Quality control analyst jobs in Redondo Beach, CA

With a legacy spanning over 35 years, Harris Spice has been a trusted partner and leading supplier of high-quality spices, herbs, and innovative seasoning blends. With international facilities and a global supply chain, we proudly serve multiple channels of trade-including industrial bulk, food service, and retail. Our commitment to excellence, quality and consistency has earned us the trust of some of the nation's largest and most recognized brands. As Harris Spice continues to grow, we are dedicated to cultivating a dynamic, inclusive workplace where innovation thrives. We're looking for diverse, talented individuals who are ready to grow with us and help strengthen a brand known for trust, quality, and bold flavor solutions. Position Overview/Job Summary: We are looking for a 1st shift (4:30am-1:00pm) Quality Control Technician to join our team. The Quality Control Technician is responsible to ensure food safety and quality of plant through enforcement of HACCP, and Good Manufacturing Practices (GMPs) are followed by all personnel and to confirm each product meets specifications and quality parameters. Essential Job Functions: Performing pre-operational inspections at beginning of shift or production line changeovers to achieve on-time start-up and first-time quality. Collect raw material samples upon receipt and report any discrepancies to Quality Manager. Verify correct raw materials and packaging are being picked, staged, and used in production. Determine the acceptability of products using visual inspections, sampling, and testing protocols (when necessary). Perform detail-oriented tasks to support production such as checking legible lot codes, “best by” dates, container seals, handling production line rejects, etc. Enforce good manufacturing practice Provide support to the production department to minimize downtime and run efficiently. Maintain orderly paperwork and verify accurate documentation among production, quality, sanitation, maintenance, warehouse, and R&D departments. Organize production and quality records by following established protocol. Perform, log, and verify metal detector checks and provide training to production coworkers. Escalate issues of non-conforming products in a timely manner to management and segregate or place on hold. Interact and support cross-functional department personnel and adapt to change in a fast-paced environment. Ability to work with minimum supervision. Follow and enforce personal safety procedures and escalate to management. Other duties as assigned. This position has no direct reports but may assist in training coworkers and/or covering absences. This describes just some of the main duties, activities and responsibilities for the role which may change at any time with or without prior notice. Skills/Qualifications: 1-2 years of experience in a quality or lab role, preferably within a food manufacturing environment. Knowledge of sanitary food lab techniques and equipment. Able to read Standard Operating Procedures and follow instructions. Able to interpret product specifications. Good communication skills Understand and apply company and customer quality standards. Comfortable working with Microsoft Office and other production or lab information systems as needed. English fluency required, bilingual Spanish a plus. Physical Requirements: Ability to stand in a lab environment, ability to lift 55lbs, and handle food samples in a sanitary manner Sit, use hands & arms, twist, bend, push or pull Walking, standing, stooping, bending, kneeling, pulling, pushing, twisting, climb etc. The statements herein are intended to describe the general nature and levels of the work performed by employees, but are not a complete list of responsibilities, duties, and skills required of personnel so classified. Furthermore, the job description does not constitute a written or implied contract for employment. Harris Spice reserves the right to revise or change job duties and responsibilities as the need arises. Equal Employment Opportunity Statement Harris Spice is a certified Minority-owned business. Our business is an equal opportunity employer committed to a diverse and inclusive workforce. Applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other protected status.

About Us Haskel, an Ingersoll Rand Company, is a High-Pressure Technology Solutions. We specialize in Air-Driven Liquid Pumps, Air-Driven Refrigerant Pumps, Hydraulic Drive Compressors, Gas Booster Compressor System, BuTech High-Pressure Valves and Hydrogen Valves Fitting and Tubing. Job Summary This role is responsible for ensuring the quality control cell is actively engaged to meet daily customer demand and production schedule. Performs receiving, in-process and/or final inspection of hardware. Conducts complex inspections as defined by quality/inspection plans or per directions of quality management/engineering. Uses a complete range of precision tools and instruments requiring advanced inspection skills and techniques. Ensures that all gauges/tools used are properly calibrated. Identify accurate and efficient means of inspection techniques. Works with general/minimal supervision. Train and provide directions to the Quality Control team under the supervision of the Quality Control Manager. Responsibilities The Quality Team Lead will inspect products by using a variety of inspection tools/devices, work instructions and computer to perform a series of inspections to correctly verify incoming parts, in-process and completed assemblies. Verify supplier material certifications, including special processes, and ensure compliance with quality/PO requirements. Creates supporting documentation (data books, certificates of conformance, etc…) Support disposition of discrepant materials (MRB) in accordance with appropriate quality procedures and maintain low inventory of on-hold parts. Verifies first articles from suppliers and internal departments. Prepares and processes records and reports to document supplier/operations performance. Qualify supplier components and/or systems for assuring conforming product. Adheres to calibrations system of inspection, measuring and test equipment. Applies Statistical Quality Control techniques as directed. Assist with interpretation of drawings, specifications and quality requirements. Properly process goods for outside processing, investigates and evaluates component parts returned and nonconforming product. The Quality Team Lead provides effective training to the quality control cell and ensures safety and quality standards are always maintained. Work with supervisor to manage and prioritize staffing assignments to ensure customer demand and the production schedule are met. Use basic problem-solving skills to ensure stable operation of the quality control cell. Report problems or concerns with quality, processes, equipment, materials and labor to Quality management. Work closely with support staff such as Purchasing/Planning, Manufacturing Engineering, Production Supervisor, Materials/Warehouse to resolve issues. Observe, maintain, coordinate and complete standard work. Update production metrics and facilitate regular team communication. Identify and support continuous improvement efforts with Quality management. Sustain and drive lean manufacturing and 5S activities. Follow documented policies and procedures as designated by the company's Quality System. Basic Qualifications Ability to read and interpret documents such as safety rules, engineering drawings, operating and maintenance instructions, Material Standards, Quality Plans, Control Plans and Inspection Test Plans. Experience with Microsoft Office (Word, Excel, Outlook). Ability to communicate effectively through oral and written communications. Ability to analyze and solve problems. Ability to work with others collaboratively. Strong organizational skills. Preferred Experience leading teams or projects strongly desired. Quality Control experience. Lean manufacturing and continual process improvement experience. Educational Requirements High School diploma or equivalent Five years + of related experience and a minimum of two leading teams. LIP Eligible Role This position is eligible for the LIP (Local Incentive Plan) of up to 4%. The pay range takes into account a wide range of factors that are considered in making compensation decisions including, but not limited to, skills; experience and training; licensure and certifications; and other business and organizational needs. The disclosed pay range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At Ingersoll Rand, it is not typical for an individual to be hired at or near the top of the pay range for their role and compensation decisions are dependent on the facts and circumstances of each case. At Ingersoll Rand, we think and act like owners - of our business, our communities, our planet, and our health too. The Ingersoll Rand benefits program provides you with the tools and resources to take accountability for your health so that we can continue to help make life better. Benefits of employment and include; Medical and Prescription drug plans Wellness and Chronic disease management programs Dental, vision, life/AD&D insurance Short- and Long-term disability Health Savings Account Flexible Spending Account Parental Leave Employee Assistance Program Discount Program Employee Stock Grant 401k plan with a company match 3 weeks of paid vacation and 11 paid holidays throughout the calendar year Voluntary benefits include legal, accident, and critical illness protection

Quality Control Inspector Needed in Camarillo Direct Hire Industry: BioTech, Pharmaceuticals Pay range: $23 - $24/hour Monday - Friday 7am - 3:30pm Must Have * Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820. * Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices. * Minimum of 2 years' experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment. Job Summary Performs quality control inspections in all aspects of operations, checks, and test during the manufacture of products. Inspect incoming materials, and products at different stages of production. Records observations and make recommendations for improving processes. Essential Functions * Responsible for all activities involving quality inspections and compliance with applicable regulatory requirements; * Conduct inspection and testing related to: ► Incoming product. ► First article. ► In-process. ► Final. * Initiate nonconformance reports (NCR). * Performs all aspects of testing related to manufacturing. o Incoming inspections o In-process inspection. o Final Inspection release of finished goods. o Document review. o Supports cross functional departments investigate potential non-conformance's observed * Ensures that all inspections and procedures are properly completed and documented. * Perform pre and post-inspection of product gamma irradiation process. * Approve or reject raw materials with respect to quality standards and communicate results to all pertinent parties. * Initiate nonconformance reports (NCR) for all non-conforming material identified throughout operations * Prepare and submit Metrics reports to the quality supervisor or QC lead * Comply with all safety requirements ensuring work areas meet standards. * May be required to report to multiple facilities within a 2-mile radius. * Job Order document review and release * Other duties as assigned Education * High School Diploma or equivalent with 2 years of experience in quality control inspections. Required Experience & Competencies * Understanding of global pharmaceutical product regulations with experience with ISO 9001 and/or 13485:2003 and 21 CFR Parts 210 and 211 and/or Part 820. * Demonstrated ability to perform GMP operations following detailed SOPs, maintaining training, and good documentation practices. * Minimum of 2 years' experience with technical documentation for quality activities. This experience should be in the areas of the Quality manufacturing that includes quality inspections and corrective actions in a pharmaceutical or medical device environment. * Solid organizational and planning skills required. * Ability to communicate effectively, verbally and in writing, demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors. * Must be able to work effectively and efficiently in a team environment. * Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction. * Must display personal accountability for results and integrity. * Must display eagerness to learn and continuously improve. * Must have uncompromising dedication to quality. * Good general mathematical skills. * General knowledge and use of measuring devices such as calipers, tape measures, rulers, pin gauges * General computer skills. All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

Become part of a team that champions wellness worldwide! CAPTEK Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world's most successful brands. Summary: The Quality Control Chemist III plays a senior role in the Quality Control (QC) laboratory, responsible for leading complex analytical testing and providing cross-functional support for the testing and release of raw materials and finished goods. In addition to performing advanced chemical analyses, the Chemist III supports the QC Supervisor with daily operations, mentoring junior chemists, and ensuring compliance with cGMP regulations. This role bridges technical execution with leadership by ensuring timely, accurate testing while driving continuous improvement in quality systems. Essential Duties and Responsibilities: Perform advanced analytical testing on raw materials and finished goods using High-Performance Liquid Chromatography (HPLC), Gas chromatography (GC), Ultraviolet and Visible (UV-Vis), Fourier Transform Infrared Spectroscopy (FTIR), Atomic Absorption Spectrometry (AA), and other techniques, ensuring data accuracy and compliance with established specifications. Lead investigations of out-of-specification (OOS) results, including root cause analysis and documentation of corrective actions. Review and approve analytical data and Certificates of Analysis (CoAs) for accuracy and completeness prior to supervisor sign-off. Provide technical support and guidance to QC Chemists I and II, ensuring adherence to SOPs, test methods, and good documentation practices. Collaborate with the QC Supervisor to coordinate daily sample flow, prioritizing testing schedules for raw material (RM) and finished goods (FG) to meet production and release timelines. Support the Supervisor in ensuring timely review and disposition of RM and FG, including the verification of data used for release decisions. Assist in training QC staff on new test methods, instruments, and safety procedures. Acts as a liaison between the QC lab and other departments (QA, Production, Planning and Purchasing) for RM/FG testing needs, troubleshooting, and process improvements. Troubleshoot OOS results on raw materials with vendors, including coordinating retesting, reviewing vendor CoAs, and collaborating on corrective actions to ensure material compliance and timely resolution. Troubleshoot finished goods OOS results and escalate findings through proper Quality management channels, involving Sales and Business teams as necessary, based on management's approval. Perform method development and validation as needed, with documentation aligned to regulatory and internal standards. Participate in internal and external audits, provides data and justifications as needed. Assist in the maintenance, calibration, and troubleshooting of laboratory instruments. Support contract testing coordination with third-party labs for specialized assays or confirmatory testing. Draft and revise SOPs, test methods, and other controlled documents. Work closely with the QC Supervisor/Quality Management to manage the workflow for raw material and finished good testing, ensuring timely completion and release. Participate in cross-functional meetings with QA, Production, and Purchasing to align testing priorities with business needs. Assist RM/FG CoAs approvals and releases materials/products as needed. Lead continuous improvement initiatives to enhance testing efficiency, reduce errors, and streamline processes. Engage in interdepartmental collaboration to resolve technical issues affecting RM/FG quality, including non-conformance investigations. Generates appropriate and complete finished product Certificates of Analysis per product requirement and verifying finished product CoA claims as accurate, true, and complete. Prepares sample, solvents/reagents, and systems for testing, calculates data and results, documents the entire procedure, disposes and safely cleans up solutions in the hazardous chemicals waste (under the hood), discards all disposables in appropriate waste containers and properly and safely cleans all glassware, work-stations, and apparatus/equipment used. Safely and appropriately uses tools such as scalpels, glassware, dishes, weighing dishes, pipets, burets, volumetric flasks, ovens, furnaces, stirrers/heat-plates, ultrasonicators, baths, balances, titrators, chemically resistant containers, graduated cylinders, beakers, spectrophotometer cuvettes and permanent markers. Ensure lab compliance with cGMP, safety, and environmental regulations, including proper chemical handling and waste disposal. Safely uses reagents (substance or compounds) such as water, acids and bases of varying concentration, buffers, and solvents ranging from weak to strong that are added to a system in order to bring about a chemical reaction or to see if a reaction, interaction, or separation occurs. Obtains sample and checks sample label and appearance to make sure that the sample is correct. Accurately weigh, label, log and document all samples and in-use apparatus, tools, equipment/instruments, and solvents/regents. Adheres to all safety, cGMP, and Captek's Standard Operating Procedures, particularly those of the 6 series, while par-taking in the accountability of all QC staff to do the same. Quality Control Chemist III must have the ability to be flexible, handle multiple projects simultaneously and adapt to increased business demands. Perform additional duties as assigned. Qualifications: 5+ years of experience in a cGMP-regulated QC laboratory, with a focus on raw material and finished product testing. Proficient with advanced analytical instruments (HPLC, GC, UV-Vis, FTIR, AA) and method troubleshooting. Experience leading technical teams or mentoring junior chemists. Strong technical writing, problem-solving, and data analysis skills. Excellent communication skills, with the ability to work cross-functionally. Knowledge of regulatory requirements (21 CFR Part 111, USP, FDA) in dietary supplements or pharmaceutical industries is a plus. Education/Experience: Bachelor's degree in Chemistry, Biochemistry, or related scientific field (required); Master's degree preferred. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts, fumes, or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate. 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 accommodation may be made to enable individuals with disabilities to perform the essential functions. Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear. EEOC Statement: CAPTEK is an equal employment opportunity employer. In order to provide equal opportunities to all individuals, employment decisions will be based on merit, qualifications, and abilities, not on any mental or physical disability. We comply with the law regarding reasonable accommodation for disabled employees and applicants. We do not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), reproductive health decisions, gender, gender identity, gender expression, religious creed, disability (mental and physical) including HIV and AIDS, medical condition (cancer and genetic characteristics ), genetic information, age, marital status, sexual orientation, military and veteran status, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment.

FirstCarbon Solutions (FCS), an ADEC Innovation, is focused on improving the world we live in. It's our goal to improve the lives of all the people we work with, whether they are clients, partners, or colleagues. Come join our team of amazing professionals dedicated to making the world a better place! FirstCarbon Solutions is searching for an Air Quality Scientist (CG06 - CG07) to join our team. The ideal candidate will be able to perform emission, air dispersion, and/or health risk modeling independently within minimal supervision. This role requires good knowledge of air quality and greenhouse gas emission regulations and legislative updates. The candidate needs to be a strong writer with extensive experience writing air quality, greenhouse gas, and energy sections pursuant to CEQA. The ideal candidate will also provide training and mentorship to junior staff and promote teamwork through interpersonal skills. This will report to the Senior Air Quality Scientist. This role is an evergreen position, meaning we are always looking for talented individuals to join our team. Applications for this position are continuously accepted and reviewed on a rolling basis. Duties and Responsibilities Review site plan and project information, coordinate with client on data needs, and gather all data necessary to conduct technically and legally defensible air quality/air dispersion/health risk modeling Author technically and legally defensible air quality, greenhouse gas, and energy analyses and technical appendices to be included in CEQA and NEPA environmental documents. Use approved software models, such as the California Emissions Estimation Model (CalEEMod) and EMFAC, to estimate a project's air pollutant emissions. Develop and quantify emission reduction potential of appropriate mitigation measures, if needed Use air dispersion models, such as AERMOD and HARP, to evaluate the project's construction-related and operational-related emission and health impacts. Strong knowledge of various Air District guidelines and latest greenhouse gas emission legislative updates Skills Ability to conduct air quality assessments. CalEEMod, AERMOD, and/or HARP experience Provide effective and quality communication through written and oral methods. Marketing and proposal preparation. Demonstrated proficiency in MS Office applications, especially Word and Excel, as well as internet usage. Education and Experience Bachelor's degree in environmental sciences or related field required, master's degree in environmental management or equivalent a plus. 5-7 years of experience in Environmental Services, air quality and/or greenhouse gas emission inventory quantification and modeling skills including AERMOD, CalEEMod, ArcGIS and other software models. Other air permitting or assessment/modeling experience highly desired. Work Environment The position operates in a dynamic and highly collaborative working environment. FCS provides our staff the opportunity to elect remote, hybrid home/office as well as as-needed field assignments (under COVID-19 safety regulations). This role routinely uses standard office equipment. This position may require some travel to attend meetings as well as fieldwork. Competitive, progressive benefits including Salary: $84,300 - $109,100 FCS offers competitive salaries and robust benefits with opportunities for personal and professional development. If you want to work in a collaborative, creative work environment where you can provide meaningful contributions while being challenged to grow on the job, then you are encouraged to apply! Remote/Hybrid/in-office work location options Escalating PTO structure Up to 10 paid holidays (up to 4 are flexible holidays) Full health care package: Up to 100% employer-paid employee medical and 55% eligible dependent coverage* 80% employer-paid dental and vision Employer-paid Life and AD&D insurance Short- and long-term Disability insurance Employee Assistance & Wellness Program 401k & Roth Pet insurance discounts 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. While performing the duties of this job, the employee is regularly required to talk and hear; have hand/finger dexterity; and reach with hands and arms. The employee will spend extended periods of time in front of a computer/laptop. Specific vision abilities required by this job include close vision, distance vision, and ability to adjust focus. Compliance with all ADECi & FCS Travel and Workspace Policies that align with the CDC, local, state, and federal guidelines must be followed and upheld. Information Security Adhering to all policies, guidelines, and procedures pertaining to the protection of information of the organization, employees must maintain confidentiality of all sensitive information to which they are given access. They are also responsible for reporting actual or suspected events or incidents, including vulnerabilities or breaches, that may affect the confidentiality, integrity, and availability of information to members of the Management Team. Mutual respect is fundamental. Fundamental to our teams. Fundamental to our clients. Fundamental to the communities we serve and live in. Fundamental to the landscapes we work within. We need you and your unique talents, history, and background to become the Company we aspire to be. We insist upon a culture of common respect, expect transparency, and celebrate the fundamental value and dignity of all individuals. Our mutual equality as humans is the path to diverse and innovative collaboration. We cultivate integrity, driving us to growth, and allowing us to achieve more together than we could ever hope to as individuals. FCS offers competitive salaries and robust benefits with opportunities for personal and professional development. If you want to work in a collaborative, creative work environment where you can provide meaningful contributions while being challenged to grow on the job, then you are encouraged to apply!

The Production Scientist is responsible for a upscaling R&D small scale work into GMP large scale manufacturing, Oversee production activities of the assigned projects, collect and analyze GMP data, Author and review quality documents such as MBPR, R.A, PPQ protocol, drive yield and process improvement projects, update the customer with the GMP activities, ensuring production processes meet quality standards, or maintaining equipment efficiency. This role contributes directly to PolyPeptide's commitment to delivering exceptional quality and on-time delivery to our customers Key Responsibilities: * Review and approve quality and validation documents as the production representative that does not need managers approval (MBPR, CC, SOP, PQE, PPQ related documents, educational certificates etc.) * Perform Operational assessments. * Prepare weekly slide deck presentations on project updates to internal and external stakeholders. * Lead and/or prepare and/or support product investigations using root cause analysis techniques (interviewing, fishbone diagram, 5 whys etc) and summarizing findings in written reports and oral presentations to internal and external stakeholders (QIRM, OOT, OOS, RCI, CAPA/Task) * Author, prepare and support Deviations, process change controls, CAPA during project execution. * Prepare Change Control Change Request and list of change document as part of MBPR generation (CC general and for MBPR) * Draft and review Standard Operating Procedures (QUMAS) * Conduct Risk Assessment (CRIA, RIA, FMEA) * Approve quality documents as the production representative that does not need managers approval (MBPR, ARM, CR, SOP, PQE, validation documents, educational certificates etc.) * Generate detailed Gannt chart of batch schedule. * BOM generation and Process mapping (soon to include route & formula) * Provide on-floor and remote 24/7 technical support to Production during project execution (including weekends, grave, and night shifts), e.g. make go/no go decisions on IPC-results regarding process steps or troubleshooting issues. * Project management of operation activities related to batch preparation/ execution (equipment/ IPC validation, hold time study, etc…) * Draft, format and improve MBPR template. * Support technology transfer activities (generation of comparability report, identification of CPPs, review and approve validation PPQ documents, generation of BPR etc). * Author and review campaign reports. * Raw material OOS assessment * Conduct Bottle neck analysis and Gap analysis of unit operations. * Prepare Process capability analysis. * Conduct cost analysis and forecasting. * Liaise with cross functional groups (Production, QA, QC, Development, Project Management, Sale, Regulatory, Supply Chain etc.) to support the planning and execution of manufacturing operations. * Collaborate with PD to Design small scale experiments to support investigations or process improvement initiatives. * Lead, mentor and train Operators and team members as part of upstream and downstream process knowledge transfer on MBPR and unit operations. * Support continuous improvement initiatives. * Manually Collect, trend, and analyze in process data as part of process monitoring to determine yields and change points. * Support QA and regulatory with responding to comments by clients on executed BPR and NDA/BLA, submission. * Support Validation activities during the planning execution of PPQ runs (prepare supporting PPQ document, e.g. equipment calibration and suitability, analytical methods, hold time study, PPQ strategy etc). * Support regulatory review of documents. * Process Mapping * Routes and Formula on AX to be added to our responsibilities. Qualifications: Education & Experience * Required Education: * Advanced degree in chemistry, Biochemistry, Engineering, or a related field. * Formal training or coursework in GMP, pharmaceutical manufacturing, or related regulatory standards is highly desirable. * Relevant industry certifications (e.g., Lean Six Sigma, GMP compliance) are a plus. * Experience: * Minimum 5 years in pharmaceutical manufacturing GMP production or MS&T team, peptide manufacturing experience preferred. * Proven ability to independently operate and troubleshoot production equipment and execute complex manufacturing procedures. * Demonstrated success in working autonomously while managing multiple production tasks and priorities. Skills & Competencies * Technical Skills: Basic understanding about SPPS GMP manufacturing, Proficiency in HPLC systems, cGMP processes, Data analysis (Minitab experience is preferred). * Soft Skills: Strong problem-solving, collaboration, Microsoft Data analysis (Minitab experience is preferred), Technical writing, and communication skills, and Microsoft office. * Competencies: * Strategic Scientific Judgment * Quality and Regulatory Leadership * Complex Problem Solving and Decision Making * Technical Influence and Innovation * Cross-Functional Leadership and Collaboration Salary: $115K-$130K We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

The Production Scientist is responsible for a upscaling R&D small scale work into GMP large scale manufacturing, Oversee production activities of the assigned projects, collect and analyze GMP data, Author and review quality documents such as MBPR, R.A, PPQ protocol, drive yield and process improvement projects, update the customer with the GMP activities, ensuring production processes meet quality standards, or maintaining equipment efficiency. This role contributes directly to PolyPeptide's commitment to delivering exceptional quality and on-time delivery to our customers Key Responsibilities: Review and approve quality and validation documents as the production representative that does not need managers approval (MBPR, CC, SOP, PQE, PPQ related documents, educational certificates etc.) Perform Operational assessments. Prepare weekly slide deck presentations on project updates to internal and external stakeholders. Lead and/or prepare and/or support product investigations using root cause analysis techniques (interviewing, fishbone diagram, 5 whys etc) and summarizing findings in written reports and oral presentations to internal and external stakeholders (QIRM, OOT, OOS, RCI, CAPA/Task) Author, prepare and support Deviations, process change controls, CAPA during project execution. Prepare Change Control Change Request and list of change document as part of MBPR generation (CC general and for MBPR) Draft and review Standard Operating Procedures (QUMAS) Conduct Risk Assessment (CRIA, RIA, FMEA) Approve quality documents as the production representative that does not need managers approval (MBPR, ARM, CR, SOP, PQE, validation documents, educational certificates etc.) Generate detailed Gannt chart of batch schedule. BOM generation and Process mapping (soon to include route & formula) Provide on-floor and remote 24/7 technical support to Production during project execution (including weekends, grave, and night shifts), e.g. make go/no go decisions on IPC-results regarding process steps or troubleshooting issues. Project management of operation activities related to batch preparation/ execution (equipment/ IPC validation, hold time study, etc…) Draft, format and improve MBPR template. Support technology transfer activities (generation of comparability report, identification of CPPs, review and approve validation PPQ documents, generation of BPR etc). Author and review campaign reports. Raw material OOS assessment Conduct Bottle neck analysis and Gap analysis of unit operations. Prepare Process capability analysis. Conduct cost analysis and forecasting. Liaise with cross functional groups (Production, QA, QC, Development, Project Management, Sale, Regulatory, Supply Chain etc.) to support the planning and execution of manufacturing operations. Collaborate with PD to Design small scale experiments to support investigations or process improvement initiatives. Lead, mentor and train Operators and team members as part of upstream and downstream process knowledge transfer on MBPR and unit operations. Support continuous improvement initiatives. Manually Collect, trend, and analyze in process data as part of process monitoring to determine yields and change points. Support QA and regulatory with responding to comments by clients on executed BPR and NDA/BLA, submission. Support Validation activities during the planning execution of PPQ runs (prepare supporting PPQ document, e.g. equipment calibration and suitability, analytical methods, hold time study, PPQ strategy etc). Support regulatory review of documents. Process Mapping Routes and Formula on AX to be added to our responsibilities. Qualifications: Education & Experience Required Education: Advanced degree in chemistry, Biochemistry, Engineering, or a related field. Formal training or coursework in GMP, pharmaceutical manufacturing, or related regulatory standards is highly desirable. Relevant industry certifications (e.g., Lean Six Sigma, GMP compliance) are a plus. Experience: Minimum 5 years in pharmaceutical manufacturing GMP production or MS&T team, peptide manufacturing experience preferred. Proven ability to independently operate and troubleshoot production equipment and execute complex manufacturing procedures. Demonstrated success in working autonomously while managing multiple production tasks and priorities. Skills & Competencies Technical Skills: Basic understanding about SPPS GMP manufacturing, Proficiency in HPLC systems, cGMP processes, Data analysis (Minitab experience is preferred). Soft Skills: Strong problem-solving, collaboration, Microsoft Data analysis (Minitab experience is preferred), Technical writing, and communication skills, and Microsoft office. Competencies: Strategic Scientific Judgment Quality and Regulatory Leadership Complex Problem Solving and Decision Making Technical Influence and Innovation Cross-Functional Leadership and Collaboration Salary: $115K-$130K We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. ***************** Job Description Performing A/V linear passes, checking and confirming accuracy, sync, and quality of audio, video, and subtitles Performing logic and navigation QC, and confirming functionality and presence of all assets against client specs Checking video assets for quality issues, including any dropouts, corruption, blocking, etc. Performing compatibility testing, checking for basic functionality on a matrix of devices based on product specs Writing up any issues observed in a clear, accurate, technically proficient manner Qualifications Experience utilizing various devices for both physical media and streaming playback (set top boxes, gaming systems, streaming media players, etc.) Experience with FileMaker Proficiency in Excel Deep understanding of DVD & Blu-Ray production processes, Surround Sound, Dolby ATMOS, HD, UHD, and regional products (domestic and international), etc. Excellent verbal and written communication skills A love of television and movies and a genuine curiosity about the technology involved in creating them Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Location: Burbank, California Employment Type: Part-Time, On-Site Schedule: Flexible hours Salary: $20.00-22.00 Per Hour

Resillion is a strategic partner for quality assurance. We offer worldwide services on the field of quality technology, testing, conformity, interoperability and assurance, from initiation to launch - for the software system, cybersecurity, the device, digital products and media content. With a passion for quality, Resillion provides end-to-end solutions to support customers in their strategic digital initiatives and offers a holistic approach for both software and hardware. Via our office in Europe, the United Kingdom, the USA, India and China, we bring together more than 500 experts who are committed to success. We combine the best human and artificial intelligence (AI) on advanced solutions for quality technology in the liver. Resillion offers deep sector knowledge and works together with the world's leading companies in telecom, media, energy & utilities, health care, finance and consumer electronics. ***************** Job Description Title responsibilities include, but are not limited to, the following: Performing A/V linear passes, checking and confirming accuracy, sync, and quality of audio, video, and subtitles Performing logic and navigation QC, and confirming functionality and presence of all assets against client specs Checking video assets for quality issues, including any dropouts, corruption, blocking, etc. Performing compatibility testing, checking for basic functionality on a matrix of devices based on product specs Writing up any issues observed in a clear, accurate, technically proficient manner Qualifications The ideal candidate would possess: Experience utilizing various devices for both physical media and streaming playback (set top boxes, gaming systems, streaming media players, etc.) Experience with FileMaker Proficiency in Excel Deep understanding of DVD & Blu-Ray production processes, Surround Sound, Dolby ATMOS, HD, UHD, and regional products (domestic and international), etc. Excellent verbal and written communication skills A love of television and movies and a genuine curiosity about the technology involved in creating them Additional Information Location: Burbank, California Employment Type: Part-Time Schedule: Day Shift Salary: $20.00-22.00 Per Hour

At Open Bank, we pride ourselves on being different and OPEN to new ideas and opportunities for our clients and employees. We celebrate innovation, diversity, teamwork, excellence and integrity. We are an equal opportunity employer and offer competitive compensation and benefits package to recruit, retain and reward top talent. We would like to be your partner in success and happiness! Join our TEAM - Together Everyone Achieves More Job Title: AVP & Senior Quality Control Analyst Department: BSA (Hybrid: 2 days in HQ Office and 3 days remote per week) We are looking for AVP & Senior Quality Control Analyst to join our BSA team at Open Bank! The AVP & Senior Quality Control Analyst will be responsible for conducting all aspects of monitoring activities relating to the Bank Secrecy Act (BSA), Anti-Money Laundering (AML), and OFAC compliance. Key Responsibilities: * Implements, performs, and documents assigned control reviews; performs and conducts testing based on detailed procedures and processes. * Conduct Quality Control/Assurance on Alerts, SARs, EDDs, CTRs and OFAC related tasks. * Identifies areas of risk and make recommendations on operational improvements, processes for compliance, quality assurance and any additional training essential to mitigate risk. * Communicates test results to management and business partners as directed. * Researches and analyzes testing results or issues, training, reads literature in order to become more knowledgeable about current banking, regulatory and audit issues, and performs other tasks as necessary to carry out daily responsibilities; maintains expertise in areas of testing. Requirements/Qualifications: * Bachelor degree from an accredited college is preferred. * Minimum five years of experience of BSA, bank audit, compliance, or banking operations is required. * Knowledge of Bank Secrecy Act, USA Patriot Act and OFAC. * Experience of BSA, bank audit, compliance, or banking operations is preferred. * Good knowledge of bank documents and bank operation. * Present a professional image in dealing with customers, interdepartmental, and external representatives. * Good written and oral communication skills; ability to communicate effectively and project a professional image when giving and taking information in writing, in person, and over the phone. * Accurate typing/keyboarding skills; basic computer skills, including the use of word processing, spreadsheet software applications, and e-mail. Employee Benefits & Perks * Medical, Dental, & Vision: Open Bank offers medical, dental, and vision insurance for all full-time employees and their immediate family members. Employees become eligible for insurance benefits on the first of the month following their hire date. * Life, Accidental Death & Dismemberment, & Long-Term Disability: Open Bank pays 100% of the cost. * Flexible Spending Account (FSA): Tax-advantaged financial accounts are offered for employees to pay for eligible out-of-pocket expenses (health, dependent care, transit, and parking) with pre-tax dollars. * 401(k) Retirement Savings Plan: Open Bank matches 100% of the first 6% of employees' contributions. Employees are eligible to participate on the first of the month following 90 days of employment. * Paid Time Off (PTO): Employees begin to accrue PTO hours at the time of hire to use for vacation, illness, or other personal reasons. * Employee Assistance Program (EAP): The EAP offers counseling sessions, online tools and resources, and legal and financial guidance for employees and their family. * Company Paid Lunch: Open Bank provides company paid lunch twice a week. To view current job openings, please visit Open Bank Careers Page: ******************************

PENNYMAC Pennymac (NYSE: PFSI) is a specialty financial services firm with a comprehensive mortgage platform and integrated business focused on the production and servicing of U. S. mortgage loans and the management of investments related to the U. S. mortgage market. At Pennymac, our people are the foundation of our success and at the heart of our dynamic work culture. Together, we work towards a unified goal of helping millions of Americans achieve aspirations of homeownership through the complete mortgage journey. Job Overview The Senior Analyst Quality Control Credit Compliance is the functional lead for audits of purchased, funded and acquired loans for testing compliance with Federal and State regulations and FNMA, FHLMC, FHA, VA and USDA requirements. Offers interpretation and guidance on complex issues and findings. Builds, revises and maintains audit tests. A Typical Day The Senior Analyst Quality Control Credit Compliance will: Assist Corporate Compliance with the development and implementation of QC Compliance test plans. Manage complex QC process review projects across multiple business units with differing compliance requirements Manage reviews of loan audits performed by vendors Prepare monthly QC reporting packages Serve as the primary QC liaison to compliance management counterparts in the business units Perform other related duties as required and assigned Demonstrate behaviors which are aligned with the organization's desired culture and values What You'll Bring Bachelor's degree or equivalent work experience 3+ years of relevant work experience Broad knowledge of Federal, State, GSE (FNMA, FHLMC) GOV (HUD, VA, and USDA) and Treasury requirements for originating and servicing loans Strong knowledge of mortgage origination and servicing practices and procedures Proficient in Microsoft Office (Excel, Word, PowerPoint) and Internet search applications Why You Should Join As one of the top mortgage lenders in the country, Pennymac has helped over 4 million lifetime homeowners achieve and sustain their aspirations of home. Our vision is to be the most trusted partner for home. Together, 4,000 Pennymac team members across the country are guided by our core values: to be Accountable, Reliable and Ethical in all that we do. Pennymac is committed to conducting a business that makes positive contributions and promotes long-term sustainable growth and to fostering an equitable and inclusive environment, where all employees and customers feel valued, respected and supported. Benefits That Bring It Home: Whether you're looking for flexible benefits for today, setting up short-term goals for tomorrow, or planning for long-term success and retirement, Pennymac's benefits have you covered. Some key benefits include: Comprehensive Medical, Dental, and Vision Paid Time Off Programs including vacation, holidays, illness, and parental leave Wellness Programs, Employee Recognition Programs, and onsite gyms and cafe style dining (select locations) Retirement benefits, life insurance, 401k match, and tuition reimbursement Philanthropy Programs including matching gifts, volunteer grants, charitable grants and corporate sponsorships To learn more about our benefits visit: ********************* page. link/benefits For residents with state required benefit information, additional information can be found at: ************ pennymac. com/additional-benefits-information Compensation: Individual salary may vary based on multiple factors including specific role, geographic location / market data, and skills and experience as defined below: Lower in range - Building skills and experience in the role Mid-range - Experience and skills align with proficiency in the role Higher in range - Experience and skills add value above typical requirements of the role Some roles may be eligible for performance-based compensation and/or stock-based incentives awarded to employees based on company and individual performance. #TPO Salary $55,000 - $85,000 Work Model OFFICE

The Vision System Operator is responsible for the operation of the Mitutoyo Vision System and the programming of the system. This position will write, develop and validate vision measuring system using QVPAK. Responsible for interpreting technical documents, engineering blueprints and 3D CAD models into precise measurements. Additionally, this role will perform first article inspections and complete non-conformance documentation working in coordination with Quality Control for the enhancement of processes and procedures. Responsible for the programming and operations of the Mitutoyo Vision System, including: Creating inspection program by writing, developing and validating new inspection programs for the Vision measuring system using software such as QVPAK Interpretation of technical documents including the translation of complex engineering blueprints, technical drawings and 3D CAD models into precise measurement routines. Fixture and calibrate, setting parts on the vision system, ensuring proper fixture and perform regular calibration checks to guarantee accuracy and reliability Collaborate with Design and Manufacturing Engineers to determine measurements and develop efficient inspection plan. Responsible for the operation and inspection, including Running automated and manual measurement program to perform first-article inspections Using the vision system's capabilities, including optical, laser and touch probes to inspect intricate shapes and tight tolerances Analyze measurement data and create comprehensive inspection reports, including First Article Inspection Reports (FAIRs) and non-conformance documents. Identify and resolve program errors, measurement discrepancies and system performance problems. Work within Quality Management System (ISO 9001) to ensure all inspections are compliant Perform supplementary dimensional inspections with manual tools such as micrometers, calipers and height gauges, etc. Other duties as assigned. KPI Reporting Responsibilities As established with Director of Quality Control Job Qualifications, Skills, and Abilities Minimum of associate's degree in technical field such as Manufacturing Technology, Metrology or related degree, preferred 3-5 years hands on experience with precision manufacturing environment. 1-3 years' experience as a Quality Inspector preferred. Prior experience using a Mitutoyo Vision Machine with QVPACK preferred Knowledge of MiCAT Planner software a plus Advanced ability to read and interpret complex engineering blueprints and able to apply Geometric Dimensioning and Tolerance (GD&T) principles Working knowledge of Microsoft Office Working knowledge of NetSuite a plus Excellent verbal and written communication skills preferred Travel Expectations 0% Physical Activities may include sitting and standing for long periods of time. Able to use eyes for visual inspections, able to navigate a small work area. May work on a computer for long periods that may emulate blue light.

Linde Gas & Equipment Inc. Chemist Analyst Linde Gas & Equipment Inc. is seeking a Chemist Analyst to join our team! The Chemist Analyst will assist the Laboratory Manager, Laboratory, Sales, and Customers with analytical and technical support. What we offer you! * Competitive compensation * Comprehensive benefits plan (medical, dental, vision and more) * 401(k) retirement savings plan * Paid time off (vacation, holidays, PTO) * Employee discount programs * Career growth opportunities * Additional compensation may vary depending on the position and organizational level Hourly Rate- $24.17 - $35.46 (commensurate with industry experience) What you will be doing: (1st shift) * Observe all company policies, safety, and standard operating procedures. * Ability to perform required analyses on all gases and mixtures. * Develop and improve methods of all analyses. * Keep up to date on new methods and new instrumentation related to all analyses. * Develop and improve analytical methods for existing, and new mixtures. * Assist in development of analytical specifications and product technical literature. * Provide technical support internally and externally. * Recommend new procedures and new equipment. * May assist with technical training to laboratory personnel. * Establish and manage internal stability and Proficiency testing Program. * Perform other duties as assigned by the laboratory manager What makes you great: * Bachelor's degree in Chemistry or related field required * Minimum of five years' experience in an analytical laboratory * Experience in G.C., GC/MS., FTIR, Titration, and other common methods of gas analysis is required * Ability to plan, schedule, and carry out laboratory assignments independently * Enthusiastic, positive attitude at all times, meticulous attention to all details of the position, quick response; fast; gets results with speed, able to work well with others. * Communicates, listens to others Communication, processes information accurately, displays commitment, seeks improvement, work efficiently, work competently, takes action, achieve results Why you will enjoy working with us: Linde is a leading global industrial gases and engineering company with 2024 sales of $33 billion. We live our mission of making our world more productive every day by providing high-quality solutions, technologies and services which are making our customers more successful and helping to sustain, decarbonize and protect our planet. Linde Gas & Equipment Inc. (LG&E) is part of the largest Welding, Industrial, Medical, and Specialty Gases companies in the U.S. We carry a comprehensive selection of industrial gases, such as oxygen, nitrogen, argon, and carbon dioxide, etc. LG&E has an extensive network of production plants, retail stores, distribution centers, and customer service locations with a focus on making our world more productive every day by providing high-quality solutions, technologies and services which are making our customers more successful by helping to sustain and protect our planet. For more information about the company, please visit our website. Don't wait, fill out an application right from your phone today! DRIVE YOUR CAREER FORWARD! All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, pregnancy, sexual orientation, gender identity or expression, or any other reason prohibited by applicable law.

Rate: $32.00 to $35.00 Analyzes Raw Materials, In-Process Samples and Finished Goods Includes the following: Other duties may be assigned. * Analyzes compounds to determine chemical and physical properties. * Complete routine review of QC test data and related documents for in-process samples, finished goods and stability samples. * Monitor and trend QC data results * Follows established procedures and documents all findings and results timely, concisely, clearly and accurately. * Prepares standards and specifications for processes, facilities, products, and tests. * Measures products for compliance to standards and specifications and reports same. * Provide updates/escalations at daily and weekly site-specific and cross-site meetings. * Experience with method development/qualification, tech transfer, QC testing, and laboratory deviations/investigations * Experience with analytical testing methods (organoleptic, viscosity, pH, moisture, specific gravity, titration assays, FTIR) in cosmetic and OTC manufacturing environment to support QC testing, data reviews, & COA generation to support testing and release. * Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/ 210/ 211). Knowledge of regulatory requirements for data integrity and practices. * Knowledge of regulatory guidance and experience maintaining QC lab GMP compliance and audits * Assessment of GMP systems currently in place to ensure compliance. * Proficiency in MS Word, Excel, Power Point and other applications * Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment * Works with development of formulas, processes, and methods for solution of technical problems. * Provides input to the development of procedures. * Strives toward continuous self-improvement in personal productivity. * Comfortable in a fast-paced environment with minimal direction and able to adjust workload and flexibility based upon changing priorities * A minimum of 3 years' experience and BS or BA. Preferred: * Demonstrated leadership and management skills, including establishing direction and goals, and building good work ethics for the team * Supervising/managing experience. * Experience with microbiological testing methods. What we're offering: ●Competitive compensation package. ●Health, dental, and vision benefits. ●401K program. ●The spirit of a startup with the security of an established, profitable industry leader. ●The opportunity to make waves in a $250B industry. At Prime, we believe that a diverse, equitable and inclusive workplace makes us a more relevant, more competitive, and more resilient company. We welcome people from all backgrounds, ethnicities, cultures, and experiences. Prime is an equal opportunity employer.

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post. Nature and Scope Perform QC related work including, but not limited to, preparing/performing analysis samples from all phases of a manufacturing or other handling processes and creating/revising SOPs. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Perform QC testing in all phases of manufacturing including raw material, in-process, bulk, finished goods and stability testing. Conduct various laboratory procedures as per manufacturing/QC SOPs. Assist fundamental tasks for special projects on analytics and instruments. Prepare and maintain testing records. Involve in procedure review and propose modifications and updates. Support design and development of experimental protocols, SOP's, etc., consistent with cGMP/GLP. Under general supervision, manage own time effectively, maintains control over all current assignments and responsibilities. Perform any other tasks/duties as assigned by management. Additional Qualifications/Responsibilities Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. BS degree in Chemistry, Biology or equivalent combination of education and experience. Up to 2 years of related quality control and quality assurance in the pharmaceutical industry. Require/Preferred Experience with specific equipment/software/programs etc. Clean, organize and legible documentation. Knowledge of cGMP environment is a plus. Able to follow, create, maintain, and organize documents per established company guidance. Knowledge of workplace safety and safe materials handling as appropriate Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals. Ability to work overtime as needed. Physical Environment and Requirements Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees. Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision. Specific vision requirements include color vision. Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly. Employee must be able to occasionally lift and/or move up to 50 pounds. Expected Salary Range: $33.70-35.00

Nature and Scope Perform QC related work including, but not limited to, preparing/performing analysis samples from all phases of a manufacturing or other handling processes and creating/revising SOPs. Essential Duties and Responsibilities Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Perform QC testing in all phases of manufacturing including raw material, in-process, bulk, finished goods and stability testing. Conduct various laboratory procedures as per manufacturing/QC SOPs. Assist fundamental tasks for special projects on analytics and instruments. Prepare and maintain testing records. Involve in procedure review and propose modifications and updates. Support design and development of experimental protocols, SOP's, etc., consistent with cGMP/GLP. Under general supervision, manage own time effectively, maintains control over all current assignments and responsibilities. Perform any other tasks/duties as assigned by management. Education Requirements and Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. BS degree in Chemistry, Biology or equivalent combination of education and experience. Up to 2 years of related quality control and quality assurance in the pharmaceutical industry. Require/Preferred Experience with specific equipment/software/programs etc. Clean, organize and legible documentation. Knowledge of cGMP environment is a plus. Able to follow, create, maintain, and organize documents per established company guidance. Knowledge of workplace safety and safe materials handling as appropriate Must be able to read documents in Standard English such as Standard Operating Procedures, maintenance schedules and operating manuals. Ability to work overtime as needed. Physical Environment and Requirements Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves. PPE and Respirators are essential for the health and safety of employees. Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision. Specific vision requirements include color vision. Employees must maintain a clean-shaven appearance each working shift to wear tight-fitting respirators properly. Employee must be able to occasionally lift and/or move up to 50 pounds. Expected Salary Range: $33.70-35.00 The salary range, is the minimum and maximum hourly rate of compensation for the role that the employer in good faith believes to be accurate at the time of the posting of an advertisement for the role. Actual compensation for the role will be based on a number of different factors including but not limited to the candidate's qualifications, education, knowledge, skills and experience.American Regent also offers a competitive total rewards package which includes healthcare, life insurance, profit sharing, paid time off, matching 401k as well as a widerange of other benefits. American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status. Applicants have rights under Federal Employment Laws. FMLA poster: ********************************************************** Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov) Employee Polygraph Protection Act: ********************************************************* Alert: We're aware of individuals impersonating our staff to target job seekers. Please note: · All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address. · Our recruiting process includes multiple in person and/or video interviews and assessments. · If you are unsure about the legitimacy of a message, contact John Rossini at *************************** before responding. · We never request payment, bank information, or personal financial details during our offer process. Your security is important to us, and we encourage you to stay vigilant when job searching. American Regent Inc. endeavors to make *********************************** accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email **************************************.

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 (*******************).

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 (*******************).

Entry level laboratory analyst for work with GC-ECD samples. Duties include extraction/analysis of samples. Instrument maintenance, cleaning labware, preparation of reagents and standards. Following all laboratory protocol, following all standard operating procedures (SOPs) and adhering to any and all laboratory quality assurance protocols. Ideal Candidate will have experience with: Sample Analysis: Perform sample preparation, chemical analysis, and quantification of chemicals in accordance with EPA and standard methods Equipment Operation: Utilize advanced laboratory equipment such as Gas Chromatography (GC - FID, ECD, TCD), ICP, ICP-MS, CVAAS, GC-MS, UV-VIS analyses, balances, ovens, and more. Data Documentation: Maintain detailed records including laboratory notebooks, software data, standard preparations, and equipment logs. Equipment Maintenance: Conduct routine and in-depth maintenance, including troubleshooting laboratory equipment. Accreditation Support: Perform tasks required to maintain laboratory accreditation, such as running and reporting audit samples, completing MDL studies bi-annually, and updating documentation (e.g., SOPs, DOC forms). Quality Control: Perform and document standardizations, calibrations, and performance verifications daily. Safety & Compliance: Ensure proper sample custody, control, and hazardous waste disposal in compliance with safety protocols. Additional Duties: Assist with editing and reviewing SOPs, guidance documents, and other tasks as assigned.  Essential Functions: Performs laboratory operations, including preparation, analysis, quantification of chemicals; prepares standards and samples for analysis, including quality control samples, and reports final results. Documents work performed; maintains laboratory notebooks, recordings, software data, etc. for raw data, standard preparations, and equipment Performs routine daily, weekly, and monthly maintenance of equipment Performs actions required to maintain accreditation; runs, reports, and passes audit samples bi-annually; completes MDL studies for each required method bi-annually, creates DOC forms for each quarter, and ensures all methods are run according to the requirements in each SOP Edits and reviews documents; reviews SOPs and guidance documents to ensure all procedures accurately reflect laboratory practices and meet NELAC and/or EPA requirements Maintains sample custody, control, and hazardous waste disposal Performs other job-related duties as assigned Required Qualifications: EDUCATION REQUIREMENT - Bachelor's degree in chemistry or science-related field Some experience in a laboratory setting Experience working with hazardous chemicals Familiarity with various sample methods STARTING PAY RATE: $20.00/hr. Knowledge, Skills & Abilities: General knowledge of chemistry and lab analysis operations and lab safety Proficiency in Microsoft Office programs, including MS Word and Excel Strong verbal and written communication skills Ability to lead a team and provide training and guidance to subordinates Professional demeanor and appearance; ability to serve as a representative of the company Ability to prioritize and multi-task Strong organizational skills and attention to detail Ability to read, count, and write to accurately complete all documentation   Work Environment - While performing the duties of this job, the employee regularly works in a laboratory setting. 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. Sitting or standing for extended periods and the use of hands to finger is common. Hearing and vision within normal ranges is helpful for normal conversations, to receive ordinary information and to prepare or inspect documents.  Duties frequently involve repetitive motions and eye/hand/foot coordination.  Testing priorities and timelines may serve as a source of emotional stress. Occasional heavy lifting is expected. Exertion of up to 30 lbs. of force may occasionally be required. While performing the duties of this job, good manual dexterity for the use of laboratory equipment is needed. The employee is occasionally required to walk, lift, carry, push, pull, climb, stoop, kneel, crouch, reach, handle, grasp, and feel. Use of applicable Personal Protective Equipment is mandatory.   Other Duties Please note this job description is intended to describe the general nature and level of work performed by employees assigned to this position. It is not designed to contain or be interpreted as a comprehensive list of all duties, responsibilities, and qualifications. Additional job-related duties may be assigned.  Alliance reserves the right to amend and change responsibilities to meet business and organizational needs as necessary with or without notice. KEY BENEFITS INCLUDE:  Medical, Dental, and Vision Insurance Flexible Spending Accounts 401(K) Plan with Competitive Match Continuing Education and Tuition Assistance Employer-Sponsored Disability Benefits Life Insurance Employee Assistance Program (EAP)  Paid Time Off (PTO), Paid Holidays, & Bonus Floating Holiday (if hired before July 1st) Profit Sharing or Individual Bonus Programs Referral Program Per Diem & Paid Travel Employee Discount Hub EEO Commitment We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, national origin, ethnicity, sex, pregnancy, sexual orientation, gender identity/expression, religion, disability, age, genetics, active military or veteran status, and any other characteristics protected under applicable federal or state law. #LABS