Quality control technician jobs in San Buenaventura, CA - 130 jobs

This opportunity is located within our Ensign-Bickford Aerospace & Defense Company business, a global leader of mission-critical hardware and systems solutions including precision energetics systems and innovative explosive solutions.Click here to learn more. Job Description: EBAD seeks a Quality Assurance Technician - Flex Shift in Moorpark, California Facility. Responsibilities: This position supports multiple Product Families. The candidate will be responsible for providing effective verification of products and/or processes against requirements and dissemination of findings thereof. Perform inspection of components and assemblies not limited to receiving, in-process and final Inspections Complete all required data entries for inspected items Maintains a clean and organized work area and follows all established safety guidelines Work within a team structure to achieve company and department goals Perform additional duties related to specific area assignments when requested Requirements: The successful candidate must have graduated from High School or equivalent G.E.D. and 5+ years of experience with inspection of mechanical components in an aerospace or defense related company. Required experience includes: Capable of utilizing all standard inspection tools and equipment including calipers, micrometers, drop indicators, CMM Programing and optical systems. Must be capable of programming CMM, utilizing PCDIMS software Have a basic knowledge of ISO/AS procedures Good knowledge and understanding of Geometric Dimension and Tolerance (GD&T) Must be able to read and understand industry standards Must be able to read and understand English Must be able to effectively communicate and interact with all levels of management Meticulous with high attention to detail Must have basic PC fundamentals Desired skills: Six Sigma Green Belt through ASQ, CQE/CQM Certification program is a plus. Significant experience working directly with internal/external customers and suppliers. Compensation: Salary Range: $50,000 - $75,000 per year. Salary is determined by the applicant's education, experience, knowledge, skills, abilities, internal equity, and alignment with market data. Ensign-Bickford Aerospace & Defense Company is an Equal Opportunity Employer (EOE). Qualified applicants are considered for employment without regard to race, religion, color, sex, age, disability, sexual orientation, genetic information, national origin, or veteran status.

Now Hiring: Quality Inspectors - Aerospace Manufacturing Are you an experienced Quality Inspector looking to advance your career in a high-precision aerospace machine shop? We are seeking mid- to advanced-level Inspectors with strong experience inspecting machined metal aerospace or military parts, proficiency in GD&T, and familiarity with AS9100, AS9102, and ANSI Y14.5 standards. This is a hands-on inspection role-not a quality administrator position-and does not involve final-release, audit packages, or administrative QA paperwork Key Responsibilities Perform in-process and first-article (AS9102) inspections of precision-machined aerospace components. Use precision tools such as micrometers, calipers, thread gauges, height gauges, CMMs, profilometers, and optical comparators. Interpret complex blueprints and technical drawings using advanced GD&T (ANSI Y14.5). Record inspection results in MRP systems. Support NCR investigations and basic root-cause discussions (no ownership of CAPA or audit documentation). Mentor junior inspectors and support team development. Assist with traceability checks and adherence to FOD, PPE, and cleanroom protocols. Ensure compliance with AS9100, ITAR, and internal quality procedures. Requirements Skills/Abilities Minimum 3 years inspecting machined aerospace or military parts (metal only). Strong proficiency in GD&T, dimensional inspection, and visual inspection. Knowledge of AS9100, AS9102, and ANSI Y14.5. CMM programming experience (PC-DMIS) strongly preferred; ability to create or modify CMM routines is a plus. Experience with 1factory, FileMaker, or similar QMS/MRP systems. Strong shop math, problem-solving, and English communication skills. Dependable, quality-focused, and able to work independently or in a team. Must pass annual visual acuity and color-perception tests (NDT standards). U.S. person required for ITAR compliance. Schedule Full-Time Second Shift Monday-Friday, 3:00 PM - 11:30 PM Initial training will take place on Day Shift: Monday-Friday, 7:00 AM - 3:30 PM Compensation $22.50-$39.50 per hour (I, II, & III) Benefits Medical, dental, vision, life insurance Disability, vacation, sick pay 401k Physical Demands Work primarily in an open warehouse environment with exposure to temperature changes, noise, vibrations, fumes, and chemicals Frequent use of wrists, hands, and fingers Extended periods of sitting, standing, walking, and bending Occasionally lift, carry, push, or pull up to 50 lbs ITAR Requirement This position requires the use of information subject to the International Traffic in Arms Regulations (ITAR). The candidate must be a U.S. person within the meaning of ITAR. ITAR defines U.S. persons as U.S. citizens, lawful permanent residents (i.e., Green Card holders), and some refugees. MGI is an equal opportunity employer. Ready to apply? Join our team today! NO RECRUITERS PLEASE

**Job Title:** Aerospace Quality Inspector **Job Description:** Will be performing quality inspection of various components (ranging in size) for aerospace & defense manufacturer. **Skills & Qualifications:** + Aerospace Quality Inspection + AS9100 & AS9102 + Precision measuring tool experience. + Documentation experience. + Experience working with a variety of sizes of parts is preferred **Location:** Simi Valley, CA **Placement Type:** Contract to Hire (Permanent placement relies on performance) **Compensation:** $25.00 - $38.00 / Depending on Experience **Job Type & Location** This is a Contract to Hire position based out of Simi Valley, CA. **Pay and Benefits** The pay range for this position is $25.00 - $38.00/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 Simi Valley,CA. **Application Deadline** This position is anticipated to close on Feb 6, 2026. **About Aerotek:** We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

**Country:** United States of America ** Onsite **U.S. Citizen, U.S. Person, or Immigration Status Requirements:** U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. **Security Clearance Type:** None/Not Required **Security Clearance Status:** Not Required At Raytheon, the foundation of everything we do is rooted in our values and a higher calling - to help our nation and allies defend freedoms and deter aggression. We bring the strength of more than 100 years of experience and renowned engineering expertise to meet the needs of today's mission and stay ahead of tomorrow's threat. Our team solves tough, meaningful problems that create a safer, more secure world. As a Semiconductor Production Technician, you will focus on the fabrication of Infrared Materials for Raytheon Vision Systems, a manufacturer that provides leading edge sensing technology. Our production environment is highly specialized, involving cleanroom operations, precision crystal growth, and metrology to ensure the highest standards of quality and performance. We are looking for a detailed oriented individual who must demonstrate a safety-first routine. Work consists of a combination of routine production tasks and non-routine engineering support under minimal or no supervision. You will draw from your advanced experiences in a related field to assume responsibilities for managing your time and working in a laboratory. **What You Will Do** + Follow ISO-controlled process procedures in an environmentally controlled, semiconductor (cleanroom) environment that requires handling of fragile materials and potentially hazardous materials and process chemicals, such as Mercury, Hydrofluoric acid and Bromine. + Use of Personal Protective Equipment (PPE), including occasional use of a respirator. + Participate in daily production meetings and work with colleagues to ensure optimal workflow and meeting schedule demands. + Responsible for production execution in a semiconductor laboratory/cleanroom environment. + Responsible for characterization of production components and completing test reports. + Develop and follow maintenance schedules for lab equipment. + This is a first shift position. The candidate may be required to work occasional overtime or weekends to meet the factory needs. **What You Will Learn** + Participation and coordination of cross training activities in other lab processes. + Communication related to maintenance schedule, equipment up-time, production goals and engineering challenges on a daily basis is essential. + Thorough understanding of the technical aspects associated with your assigned process and ability to work with process engineering to resolve production issues. **Qualifications You Must Have** + Typically requires an AA/AS degree (or other 2-year post high school training) with a minimum of 6 years of relevant experience + Experience in Semiconductor or Microelectronics, automotive, medical Tech Manufacturing, or similar field. + U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. **Qualifications We Prefer** + Basic computer skills include MS Office products: Outlook, Excel, Word. + Experience with safe handling of process chemicals such as acids and solvents. + Experience with vacuum, electrical, and mechanical systems. + Experience with metrology equipment, measurement systems and visual inspections. + Experience with high-tech production equipment such as vacuum or high-pressure systems. + Experience working in a laboratory with complex facility requirements such as particle control, temperature and humidity. + Direct experience working with Personal Protective Equipment (PPE) including respirators. + Experience with common instruments and tooling for high-tech fabrication and assembly to achieve measurement and dimensional targets. **What We Offer** Our values drive our actions, behaviors, and performance with a vision for a safer, more connected world. At RTX we value: Safety, Trust, Respect, Accountability, Collaboration, and Innovation. **_Relocation assistance not available for this position_** **Learn More & Apply Now!** Please consider the following role type definition as you apply for this role. + Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. Goleta, CA: ************************************************************* **_As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote._** The salary range for this role is 58,400 USD - 111,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. _RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act._ **Privacy Policy and Terms:** Click on this link (******************************************************** to read the Policy and Terms Raytheon Technologies is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other federally protected class.

Quality Control Microbiologist II - Camarillo, CA The Quality Control Microbiologist II performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We proudly offer - Generous benefit options (eligible first day of employment) - Paid training, vacation and holidays (vacation accrual begins on first day of employment) - Career advancement opportunities - Education reimbursement - 401K program with matching contributions - Learning platform - And more! Essential job duties - Lead and/or support quality event investigations for out-of-specification (OOS), out-of-trend (OOT) or nonconformance events - Perform environmental monitoring of clean rooms (under ISO and EU specifications) - Perform and review QC testing (Endotoxin, Bioburden, TOC, Conductivity, Growth Promotion Assay, etc.) for manufacturing, raw materials, in-process materials, intermediates and final product - Demonstrate technical proficiency in test procedures and ensure QC activities are carried out using applicable regulatory requirements (FDA, USP, ICH etc.) - Participate in audits, client investigations, and project-related activities - Lead and/or support activities associated with Change Control, CAPAs, client audit response, work orders, etc. - Receive and process samples to meet production/client timelines - Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results - Prepare and send out samples for microbiological identification - Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met - Work closely and collaborate in a team environment with QC Analytical and Quality Assurance, Manufacturing, Technical Services, Materials Receiving, and Research and Development - Ensure the successful implementation and execution of new QC methods/procedures and equipment - Perform trending of QC data and present information to Management - Perform general laboratory housekeeping - Author, review, and approve microbiology test results and analytical methods as needed - Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met - Support Manufacturing with client-specific testing requirements - Inspection of media fills Education, experience, certification and licensure - Bachelor's Degree in Microbiology or related field - Minimum 3-5 years' industry experience in a GMP sterile finish or pharmaceutical cleanroom environment - Willing to work flexible hours (nights and weekends), as-needed Knowledge, skills and abilities - Proficient in the validation/qualification of lab microbiological techniques preferred - Knowledgeable in FDA cGMPs (21 CFR 211); ISO 9001, 13485 and 17025 a plus - Knowledgeable in USP , , , and - Strong organizational skills and the ability to prioritize/multitask - Proficient in Microsoft Office Suite (excel) - Attention to details and following GMP methods and instructions - Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently - Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, and customers - Ability to write reports, business correspondence, and procedures - Ability to define problems, collect data, establish facts, and draw valid conclusions Physical requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to stand; walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. Work environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and may be expected to work with electronic equipment (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate. Employee may be responsible for moving and/or generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the customized Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials. Other Qualifications - Must pass a background check - Must pass a drug screen - May be required to pass Occupational Health Screening Pay Range: $70,304-$88,000/year Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

Quality Control Microbiologist II - Camarillo, CA The Quality Control Microbiologist II performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We proudly offer * Generous benefit options (eligible first day of employment) * Paid training, vacation and holidays (vacation accrual begins on first day of employment) * Career advancement opportunities * Education reimbursement * 401K program with matching contributions * Learning platform * And more! Essential job duties * Lead and/or support quality event investigations for out-of-specification (OOS), out-of-trend (OOT) or nonconformance events * Perform environmental monitoring of clean rooms (under ISO and EU specifications) * Perform and review QC testing (Endotoxin, Bioburden, TOC, Conductivity, Growth Promotion Assay, etc.) for manufacturing, raw materials, in-process materials, intermediates and final product * Demonstrate technical proficiency in test procedures and ensure QC activities are carried out using applicable regulatory requirements (FDA, USP, ICH etc.) * Participate in audits, client investigations, and project-related activities * Lead and/or support activities associated with Change Control, CAPAs, client audit response, work orders, etc. * Receive and process samples to meet production/client timelines * Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results * Prepare and send out samples for microbiological identification * Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met * Work closely and collaborate in a team environment with QC Analytical and Quality Assurance, Manufacturing, Technical Services, Materials Receiving, and Research and Development * Ensure the successful implementation and execution of new QC methods/procedures and equipment * Perform trending of QC data and present information to Management * Perform general laboratory housekeeping * Author, review, and approve microbiology test results and analytical methods as needed * Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met * Support Manufacturing with client-specific testing requirements * Inspection of media fills Education, experience, certification and licensure * Bachelor's Degree in Microbiology or related field * Minimum 3-5 years' industry experience in a GMP sterile finish or pharmaceutical cleanroom environment * Willing to work flexible hours (nights and weekends), as-needed Knowledge, skills and abilities * Proficient in the validation/qualification of lab microbiological techniques preferred * Knowledgeable in FDA cGMPs (21 CFR 211); ISO 9001, 13485 and 17025 a plus * Knowledgeable in USP , , , and * Strong organizational skills and the ability to prioritize/multitask * Proficient in Microsoft Office Suite (excel) * Attention to details and following GMP methods and instructions * Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently * Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, and customers * Ability to write reports, business correspondence, and procedures * Ability to define problems, collect data, establish facts, and draw valid conclusions Physical requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to stand; walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. Work environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and may be expected to work with electronic equipment (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate. Employee may be responsible for moving and/or generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the customized Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials. Other Qualifications * Must pass a background check * Must pass a drug screen * May be required to pass Occupational Health Screening Pay Range: $70,304-$88,000/year Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

Eleven Recruiting is searching for three Quality Technicians for one of our largest aerospace manufacturing clients sitting onsite in Simi Valley, CA. This role will play a pivotal role in ensuring adherence to quality standards and specifications of incoming products, materials, and components. Responsible for conducting thorough examinations, quality control inspections, and providing detailed analysis to support Supplier Quality Engineering functions. This position supports the Material Review Board (MRB) processes and collaborates closely with Supplier Quality Engineers to uphold superior quality across all stages of the production process. Job Responsibilities: Conduct comprehensive examinations and quality control inspections on non-conforming products, materials, and components for both standard and specialized products, ensuring alignment with established quality standards. Provide in-depth analysis, troubleshooting, and evaluation of components and assemblies, generating quality notifications for the Material Review Board (MRB) as necessary. Maintain meticulous documentation records and data related to performed tests, ensuring accuracy and accessibility. Collaborate with Supplier Quality Engineers to review quality notifications, determine the issuance of supplier corrective actions, and contribute to continuous improvement initiatives. Support Supplier Quality Engineers in conducting supplier audits to assess and enhance supplier quality performance. Update, refine, and create work inspections and supplier quality to ensure compliance with evolving standards and best practices. Perform other duties as assigned to support the smooth functioning of supplier quality operations. Job Requirements: Education: High School Diploma Certifications: AS9100 Lead Auditor - preferred Experience: 4+ years of hands-on experience in quality control inspections and related functions within a manufacturing or similar environment. Skills: Proficiency in conducting examinations and quality control inspections across various types of products, materials, and components. Able to apply a systematic QA approach while using existing procedures to solve a range of technical issues Performs routine quality inspections on engineering designs, assemblies, piece parts, final assemblies and tooling Conducts Internal audits and corrective action follow-ups Experience interpreting blueprints, drawings, and parts lists to ensure compliance with specifications. Proficient computer skills for documentation, data management, and report generation. #LI-BP1 #LI-Onsite Seniority Level: Mid-level Salary: $60,000-75,000 Job Function: Quality Technician Industry: Aerospace Manufacturing Employment Type: Full-Time Location: Simi Valley, CA

Johanson Technology Inc. (JTI) is looking for a Quality Technician I, will be responsible for the facilitation of MRB and RMA activities up to and including testing and failure analysis of multi-layer / single-layer ceramic capacitors. Will also be maintaining accuracy on day-to-day quality sharepoint databases (MRB, RMA, CAR, Incoming Inspection, etc.) Hourly Rate (Non-Exempt): $20.00 - $21.50 per hour (DOE) Work Schedule (Monday-Friday) 8:00 a.m. - 4:30 p.m. Company Offer Benefits: Medical (HMO/PPO/HSA) Dental (HMO/PPO) Vision Company Paid Basic Life Insurance Supplemental Life Insurance Paid time off (i.e. Vacation, Sick, Holiday, and Bereavement) 401k Savings plus company match Tuition Assistance Required Education and Experience: H.S Diploma or GED equivalent At least six (6) months of understanding of cross sectioning and root cause analysis of sectioned samples. Familiarity with ISO9001 Standard Excellent teamwork, multitasking and problem-solving skills. Excellent written, verbal and communication skills. Excellent knowledge of Microsoft Office (Outlook, Excel, Word, Project, PowerPoint), SharePoint, MS Teams, and Adobe Acrobat. Preferred Education And Experience Associates degree preferable in Chemistry, Physics, Electronics or Material Science. Two (2)+ years of production quality or failure analysis experience. Essential Functions: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Coordinates flow of MRB activity through department and moves material once it is dispositioned. Coordinates flow of RMA activity through the RMA process. Performs special testing, failure analysis, and root cause analysis when needed. Cross sections defective samples to point of failure provides cause of failure and provide a documented report of findings. Coordinates test using SEM/EDX, DPA analysis and other electrical test equipment and provide documented reports. Work directly with Managers, Engineers, Production Control, and other JTI/JMX team members. Generate daily / weekly / monthly quality department reports (Excel, Power point, MS Teams). Perform Secondary (Non MRB) failure analysis (Visual inspection, electrical testing, cross sectioning) Maintain and track ongoing quality related tasks through Microsoft SharePoint. Assist with maintaining and auditing the Quality Management System (QMS) Housekeeping chores will be performed as assigned; work areas must be kept clean and organize at all times. Cross training for other jobs is required so that employees can occasionally fill-in in other departments, when required. Additional or different functions may be assigned to the employee periodically. Knowledge, Skills & Abilities: Ability to understand manufacturing and testing, preferable in the ML/SL Ceramic Capacitors. Must have the ability to follow safety procedures when using manufacturing/testing equipment. Self-motivation and ability to stay focused in the middle of distraction. Capable of prioritizing and determining what needs to be completed according to department needs and workload. Ability to effectively prioritize competing requests, while keeping lines of communication open and the team satisfied. Excellent written, verbal and presentation skills. Very detail oriented Ability to analyze and think quickly to resolve conflict. Physical And Mental Demands The physical and mental 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 sit; use hands to handle or feel and talk or hear. The employee is frequently required to reach with hands and arms. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Alternative or combined skills in understanding, counseling, and/or influencing people are important in achieving job objectives, causing action, understanding others, or changing behavior; and, skills of persuasiveness or assertiveness, as well as sensitivity to the point of view of others. Performs a wide range of tasks as dictated by variable demands and changing conditions. Free to plan work assignments and schedule to meet long-term goals and objectives. Performs a wide range of complex tasks with little predictability as to their occurrence. Relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on complex issues. Must independently apply abstract principles to solve complex conceptual issues. Must independently manage a large group of performing varied tasks. Must write letters to explain complex issues. Persuade or explain complex issues in person or by phone. Responsibility For Confidentiality This position requires confidentiality; the company has many Non-Disclosure Agreements with customers who require confidentiality and occasionally will work with ITAR controlled documents. As such, US citizenship or permanent resident status is required. Travel On rare occasions will travel to Tijuana, Mexico facility. If you are interested in the Quality Technician I, please submit your resume ******************************************************** To learn more about Johanson Technology's products, services, and culture, visit our websites at ************************** and **************************** Johanson Technology Inc., and Johanson Dielectrics Inc. are Equal Opportunity Employer/Veterans/Disabled

Summary The Quality Systems Associate supports multiple quality functions including investigations, documentation control, labeling, and training. This role performs RMA inspections, deviations and product complaint investigations, manages document control activities, and supports labeling and packaging specification processes. The Associate ensures compliance with internal procedures, regulatory requirements, and quality standards while collaborating with cross-functional teams to maintain the integrity of the Quality Management System (QMS). Essential Duties Investigation ·Perform investigation of deviations and product complaints (PC). ·Follow up with internal teams and suppliers for open actions and gather data through interviews. ·Complete status reports, draft RCIs, and participate in MRB meetings and status updates. ·Answer and document PC-related phone calls. ·Perform RMA inspections for all returned materials/products and document findings. Labeling and Packaging Support ·Support label specification creation and revisions for new product introductions and updates. ·Review supplier artwork, packaging assessments, and initiate DCRs for PI revisions and label updates. ·Upload PMGs to the website to ensure current information for patients. ·Verify SPL postings or deletions for compliance. Documentation Management ·Perform daily document control activities including physical file put-away, check-in/out, and record retention records. ·Locate archived documents and assist with digital formatting. Support document storage solutions and transfer boxes to permanent storage areas. This position may be assigned additional responsibilities at the discretion of management to support evolving departmental needs and organizational objectives Knowledge, Skills, Experience Needed Education ·Bachelor's degree in Life Sciences, Engineering, or related field. (preferred) Experience ·2+ years in quality, documentation, or operations within a regulated industry Skills / Competencies: Technical Skills ·Basic understanding of GMP/GDP and QMS workflows. ·Proficiency in document control systems, LMS administration, and Microsoft Office Suite. ·Ability to interpret and update labeling specifications and artwork. · Familiarity with QMS systems, LMS platforms, and basic GMP/GDP principles. Soft Skills ·Attention to Detail - Ensures accuracy in documentation and labeling. ·Communication - Clear and professional interaction with internal teams and suppliers. ·Organization - Manages multiple tasks and deadlines efficiently. ·Problem-Solving - Identifies issues and escalates appropriately. ·Collaboration - Works effectively across departments. Miscellaneous Requirements: ·Maintain a strong attendance record ·Adhere to company's drug-free workplace policies Physical Requirements: Office-based with occasional work in controlled environments. ·May be required to work longer than the typical 8-hour workday. ·Sedentary position that may require pro-longed periods of desk work. ·Requires light physical duties in keeping work areas clean and organized. Regularly required to walk the production and warehouse areas. May require lifting boxes or equipment weighing up to 50 pounds. About GSMS Founded in 1986 by a veteran of the US Air Force, GSMS has grown to be the leading provider of generic pharmaceuticals to the federal government. Based in Camarillo, CA, the GSMS team is relentlessly focused on providing critical medicines to our veterans, active-duty military members, and their families while delivering significant cost-savings to the government. Our expertise covers all aspects of the federal healthcare market, including contracting, compliance, data analytics, packaging, labeling, distribution, sales, and customer relations. With over 200 team members and 90 manufacturer partners, GSMS is well positioned to grow our market leadership position and bring innovative solutions to our customers and investors. The hiring range for this position in Camarillo, CA (Remote) is $24.04 - 27.88 per hour. The base pay actually offered will take into account internal equity and also may vary depending on the candidate's geographic region, job-related knowledge, skills and experience among other factors. A bonus may be provided as part of the compensation package, in addition to a full range of other health and welfare benefits.

Kate Farms is a company with heart. Our company was founded on the belief that good nutrition leads to good health, and good health opens the door to endless possibilities. That's why our mission is to make nutrition the cornerstone of healthcare so people can live their best lives. We are a medical food company that makes complete nutrition formulas for people who have a medical need for liquid nutrition. Kate Farms works to be the place where a diverse mix of talented individuals want to come, stay, and do their best work. Ensuring a diverse and inclusive workplace where we learn from each other is at the core of Kate Farms' values. We are an equal-opportunity employer and fully focused on equality; we believe deeply in diversity of race, gender, sexual orientation, religion, ethnicity, national origin, and all the other fascinating characteristics that make us different. We invite you to do the best work of your life with us at Kate Farms. POSITION OVERVIEW The QC Lab Technician will operate within the Quality Control arm of the Quality and Regulatory Affairs Department. In this role, the QC Lab Technician will conduct physical laboratory tests in support of research and development and commercial product testing programs using various scientific equipment and bench chemistry techniques. The QC Lab Technician will be expected to learn and understand the requirements for Corporate Food Safety and Quality, ensuring all QC objectives are met. The ideal candidate must be adaptable to a dynamic work environment, willing to learn, and willing to collaborate with all functional groups. Quality Control is an integral part of the Quality and Regulatory Affairs team, which ensures a full slate of safe, wholesome, and clinically effective food products in their development and finished phases meet set standards of quality, uniformity, and performance. To further our advancement in plant-based nourishment, Kate Farms has established the Innovation and Quality Center in Goleta, where a Pilot Plant, along with a state-of-the-art laboratory, is situated to support evaluation of R&D-scale production, Product Development, Quality Control, and full-scale analytical and functional testing. The QC Lab Technician will be immersed in game-changing food technology and support advanced testing activities. WHAT YOU WILL DO Perform required routine and non-routine finished product tests in support of hold and release of commercial products according to SOPs. Operate and maintain laboratory instruments (pH, viscosity and density meters, solid analyzer, balances, etc.) and support miscellaneous testing needs with these instruments. Accurately record test results in LIMS, report any out-of-specification results, and assist with investigations. Use Excel spreadsheets and basic formulas to perform calculations. Support third-party laboratory test submissions, including electronic submittals, sample shipping, tracking, notifications, receiving reports, and data entry. Manage lab supplies and product inventory for the QC team and ensure adequate supply for various test needs. Help with organizing and maintaining the retention sample library. Maintain current knowledge of Good Laboratory Practices and required regulatory compliance. Handle and dispose of hazardous materials according to local, state, and federal regulations. Perform other duties as assigned. WE ARE LOOKING FOR SOMEONE WHO Minimum High School Diploma or GED. Must be comfortable in a chemistry laboratory environment where hazardous materials (biological and chemical) are present and require direct handling and exposure. Possess basic competency in mathematical skills. Must pass a skills evaluation for basic math proficiency and attention to detail during the interview. Must have operating knowledge of Microsoft Office programs, including Excel, Word, PowerPoint, and Outlook. Has the ability to operate laboratory equipment and follow written procedures and protocols. Can work with a sense of urgency in response to changing priorities. Is self-motivated and able to think independently and to work with minimal supervision. Has excellent interpersonal and collaboration skills for working across departments and teams. Has good written and oral communication skills in the English language. Has a strong commitment to company mission and values. Can work independently and collaboratively in a fast-paced, dynamic environment. Respectfully shares and accepts feedback willingly from all levels of the organization. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by the employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Effectively handle lifting of various objects weighing up to 12 pounds. While performing the essential functions of the job, the employee will be required to bend, stoop, kneel, reach, and climb stairs. Possess the ability to sit at a computer for extended periods of time. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. This position will work onsite, Goleta, CA. Compensation for this role is in the form of base salary plus a variable component that together comprise the On-Target-Earnings (OTE). The typical starting salary range for new hires in this role is listed below. This range represents the lowest to highest salary range we reasonably and in good faith believe we would pay for this role at the time of this posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Please note that base pay offered may vary depending on factors including your geographic location, job-related knowledge, skills, and experience. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. All job offers are contingent upon successful completion of background verification. $22.00 / hour - $24.00 / hour USD For full-time salaried or hourly workers, our total rewards package also include the option to enroll in a company-matched 401k plan, as well as participate in Company-sponsored medical, dental, vision, and basic life insurance plans for the employee and the employee's eligible dependents. Employees will also receive a generous PTO benefit with a starting accrual of 15 days per year (prorated upon hire and increased by tenure), two weeks of paid “Refresh” leave, 80 hours of paid sick leave annually, and 11 paid holidays throughout the calendar year. Kate Farms offers a range of other benefits offered with an emphasis on employee well-being such as paid disability leave, paid parental / pregnancy leave, Flexible Spending Accounts (FSA), tuition reimbursement, an Employee Assistance Program, and more. NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization as directed by the management of the company.

Job Description Job Title: Quality Control Inspector II F Reports To: Quality & Process Planning Manager Job Purpose The Quality Control Inspector II is responsible for ensuring that all products meet established quality standards and customer specifications. This role performs inspections, checks, and tests during the manufacturing process, records observations, and recommends improvements. The position requires proficiency with ERP systems to produce quality reports for internal and external use, while supporting company-wide quality initiatives and continuous improvement efforts. Duties & Responsibilities Ensure compliance with all quality check procedures throughout the production process. Perform required physical testing in accordance with Work Instructions. Develop inspection plans aligned with company and customer-specific requirements. Conduct required visual checks and verify masking accuracy against blueprints and purchase orders. Act as subject matter expert for multi-process orders. Approve internal masking with resource owners to prevent process failures. Record inspection data, document pass/fail status, and report rejections with photo evidence as needed. Tag and hold parts for review when disposition is required. Complete logbooks for Copper Sulfate and 24-hour humidity tests. Review Shop Travelers for accuracy, completion, and compliance. Verify packaging instructions are followed before shipment and ensure traceability. Inspect expedited, regular, and rework orders for proper processing. Perform random sampling inspections on large quantity orders. Gather required measurement tools and take photos, sharing findings with customers and production teams. Promote accuracy in job scanning and identify opportunities to improve shop floor efficiency. Utilize ERP software to document corrective actions and prevent recurring quality issues. Educate production staff on quality control issues and support improvement efforts. Assist Quality Engineering and Specialists with troubleshooting and corrective actions. Maintain communication via email and phone as required. Ensure inspection benches are organized and clean; maintain 5S standards and audits. Perform other duties as assigned by management. Qualifications 3-5 years of quality control inspection or related experience. High School Diploma or equivalent required. Basic blueprint reading and interpretation. Proficiency with Microsoft Office Suite and ERP systems. Strong verbal, written, and customer service skills. Experience using measuring tools (meters, gauges, calipers, etc.). Ability to work full-time, including overtime and weekends as needed. Key Competencies Strong verbal and written communication skills. Attention to detail and accuracy. Basic math and analytical skills. Documentation and reporting skills. Hand-eye coordination. Ability to stay organized and maintain good housekeeping practices.

Basic Qualifications Associate's degree in related discipline or equivalent is required plus a minimum of 1 year of relevant experience. CLEARANCE REQUIREMENTS: Department of Defense Secret security clearance is required at time of hire. Applicants selected will be subject to a U.S. Government security investigation and must meet eligibility requirements for access to classified information. Due to the nature of work performed within our facilities, U.S. citizenship is required. Responsibilities for this Position Help make the technologies, products and services that make a difference. That's the opportunity that's waiting for you at General Dynamics Mission Systems. We help our nation's heroes keep our nation safe by creating solutions so advanced, they redefine innovation for the world. It's an amazing challenge. And it's waiting for you now. We apply advanced technologies such as Artificial Intelligence, Blockchain, AR/VR, Cloud Native and Quantum Physics to solve our customers' missions in cyber, RF, undersea, interstellar and everything in between. General Dynamics Mission Systems has an immediate opening for a LCS Mission Package General Technician at Port Hueneme Naval Station Oxnard, CA. This position provides an opportunity to further advance the cutting-edge technology that supports some of our nation's core defense/intelligence services and systems. General Dynamics Mission Systems employees work closely with esteemed customers to develop solutions that allow them to carry out high-stakes national security missions. REPRESENTATIVE DUTIES AND TASKS: The LCS DEPS Mission Package General Technician will engage in Maintenance, Mission Module Movements/Embarks and Debarks, Pre-embark Staging, Maintenance Planning, Fly-Away/Distance Support and Logistic Engineering Support. The candidate will perform a variety of duties in Corrective Maintenance, Emergent Repair, and Preventative Maintenance involving GDMS Mission Module support of Littoral Combat Ship (LCS). Assists in the development, implementation, installs, tests, modifies and/or operates complex equipment and systems Participates on the engineering work team and supports other team members in experimental design, materials, equipment setup/maintenance and related issues Installs and removes MM equipment on LCS ships Performs a variety of equipment/process operations involving an application or technical skills in a specific area (electrical, software, manufacturing, optical, etc.) Construct, modify, debug, test and adjust a variety of tools and equipment given appropriate drawings, parts and instructions Implements basic practical solutions for process improvement Conducts and documents experiments under guidance of senior technician Constructs basis tooling and fixtures to accomplish unique tasks Works under general supervision The candidate will be based in Port Hueneme, Ca Naval Base and will support the LCS platforms, including travel to other domestic ports and OCONUS ports as appropriate. The selected candidate will be expected to travel 40% of the time supporting Littoral Combat Ships (LCS-class ships) and will work within the parameters and rules common to U.S. Naval vessels. Performs physically demanding work including working in tight, restricted access quarters onboard a US Navy warship and other spaces (e.g., RIB engine compartment), climbing 20 ft. ladders and standing for long periods of time on a Navy ship or pier lifting 50 lbs. or more. As required, candidates hired for a specific position must be able to pass forklift and/or Category II or III Crane operator's physical and proficiency tests. Travel will be required to other Navy bases and deployed sites. Must be able to obtain and maintain a secret clearance and be able to travel 40% of time. KNOWLEDGE SKILLS AND ABILITIES: This position will require the ability to work from tech manuals, vendor documentation, schematics, and engineering drawing to supports the ship's maintenance efforts. The LCS DEPS Mission Module Maintenance Technician will be expected to be proficiency in test equipment operations, cable repair/rework, and connector repair/rework. Additional duties may be assigned, including but not limited to logistics, material, and safety responsibilities as it relates to the Mission Modules. The LCS DEPS Mission Package Maintenance Technician will be expected to become completely familiar with their system, with the goal of becoming the Subject Matter Expert (SME). Candidate will be required to perform physically demanding work, to include working aloft, in tight, restricted spaces onboard LCS Platforms, climbing scaffolding, ladders and standing for long periods of time onboard a LCS ship or pier and be able to lift 50 lbs. or more. Must be able to pass forklift operators physical and proficiency tests The candidate may be responsible for working with a team of technicians, engineers, and government staff as appropriate Exercise creative thinking to advance our technical performance Experience with Navy maintenance, to include Ships Maintenance and Material Management (3M), Preventive Maintenance and Corrective Maintenance. This individual must have strong oral and written communication skills and be proficient with typical PC applications to include Word, Project, Excel and Access Professional etiquette and ability to operate effectively in a distributed team environment and effectively communicate customer initiatives, strategy and mission needs PREFERRED EXPERIENCE: Formally trained, operated, and maintained Navy's Surface Warfare (SUW), Mine Countermeasure (MCM) and systems and inter-workings of the LCS Class MM program Experience with 30mm guns on the LCS, LPD-17 Class, USMC Advanced Amphibious Assault Vehicle (AAAV) or similar chain guns is highly desired Experience with 11m Rigid Hull Inflatable Boats (RHIBS); Qualify as an operator and maintainer Experience in Heating, Ventilation and Air Conditioning (HVAC) Licensed Forklift Operator Commercial Driver's License (CDL) Familiar with U.S. Naval protocol and the ability to work directly with interfaces in uniform and with engineers in other companies Superior organizational and time management skills Familiar with U.S. Navy Work Authorization Forms (WAF) and Tag-Out Programs What sets you apart: Team player who thrives in collaborative environments and revels in team success Commitment to ongoing professional development Superior communication and collaboration skills Workplace Options: This position is fully on site. Salary Note This estimate represents the typical salary range for this position based on experience and other factors (geographic location, etc.). Actual pay may vary. This job posting will remain open until the position is filled. Combined Salary Range USD $31.25 - USD $31.25 /Hr. Company Overview General Dynamics Mission Systems (GDMS) engineers a diverse portfolio of high technology solutions, products and services that enable customers to successfully execute missions across all domains of operation. With a global team of 12,000+ top professionals, we partner with the best in industry to expand the bounds of innovation in the defense and scientific arenas. Given the nature of our work and who we are, we value trust, honesty, alignment and transparency. We offer highly competitive benefits and pride ourselves in being a great place to work with a shared sense of purpose. You will also enjoy a flexible work environment where contributions are recognized and rewarded. If who we are and what we do resonates with you, we invite you to join our high-performance team! Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description We are looking for a Quality Control Microbiologist I at our Santa Monica facility. Shift Tuesday to Saturday days Responsibilities (include but are not limited to): Perform and review environmental monitoring of cleanrooms including surface, viable air, non-viable air, and personnel monitoring. Perform microbiological testing of raw material, in process, final product, protocol/validation-related, and critical utility samples. Collect water samples to ensure all sample collected per schedule. Performs bioburden testing of water and product. Prepares growth promotion and other applicable nutrient substrate media qualification. Data entry and data trend as needed. Assist in investigations regarding out of specifications (OOS) results, address and manage deviations related to micro procedures. Routine maintenance of lab equipment and lab spaces. Conducts procedure updates in QC lab and GMP reviews of logbooks. Coordinates waste management, LEAN and 5S efforts as required. Perform other duties as assigned. Knowledge: Basic Knowledge of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs). Basic Knowledge of general Microbiology techniques such as Gram staining, aseptic technique, and plate streaking technique. Knowledge of USP and other regulatory requirements. Proficiency in Microsoft Office applications. Ability to work effectively in a team environment. Strong verbal, written, and interpersonal communication skills are required. Basic Qualifications: Bachelor's OR Associate and 2+ years of relevant experience OR High School Diploma/GED and 3+ years of relevant experience Preferred Qualifications: Prior Quality Control Microbiology laboratory experience preferred. Experience in aseptic techniques and clean room operations. Ability to gown for entry into Aseptic core and supporting areas, and lift approximately 25 lbs. Knowledge of GMP, SOPs, LIMS, and quality control processes for clinical manufacturing. Proficient in MS Word, Excel, Power Point and other applications. Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment. Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities. Ability to be flexible with schedule and work overtime as needed. The salary range for this position is: $69,445.00 - $89,870.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: ****************************************************************** * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit ******************* Sign up to follow @KitePharma on Twitter at *************************** For jobs in the United States: Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.

We're here for one reason and one reason only - to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We've made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet. Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows. Job Description We are looking for a Quality Control Microbiologist I at our Santa Monica facility. Shift Tuesday to Saturday days Responsibilities (include but are not limited to): * Perform and review environmental monitoring of cleanrooms including surface, viable air, non-viable air, and personnel monitoring. * Perform microbiological testing of raw material, in process, final product, protocol/validation-related, and critical utility samples. * Collect water samples to ensure all sample collected per schedule. * Performs bioburden testing of water and product. * Prepares growth promotion and other applicable nutrient substrate media qualification. * Data entry and data trend as needed. * Assist in investigations regarding out of specifications (OOS) results, address and manage deviations related to micro procedures. * Routine maintenance of lab equipment and lab spaces. * Conducts procedure updates in QC lab and GMP reviews of logbooks. * Coordinates waste management, LEAN and 5S efforts as required. * Perform other duties as assigned. Knowledge: * Basic Knowledge of current Good Manufacturing Practices (GMPs) and Good Laboratory Practices (GLPs). * Basic Knowledge of general Microbiology techniques such as Gram staining, aseptic technique, and plate streaking technique. * Knowledge of USP and other regulatory requirements. * Proficiency in Microsoft Office applications. * Ability to work effectively in a team environment. * Strong verbal, written, and interpersonal communication skills are required. Basic Qualifications: * Bachelor's OR * Associate and 2+ years of relevant experience OR * High School Diploma/GED and 3+ years of relevant experience Preferred Qualifications: * Prior Quality Control Microbiology laboratory experience preferred. * Experience in aseptic techniques and clean room operations. * Ability to gown for entry into Aseptic core and supporting areas, and lift approximately 25 lbs. * Knowledge of GMP, SOPs, LIMS, and quality control processes for clinical manufacturing. * Proficient in MS Word, Excel, Power Point and other applications. * Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment. * Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities. * Ability to be flexible with schedule and work overtime as needed. The salary range for this position is: $69,445.00 - $89,870.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: ****************************************************************** * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit ******************* Sign up to follow @KitePharma on Twitter at *************************** For jobs in the United States: Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance. For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Kite Pharma Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.

This role is designed for Second Shift. The **Quality Technician I** supports the Quality Engineering group through processing First Article Inspection (FAI) and Part Approval Process, selective inspection, analysis and processing of internal Nonconformance Reporting (NC) material and other administrative and logistical support duties. Represents the Quality Department in witnessing and documenting UAV flight acceptance test activity. **Position Responsibilities** + Processes inbound or outbound FAI and deliverable submissions accurately and timely including: receipt and analysis of parts and/or supporting documentation; completion of associated records and logs; communication of submission status as needed to QEs, managers, engineers or interested parties; processing of parts after completion; maintaining records and files associated with submissions; and other related tasks + Conducts selective inspection under the direction of the QE group including: receipt and verification of material, completion and maintenance of related documentation, communication of inspection results to concerned parties and processing of material after verification using Agile/Oracle database + Processes internal non-conforming material as needed in support of QE including: retrieval and analysis of material, interpretation of preliminary findings and restatement of problem statements to ensure understanding of problem, processing material through the necessary NC processes, communication of status to concerned parties, maintaining necessary documentation and processing material to internal and external suppliers + Provides general support of QEs including communication, Corrective Action Request processing, product evaluation, and sorting activities under exceptional circumstances, and interfacing with other team members as necessary to complete assigned tasks in support of continuous improvement initiatives using A3, Six Sigma DMAIC forms + Support DCMA Source Inspection process + Coordinates with Shipping and Contracts department as needed to ensure timely delivery + Also will assist flight test operators as necessary + Responsible for creating the Final Inspection documentation package including COC, TDR's, etc., and as necessary support internal/external customer inspection + Represents and supports QEs during internal and 3rd party audits regarding the essential functions above and as needed regarding our measurements system and documented system + Works on assignments that are routine in nature, requiring limited judgment + Other duties as assigned **Basic Qualifications (Required Skills & Experience)** + High School Diploma or GED equivalent is required + 0 - 1 years of related work experience or equivalent combination of education, training, and experience + Aerospace quality management system experience (AS9100DD) and/or internal audit experience is preferred + Demonstrated knowledge in mechanical inspection methods and skills including surface plate work, hand tools, and gages, etc. + Solid ability to read and understand drawing requirements including a solid understanding of Geometric Dimensioning and Tolerance to ANSI Y14.5 + Possesses basic knowledge of engineering drawings and specification systems + Basic knowledge of FAI validation and verification process requirements + Basic knowledge of engineering drawings and specification systems + Strong computer skills and has basic proficiency in MS Office Suite (Word, Access, PowerPoint, Excel) + Must be able to fill out the necessary flight test documentation + Must have the skills necessary to perform pre and post-flight visual inspections on flight hardware and components + Must possess the skills necessary to remove and replace field replaceable components on aircraft. Will populate excel spreadsheets on a daily basis documenting flight test results + Must be able to document any/all non-conformances encountered + Required to travel to and from remote flying sites on a daily basis + Must have a valid California driver's license and clean driving record + Willingness to work overtime also a must **Other Qualifications & Desired Competencies** + 2 year technical degree preferred; Quality system courses and/or equivalent experience preferred + Receives detailed instructions on all work. Works under close supervision. Acquires job skills and learns company policies and procedures to complete routine tasks + Solid ability to accurately record and manage data, records, files and other documents to support tasks + Has an analytical approach to problem solving and high organizational skills as well as effective time management, interpersonal and communication skills + Strong ability to manage time and prioritize tasks + Able to excel in a fast-paced, deadline-driven environment, where small teams share a broad variety of duties + Displays strong initiative and drive to accomplish goals and meet company objectives + Takes ownership and responsibility for current and past work products + Is committed to learning from mistakes and driven to improve and enhance performance of oneself, others, and the company + Builds effective problem-solving, analytical, interpersonal and communication skills. Focuses on teamwork, collaboration and puts the success of the team above one's own interests **Physical Demands** + Ability to work the majority of the time outdoors in varying weather conditions, when needed, during flight test activity (Frequent) + Ability to lift up to 50 lbs. and carry/move objects of varying shapes and sizes (Frequent) + Regularly required to, stand, sit; talk, hear, and use hands and fingers to operate a computer and telephone keyboard (Frequent) **Clearance Level** Clearance Level AeroVironment considers several factors, including but not limited to, the location, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. **ITAR Requirement:** _T_ _his position requires access to information that is subject to compliance with the International Traffic Arms Regulations ("ITAR") and/or the Export Administration Regulations ("EAR"). In order to comply with the requirements of the ITAR and/or the EAR, applicants must qualify as a U.S. person under the ITAR and the EAR, or a person to be approved for an export license by the governing agency whose technology comes under its jurisdiction. Please understand that any job offer that requires approval of an export license will be conditional on AeroVironment's determination that it will be able to obtain an export license in a time frame consistent with AeroVironment's business requirements. A "U.S. person" according to the ITAR definition is a U.S. citizen, U.S. lawful permanent resident (green card holder), or protected individual such as a refugee or asylee. See 22 CFR § 120.15. Some positions will require current U.S. Citizenship due to contract requirements._ **Benefits** : AV offers an excellent benefits package including medical, dental vision, 401K with company matching, a 9/80 work schedule and a paid holiday shutdown. For more information about our company benefit offerings please visit: ********************************* . We also encourage you to review our company website at ******************** to learn more about us. Principals only need apply. NO agencies please. **Who We Are** Based in California, AeroVironment (AVAV) is a global leader in unmanned aircraft systems (UAS) and tactical missile systems. Founded in 1971 by celebrated physicist and engineer, Dr. Paul MacCready, we've been at the leading edge of technical innovation for more than 45 years. Be a part of the team that developed the world's most widely used military drones and created the first submarine-launched reconnaissance drone, and has seven innovative vehicles that are part of the Smithsonian Institution's permanent collection in Washington, DC. Join us today in developing the next generation of small UAS and tactical missile systems that will deliver more actionable intelligence to our customers so they can proceed with certainty - and succeed. **What We Do** Building on a history of technological innovation, AeroVironment designs, develops, produces, and supports an advanced portfolio of unmanned aircraft systems (UAS) and tactical missile systems. Agencies of the U.S. Department of Defense and allied military services use the company's hand-launched UAS to provide situational awareness to tactical operating units through real-time, airborne reconnaissance, surveillance, and target acquisition. _We are proud to be an EEO/AA Equal Opportunity Employer, including disability/veterans. AeroVironment, Inc. is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Qualified applicants will receive fair and impartial consideration without regard to race, sex, color, religion, national origin, age, disability, protected veteran status, genetic data, sexual orientation, gender identity or other legally protected status._ **ITAR** U.S. Citizenship required **About AV:** **AV isn't for everyone. We hire the curious, the relentless, the mission-obsessed. The best of the best.** We don't just build defense technology-we redefine what's possible. As the premier autonomous systems company in the U.S., AV delivers breakthrough capabilities across air, land, sea, space, and cyber. From AI-powered drones and loitering munitions to integrated autonomy and space resilience, our technologies shape the future of warfare and protect those who serve. Founded by legendary innovator Dr. Paul MacCready, AV has spent over 50 years pushing the boundaries of what unmanned systems can do. Our heritage includes seven platforms in the Smithsonian-but we're not building history, we're building what's next. **If you're ready to build technology that matters-with speed, scale, and purpose-there's no better place to do it than AV.** **Careers at AeroVironment (*****************************************

At Ensign-Bickford Aerospace & Defense Company (EBAD), we believe that our strengths are built on our most important resource - our people. Join EBAD and you'll be a part of a team who creates cutting edge technology that will blast us into the future. No other company can match the innovative energetic solutions that we provide. At EBAD you will actively contribute to successful missions putting men, women and satellites into space, and protecting our armed service men and women around the world. If this is the culture and work environment you are seeking, then EBAD is the place for you! Job Description EBAD seeks a Quality Assurance Technician - Flex Shift in Moorpark, California Facility. Responsibilities: This position supports multiple Product Families. The candidate will be responsible for providing effective verification of products and/or processes against requirements and dissemination of findings thereof. Perform inspection of components and assemblies not limited to receiving, in-process and final Inspections Complete all required data entries for inspected items Maintains a clean and organized work area and follows all established safety guidelines Work within a team structure to achieve company and department goals Perform additional duties related to specific area assignments when requested Requirements: The successful candidate must have graduated from High School or equivalent G.E.D. and 5+ years of experience with inspection of mechanical components in an aerospace or defense related company. Required experience includes: Capable of utilizing all standard inspection tools and equipment including calipers, micrometers, drop indicators, CMM and optical systems Programming CMM, utilizing PCDIMS software a plus Have a basic knowledge of ISO/AS procedures Good knowledge and understanding of Geometric Dimension and Tolerance (GD&T) Must be able to read and understand industry standards Must be able to read and understand English Must be able to effectively communicate and interact with all levels of management Meticulous with high attention to detail Must have basic PC fundamentals Desired skills: Six Sigma Green Belt through ASQ, CQE/CQM Certification program is a plus. Significant experience working directly with internal/external customers and suppliers. Compensation: Salary Range: $50,000 - $75,000 per year. Salary is determined by the applicant's education, experience, knowledge, skills, abilities, internal equity, and alignment with market data. Ensign-Bickford Aerospace & Defense Company is an Equal Opportunity Employer (EOE). Qualified applicants are considered for employment without regard to race, religion, color, sex, age, disability, sexual orientation, genetic information, national origin, or veteran status.

Quality Control Microbiologist II - Camarillo, CA The Quality Control Microbiologist II performs quality activities in support of product production and releases. The QC Microbiologist performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. We proudly offer • Generous benefit options (eligible first day of employment) • Paid training, vacation and holidays (vacation accrual begins on first day of employment) • Career advancement opportunities • Education reimbursement • 401K program with matching contributions • Learning platform • And more! Essential job duties • Lead and/or support quality event investigations for out-of-specification (OOS), out-of-trend (OOT) or nonconformance events • Perform environmental monitoring of clean rooms (under ISO and EU specifications) • Perform and review QC testing (Endotoxin, Bioburden, TOC, Conductivity, Growth Promotion Assay, etc.) for manufacturing, raw materials, in-process materials, intermediates and final product • Demonstrate technical proficiency in test procedures and ensure QC activities are carried out using applicable regulatory requirements (FDA, USP, ICH etc.) • Participate in audits, client investigations, and project-related activities • Lead and/or support activities associated with Change Control, CAPAs, client audit response, work orders, etc. • Receive and process samples to meet production/client timelines • Read, trend and report environmental, personnel, in-process, raw material, finish product and water bioburden testing results • Prepare and send out samples for microbiological identification • Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met • Work closely and collaborate in a team environment with QC Analytical and Quality Assurance, Manufacturing, Technical Services, Materials Receiving, and Research and Development • Ensure the successful implementation and execution of new QC methods/procedures and equipment • Perform trending of QC data and present information to Management • Perform general laboratory housekeeping • Author, review, and approve microbiology test results and analytical methods as needed • Ensure QC sample testing (e.g. in-process, lot release, stability, EM, water) and data approval deadlines are met • Support Manufacturing with client-specific testing requirements • Inspection of media fills Education, experience, certification and licensure • Bachelor's Degree in Microbiology or related field • Minimum 3-5 years' industry experience in a GMP sterile finish or pharmaceutical cleanroom environment Knowledge, skills and abilities • Proficient in the validation/qualification of lab microbiological techniques preferred • Knowledgeable in FDA cGMPs (21 CFR 211); ISO 9001, 13485 and 17025 a plus • Knowledgeable in USP , , , and • Strong organizational skills and the ability to prioritize/multitask • Proficient in Microsoft Office Suite (excel) • Attention to details and following GMP methods and instructions • Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently • Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, and customers • Ability to write reports, business correspondence, and procedures • Ability to define problems, collect data, establish facts, and draw valid conclusions Physical requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to stand; walk; climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus. Work environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee has the potential of being exposed to fumes or airborne particles and toxic or caustic chemicals (wearing proper Personal Protective Equipment will be required in these situations). The employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; high, precarious places; outside weather conditions; and may be expected to work with electronic equipment (always being aware of one's environment and taking proper precautions is required). The noise level in the work environment is usually moderate. Employee may be responsible for moving and/or generating hazardous waste for treatment, storage and disposal. Affected employee will need to be familiar with the applicable training requirements included in the customized Resources, Conservation and Recovery Act. Employee will understand waste labeling, secondary containment, chemical compatibility, storage time limits, container size and quantity limits, container integrity when waste is left unattended and improper disposal of hazardous materials. Other Qualifications • Must pass a background check • Must pass a drug screen • May be required to pass Occupational Health Screening Pay Range: $70,304-$88,000/year Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral. All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

Job Description Johanson Technology Inc. (JTI) is looking for a Quality Technician I, will be responsible for the facilitation of MRB and RMA activities up to and including testing and failure analysis of multi-layer / single-layer ceramic capacitors. Will also be maintaining accuracy on day-to-day quality sharepoint databases (MRB, RMA, CAR, Incoming Inspection, etc.) Hourly Rate (Non-Exempt): $20.00 - $21.50 per hour (DOE) Work Schedule (Monday-Friday) 8:00 a.m. - 4:30 p.m. Company Offer Benefits: Medical (HMO/PPO/HSA) Dental (HMO/PPO) Vision Company Paid Basic Life Insurance Supplemental Life Insurance Paid time off (i.e. Vacation, Sick, Holiday, and Bereavement) 401k Savings plus company match Tuition Assistance Required Education and Experience: H.S Diploma or GED equivalent At least six (6) months of understanding of cross sectioning and root cause analysis of sectioned samples. Familiarity with ISO9001 Standard Excellent teamwork, multitasking and problem-solving skills. Excellent written, verbal and communication skills. Excellent knowledge of Microsoft Office (Outlook, Excel, Word, Project, PowerPoint), SharePoint, MS Teams, and Adobe Acrobat. Preferred Education And Experience Associates degree preferable in Chemistry, Physics, Electronics or Material Science. Two (2)+ years of production quality or failure analysis experience. Essential Functions: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Coordinates flow of MRB activity through department and moves material once it is dispositioned. Coordinates flow of RMA activity through the RMA process. Performs special testing, failure analysis, and root cause analysis when needed. Cross sections defective samples to point of failure provides cause of failure and provide a documented report of findings. Coordinates test using SEM/EDX, DPA analysis and other electrical test equipment and provide documented reports. Work directly with Managers, Engineers, Production Control, and other JTI/JMX team members. Generate daily / weekly / monthly quality department reports (Excel, Power point, MS Teams). Perform Secondary (Non MRB) failure analysis (Visual inspection, electrical testing, cross sectioning) Maintain and track ongoing quality related tasks through Microsoft SharePoint. Assist with maintaining and auditing the Quality Management System (QMS) Housekeeping chores will be performed as assigned; work areas must be kept clean and organize at all times. Cross training for other jobs is required so that employees can occasionally fill-in in other departments, when required. Additional or different functions may be assigned to the employee periodically. Knowledge, Skills & Abilities: Ability to understand manufacturing and testing, preferable in the ML/SL Ceramic Capacitors. Must have the ability to follow safety procedures when using manufacturing/testing equipment. Self-motivation and ability to stay focused in the middle of distraction. Capable of prioritizing and determining what needs to be completed according to department needs and workload. Ability to effectively prioritize competing requests, while keeping lines of communication open and the team satisfied. Excellent written, verbal and presentation skills. Very detail oriented Ability to analyze and think quickly to resolve conflict. Physical And Mental Demands The physical and mental 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 sit; use hands to handle or feel and talk or hear. The employee is frequently required to reach with hands and arms. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Alternative or combined skills in understanding, counseling, and/or influencing people are important in achieving job objectives, causing action, understanding others, or changing behavior; and, skills of persuasiveness or assertiveness, as well as sensitivity to the point of view of others. Performs a wide range of tasks as dictated by variable demands and changing conditions. Free to plan work assignments and schedule to meet long-term goals and objectives. Performs a wide range of complex tasks with little predictability as to their occurrence. Relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on complex issues. Must independently apply abstract principles to solve complex conceptual issues. Must independently manage a large group of performing varied tasks. Must write letters to explain complex issues. Persuade or explain complex issues in person or by phone. Responsibility For Confidentiality This position requires confidentiality; the company has many Non-Disclosure Agreements with customers who require confidentiality and occasionally will work with ITAR controlled documents. As such, US citizenship or permanent resident status is required. Travel On rare occasions will travel to Tijuana, Mexico facility. If you are interested in the Quality Technician I, please submit your resume ******************************************************** To learn more about Johanson Technology's products, services, and culture, visit our websites at ************************** and **************************** Johanson Technology Inc., and Johanson Dielectrics Inc. are Equal Opportunity Employer/Veterans/Disabled Job Posted by ApplicantPro

Kate Farms is a company with heart. Our company was founded on the belief that good nutrition leads to good health, and good health opens the door to endless possibilities. That's why our mission is to make nutrition the cornerstone of healthcare so people can live their best lives. We are a medical food company that makes complete nutrition formulas for people who have a medical need for liquid nutrition. Kate Farms works to be the place where a diverse mix of talented individuals want to come, stay, and do their best work. Ensuring a diverse and inclusive workplace where we learn from each other is at the core of Kate Farms' values. We are an equal-opportunity employer and fully focused on equality; we believe deeply in diversity of race, gender, sexual orientation, religion, ethnicity, national origin, and all the other fascinating characteristics that make us different. We invite you to do the best work of your life with us at Kate Farms. POSITION OVERVIEW The QC Lab Technician will operate within the Quality Control arm of the Quality and Regulatory Affairs Department. In this role, the QC Lab Technician will conduct physical laboratory tests in support of research and development and commercial product testing programs using various scientific equipment and bench chemistry techniques. The QC Lab Technician will be expected to learn and understand the requirements for Corporate Food Safety and Quality, ensuring all QC objectives are met. The ideal candidate must be adaptable to a dynamic work environment, willing to learn, and willing to collaborate with all functional groups. Quality Control is an integral part of the Quality and Regulatory Affairs team, which ensures a full slate of safe, wholesome, and clinically effective food products in their development and finished phases meet set standards of quality, uniformity, and performance. To further our advancement in plant-based nourishment, Kate Farms has established the Innovation and Quality Center in Goleta, where a Pilot Plant, along with a state-of-the-art laboratory, is situated to support evaluation of R&D-scale production, Product Development, Quality Control, and full-scale analytical and functional testing. The QC Lab Technician will be immersed in game-changing food technology and support advanced testing activities. WHAT YOU WILL DO * Perform required routine and non-routine finished product tests in support of hold and release of commercial products according to SOPs. * Operate and maintain laboratory instruments (pH, viscosity and density meters, solid analyzer, balances, etc.) and support miscellaneous testing needs with these instruments. * Accurately record test results in LIMS, report any out-of-specification results, and assist with investigations. * Use Excel spreadsheets and basic formulas to perform calculations. * Support third-party laboratory test submissions, including electronic submittals, sample shipping, tracking, notifications, receiving reports, and data entry. * Manage lab supplies and product inventory for the QC team and ensure adequate supply for various test needs. * Help with organizing and maintaining the retention sample library. * Maintain current knowledge of Good Laboratory Practices and required regulatory compliance. * Handle and dispose of hazardous materials according to local, state, and federal regulations. * Perform other duties as assigned. WE ARE LOOKING FOR SOMEONE WHO * Minimum High School Diploma or GED. * Must be comfortable in a chemistry laboratory environment where hazardous materials (biological and chemical) are present and require direct handling and exposure. * Possess basic competency in mathematical skills. * Must pass a skills evaluation for basic math proficiency and attention to detail during the interview. * Must have operating knowledge of Microsoft Office programs, including Excel, Word, PowerPoint, and Outlook. * Has the ability to operate laboratory equipment and follow written procedures and protocols. * Can work with a sense of urgency in response to changing priorities. * Is self-motivated and able to think independently and to work with minimal supervision. * Has excellent interpersonal and collaboration skills for working across departments and teams. * Has good written and oral communication skills in the English language. * Has a strong commitment to company mission and values. * Can work independently and collaboratively in a fast-paced, dynamic environment. * Respectfully shares and accepts feedback willingly from all levels of the organization. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by the employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. * Effectively handle lifting of various objects weighing up to 12 pounds. * While performing the essential functions of the job, the employee will be required to bend, stoop, kneel, reach, and climb stairs. * Possess the ability to sit at a computer for extended periods of time. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. This position will work onsite, Goleta, CA. Compensation for this role is in the form of base salary plus a variable component that together comprise the On-Target-Earnings (OTE). The typical starting salary range for new hires in this role is listed below. This range represents the lowest to highest salary range we reasonably and in good faith believe we would pay for this role at the time of this posting. We may ultimately pay more or less than the posted range, and the range may be modified in the future. Please note that base pay offered may vary depending on factors including your geographic location, job-related knowledge, skills, and experience. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. All job offers are contingent upon successful completion of background verification. $22.00 / hour - $24.00 / hour USD For full-time salaried or hourly workers, our total rewards package also include the option to enroll in a company-matched 401k plan, as well as participate in Company-sponsored medical, dental, vision, and basic life insurance plans for the employee and the employee's eligible dependents. Employees will also receive a generous PTO benefit with a starting accrual of 15 days per year (prorated upon hire and increased by tenure), two weeks of paid "Refresh" leave, 80 hours of paid sick leave annually, and 11 paid holidays throughout the calendar year. Kate Farms offers a range of other benefits offered with an emphasis on employee well-being such as paid disability leave, paid parental / pregnancy leave, Flexible Spending Accounts (FSA), tuition reimbursement, an Employee Assistance Program, and more. NOTE: This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization as directed by the management of the company.