demonstrated ability to perform described responsibilities. Knowledge of applicable military standards or specifications. Required experience in CMM operations, background in dimensioning and tolerancing per ANSI Y 14.5. Proficient in reading and interpreting blueprints, customer's specifications and internal drawings and procedures. Thorough knowledge of machine shop mathematics including trigonometry. Knowledge of electro‐hydraulic servo systems and the computer IEEE systems. Personal hand tools may be required. Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

The Quality Control Associate will support the PTDA Bioassay US Testing Group by performing biochemical, immunological, and cell-based assays in support of clinical and commercial products. This role operates in a cGMP-regulated laboratory and supports process development, product characterization, stability, and lot release testing using established procedures. Key Responsibilities Perform biochemical, immunological, and cell-based bioassays Support process development, product characterization, stability, and lot release testing Review, verify, and release assay data (electronic and paper-based) Prepare reagents and maintain assay readiness Present assay results and monitor assay performance and quality Follow Good Documentation Practices (GDP) and ALCOA+ data integrity principles Perform routine laboratory maintenance and support 5S initiatives Comply with EHS safety requirements and cGMP standards Required Qualifications B.S. in Biological Sciences or related field 1-2 years of relevant experience in Quality Control Hands-on experience with immunological and/or cell-based assays Experience with aseptic cell culture Working knowledge of cGMP environments Ability to work independently and collaboratively in a fast-paced setting Strong attention to detail and ability to manage multiple priorities Effective written and verbal communication skills Technical & Systems Skills Proficiency with computer applications, data management, and electronic documentation Experience with GxP-compliant systems such as SoftMax Pro, LIMS, and Veeva QMS (preferred)

Kelly Engineering has an outstanding opportunity for a contract to hire Senior QA Associate role with an organization that is committed to advancing solutions for some of the most challenging issues in healthcare in Petaluma, CA. You will be working with innovative technologies to improve outcomes across a wide range of medical applications, from patient care settings to medical product development. With substantial growth ahead and an upcoming public offering, this is an exceptional opportunity to join a dynamic company offering significant equity potential. The QA Associate will assist in leading the Quality Assurance department and drive compliance for pharmaceutical and combination product regulations. You'll be critical for our major product launch and key to building robust quality processes for future growth Key Responsibilities: Assist the QA Manager in building, scaling and managing the QA team Ensure regulatory compliance with GMP, FDA, ISO13485 and combination product requirements Assist in launch readiness and quality activities to meet urgent product timelines Develop and implement SOPs, validation protocols, and quality documentation systems Assist in audit and inspection preparation Drive root cause analysis, CAPA programs, and continuous improvement. Engage with R&D, manufacturing, and regulatory teams to align quality and business goals What We Are Looking For: 5+ years of Quality experience in a pharmaceutical environment (combination product experience a plus). Expertise in FDA regulations, ISO standards, drug/device compliance BS/MS in a related discipline What happens next: Once you apply, you'll proceed to next steps if your skills and experience look like a good fit. But don't worry - even if this position doesn't work out, you're still in the Kelly Engineering network. That means our team of expert engineering recruiters will have access to your profile, making your opportunities limitless.

Senior Formulation Technician Duration: 12 Months Job Type: Contract Work Type: Onsite Shift: Monday to Friday from 06:00 AM to 02:30 PM Pay Range: $20 to $26 per hour Overview TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. The job opportunity below is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary Work in a team-based manufacturing laboratory environment responsible for synthesizing, testing, and qualifying ion exchange media used in chromatography consumables, while maintaining high quality, safety, and compliance standards. Responsibilities Perform testing and qualification of resin products using specialized instruments to meet customer and production demands. Accurately record, analyze, and report test results; maintain complete and compliant documentation. Execute complex production work orders in accordance with established SOPs and procedures. Analyze data, derive conclusions, and prepare technical reports based on findings. Collaborate with cross-functional teams to support production and quality objectives. Adhere to ISO 9001 guidelines, GMP, and corporate quality policies. Comply with EH&S safety requirements and participate in safety improvement initiatives. Identify process improvement opportunities and propose corrective or preventive actions. Maintain a clean, organized, and inspection-ready laboratory environment. Required Skills Hands-on experience in a chemistry or biotechnology laboratory. Bachelor's degree in Chemistry, Biotechnology, or a related life sciences field. Experience in a manufacturing or regulated production environment. Familiarity with chromatography techniques and chromatography-related software. Exposure to Lean Manufacturing, PPI, or Continuous Improvement tools. Willingness and ability to learn new processes, tools, and technologies. Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Ability to read, understand, and follow written SOPs and verbal instructions in English. Strong mathematical skills, including basic arithmetic with whole numbers, fractions, and decimals. Proficiency in Microsoft Word, Excel, Outlook, and basic data handling. Strong documentation, organizational, and problem-solving skills. Effective verbal and written communication skills. Familiarity with common hand tools (e.g., wrenches, torque drivers, tweezers). Ability to work independently with minimal supervision while meeting deadlines and production targets. Strong punctuality, attendance, and ownership mindset. Understanding of production schedules and task prioritization. Compliance with GMP, QSRs, ISO, and IVD regulatory requirements. TekWissen Group is an equal opportunity employer supporting workforce diversity.

Job Title: Senior Business Intelligence Developer Duration: 03+ Months Contract with Possible extension Pay Range: $60-$65 Per hour on W2 Only USC, GC & EAD on W2, No C2C Please Job Brief: • We are seeking an experienced, highly skilled, and self-directed Business Intelligence Developer to join our People Analytics team, empowering our People & Culture function. This is a high-impact, full-time contract role crucial to enhancing our People Analytics capabilities by developing, maintaining, and automating robust data solutions. • You will proactively collaborate with the People Analytics data team and cross-functional partners to address critical tactical and strategic priorities. This includes leading the implementation of enhancements and resolution of backlogs for existing Tableau dashboards, significantly improving data quality across our current Tableau and Snowflake environments, and building reliable, optimized data pipelines to ensure our stakeholders have performant, validated, and trustworthy analytical tools. Responsibilities: • Routinely diagnose, troubleshoot, and resolve complex bugs and performance issues in existing Tableau dashboards. • Translate business requirements from stakeholders into effective, actionable dashboard enhancements. • Maintain and continuously optimize the performance, accuracy, and data integrity of the dashboard portfolio. • Design and execute rigorous data validation and testing protocols to ensure the quality of all published dashboards and reports. • Maintain a deep, current understanding of our dashboard architecture and data models to take immediate, autonomous action on assigned tasks. Required Qualifications: • 5+ years of demonstrated experience developing, maintaining, and troubleshooting complex, high-visibility dashboards in Tableau. • Expert knowledge of People Analytics and core HR metrics (e.g., recruiting, headcount, attrition, engagement). • Exceptional analytical and problem-solving skills with a proven ability to quickly identify and implement fixes for root causes. • Demonstrated ability to operate with a high degree of independence and effectively manage competing, high-priority tasks. Technical Skills: • Expert proficiency in SQL for complex data querying, manipulation, and transformation (Window Functions, CTEs, optimization). • Advanced skill and deep understanding of Tableau for dashboard development, maintenance, and performance optimization. • Hands-on experience with Python for data automation, scripting, and building robust data pipelines (e.g., using Pandas or similar libraries). • Solid knowledge of data warehousing concepts and technologies (e.g., Snowflake, AWS Redshift, or similar) and experience with ETL/ELT processes. Soft Skills: • Proven self-starter with the ability to drive projects forward and operate effectively with minimal supervision. • Executive-level communication skills with a proven ability to work directly with non-technical stakeholders, gather requirements, and effectively navigate sensitive HR situations with professionalism and discretion. (Rationale: Emphasizing communication and direct stakeholder interaction is key for a remote manager-report relationship.) • Excellent organizational skills and attention to detail. Preferred Qualifications: • Direct experience working with HRIS data and familiarity with platforms such as Workday, SuccessFactors, or similar. (Rationale: Prioritizing direct HRIS experience.) • Experience with other BI tools (e.g., Power BI, Looker) is a plus.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Vaccine Immuno therapeutics (VITx) seeks to Client Client vaccines (prophylactic and therapeutic) for the prevention and treatment of significant human using a variety of vaccine technology platforms combined with immunomodulatory agents. A virus purification scientist is required to join Vaccine Immunotherapeutics in La Jolla, California, to develop and support vaccine platform production processes at the research scale. The candidate will have solid training and knowledge in virus/protein purification. The candidate will be able to independently and proactively apply this knowledge in the design and execution of experimental work, to enable progression of vaccine discovery projects. Experience in most or all of the following areas are desirable- protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. The candidate will be required to work semi-independently and, as a member of a team, be accountable for the critical appraisal of their results and present them for review, at specific project milestones. The role is laboratory based, and a major emphasis is placed upon laboratory training to increase the scope of practical abilities, as well as the theory behind such practical work. Position Comments visible to MSP and Supplier: Additional Skills: Protein/virus purification using chromatographic techniques, experience with Unicorn based FPLC systems, tangential flow ultrafiltration, dead-end filtration and ultracentrifugation based purification. Additional desirable skills would include virus/protein characterization techniques and experience in handling Cat.2 infectious viruses. Expected qualifications/experience BSs or MSc in biological sciences or biochemical/chemical engineering At least 1-5 years working in a laboratory in an academic or industrial setting Qualifications BSs or MSc in biological sciences or biochemical/chemical engineering Additional Information For more information, Please contact Akriti Gupta ************** Morristown, NJ 07960

: Support the daily operations of the Quality Control Department by performing, often complex, elemental analysis of raw materials, drug substance, drug product and components in accordance with cGMP requirements, company policies and procedures as directed by laboratory management. Responsibilities: • Perform, often complex, elemental analysis of raw materials, drug substance, drug product, and components according to established specifications and procedures using elemental analysis techniques (ICP-MS, ICP-OES, AA) in accordance to USP, Pharm. Eur. and other compendial methods per Customer, Company, and cGMP requirements. • Assume ownership of assigned quality documentation, such as investigations, change controls, and CAPAs, ensuring that documentation is initiated and closed on time, required actions are thorough and meet procedural requirements as well as customer needs. • Compose test methodologies, study protocols, and Standard Operating Procedures in order to execute testing in compliance with necessary policies and procedures. Record/review data in controlled notebooks, data sheets, and electronic systems (i.e. LIMS, etc.) in accordance with cGMP requirements. • Work on problems complex in nature where analysis of situations or data requires in-depth review and evaluation of various factors, considerable judgment is required in resolving problems and making routine recommendations. Exercise judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results. • Notify Supervisor of any discrepancy in laboratory testing or general laboratory operations. In case of any observed discrepancies, initiate and follow through with the required quality exception documentation as needed. • Recommend equipment, facility, and process improvements to your supervisor. • Maintain clear, accurate and traceable documentation records to ensure compliance with Good Documentation Practices (GDP). • Maintain laboratory and workspace cleanliness by adhering to the 5S method of organization. • Abide by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor. • This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary. Qualifications • A minimum of 12 years, 14+ years preferred, industry related work experience. • Bachelor's degree or equivalent in scientific discipline required. Advanced degree is strongly preferred.• Advanced knowledge of elemental analysis in raw materials, drug substance, drug product and components. • Advanced knowledge of analytical chemistry principles and techniques using Atomic Absorption (Flame and Graphite Furnace), Inductively Coupled Plasma-Mass Spectroscopy (ICP-MS) and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) • Advanced knowledge of USP, Pharm. Eur. and other compendial methods and procedures with emphasis on USP , , Pharm. Eur. , , , JP , , • Proficient in method development and phase appropriate validation in compliance with ICH guidelines, FDA regulations, compendia and cGMP requirements • Strong technical writing skills for protocols, test methods, reports, laboratory investigation and deviations according to applicable methodologies/regulations. The annualized salary range for this position is $91,800 - $143,400.

Scientist, Protein Production and Characterization AlivaMab Biologics is a rapidly growing leader in the discovery of human antibody therapeutics, trusted by top-tier pharmaceutical and biotechnology companies to deliver panels of drug-quality human antibodies. We deliver on our partners' design goals, from simple to extraordinarily challenging, through collaborative access to our scientists' creativity and experience combined with proven technologies, including the AlivaMab Mouse suite of transgenic mice. Our organization is dedicated to creating a healthier world through partnerships that bring better medicines to patients faster, and we recognize our success starts with hiring people who share our passion for science. We are seeking a highly motivated and skilled Scientist to join our Protein Sciences team and contribute to both day-to-day operations and the advancement of Protein Science workflows. This position will focus on the design, optimization, and execution of transient transfection processes at various scales for antibody and protein production in mammalian expression systems. The successful candidate will leverage expertise in biophysical characterization and biochemical modification to evaluate key protein attributes. This position will report to the Associate Director of Protein Sciences and work closely with scientists in the Antibody Discovery, Antibody Engineering, Protein Sciences, and Project Management teams. The ideal candidate will drive innovation through process refinement, high-throughput automation, and growing proficiency of chemical conjugation techniques. This role offers the opportunity to work in a fast-paced, collaborative research environment, where creative solutions and a strong scientific approach are key to success. Responsibilities Responsibilities: Independently design, plan, and execute transient transfection workflows for antibody and protein production across various mammalian expression systems Develop, design, and optimize protein purification methods to enhance throughput, quality, and efficiency, as required Lead developability assessment studies by designing and conducting analytical experiments to evaluate protein stability, purity, and key biophysical characteristics Support production of complex construct design strategies (e.g VLPs, nanodiscs etc.), to enable immunization antibody discovery campaigns against challenging targets Drive implementation of automated high throughput processes to support protein production workflows using Bravo, and other robotic systems Maintain meticulous experimental records using electronic notebook (Benchling), and communicate results clearly through written reports and presentations to support project progression and scientific decision-making Contribute innovative ideas and collaborate effectively across teams to foster research excellence and ensure project success in a fast-paced environment Qualifications Qualifications: Ph.D. in Biochemistry, Chemistry, Molecular Biology, Protein Engineering, or a related field with a minimum of 2 years of industry experience or MS with minimum of 6 years of direct industry experience is required Proven hands-on experience with multiple mammalian expression platforms is required Proficiency with AKTA instrumentation, and a broad range of purification techniques, including affinity chromatography, ion exchange, HIC, and SEC, as well as standard protein QC methodologies is required Experience with therapeutic antibody developability assessment is highly desirable Strong analytical, troubleshooting, and communication skills with exceptional attention to detail Motivated self-starter with excellent organization, teamwork, and a passion for scientific innovation About AlivaMab Biologics AlivaMab Biologics sets its partners' antibody discovery programs on the fastest and most de-risked path through discovery and development. Trusted by top-tier pharmaceutical and biotechnology companies, AMB delivers drug-quality, fully human antibodies on exceptional timelines. AMB achieves its partners' design goals, from simple to extraordinarily challenging, through the generation and function-first screening of large, molecularly diverse panels of antibodies. AMB focuses on rapid and efficient delivery of antibodies, characterized for function, kinetics and developability, and engineering for alternative formats, including multi-specifics and CARs. The AMB team's experience and passion for antibody drug discovery and development combined with the use of trusted, proven technologies, including Ablexis' AlivaMab Mouse platforms, ensure the highest probability of success. The salary range for this position considers various factors, including skills, experience, training, certifications, and organizational needs. Note that this range does not reflect any geographic adjustments based on the location where the role will be based. At AlivaMab Biologics, it is uncommon for a new hire to start at or near the top of the salary range, as compensation is tailored to each individual's skills and breadth and depth of experience. The current estimated range is $98,500 - $140,000, plus a bonus target, benefits, and equity. AlivaMab Biologics provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to religion, race, creed, color, sex, sexual orientation, gender identification, alienage or citizenship status, national origin, age, marital status, pregnancy, disability, veteran or military status, predisposing genetic characteristics or any other characteristic protected by applicable federal, state or local law. #LI-DNI

About this opportunity : Support the daily operations of the Quality Control Department by performing, often complex, elemental analysis of raw materials, drug substance, drug product and components in accordance with cGMP requirements, company policies and procedures as directed by laboratory management. Responsibilities: * Perform, often complex, elemental analysis of raw materials, drug substance, drug product, and components according to established specifications and procedures using elemental analysis techniques (ICP-MS, ICP-OES, AA) in accordance to USP, Pharm. Eur. and other compendial methods per Customer, Company, and cGMP requirements. * Assume ownership of assigned quality documentation, such as investigations, change controls, and CAPAs, ensuring that documentation is initiated and closed on time, required actions are thorough and meet procedural requirements as well as customer needs. * Compose test methodologies, study protocols, and Standard Operating Procedures in order to execute testing in compliance with necessary policies and procedures. Record/review data in controlled notebooks, data sheets, and electronic systems (i.e. LIMS, etc.) in accordance with cGMP requirements. * Work on problems complex in nature where analysis of situations or data requires in-depth review and evaluation of various factors, considerable judgment is required in resolving problems and making routine recommendations. Exercise judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results. * Notify Supervisor of any discrepancy in laboratory testing or general laboratory operations. In case of any observed discrepancies, initiate and follow through with the required quality exception documentation as needed. * Recommend equipment, facility, and process improvements to your supervisor. * Maintain clear, accurate and traceable documentation records to ensure compliance with Good Documentation Practices (GDP). * Maintain laboratory and workspace cleanliness by adhering to the 5S method of organization. * Abide by safe work practices and adhere to general safety rules, performing all duties in a safe manner and never placing yourself or those around you in an unsafe condition. Report all unsafe conditions to your supervisor. * This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary. Qualifications * A minimum of 12 years, 14+ years preferred, industry related work experience. * Bachelor's degree or equivalent in scientific discipline required. Advanced degree is strongly preferred.• Advanced knowledge of elemental analysis in raw materials, drug substance, drug product and components. * Advanced knowledge of analytical chemistry principles and techniques using Atomic Absorption (Flame and Graphite Furnace), Inductively Coupled Plasma-Mass Spectroscopy (ICP-MS) and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) * Advanced knowledge of USP, Pharm. Eur. and other compendial methods and procedures with emphasis on USP , , Pharm. Eur. , , , JP , , * Proficient in method development and phase appropriate validation in compliance with ICH guidelines, FDA regulations, compendia and cGMP requirements * Strong technical writing skills for protocols, test methods, reports, laboratory investigation and deviations according to applicable methodologies/regulations. The annualized salary range for this position is $91,800 - $143,400.

The City of Chico is seeking one qualified individual to join our Wastewater Treatment Plant as a Laboratory Analyst. Under direction, performs a variety of journey level laboratory analyses in the City's wastewater treatment plant laboratory; supports wastewater treatment plant operations; assists in maintaining accreditation with the Environmental Laboratory Accreditation Program (ELAP); inputs, evaluates, and maintains a variety of data and information; and performs related duties as assigned. Receives direction from assigned management personnel. Exercises no direct supervision over staff. This journey level classification is responsible for independently performing technical and analytical duties in the City's wastewater treatment laboratory. Positions at this level exercise judgment and initiative in their assigned tasks, receive occasional instruction or assistance as new or unusual situations arise, and are fully aware of the operating procedures and policies of the work unit. Management reserves the right to add, modify, change, or rescind the work assignments of different positions and to make reasonable accommodations where appropriate so qualified employees can perform the essential functions of the job. * Performs a variety of laboratory tests and analyses using certified and non-certified test methods including chemical and biological tests on a variety of industrial and domestic wastewater samples; assists in fulfilling sample events and activities. * Maintains and applies quality assurance and quality control (QA/QC) requirements outlined in the Standard Methods, TNI, and the Quality Management Plan; applies quality management system statistics and analysis of laboratory generated data. * Creates and supports the laboratory generated documentation and recording, including quality data, corrective actions, test records, and calibrations. * Designs documents and records, as assigned; inputs, audits, and evaluates data and maintains databases through a variety of software applications. * Provides technical and analytical assistance to plant operation and industrial waste program personnel; conducts field sampling and keeps written records of observations. * Prepares and maintains laboratory supplies, materials, instruments, and equipment; operates and maintains laboratory and sampling equipment; prepares standard solutions, reagents, and materials for each type of test. * Assists in and implements laboratory upkeep and cleanliness efforts; applies laboratory safety standards including hazardous waste storage and discharge; assists with chemical hygiene. * Observes and complies with all City and mandated safety rules, regulations, and protocols. * Performs other duties as assigned. Knowledge of: * Modern laboratory techniques and procedures as related to the analysis and examination of wastewater samples. * The care, maintenance, operation, and calibration of a variety of laboratory equipment and apparatus. * Requirements set forth in the National Pollution Discharge Elimination System (NPDES) permit program and the Environmental Laboratory Accreditation Program (ELAP). * Applicable federal, state, and local laws, codes, and regulations. * The National Environmental Laboratory Accreditation Management System (NELAC) Institute's Transnational Institute (TNI) standard. * Methods and techniques of research and statistical analysis. * Proper sampling and preservation techniques for environmental sampling. * Methods and processes of wastewater treatment. * Principles and procedures of recordkeeping, document processing, and filing systems. * Mathematical principles and statistical techniques. * City and mandated safety rules, regulations, and protocols. * Techniques for providing a high level of customer service by effectively dealing with the public, vendors, contractors, and City staff. * The structure and content of the English language, including the meaning and spelling of words, rules of composition, and grammar. * Modern equipment and communication tools used for business functions and program, project, and task coordination, including computers and software programs relevant to work performed. Ability to: * Analyze samples according to Standard Methods and follow established Quality Assurance and Quality Control protocols. * Understand and conduct testing for wastewater treatment projects to optimize plant efficiency. * Perform routine and complex laboratory tests and analysis. * Perform test methods and principles in microbiology and wet chemistry and interpret results. * Interpret and apply federal, state, and local policies, procedures, laws, and regulations. * Analyze problems within the scope of laboratory testing; research and identify solutions, initiate corrective action and implement Laboratory Manager recommendations. * Understand and apply statistical methods. * Maintain and update accurate records and files. * Use tact, initiative, prudence, and independent judgment within general policy, and procedural, guidelines. * Independently organize work, set priorities, meet critical deadlines, and follow-up on assignments. * Effectively use computer systems, software applications relevant to work performed, and modern business equipment to perform a variety of work tasks. * Communicate clearly and concisely, both orally and in writing, using appropriate English grammar and syntax. * Establish, maintain, and foster positive and effective working relationships with those contacted in the course of work. Education and Experience: Any combination of training and experience that would provide the required knowledge, skills, and abilities is qualifying. A typical way to obtain the required qualifications would be: Education: * Equivalent to a bachelor's degree from an accredited college or university with major coursework in chemistry, microbiology, biology, or a related field. Experience: * Two (2) years of experience conducting chemical or biological analyses including one (1) year of experience performing wastewater plant laboratory analyses. Licenses and Certifications: * Possession of a valid California Driver's License, to be maintained throughout employment. * Possession of a valid Grade I Laboratory Analyst Certification issued by the California Water Environment Association (CWEA) or similar agency, to be maintained throughout employment. Physical Demands Must possess mobility to work in a laboratory and standard office setting and use standard office equipment, including a computer, as well as a diverse range of laboratory equipment; vision to read printed materials and a computer screen, and to operate a motor vehicle and visit various City sites; smell to detect chemicals, and hearing and speech to communicate in person and over the telephone. This is primarily a laboratory focused classification with frequent standing, sitting, and walking between work areas. Finger dexterity is needed to open and close sample bottles and operate pipettes, and to access, enter, and retrieve data using a computer keyboard or calculator, and to operate standard office equipment. Positions in this classification bend, stoop, climb to access materials, kneel, reach, push, and pull drawers open and closed to retrieve and file information. Employees must possess the ability to lift, carry, push, and pull materials and objects with an average weight of up to 30 pounds, or heavier weights, in all cases with the use of proper equipment and/or assistance from staff. Environmental Conditions Employees work primarily in a laboratory environment with moderate to excessive noise levels, controlled temperature conditions, and exposure to dust, fumes, and/or allergens, hazardous chemicals, biologic/infectious agents, and unpleasant odors. Employees also work in an office environment with moderate noise levels, controlled temperature conditions, and no direct exposure to hazardous physical substances. Employees may interact with upset staff and/or public and private representatives in interpreting and enforcing departmental policies and procedures.

Do you want to build a stronger, more sustainable future and cultivate your career? Become a part of the Dermalogica Research and Development team. We are looking for a talented Chemist to be based at the Corporate Headquarters in Carson working on-site with the R&D department in a temporary capacity. Role Overview Seeking a temporary R&D Chemist to support bench scale formulation, batching, and stability placement for skincare products. This is a hands-on, execution focused role supporting active development programs in the lab. Key Responsibilities Prepare bench scale batches following established formulas and SOPs Support stability setup including labeling, documentation, and sample placement Accurately record batch data, observations, and deviations Maintain lab organization, raw material handling, and equipment cleanliness Partner with formulation and stability teams to support active projects Required Skills & Experience BS in Chemistry, Cosmetic Science, Chemical Engineering, or related field 1 3 years hands on formulation or lab experience (cosmetics or personal care preferred) Strong bench skills including weighing, mixing, heating/cooling, and pH adjustment Familiarity with stability programs and sample tracking Detail-oriented with strong documentation and organizational skills Able to work independently with clear direction Proficient in Microsoft Office (Excel, Word, Outlook) for documentation and data entry The position is based at the corporate headquarters in Carson, CA, and will be fully on-site, 5 days per week (no remote or hybrid). The pay rate for this role is $35 per hour. Ready to make a meaningful impact and advance your career with a global brand revolutionizing the skincare industry? Apply now and complete your online application. All applications will be reviewed, and our HR team will contact you if your skills align with the position. Dermalogica is an equal opportunity employer committed to fostering an inclusive culture where all employees are valued, supported, and empowered to succeed.

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for formulation of powdered media. 3rd Shift: 9:00 pm- 5:30 am At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of "giving our world more smiles." Visit: *************************************************** Job Description Responsibilities: * Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. * Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. * Suggest changes in departmental procedures and processes (SOPs) as needed. * Performs and documents line clearance at the start of each formulation event. * Maintains all required logs and associated documentation. * Assures that all chemicals are stored and labeled properly. * Performs process scale checks on all required equipment including scales and balances. * Keeps work area, utensils, tanks, mills, and equipment clean and organized. * Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. * Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. * Understands and follows procedures to ensure that chemicals are handled properly. * Good understanding of metric system and its conversions. * Follows and actively participates in sustaining the 6S program in the area. * Other duties as requested by Lead or Supervisor. Required Skills/Education: * High School Diploma or equivalent. * Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. * 1-2 years of hands on experience * General education about chemicals and proper handling (college level science preferred). * Working knowledge of metric system. * Good understanding of current Good Manufacturing Practices (cGMPs). * Ability to speak, read, and write English. * Good oral and written communication skills. Salary and Benefits: * For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). * Medical, Dental, Vision * Life Insurance * 401k * Paid Time Off * #LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

Mon-Fri 6a - 230pm Senior Formulation Technician Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a Key Responsibilities: • Perform testing and qualification of resin products on specialized instruments to meet customer demand. • Record and report test results accurately and maintain proper documentation. • Complete complex production work-orders according to established procedures. • Analyze data, derive conclusions, and prepare reports based on findings. • Collaborate with cross-functional teams. • Adhere to ISO 9001 guidelines and corporate quality policy to ensure high-quality standards. • Follow EH&S safety requirements and actively participate in safety improvement activities. • Continuously identify areas for improvement and propose countermeasures. • Maintain a clean and organized laboratory environment. Knowledge, Skills and Abilities: • Knowledge of Good Laboratory and Manufacturing Practices and standards. • Proficiency in Microsoft Office: Excel, Word, PowerPoint. • Good mathematical, problem-solving, and organizational abilities. • Excellent communication skills (verbal and written). • Ability to read and understand written procedures (SOPs) and follow verbal instructions. • Strong punctuality and attendance record. • Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) • Willingness to learn and apply Lean manufacturing and PPI Continuous Improvement tools. • Ability to work independently with occasional assistance. • Ownership mentality and ability to meet established deadlines and targets. • Willingness to acquire new knowledge and skills. • Understanding of production schedules and ability to prioritize tasks accordingly. • Hands-on experience in a Chemistry laboratory is preferred. • Knowledges of Chromatography software a plus. Education • At least 1+ years of experience in manufacturing environment • A bachelor's in chemistry and or biotechnology preferred. Physical requirements: • Ability to lift and/or move up to 40 pounds. • Regularly required to stand; walk; use hands & finger to handle & feel. • Frequently required to sit and reach with hands and arms. • Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. • Work Environment: While performing the duties of this job, the employee is regularly exposed to toxic or caustic chemicals. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. Personal protective equipment's: • Job requires wearing lab coats, Safety glasses, gloves & safety shoes all company provided. Non-Negotiable Hiring Criteria: • Must be in compliance with GMP, QSRs, ISO and IVD regulations in the performance of department responsibilities. • Ability to read and write English and understand instructions written or orally in English. • Ability to add, subtract, multiply and divide in all units of measure, whole numbers, fractions and decimals. • Knowledge of Word, Excel and Outlook. Job Type & Location This is a Contract position based out of Sunnyvale, CA. Pay and Benefits The pay range for this position is $28.00 - $28.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Sunnyvale,CA. Application Deadline This position is anticipated to close on Dec 31, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Shift: Mon-Fri 6a - 230pm Duration: 12 Months Pay range: $28.00 Hourly - $28.00 Hourly Onsite Job Work in a team-based environment within a manufacturing lab responsible for synthesizing and testing ion exchange media used in chromatography consumables. Key Responsibilities: •Perform testing and qualification of resin products on specialized instruments to meet customer demand. •Record and report test results accurately and maintain proper documentation. •Complete complex production work-orders according to established procedures. •Analyze data, derive conclusions, and prepare reports based on findings. •Collaborate with cross-functional teams. •Adhere to ISO 9001 guidelines and corporate quality policy to ensure high-quality standards. •Follow EH&S safety requirements and actively participate in safety improvement activities. •Continuously identify areas for improvement and propose countermeasures. •Maintain a clean and organized laboratory environment. Knowledge, Skills and Abilities: •Knowledge of Good Laboratory and Manufacturing Practices and standards. •Proficiency in Microsoft Office: Excel, Word, PowerPoint. •Good mathematical, problem-solving, and organizational abilities. •Excellent communication skills (verbal and written). •Ability to read and understand written procedures (SOPs) and follow verbal instructions. •Strong punctuality and attendance record. •Familiarity with hand tools regularly used (wrenches, torque drivers, tweezer, etc.) •Willingness to learn and apply Lean manufacturing and PPI Continuous Improvement tools. •Ability to work independently with occasional assistance. •Ownership mentality and ability to meet established deadlines and targets. •Willingness to acquire new knowledge and skills. •Understanding of production schedules and ability to prioritize tasks accordingly. •Hands-on experience in a Chemistry laboratory is preferred. •Knowledges of Chromatography software a plus. Education •At least 1+ years of experience in manufacturing environment •A bachelor's in chemistry and or biotechnology preferred. Physical requirements: •Ability to lift and/or move up to 40 pounds. •Regularly required to stand;walk;use hands & finger to handle & feel. •Frequently required to sit and reach with hands and arms. •Specific vision abilities required by this job include close vision, color vision and ability to adjust focus. •Work Environment: While performing the duties of this job, the employee is regularly exposed to toxic or caustic chemicals. The employee is frequently exposed to fumes or airborne particles. The employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. Personal protective equipment's: •Job requires wearing lab coats, Safety glasses, gloves & safety shoes all company provided. Non-Negotiable Hiring Criteria: •Must be in compliance with GMP, QSRs, ISO and IVD regulations in the performance of department responsibilities. •Ability to read and write English and understand instructions written or orally in English. •Ability to add, subtract, multiply and divide in all units of measure, whole numbers, fractions and decimals. •Knowledge of Word, Excel and Outlook. Employee Benefits: At LanceSoft, full time regular employees who work a minimum of 30 hours a week or more are entitled to the following benefits: Four options of medical Insurance Dental and Vision Insurance 401k Contributions Critical Illness Insurance Voluntary Permanent Life Insurance Accident Insurance Other Employee Perks About LanceSoft LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

Job Description THE ROLE: QA Lab Supervisor Travel Requirement: N/A FLSA Status: Hourly Non-Exempt Employment Category: Full Time Regular Pay Range: $20.25 - $22.75 Generous Brands is dedicated to inspiring people to thrive through the power of vibrant nutrition through its leading brands, Bolthouse Farms, Health-Ade, and Evolution Fresh. Generous Brands partners with SAMBAZON to manufacture, distribute and sell SAMBAZON branded beverages. Bolthouse Farms is a pre-eminent provider of chilled juice, smoothies, shakes, and protein drinks. Health-Ade is the fastest growing kombucha brand, dedicated to creating bubbly beverages that boost gut health. Evolution Fresh is a premier cold-pressed juice brand with national availability. And, SAMBAZON beverages bottle the superfruit power of acaí in juice and natural energy cans. The company operates its North American business from facilities in Southern California, and the Greater Chicago Area. To learn more, please visit *********************** WHAT YOU'LL BE RESPONSIBLE FOR IN THIS ROLE The Microbiology Lab Tech will execute the daily laboratory operation and ensure that the Laboratory Quality Management System is implemented and maintained in accordance with ISO 17025 standards. This position will handle data/report and resources (equipment, supplies) to ensure that required testing is completed. WHAT WE'RE LOOKING FOR Maintain records and manages all aspects of testing activities Prepare media and agar plates for testing and recording on media logs Perform pour & petrifilm plating, count plates and record results Report out of specification conditions and summarize test results Perform sample preparation and testing of raw materials, finished products and others Complete data/information recording, follow the status of testing, generating reports and communicating findings of those test results supporting the manufacture of quality products Run membrane filtration (water testing method) and PCR method and record results Maintain the safety, cleanliness and hygienic laboratory work environment including periodic/planned maintenance, cleaning and monitoring of equipment and the work areas Follow lab safety protocols to maintain lab hygiene and eliminate cross contamination Participate in proficiency program and test control samples Assist or perform other duties/projects as assigned ADDITIONAL REQUIRED QUALIFICATIONS: Ability to operate microbiology instruments and equipment including equipment preventive maintenance, calibration, checks and verification Ability to perform microbiological swabbing and air monitoring (e.g. environment program for the micro lab) Ability to work alone and as part of a team to ensure the department goals, accuracy, and timeliness and cost effectiveness are met Show competency through successful completion of proficiency testing MINIMUM QUALIFICATIONS: Associate degree is required or bachelor's degree in one of the following areas: Food Science, Microbiology, Chemistry, Biochemistry or related areas. Equivalent experience in a related field can be substituted for education Math skills combined with the ability to perform and understand scientific based tests and results Ability to communicate effectively in oral and written forms Knowledge of computer applications such as Microsoft Office Excel, Word, etc. Communicate and interact well with others in the laboratory and manufacturing environment Ability to work with minimal supervision and apply Good Laboratory Practices Valid Driver's License PREFERRED QUALIFICATIONS: Some experience in Microbiology/Chemistry lab in the food-processing environment PHYSICAL DEMANDS & ENVIRONMENTAL HAZARDS: The work environment for this position will be typical of the manufacturing facility. There are portions of the job that will require working in cold (< 40°ree;F) environments, in warm environments (>90°ree;F), and loud environments. Must be able to work in a wet, cold, or hot environment Must be able to lift up to 50lbs HOURS & WORKDAYS: 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory. WHAT WE OFFER plus more ! Our rich benefits packages are designed to support the health and well-being of both our eligible team members and families. Medical, Dental & Vision Group Life and AD&D Voluntary Life and AD&D Group Short & Long-Term Disability 401(k) Paid Time Off Flexible Spending Accounts Employee Assistance Program Gym Membership Discounts EQUAL EMPLOYMENT OPPORTUNITY We are an equal opportunity employer committed to fostering a culturally diverse organization. We strive for inclusiveness and a workplace where mutual respect is paramount. We encourage applications from a diverse pool of candidates, and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, religion, sex, age, national origin, disability, sexual orientation, gender identity and expression, or veteran status. We will provide reasonable accommodation for qualified individuals with disabilities, as needed, to assist them in performing essential job functions. REASONABLE ACCOMMODATIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. If you are interested in applying for employment with Generous Brands and need special assistance to apply for a posted position, or if you believe you do not meet any of the required qualifications of a posted position due to a protected disability and would like to explore the possibility of an accommodation, please contact our Talent Acquisition team at *******************************. RECRUITMENT AGENCIES: Confidential does not accept unsolicited agency resumes. Generous Brands is not responsible for any fees related to unsolicited resumes. 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory.

THE ROLE: QA Lab Supervisor * Travel Requirement: N/A * FLSA Status: Hourly Non-Exempt * Employment Category: Full Time Regular * Pay Range: $20.25 - $22.75 Generous Brands is dedicated to inspiring people to thrive through the power of vibrant nutrition through its leading brands, Bolthouse Farms, Health-Ade, and Evolution Fresh. Generous Brands partners with SAMBAZON to manufacture, distribute and sell SAMBAZON branded beverages. Bolthouse Farms is a pre-eminent provider of chilled juice, smoothies, shakes, and protein drinks. Health-Ade is the fastest growing kombucha brand, dedicated to creating bubbly beverages that boost gut health. Evolution Fresh is a premier cold-pressed juice brand with national availability. And, SAMBAZON beverages bottle the superfruit power of acaí in juice and natural energy cans. The company operates its North American business from facilities in Southern California, and the Greater Chicago Area. To learn more, please visit *********************** WHAT YOU'LL BE RESPONSIBLE FOR IN THIS ROLE The Microbiology Lab Tech will execute the daily laboratory operation and ensure that the Laboratory Quality Management System is implemented and maintained in accordance with ISO 17025 standards. This position will handle data/report and resources (equipment, supplies) to ensure that required testing is completed. WHAT WE'RE LOOKING FOR * Maintain records and manages all aspects of testing activities * Prepare media and agar plates for testing and recording on media logs * Perform pour & petrifilm plating, count plates and record results * Report out of specification conditions and summarize test results * Perform sample preparation and testing of raw materials, finished products and others * Complete data/information recording, follow the status of testing, generating reports and communicating findings of those test results supporting the manufacture of quality products * Run membrane filtration (water testing method) and PCR method and record results * Maintain the safety, cleanliness and hygienic laboratory work environment including periodic/planned maintenance, cleaning and monitoring of equipment and the work areas * Follow lab safety protocols to maintain lab hygiene and eliminate cross contamination * Participate in proficiency program and test control samples * Assist or perform other duties/projects as assigned ADDITIONAL REQUIRED QUALIFICATIONS: * Ability to operate microbiology instruments and equipment including equipment preventive maintenance, calibration, checks and verification * Ability to perform microbiological swabbing and air monitoring (e.g. environment program for the micro lab) * Ability to work alone and as part of a team to ensure the department goals, accuracy, and timeliness and cost effectiveness are met * Show competency through successful completion of proficiency testing MINIMUM QUALIFICATIONS: * Associate degree is required or bachelor's degree in one of the following areas: Food Science, Microbiology, Chemistry, Biochemistry or related areas. Equivalent experience in a related field can be substituted for education * Math skills combined with the ability to perform and understand scientific based tests and results * Ability to communicate effectively in oral and written forms * Knowledge of computer applications such as Microsoft Office Excel, Word, etc. * Communicate and interact well with others in the laboratory and manufacturing environment * Ability to work with minimal supervision and apply Good Laboratory Practices * Valid Driver's License PREFERRED QUALIFICATIONS: * Some experience in Microbiology/Chemistry lab in the food-processing environment PHYSICAL DEMANDS & ENVIRONMENTAL HAZARDS: * The work environment for this position will be typical of the manufacturing facility. There are portions of the job that will require working in cold (< 40°F) environments, in warm environments (>90°F), and loud environments. * Must be able to work in a wet, cold, or hot environment * Must be able to lift up to 50lbs HOURS & WORKDAYS: * 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory. WHAT WE OFFER plus more! Our rich benefits packages are designed to support the health and well-being of both our eligible team members and families. * Medical, Dental & Vision * Group Life and AD&D * Voluntary Life and AD&D * Group Short & Long-Term Disability * 401(k) * Paid Time Off * Flexible Spending Accounts * Employee Assistance Program * Gym Membership Discounts EQUAL EMPLOYMENT OPPORTUNITY We are an equal opportunity employer committed to fostering a culturally diverse organization. We strive for inclusiveness and a workplace where mutual respect is paramount. We encourage applications from a diverse pool of candidates, and all qualified applicants will receive consideration for employment without regard to race, color, ethnicity, religion, sex, age, national origin, disability, sexual orientation, gender identity and expression, or veteran status. We will provide reasonable accommodation for qualified individuals with disabilities, as needed, to assist them in performing essential job functions. REASONABLE ACCOMMODATIONS Reasonable accommodations will be made to enable individuals with disabilities to perform the essential functions. If you are interested in applying for employment with Generous Brands and need special assistance to apply for a posted position, or if you believe you do not meet any of the required qualifications of a posted position due to a protected disability and would like to explore the possibility of an accommodation, please contact our Talent Acquisition team at *******************************. RECRUITMENT AGENCIES: Confidential does not accept unsolicited agency resumes. Generous Brands is not responsible for any fees related to unsolicited resumes. 2nd shift, workdays will vary, 2:00pm - 10:30pm & 4:00pm - 12:30am when business requires overtime and weekends will be mandatory.

We are hiring a Powder Formulation Technician. The Powder Formulation Technician will be responsible for formulation of powdered media. 3rd Shift: 9:00 pm- 5:30 am At FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences), we turn curiosity into breakthroughs that advance the field of life sciences. By offering a comprehensive portfolio of products and services in cell culture media, discovery research reagents, recombinant growth factors and proteins, fine chemicals, and critical assay materials, we partner with the brightest minds in biotech and pharma to tackle the world's biggest health challenges. Imagine being part of a team that enables life-changing discoveries like new vaccines, therapies, and advancements in regenerative medicine. Our culture fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an impact, your future belongs with us at FUJIFILM Irvine Scientific (dba FUJIFILM Biosciences). Our headquarters in Santa Ana, California, is surrounded by world-class schools, lush parks, and scenic beaches like Laguna and Huntington, making it an ideal place to live, work, and explore. With additional campuses across the US, Europe, China, and Japan, we offer opportunities to make a difference worldwide. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Responsibilities: Formulates Powder media formulas per manufacturing protocols utilizing various weighing equipment such as scales and balance. Uses Mettler-Toledo IND780 terminal system in conjunction with the SAP ERP system to ensure correct raw materials assigned in the batch record are weighed at the specified quantity. Suggest changes in departmental procedures and processes (SOPs) as needed. Performs and documents line clearance at the start of each formulation event. Maintains all required logs and associated documentation. Assures that all chemicals are stored and labeled properly. Performs process scale checks on all required equipment including scales and balances. Keeps work area, utensils, tanks, mills, and equipment clean and organized. Ensures that supplies needed such as weigh boats, gloves, lab coats, etc. are well stocked in their designated areas. Orders supplies or informs Lead/Supervisor if supplies need to be ordered. Follows all safety procedures and works in a safe manner including wearing all required personal protective equipment. Understands and follows procedures to ensure that chemicals are handled properly. Good understanding of metric system and its conversions. Follows and actively participates in sustaining the 6S program in the area. Other duties as requested by Lead or Supervisor. Required Skills/Education: High School Diploma or equivalent. Background in medical devices, diagnostics, food/vitamin processing, or pharmaceuticals. 1-2 years of hands on experience General education about chemicals and proper handling (college level science preferred). Working knowledge of metric system. Good understanding of current Good Manufacturing Practices (cGMPs). Ability to speak, read, and write English. Good oral and written communication skills. Salary and Benefits: For California, the base salary range for this position is $19.65 - $25.51 per hour. Compensation for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience, location, etc.). Medical, Dental, Vision Life Insurance 401k Paid Time Off *#LI-onsite EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (*******************).

Job DescriptionDescription: The Microbiology Lab Technician will be responsible for general laboratory testing at Grower Direct Nut Facilities. ESSENTIAL FUNCTIONS • Testing product samples. • Preparation of test samples. • Testing of chemical and sensory parameters. • Environmental monitoring program: o Trending of results o Water and air testing • Follow Good Laboratory practices to maintain a clean, sterile work environment. • Performing all microbiological, chemical and physical tests as required on products. • Recording results accurately and timely. • Notifying supervisor or manager when results are not within specification, or abnormal. • Environmental monitoring program swabbing. • Follow procedures according to BRC/ISO/AOAC Programs and requirements. • Obtain passing scores on AOAC Proficiency testing programs. • Follows and ensures adherence to established Grower Direct Nut Co., local, state, and federal regulations and requirements as well as food safety, sanitation, food production and nutritional guidelines. • Established and ensures adherence to procedures and standards, which agree with these regulations, requirements and guidelines. Requirements: 1. Ability to work as part of a team. 2. Ability to perform complex math functions. 3. Experience in a food processing plant in a QA Role. 4. Working knowledge of GMPs, Food Safety and HACCP Systems. 5. Must be Skilled at Excel, Word, PowerPoint, Email Programs. 6. Must be able to work overtime and/or weekends as needed. 7. Positive attitude, high energy, flexibility, and personal initiative. 8. Read, write and general comprehension of English. 9. Accurately complete documents and paperwork that is related to the job. 10. Punctual and good attendance is necessary. 11. Strong communication skills, both verbal and written. 12. Must be able to work under the guidelines of lab safety and GLP (Good Lab Practices). 13. Microbiology experience or college equivalent coursework preferred.

Senior Formulation Technician Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Shift: First Shift - 06:00 AM to 02:30 PM Pay Rate: $20 to $22 per hour Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands. Summary: The Media Process Technician I works as part of a team to manufacture dehydrated and liquid cell culture media. The technician follows batch record instructions, weighs raw materials ranging from micrograms to kilograms, calibrates equipment, operates milling equipment, performs sterile filtration, and completes media manufacturing tasks. Responsibilities also include performing standard product testing (osmolality, pH, turbidity) and working closely with cross-functional groups such as R&D, procurement, quality, process technology, marketing, as well as internal/external customers and vendors. Responsibilities Stage and compound raw materials within specified weight tolerances (micrograms to kilograms). Perform milling, blending, aseptic liquid filling, and process control monitoring. Follow GMP and departmental procedures to manufacture dehydrated and liquid culture media according to production schedules. Complete all required documentation neatly, accurately, and in compliance with GMP. Perform cleaning, inspection, calibration, and assist in equipment maintenance; maintain logs and records. Troubleshoot equipment issues. Handle raw materials following GMP and Safety requirements. Use laboratory and production equipment (pipettors, balances, osmometer, turbidimeter, pH meters). Work safely to maintain an injury-free and incident-free workplace. Carry out assigned responsibilities under supervision. Promote a positive team environment through effective communication and engagement. Work overtime when required. Perform other duties as assigned to support business goals. Required Skills & Qualifications BS in Chemistry or related field (or equivalent combination of education, training, and experience). Minimum 6 months of experience in a high-paced chemistry lab or manufacturing environment. Ability to read, write, and follow testing and inspection procedures. Ability to maintain neat, accurate, complete records and logs. Mechanical aptitude; ability to disassemble and reassemble equipment. Good communication skills; able to work independently or as part of a team. Flexibility to work varying schedules, including overtime. Strong attention to detail and ability to focus on tasks continuously. Basic experience weighing multiple components. Basic computer skills, including MS Excel, Word, and PowerPoint. Ability to lift or move approximately 40 lbs. Desired Skills (Preferred but Not Required) Statistical analysis experience using Excel or Minitab. Experience handling multiple components and performing precise weighing. Familiarity with GMP environments, sterile filtration, and laboratory instrumentation. TekWissen Group is an equal opportunity employer supporting workforce diversity.