Quality technician jobs in San Buenaventura, CA

The Quality Technician III 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 Leads & facilitates problem solving activities such as Fishbone, 5-Why, Fault-tree, etc. Plans and coordinates QA Technician I and II activities and provides general guidance Support DCMA Source Inspection process 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 Develops and maintains process instructions for quality-related activities Works on assignments that are moderately difficult, requiring judgement in resolving issues or in making recommendations Other duties as assigned Basic Qualifications (Required Skills & Experience) High School Diploma or GED equivalent 2 - 4 years of related work experience is required or equivalent combination of education, training, and experience Has Aerospace quality management system experience (AS9100DD) and/or internal audit experience Demonstrated expertise 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 Strong computer skills and is proficient in MS Office Suite (Word, Access, PowerPoint, Excel) Must be able to fill out the necessary flight test documentation Must document any/all non-conformances encountered 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 have a valid California driver's license and clean driving record Other Qualifications & Desired Competencies 2-year technical degree preferred; Quality system courses and/or equivalent experience preferred Must able to work efficiently in a fast-paced, high-volume environment Required to travel to and from remote flying sites on a daily basis Solid ability to accurately record and manage data, records, files and other documents to support tasks Good knowledge of FAI validation and verification process requirements Good knowledge of engineering drawings and specification systems Has an analytical approach to problem solving and high organizational skills in a fast-paced environment as well as effective time management, interpersonal and communication skills Strong ability to manage time and prioritize tasks Receives little instruction on daily work, general instructions on newly introduced assignments. Has substantial understanding of the job and applies knowledge & skills to complete wide range of 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 Has effective problem-solving, analytical, interpersonal and communication skills. Focuses on teamwork, collaboration and puts the success of the team above one's own interests Willingness to work overtime also a must 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 The salary range for this role is: $26 - $37 AeroVironment considers several factors when extending an offer, 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. Citizen, U.S. Permanent Resident (Green Card holder), asylee/refugee status as defined by 8 U.S.C. 1324b(a)(3) or a person approved for an export license from the appropriate governing agency.

Experience in a Medical Device manufacturing environment working with Quality System processes such as Corrective and Preventive Action (CAPA). Experience using Trackwise software for tracking of quality system records. 4 year degree required Experience working with cross functional teams to identify and address quality issue root causes. Experience and ability to produce clear, concise quality records. Ability to articulate information when communicating with others. Additional Information All your information will be kept confidential according to EEO guidelines.

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

Now Hiring: Quality Inspectors - Aerospace Manufacturing Are you an experienced Quality Inspector looking to advance your career in a high-precision aerospace machine shop? Join our team, where product integrity, process excellence, and safety are top priorities in a fast-paced, technical environment. We are seeking mid- to advanced-level Inspectors with a strong background in machined metal aerospace or military parts, proficiency in GD&T, and knowledge of AS9100, AS9102, and ANSI Y14.5 standards. Key Responsibilities Perform in-process, first-article (AS9102), and final inspections of precision-machined aerospace components Use 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 results in MRP systems and support NCR, root cause analysis, and CAPA activities Lead and mentor junior inspectors Support receiving inspections, traceability verification, and adherence to FOD, PPE, and cleanroom protocols Ensure compliance with AS9100, ITAR, and internal quality systems Requirements Minimum 3 years inspecting machined aerospace or military parts (metal only) Proficiency in GD&T, dimensional inspection, and visual inspection Knowledge of AS9100, AS9102, and ANSI Y14.5 standards CMM programming experience (PC-DMIS) a plus Experience with 1factory, FileMaker, or similar QMS/MRP systems Strong shop math, problem-solving, and communication skills in English Dependable, quality-focused, able to work independently and in a team Must pass annual visual acuity and color perception tests (NDT standards) U.S. person required for ITAR compliance Shifts Available 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 Pay & Benefits $22.50-$39.50 per hour (I, II, & III) 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 and take your aerospace inspection career to the next level! NO RECRUITERS PLEASE

Employment Type: Contract Business Unit: Plant Quality Assurance Incoming and Packaging Duration: 3 years with possible conversion to FTE 3 Key Consulting is hiring a Quality Assurance Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: Primary responsibilities of this position include inspecting raw materials, components, and labels, in addition to sampling raw materials, labels, and sanitary utilities, and generating/compiling quality data and reports (e.g. lot track/trace, incidents). Will also assist with document review and initiate incidents, as well as coordinate and compile general documents and oversee room clearance inspection. Skills: quality assurance or manufacturing experience in the pharmaceutical or medical device industry Preferred qualifications: Experience with GMP processes and documentation. Without that fundamental skillset the training for document review tasks, label approval and packaging inspection will have no foundation. Must be able to methodically and meticulously inspect printed materials for print quality defects, clinical product components (e.g. syringes and vials) for physical defects, and batch record documentation for accuracy and completeness. Must be able to work in a team with shifting priorities and shifting responsibilities, such that the team members must be confident verbal communicators able to discuss responsibilities, divide them, reassess them, and potentially reassign them throughout the day or week. Top Must-Have Skill Sets: Bachelor's degree not required but preferred Firm quality mindset is vital**** the job needs to be treated like everyday is their 1st day Highly motivated and willing to lear Team player Day to Day Responsibilities: Performing incoming inspection of raw materials (incoming quality assurance for all raw materials on the campus) Employee Value Proposition: Career growth/ opportunity Red Flags: Candidate cannot be color blind - vision requirements listed above Lack of willingness to learn - candidate needs to be a "go - getter" Interview process: Phone screen Virtual 1:1 (45 minutes- 60) with panel We invite qualified candidates to send your resume to *****************************. If you decide that you're not interested in pursuing this position, please feel free to look at the other positions on our website ******************************* You are welcome to also share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

The Quality Assurance and Regulatory Compliance Associate is responsible for developing, implementing, and maintaining quality systems and regulatory compliance for human subject research conducted at SDRI. Under the supervision of the Director, Clinical Research Operations, this role integrates regulatory oversight, quality assurance, and compliance management to ensure adherence to FDA, ICH-GCP, HIPAA, and institutional policies. The incumbent serves as a key liaison between research operations, sponsors, and regulatory authorities, providing expertise in clinical trial compliance, quality management, and staff education. This role supports inspection readiness, oversees document control and SOP management, maintains research staff qualifications, and ensures data integrity and participant safety across all studies. This is an onsite position; work hours will need to be flexible to meet individual project needs. Attendance at departmental and weekly general staff meetings is expected. ESSENTIAL DUTIES AND RESPONSIBILITIES Maintains regulatory compliance in all research activities in accordance with FDA, ICH-GCP, and OHRP regulations. Prepares, submits, and maintains regulatory documents including IND/IDE applications, annual reports, and study-specific submissions to regulatory agencies. Oversees and maintains Federal-wide Assurance (FWA) documentation and IRB registration. Manages clinicaltrials.gov entries under direction of Principal Investigators. Tracks and maintains documentation of research staff qualifications, training, licenses, and certifications. Oversees study record retention and archiving in accordance with FDA Title 21 CFR 312.62(c), including destruction schedules and offsite storage utilization. Maintains SDRIs SOPs and guidelines to ensure compliance and consistency in research conduct, engaging subject matter experts in SOP development and revisions. Serves as Human Protections Associate and ensures ethical conduct and regulatory compliance in all research activities. Establishes and leads a quality assurance program that monitors compliance with regulatory requirements, GCP, and internal SOPs. Conducts internal quality audits of informed consent forms, source documentation, and regulatory binders for completeness and accuracy. Identifies and manages protocol deviations, noncompliance, and CAPAs (Corrective and Preventive Action Plans). Supports preparation for and participation in external inspections (FDA, sponsor, CRO, IRB) and leads post-inspection follow-up and documentation. Provides guidance on risk management and continuous process improvement. Develops and maintains systems for study tracking, project management, and performance reporting. Partners with IT and operations to ensure secure management of regulatory documents within systems such as Microsoft 365 and Veeva SiteVault. Training Provides training and quality assurance support to research staff. Develops and delivers GCP, compliance, and SOP training sessions. Collaborates with Human Resources and leadership to ensure HIPAA and research ethics training compliance. Supports staff management and supervision as requested by the Director of Research Operations. HIPAA and Privacy Oversight Serves as HIPAA compliance liaison, ensuring privacy and data protection practices are upheld across research activities. Partners with Managed Services Providers and HR to maintain security and privacy SOPs, staff training, and documentation of compliance. Additional Responsibilities Maintains records of publications, abstracts, and clinical trial submissions. Reports issues of noncompliance to executive leadership and Human Resources. Attends and contributes to departmental and organizational meetings. Performs other duties as assigned. QUALIFICATIONS Working knowledge of FDA, ICH-GCP, OHRP, HIPAA, and related research regulations. Strong experience in quality management, internal auditing, and inspection readiness. Ability to interpret and apply regulatory requirements to operational processes. Excellent communication, organizational, and critical thinking skills. Ability to lead, train, and collaborate effectively across teams. Detail-oriented with excellent documentation and problem-solving abilities. Proficiency with Microsoft Office and regulatory document management systems (e.g., Veeva SiteVault). EDUCATION AND EXPERIENCE Bachelors degree required; Masters degree in biological/physical science or related field preferred. Preferred minimum 3 years of experience in clinical research, with emphasis in regulatory or quality assurance. Regulatory or clinical research certification (e.g., ACRP, SOCRA, RQAP-GCP) preferred. Experience supporting FDA or sponsor audits strongly desired. LANGUAGE SKILLS The ability to read, write and speak English clearly is required. The ability to interpret documents such as safety rules, SOPs, and procedures is critical and an understanding of and ability to communicate in scientific language is desired. Spanish proficiency and/or fluency highly desired. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The incumbent is regularly required to sit, talk, hear, and climb stairs. The incumbent frequently is required to use hands to finger, handle or feel equipment, paper, or files. The incumbent is required to stand, walk, and reach with hands and arms. The employee must occasionally lift and/or move up to 10- 20 pounds. Specific vision abilities required by this job include close vision. This position requires manual dexterity, skill level and adequate vision to record data onto data sheets and adequate hearing and verbal communication skills to converse with study subjects. Standing for extended periods of time as well as light lifting is necessary. The incumbent must be in sufficient overall health to report for work consistently and reliably and work through a standard day with appropriate breaks. WORK ENVIRONMENT The work environment would be generally described as an office setting with clinical facilities adjacent to the primary work area and laboratory facilities on a different floor. The ability to move within all three of these areas may be required in the execution of the employees functional activities. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate and the illumination of the work area is primarily with fluorescent artificial lighting. This position is associated with exposure to biohazardous materials and communicable disease always requiring the use of universal precautions as well as other conditions common to a medical clinic and research facility. This job description is intended to describe the general requirements of the performance of the job. It is not a complete list of duties, responsibilities or requirements. Other duties not listed here may be assigned as needed.

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 Control Technician, located in our Moorpark, CA facility. Responsibilities: The candidate will be responsible for providing effective verification of products and certification packages against requirements and the communication of findings associated to the verification. Perform inspection of components and assemblies as part of receiving inspection Maintain accurate, neat and complete inspection records Keep work area organized and clean and follow 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 Must be capable of programming a CMM. The ability to operate and program a Mitutoyo Vision CMM, QV Pak Software, is highly desirable. Knowledge of ISO/AS procedures Must be able to read and interpret Geometric Dimension and Tolerance (GD&T) Must be able to read and understand military specifications and industry standards Read and understand English Effectively communicate and interact with all levels of management High attention to detail Basic PC fundamentals, knowledge of Microsoft Office is essential. 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 - $80,000 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.

Job Title: Quality Control Inspector Business Unit: Space Vector Schedule: 9/80: Employees work 9 out of every14 days - totaling 80 hours worked - and have every other Friday off. About Fisica Inc. Fisica, Inc. is a premier manufacturer of advanced defense products, specializing in the design and production of airborne and ground-based antennas, as well as cutting-edge electromagnetic systems and simulators. Headquartered in San Leandro, California, with additional operations in Simi Valley, Fisica plays a vital role as a trusted partner to leading defense primes and the U.S. Department of Defense. Our company operates as - ATI, Randtron, Datron and Space Vector-each bringing deep expertise and innovation to the defense sector. Led by a seasoned management team, Fisica is committed to excellence in engineering, manufacturing, and mission-critical solutions that enhance national security. At Fisica, we foster a strong, collaborative work culture that values individual contributions and empowers our employees. Our commitment to innovation, integrity, and teamwork makes us a leader in the defense industry and an exceptional place to build a career. Primary Function: Responsible for performing inspections, tests and/or audits of purchased parts, units, materials, equipment, panel/module level assemblies and quality control programs to specifications. Interprets manufacturing drawings, diagrams, specifications and lists to approve or reject units, test setups, or systems for in process or final assemblies. Inspects and may perform minor rework on defective or malfunctioning units or systems. Maintains support documentation and performs sampling and testing of incoming components, raw materials, and build of assemblies. Reviews and reports performance data. Ensure raw materials, in-process and finished products meet company and test standards. Determines or assists in determining methods and procedures necessary for inspection. May interface with customer quality representatives or suppliers. Overall Summary Fully proficient support individual contributor. Works under limited supervision. May be a resource to other employees in areas of expertise. Assignments are moderately difficult requiring some judgment. Nature of Supervision Works under limited supervision. Less detailed instructions are provided and minimal peer review is required. Communication & Influence Communicates with contacts typically within and outside the department on matters that involve obtaining or providing information requiring explanation or interpretation to understand and reach agreement. May be a resource to other employees in areas of proficiency. Innovation & Complexity Work may be structured within identified boundaries and procedures. Follows established processes to complete tasks. Identifies problems and issues in straightforward situations. Resolves most issues. Organization Impact Works to achieve operational targets within job area which has moderate impact on the overall achievement of results for the team. Work is of moderate scope, typically on larger, task-related activities. Education & Experience Requires fully proficient job knowledge/skills. Requires a High School Diploma or equivalent and a minimum of 6 years of prior relevant experience or 2 years post-Secondary/Associates Degree with a minimum of 2 years of prior related experience. In compliance with pay transparency requirements, the salary range for this role $51,000 - $94,500. This is not a guarantee of compensation or salary, as the final offer amount may vary based on factors including but not limited to experience and geographic location. Fisica Inc also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on the date of hire, and schedule type. EEO Statement Fisica is proud to be an Equal Opportunity Employer. Fisica is committed to treating all employees and applicants for employment with respect and dignity and maintaining a workplace that is free from unlawful discrimination. All applicants will be considered for employment without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender (including pregnancy, childbirth, breastfeeding or other related medical conditions), gender identity, gender expression, sexual orientation, marital status, military and veteran status, disability, genetic information, citizenship status, characteristic or membership in any other group protected by federal, state or local laws. Fisica maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks, where permitted by law. Fisica is an E-Verify Employer. Please click here for the E-Verify Poster in English or Spanish. For information regarding your Right To Work, please click here for English or Spanish. #LI-KW1

Job Description Job Title: Quality Control Inspector Business Unit: Space Vector Schedule: 9/80: Employees work 9 out of every14 days - totaling 80 hours worked - and have every other Friday off. About Fisica Inc. Fisica, Inc. is a premier manufacturer of advanced defense products, specializing in the design and production of airborne and ground-based antennas, as well as cutting-edge electromagnetic systems and simulators. Headquartered in San Leandro, California, with additional operations in Simi Valley, Fisica plays a vital role as a trusted partner to leading defense primes and the U.S. Department of Defense. Our company operates as - ATI, Randtron, Datron and Space Vector-each bringing deep expertise and innovation to the defense sector. Led by a seasoned management team, Fisica is committed to excellence in engineering, manufacturing, and mission-critical solutions that enhance national security. At Fisica, we foster a strong, collaborative work culture that values individual contributions and empowers our employees. Our commitment to innovation, integrity, and teamwork makes us a leader in the defense industry and an exceptional place to build a career. Primary Function: Responsible for performing inspections, tests and/or audits of purchased parts, units, materials, equipment, panel/module level assemblies and quality control programs to specifications. Interprets manufacturing drawings, diagrams, specifications and lists to approve or reject units, test setups, or systems for in process or final assemblies. Inspects and may perform minor rework on defective or malfunctioning units or systems. Maintains support documentation and performs sampling and testing of incoming components, raw materials, and build of assemblies. Reviews and reports performance data. Ensure raw materials, in-process and finished products meet company and test standards. Determines or assists in determining methods and procedures necessary for inspection. May interface with customer quality representatives or suppliers. Overall Summary Fully proficient support individual contributor. Works under limited supervision. May be a resource to other employees in areas of expertise. Assignments are moderately difficult requiring some judgment. Nature of Supervision Works under limited supervision. Less detailed instructions are provided and minimal peer review is required. Communication & Influence Communicates with contacts typically within and outside the department on matters that involve obtaining or providing information requiring explanation or interpretation to understand and reach agreement. May be a resource to other employees in areas of proficiency. Innovation & Complexity Work may be structured within identified boundaries and procedures. Follows established processes to complete tasks. Identifies problems and issues in straightforward situations. Resolves most issues. Organization Impact Works to achieve operational targets within job area which has moderate impact on the overall achievement of results for the team. Work is of moderate scope, typically on larger, task-related activities. Education & Experience Requires fully proficient job knowledge/skills. Requires a High School Diploma or equivalent and a minimum of 6 years of prior relevant experience or 2 years post-Secondary/Associates Degree with a minimum of 2 years of prior related experience. In compliance with pay transparency requirements, the salary range for this role $51,000 - $94,500. This is not a guarantee of compensation or salary, as the final offer amount may vary based on factors including but not limited to experience and geographic location. Fisica Inc also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on the date of hire, and schedule type. EEO Statement Fisica is proud to be an Equal Opportunity Employer. Fisica is committed to treating all employees and applicants for employment with respect and dignity and maintaining a workplace that is free from unlawful discrimination. All applicants will be considered for employment without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender (including pregnancy, childbirth, breastfeeding or other related medical conditions), gender identity, gender expression, sexual orientation, marital status, military and veteran status, disability, genetic information, citizenship status, characteristic or membership in any other group protected by federal, state or local laws. Fisica maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks, where permitted by law. Fisica is an E-Verify Employer. Please click here for the E-Verify Poster in English or Spanish. For information regarding your Right To Work, please click here for English or Spanish. #LI-KW1

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

Join our dynamic team as a Quality Control Technician, where you will play a crucial role in ensuring the highest standards of product quality in a cleanroom environment. You will be responsible for inspecting incoming and final products, contributing significantly to our quality assurance processes. Responsibilities * Manage the equipment calibration and maintenance program, maintaining inventory and status of measuring devices. * Provide support for all testing related to manufacturing, including first article inspections, in-process release inspections, final QC release of finished goods, and document reviews. * Ensure all inspections and procedures are properly completed and documented. * Support environmental monitoring of cleanrooms and address microbial failures with effective solutions. * Review quality assessment results to determine acceptance or rejection of manufactured products during the inspection process. * Participate in the investigation of source materials for products and components. * Complete customer surveys and questionnaires. Essential Skills * Bachelor's degree in a technical or scientific field, or High School Diploma with 1-3 years of experience in quality assurance. * Understanding of global pharmaceutical product regulations with experience in ISO 9001 and/or 21 CFR Parts 210, 211, and/or Part 820. * Experience in quality systems including corrective actions, change control, quality audits, and validation of manufacturing processes or product development in a pharmaceutical or medical device environment. * Solid organizational and planning skills. * Ability to communicate effectively, both verbally and in writing, and demonstrate good interpersonal skills interdepartmentally and with external vendors and contractors. * Ability to work effectively and efficiently in a team environment. * Passion for innovation and drive for solutions. * Personal accountability for results and integrity. * Eagerness to learn and continuously improve. * Uncompromising dedication to quality. * Good general mathematical and computer skills. Additional Skills & Qualifications * Experience with labeling, quality control, quality assurance, blueprint reading, GMP, documentation, quality inspection, deviation management, attention to detail, and document control. * Proficiency in the use of calipers and quality inspection techniques. * Ability to work effectively in a high-paced cleanroom environment. Work Environment This role requires working within a cleanroom environment where precision and attention to detail are paramount. Candidates should be comfortable working in a fast-paced setting, utilizing small measuring devices and computer skills to ensure the highest level of product quality. Job Type & Location This is a Permanent position based out of Camarillo, CA. Pay and Benefits The pay range for this position is $49920.00 - $49920.00/yr. Medical, Dental, Vision, FSA, Life and AD&D, 401(k) Workplace Type This is a fully onsite position in Camarillo,CA. Application Deadline This position is anticipated to close on Dec 31, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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.

Quality Inspector Opening! We are seeking a skilled and detail-oriented Quality Inspector to join our team. As a Quality Inspector, you will be responsible for ensuring that our products meet the highest quality standards through inspection, testing, and documentation. You will play a crucial role in maintaining our commitment to excellence and customer satisfaction. Responsibilities: Perform thorough inspections of incoming materials, in-process components, and finished products to ensure compliance with established quality standards and specifications. Conduct inspections using precision measuring instruments, gauges, and testing equipment. Analyze and interpret technical drawings, specifications, and other relevant documents to determine compliance with quality requirements. Document and report inspection findings, test results, and non-conformities, and collaborate with cross-functional teams to resolve any quality issues. Monitor and maintain inspection equipment, including calibration and troubleshooting as needed. Participate in root cause analysis and corrective action initiatives to identify and address quality concerns. Provide guidance and support to production teams in implementing quality control procedures and best practices. Conduct product audits and review quality documentation to ensure adherence to regulatory and industry standards. Contribute to continuous improvement efforts by identifying opportunities for process optimization and efficiency gains. Qualifications: High school diploma or equivalent, with additional technical or vocational training in quality assurance or a related field preferred. Proven experience as a Quality Inspector in a manufacturing or production environment. Strong understanding of quality control principles, inspection techniques, and measurement tools. Ability to read and interpret technical drawings, specifications, and documentation. Familiarity with relevant regulatory and industry standards, such as ISO 9001, AS9100, or similar. Excellent attention to detail, with the ability to identify and address non-conformities and discrepancies. Strong communication skills, both written and verbal, with the ability to effectively collaborate with cross-functional teams. Ability to work independently, prioritize tasks, and meet deadlines.

MWH is a leading water and wastewater treatment focused general contractor in the US with a rich history dating back to the 19th century Fueled by the mission of Building a Better World our teams are rapidly growing across the nation As a company committed to our teams well being and growth we offer a supportive work environment opportunities for advancement and the chance to contribute to a mission that shapes the future Your expertise and ambition are valued here The work we do matters The critical systems infrastructure we build changes lives betters communities and improves ecosystems If youre passionate about this we want to hear from you About the Role MWH Constructors Construction Management Services CMS group is seeking qualified candidates for the position of Quality Inspector to conduct and document inspections related to the construction of waterwastewater related infrastructure projects in the Santa Clarita CA area Essential Functions Represent the project owner in the field provide single point field inspection of the Contractors work Daily monitor and record contractors methods procedures and processes for compliance with the contract and prepare a comprehensive Daily Inspection Report with measurement of daily installed quantities and resources utilized Inspect the work for completeness and conformance with the plans specifications and applicable regulations and ordinances Assist the construction manager in developing as built drawings Document compliance and non compliance of completed work with established quality control and quality assurance processes and procedures Basic Qualifications High School diploma or equivalent education Strong written and oral communication skills Minimum of 3 years of inspection experience in the construction of water infrastructure projects ACIACPII CertificationsA thorough understanding of construction safety quality control and general contract management requirements is necessary Confined Space CertificationAn equivalent combination of related experience and technical training may be substituted Valid California Drivers LicensePreferred Qualifications Bachelor of Science degree in Civil Engineering or Construction ManagementCompensation The base hourly rate is 6596 and fringe benefits are 3535 as per the General Prevailing Wage Determination PWD issued by the Director of Industrial Relations httpswwwdircagovoprl2025 2PWDDeterminationsSouthernSC 023 63 2DpdfBenefits Health Insurance medical dental and vision Paid Time Off includes vacation and sick time Paid Parental Leave Program10 Paid Holidays 401k Plan company matching contributions up to 4Employee Referral Program MWH Constructors is a global project delivery company in heavy civil construction with a focus on water and wastewater treatment infrastructure With the ultimate goal of delivering maximum value to clients and their local communities MWH Constructors provides single source integrated design and construction services through a full range of project delivery methods Incorporating industry leading preconstruction and construction services the Companys multi disciplined team of engineering and construction professionals delivers a wide range of projects including new facilities infrastructure improvement and expansion and capital construction services Equal Opportunity Employer including disabled and veterans Please note that all positions require pre employment screening including drug and background check as a condition of employment LI JB1 LI Onsite

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 (*****************************************

Experience in a Medical Device manufacturing environment working with Quality System processes such as Corrective and Preventive Action (CAPA). Experience using Trackwise software for tracking of quality system records. 4 year degree required Experience working with cross functional teams to identify and address quality issue root causes. Experience and ability to produce clear, concise quality records. Ability to articulate information when communicating with others. Additional Information All your information will be kept confidential according to EEO guidelines.

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 Control Technician, located in our Moorpark, CA facility. Responsibilities: The candidate will be responsible for providing effective verification of products and certification packages against requirements and the communication of findings associated to the verification. Perform inspection of components and assemblies as part of receiving inspection Maintain accurate, neat and complete inspection records Keep work area organized and clean and follow 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 Must be capable of programming a CMM. The ability to operate and program a Mitutoyo Vision CMM, QV Pak Software, is highly desirable. Knowledge of ISO/AS procedures Must be able to read and interpret Geometric Dimension and Tolerance (GD&T) Must be able to read and understand military specifications and industry standards Read and understand English Effectively communicate and interact with all levels of management High attention to detail Basic PC fundamentals, knowledge of Microsoft Office is essential. 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 - $80,000 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.

Employment Type: Contract Business Unit: Plant QA Drug Substances Duration: 18+ months (with likely extensions) Rate: $28-32/Hr W2. Notes: 100% Onsite. Must have Biotech/ Pharma experience required. Must be able to work swing, morning, evenings, night shift (24/7 Operation building). Once trained it will 4 day work week. Must have proven Quality Assurance experience. Must have lab setting and quality background as they will be supporting the lab staff and provide quality oversight. Posting Date: 06/02/22 3 Key Consulting is hiring a Quality Assurance Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company. Job Description: The Senior Associate QA role supports client's Quality Assurance program, providing daily oversight of Drug Substance manufacturing facilities at client's Thousand Oaks, CA. facility. Under general supervision, the role provides support and compliance oversight to MFG and F&E staff in the execution of their processes, procedures, and use of quality systems. Duties include purposeful presence on the manufacturing floor, batch record review, SOP and MP revision approval, work order approval, and quality approval of deviations and CAPAs. Responsibilities will include evaluation of compliance issues, providing recommendations, and assuring progress of quality records to completion. The incumbent will also represent functional area quality for the Bulk Quality Assurance department in the execution of projects necessary to achieve departmental operational excellence goals and will work in a team matrix environment to ensure workplace safety. This staff member will be assigned to provide quality support during either day or night shift schedule periods, as operation support is 24/7. Why is the Position Open? Supplement additional workload on team. Top Must-Have Skill Sets: Technical writing experience (i.e. deviation records, CAPA records, controlled documents) Excellent verbal and written cross functional communication skills Must have biotech/pharma manufacturing, quality assurance, or quality control experience Biotech/ Pharma experience required*** Must be able to work swing, morning, evenings, night shift (24/7 Operation building). Once trained it will 4 day work week. Day to Day Responsibilities: Purposeful presence on the manufacturing floor (80% of working time spent on MFG floor in controlled, classified cell culture and protein purification areas). Batch record review SOP and MP revision approval work order approval quality approval of deviations and CAPAs Safety auditing and observational work GEMBA walks Red Flags: Not able to work onsite Unable to work shifts including morning, evening, or potentially nights No Biotech/ Pharma background/experience No quality assurance, quality control experience Interview process: Phone screening followed by in-person interview. We invite qualified candidates to send your resume to **************************. If you decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our website ******************************* You are also welcome to share this opportunity with anyone you think might be interested in applying for this role. Regards, 3KC Talent Acquisition Team

Job DescriptionQuality Inspector (Electronic) Reports To: Quality Manager Department: Quality Summary: The prime responsibility of the Quality Inspector is to maintain quality standards by inspecting and approving incoming materials, in process production, finished products, and recording quality results. Duties: Using established sampling standards, inspect and approve incoming materials, in process production, and finished products by confirming specifications, conducting visual and measurement tests, and rejecting unacceptable materials and/or products Document inspection results by completing reports and logs, summarizing reject results, and inputting data into quality database When in process production materials fail, determine which Operator(s) were involved and document results Comply with ESD and FOD requirements and report instances where ESD and FOD requirements are not met, to supervisor Operate inspection equipment (microscopes, calipers, etc.) Generate non-conformance reports Initiate corrective actions after approval from supervisor Complete work consistent with the Master Schedule Attend and effectively communicate in required meetings Other duties as assigned. Qualifications: Education/Experience: High school diploma or General Education Degree (GED); or one to three months related experience and/or training; or equivalent combination of education and experience. Prefer, 6 months prior experience inspecting electronic boards. Language Ability: Read and understand English. Math Ability: Good Math and analytical skills. Reasoning Skills: Able to Read and interpret written instructions and drawings. Supervisory Responsibilities: This job has no supervisory responsibilities. Additional Requirements: Familiar with inspecting electronic boards, components, etc. Familiar with counterfeit mitigation Able to read and understand written instructions and electrical drawings Familiar with use of measuring tools Must be extremely detail oriented Prefer, IPC Standards Knowledge Familiar with AS 9100/ISO 9001 requirements General PC Knowledge Familiar with manufacturing software (or able to become familiar with manufacturing software) used by the company. Physical Demands: The employee must regularly lift and/or move up to 10 pounds and occasionally lift and or move up to 15 pounds. Specific vision abilities required by this job include Close vision, Distance vision, Peripheral vision, Depth perception and Ability to adjust focus. While performing the duties of this job, the employee is regularly required to sit for prolonged periods of time; use hands to finger, handle, or feel and reach with hands and arms. The employee is frequently required to talk or hear. The employee is regularly required to stand and walk. Must be able to work Four 10 hour shifts per week. Measures of Performance: Accurately inspects products; defects are caught before going to next in-process assembly Accurately records inspection results, with specific Operator(s) identified Communicates well with other personnel Attendance record Completes work within timeframes allotted from Master Schedule.