Quality assurance technician jobs in San Buenaventura, CA

Hourly Wage Estimate: $62.20 - $73.26 / hour Learn more about the benefits offered for this job. The estimate displayed represents the typical wage range of candidates hired. Factors that may be used to determine your actual salary may include your specific skills, how many years of experience you have and comparison to other employees already in this role. The typical candidate is hired below midpoint of the range. Introduction Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring for patients with purpose and integrity. We care like family! Jump-start your career as a Cardiac Cath Lab Technologist today with Los Robles Regional Medical Center. Benefits Los Robles Regional Medical Center offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include: Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation. Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more. Free counseling services and resources for emotional, physical and financial wellbeing 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service) Employee Stock Purchase Plan with 10% off HCA Healthcare stock Family support through fertility and family building benefits with Progyny and adoption assistance. Referral services for child, elder and pet care, home and auto repair, event planning and more Consumer discounts through Abenity and Consumer Discounts Retirement readiness, rollover assistance services and preferred banking partnerships Education assistance (tuition, student loan, certification support, dependent scholarships) Colleague recognition program Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence) Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income. Learn more about Employee Benefits Note: Eligibility for benefits may vary by location. Come join our team as a Cardiac Cath Lab Technologist. We care for our community! Just last year, HCA Healthcare and our colleagues donated $13.8 million dollars to charitable organizations. Apply Today! Job Summary and Qualifications Every heartbeat matters-and as a Cardiac Cath Lab Technologist, you'll be part of the team that protects them. In this role, you'll stand alongside physicians and colleagues to deliver advanced care during lifesaving cardiac procedures. With access to state-of-the-art cath lab technology, a strong team by your side, and the support you need to balance work and life, you'll be empowered to deliver the safe, high-quality care you take pride in delivering. From guiding patients and families through their journey to ensuring precision in every step of treatment, you'll bring both skill and compassion to moments that improve more lives in more ways. Your responsibilities will include: Assisting physicians with complex cardiac and vascular procedures, including angiograms, angioplasties, and stent placements Preparing and supporting patients and families with care, education, and reassurance before, during, and after procedures Operating and maintaining advanced equipment to deliver safe and effective treatment Monitoring patient responses with vigilance and compassion to ensure the highest level of care Safeguarding a sterile, safe environment while serving as an advocate for every patient What qualifications you will need: Registered through American Registry of Radiologic Technologists (ARRT) Must be certified by the State of California (i.e. CRT) Must have current California Fluoroscopy permit Current BLS provider card Current ACLS provider card within three months of hire Registered Cardiovascular Invasive Specialist within 18 months of employment desired Los Robles Regional Medical Center is a 380+ bed acute care hospital dedicated to serving the residents of Ventura and Los Angeles Counties along with the Greater Conejo Valley. We are the only Level II Trauma Center in East Ventura County. We are known for providing excellent care with compassion and kindness to each of our patients. In addition, Los Robles Regional Medical Center features a 24-hour emergency department, comprehensive stroke center, ICU/CCU, maternity, Level III NICU, comprehensive cancer center, heart & cardiovascular center, same day surgery, and rehab center. HCA Healthcare has been recognized as one of the World's Most Ethical Companies by the Ethisphere Institute more than ten times. In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses. "The great hospitals will always put the patient and the patient's family first, and the really great institutions will provide care with warmth, compassion, and dignity for the individual."- Dr. Thomas Frist, Sr. HCA Healthcare Co-Founder If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Cardiac Cath Lab Technologist opening. We promptly review all applications. Highly qualified candidates will be contacted for interviews. Unlock the possibilities and apply today! We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

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. **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 (*****************************************

Company: Fusion Medical Staffing Job Details Fusion Medical Staffing is seeking a skilled Cath Lab Tech for a 13-week travel assignment in Thousand Oaks, California. As a member of our team, you'll have the opportunity to make a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team. Required Qualifications: One year's recent experience as a Cardiac Cath Lab Tech Current BLS (AHA/ARC) certification ARRT, RCES, or RCIS certification Current ACLS (AHA/ARC) certification Preferred Qualifications: Valid Radiologic Technologist license in compliance within state regulations PALS (AHA/ARC) or ENPC Certifications Other certifications and licenses may be required for this position Summary: The Cath Lab Technologist is responsible for assisting in diagnostic and interventional cardiovascular procedures in the cardiac catheterization lab. This role involves preparing patients and equipment, monitoring hemodynamic data, assisting physicians during procedures, and ensuring patient safety throughout the process. The technologist operates specialized imaging equipment, maintains sterile technique, and collaborates with the healthcare team to provide high-quality patient care. This position requires technical expertise in cardiovascular procedures, critical thinking skills, and the ability to work efficiently in high-pressure situations. Essential Work Functions: Prepare and position patients for cardiac catheterization, angioplasty, stent placement, electrophysiology studies, and other interventional procedures Assist physicians during procedures by passing catheters, wires, balloons, and stents, and operating fluoroscopy and hemodynamic monitoring equipment Operate and maintain imaging equipment, contrast injectors, and hemodynamic monitoring systems, ensuring proper functionality Scrub in and assist with sterile field setup, ensuring adherence to infection control and procedural protocols Perform sheath removal and hemostasis using manual compression or closure devices as directed Maintain accurate documentation, including patient records, imaging data, and equipment logs Assist with inventory management, stocking supplies, and ensuring proper storage of sterile instruments and medications Adhere to radiation safety protocols, ensuring proper use of lead aprons, shields, and dosimeters Ensure compliance with hospital policies, safety guidelines, and regulatory requirements Adhere to hospital safety protocols, infection control guidelines, and regulatory standards Perform other duties as assigned within the scope of practice Required Essential Skills: Critical thinking, service excellence, and good interpersonal communication skills The ability to read, write, and communicate in the English language Ability to read/comprehend written instructions, follow verbal instructions, and proficiency in PC skills Physical Abilities - Must be able to remain in a stationary position, move about, move equipment (50-100lbs), push, pull, and bend Interpersonal Skills - Must be able to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and professionalism Technical/Motor Skills - Must have the ability to grasp, perform fine manipulation, push/pull, and move about when assisting with procedures and/or using department equipment Mental Requirements - Must be able to cope with frequent contact with the general public and customers while meeting deadlines under pressure. Must be able to work under close supervision occasionally, as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail Sensory - Must possess visual acuity and ability to effectively communicate Benefits Include: Highly competitive pay for travel professionals Comprehensive medical, dental, and vision insurance with first day coverage Paid Time Off (PTO) after 1560 hours Life and Short-term disability offered 401(k) matching Aggressive Refer-a-friend Bonus Program 24/7 recruiter support Reimbursement for licensure and CEUs Why Choose Fusion? At Fusion Medical Staffing, our goal is to improve the lives of everyone we touch, and we're always looking for people like you to join our mission. Your passion for helping others deserves a partner just as committed to supporting you - that's why we offer day one insurance, $0 copay for mental health services, scholarships and awards, exclusive discounts, and more. From your personal recruiter to our clinical and traveler experience teams, we're here to guide and celebrate you along your journey. You take care of others; we take care of you. Other Duties Disclaimer: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed 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. Other duties may be assigned. This job description is not a comprehensive list of all activities, duties, or responsibilities that are required of the employee for this job and is subject to change at any time with or without notice. Start your rewarding career as a Travel Cath Lab Tech with Fusion Medical Staffing and join our mission to improve lives. Apply now! *Fusion is an EOE/E-Verify Employer #pb15

Your Opportunity as a Quality Assurance Intern As an intern within our quality department, you will work closely with management, office, quality control, maintenance and hourly personnel to achieve goals. You will assist in identifying potential quality problems; develop, recommend and report on improvement measures; and recommend corrective action. Location: Oxnard, CA Work Arrangements: Onsite, 100% of the time In this role you will: Responsible for adherence to company and departmental policies, procedures and practices. Ensures that company GMPs are being followed. Participates in daily Production meetings. Conduct daily sanitation inspection. Inspects incoming packaging and ingredients for compliance with JMS specifications. Monitors HACCP plan. Assists in the training of hourly personnel. Data entry into computer systems. Monitors accuracy of lab paperwork. Investigates quality incidents. Prevents accidents by recognizing physical and behavioral hazards and taking corrective action. May do manual work. Work with the Personnel Clerk and work out labor needs for the following workday. Assists in the coordination of the activities of all QA staff, as necessary. May assist in the training and dissemination of work in the Department. Perform laboratory tests as required. Maintain laboratory in an organized, clean condition. Maintain inventory of laboratory chemicals, supplies and equipment. Inspect and grade products as necessary. Provide up-to-date quality control records and reports as necessary on a timely basis. Promote a positive and safe work environment. Maintains updated specification manuals, formulas, and test procedures. Responsible for having an understanding and working knowledge of JMS grading procedures and product specifications. Conduct special tests, evaluations, and projects as requested by the Quality Assurance Manager. Coordinates shipping and receiving activities with floor persons, quality control personnel and forklift drivers. Assist with preparation for third party audits. Maintain quality control records. Supervise or conduct incoming packaging or ingredient materials inspection. Stay current with trends and developments in the quality control field including sanitation, food technology, processing, governmental regulations and requirements. Other duties as required. What we are looking for: Currently have a 4-year degree or are currently enrolled in a 4-year Food Science or Engineering degree program is required. Ability to read, write and speak Spanish highly desired Available in late March through the end of August. Able to work weekends, overtime, and night shifts. Must be able to work six days per week, various shifts. Strong leadership skills and communication skills. Must be detail orientated. Organized with good analytical skills. Technical knowledge in food processing is preferred. Must be able to read, write, and speak English. Compensation: Pay range: $20/hr. to $24.50/hr. Housing allowance (for applicable students) Application Period: Application period closes on January 31st, 2026 Why Choose the J.M. Smucker Company's Internship Program? Are you seeking an exceptional internship experience at a Fortune 500 company? At Smucker, we are dedicated to providing a world-class, award-winning internship that offers you the opportunity to: Learn: Unlock your potential in a collaborative and supportive environment where you are treated like a true peer and challenged to be your best. Grow: Benefit from hands-on training with a dedicated mentor and connect with peers and leaders throughout the company. Lead: Contribute to high-profile projects that support our Company's growing categories like snacks, coffee and pet food. Additional Perks: Along with engaging work, we offer a variety of benefits to ensure your internship is both rewarding and memorable. These include: Unique opportunities to network and interact with company leadership Customized professional development sessions Networking events and social outings with fellow interns Access to a fully equipped fitness center, complete with a basketball court, indoor walking track, and recreational league sports The Orchard, our gourmet cafeteria, offering breakfast and lunch with seasonal and locally-sourced ingredients A competitive compensation package, including paid corporate holidays Employee discounts at our Company Store A housing stipend for interns relocating for the program Experience an internship where you can learn, grow, and lead - all while being part of something special at Smucker. Learn more about working at Smucker: Our Internship Program Delivering on Our Purpose Our Continued Commitment to Ensuring a Workplace for All Follow us on LinkedIn

Responsible for inspecting, documenting and communicating product conditions upon arrival. Perform other duties as necessary. ESSENTIAL DUTIES & RESPONSIBILITIES · Conduct routine visual inspections on the product to ensure conformance to standards. · Record findings. · Set up stations and equipment to measure quality specifications. · Test product for internal defects and oil content. · Maintain a clean and orderly workstation. · Communicate issues to leads and supervisors. · Utilize ladders, computers, tablets and other tools to record quality of product. · Maintain food facility regulations. · Perform other duties as requested. MINIMUM QUALIFICATIONS & REQUIREMENTS · High school diploma or equivalent. · Basic computer skills. · Effective interpersonal communication skills. · Bilingual in English and Spanish preferred. · Able to work in a fast-paced, dynamic and high stress environment. · Able to work independently. WORKING CONDITIONS · Ability to be flexible with hours. · Ability to work in a cold and wet environment. · Ability to lift or move 25-50 pounds. · Ability to climb ladders. · Safely work near moving mechanical parts and equipment. · Ability and willingness to stand, walk, stoop, kneel, crouch/bend as needed to perform essential task.

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 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.

U.S. Citizenship is Required. Ability to qualify for a US Department of Defense security clearance required. is in person. The Quality Assurance Specialist will support the operation of the Quality Management System (QMS) of the Aerospace Systems team. This role will report directly to the Aerospace Systems Quality Manager and will contribute significantly to upholding the quality of our manufacturing processes. A successful candidate will possess strong critical thinking skills, a motivation for continuous improvement, and an acute attention to detail. Key Responsibilities: Coordinate closely with Aerospace team members to ensure compliance with relevant quality requirements Conduct quality reviews for controlled documentation and completed manufacturing travelers Assist with third party and internal audits including performance of root cause evaluations and enacting corrective action plans Track and consolidate key performance indicator data including supplier performance, and nonconformance rates Manage the creation, review, and retention of a wide variety of controlled documents in support of the QMS and customer requirements, including first article inspection reports, configuration management reports, nonconforming material records, process deviations, build records, and calibrated tool maintenance Identify improvements to existing processes and review effectivity of process changes. Lead the management of suppliers including evaluation and approval of prospective suppliers, engagement with project managers on active orders, issuance and tracking of supplier corrective actions, performance of supplier audits Track changes to required standards (e.g., customer quality requirements documents, AS9102, AS5553, EIA- 649, etc.) and assist with updating internal processes for continued compliance Requirements Bachelor's degree: Business, engineering, or a related field preferred Minimum of 4 years of work experience Previous experience working under a QMS, ISO 9001 or AS9100 preferred Proficient in crafting presentations, handling spreadsheets, preparing reports, and composing procedures using MS Word, Excel, and PowerPoint software applications Showcase strong organizational skills and a consistent approach to planning Able to communicate and facilitate collaboration of cross-discipline team members Preferred Qualifications: Possess an in-depth understanding of AS9100 Experience in a high value aerospace manufacturing environment Experience in procurement WE OFFER AN EXCEPTIONAL EMPLOYEE BENEFITS PACKAGE! Competitive Industry Pay 100% Employer-Paid Medical Insurance Premium HSA with Employer Contributions Dental and Vision Coverage Options Paid Holidays Paid Vacation and Sick leave Company Funded 401(k) and Profit Sharing Plans Employee Stock Ownership Plan (ESOP) Life and Disability Insurance Paid Parental Leave Discretionary Bonus Eligibility The annual pay range for the Quality Assurance Specialist position is $75,000 to $115,000. The posted pay range values provide the candidate with guidance on annual base compensation for the position, at a full time level of effort, exclusive of overtime, bonus, and benefits-related compensation, over a range of qualifications that may fit hiring objectives. Toyon Research Corporation will consider the individual candidate's education, work experience, applicable knowledge, skills and training, among other factors, when preparing an offer of employment. Pay Transparency Nondiscrimination Provision Equal Opportunity Employer including Disability and Veterans Applicant Privacy Notice Learn more about our company in our latest video, We are Toyon. Ref #2568-H

We are seeking a Quality Specialist to support client's digital quality transformation by leading validation testing, driving change management, and managing cross-functional projects across our digital Quality platforms. This role ensures that enhancements to our **digital quality systems-such as batch release, quality workflows, and integrated data solutions-**are compliant, reliable, and successfully adopted by global users. **Key Responsibilities** + Lead validation activities for digital quality system updates, including test planning, execution, documentation, and issue resolution. + Drive change management to support new system capabilities, user adoption, communications, and training. + Manage multiple digital quality projects involving system enhancements, process improvements, and cross-functional coordination. + Ensure digital workflows and integrations supporting material and product release meet GxP requirements. + Collaborate with internal partners and external vendors to ensure timely, compliant, and high-quality delivery. **Required Skills & Competencies** + Strong GxP background with direct experience in material and product release. + Hands-on experience with digital quality systems (e.g., eQMS, complaint systems, digital batch release, quality data integrations). + Proven capabilities in validation testing, change management, and project leadership. + Excellent communication skills (English & Spanish preferred) and ability to work effectively in a matrixed, cross-functional environment. + Exceptional attention to detail, analytical mindset, and ability to manage competing priorities. **Preferred Qualifications** + 5+ years of biopharmaceutical experience in Quality, Validation, Manufacturing, Regulatory, or related areas. + Knowledge of GMP regulations, digital quality systems, and modern quality technologies. **Must Have skills:** + Looking for someone with PM experience and quality background + This position will largely be focused on validation testing, writing, change management responsibilities and some PM work. **About US Tech Solutions:** US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit *********************** . "US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran"

We have a great opportunity to join a stable, family-owned company looking for a new team member. Located in Ventura County, in business 59 years, and supplier to the aeronautical and aerospace industries, Hudson Plating Works specializes in prototypical, research & development, and special projects. We are currently looking to add a Senior Process Technician. This is a top-level position that requires a solid production background. Previous metal finishing experience is a plus, but not required. Duties & Responsibilities: Ability to understand industry and customer specifications. Proficient with blueprint interpretation. Experience in handling hazardous chemicals required in processing. Demonstrate ability to prepare surfaces of parts; mask, blast, clean, plate. Basic electrical knowledge; circuitry, rectifiers, anode/cathode placement. Assist laboratory in adding chemicals to plating baths to ensure proper balances. Experience with all safety and PPE requirements used in plating with hazardous chemicals. Report all equipment problems to management and make minor/temporary repairs when possible. Coordinate troubleshooting for all process and equipment operations Maintain safe and healthy work environment by ensuring that policies and safety procedures are followed Provide exceptional attention to detail and maintain strong relationships with team members and customers Required Skills & Qualifications: •Minimum 3-5 years production experience •Excellent planning, organizational, and communication skills We offer the unique prospect of learning and growing with our expanding company. Further your knowledge with a chance to earn certification, accreditation and a distinctive edge in this challenging industry. The successful candidate will be one that can show dependability and a desire to become a team member with our expanding organization. **This role requires industrial experience. The position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. citizen or U.S. Permanent Resident (i.e. Green Card Holder).** When applying, provide a salary requirement along with your resume. Salary is commensurate with experience and skill level. Send resume and salary expectations to: employment@castorstaffing.com Job Type: Full-time Pay: Up to $37.00 per hour Expected hours: 40 per week Benefits: 401(k) 401(k) matching Dental insurance Health insurance Paid time off Vision insurance Schedule: 8 hour shift Monday to Friday Ability to Commute: Moorpark, CA 93021 (Required) Ability to Relocate: Moorpark, CA 93021: Relocate before starting work (Required) Work Location: In person

Halo Group is a premier provider of IT talent. We place technology experts within the teams of the world's leading companies to help them build innovative businesses that keep them one step closer to their customers and one step ahead of the competition. We offer a meaningful work environment for employees, attractive and interesting engagements for consultants, and cutting-edge digital innovation for our customers. We delight in helping our customers execute their digital vision. Big projects or small, Halo Group knows that by combining the highest quality talent with our unwavering support, we will become an invaluable extension of the team. Halo Group's experienced consultants in Detroit, Atlanta and Dallas specialize in all areas of product/project governance, UX/UI, multi-platform applications, quality assurance/testing, cloud computing, and data analytics. Since its inception, Halo Group has been recognized for numerous awards, including: - INC 5000 - Future 50 - 101 Best and Brightest - Michigan 50 Companies to Watch - Goldline Research - “Most Dependable Companies” - Ernst & Young - “Entrepreneur of the Year” Finalist : Extensive experience with QTP and UFT is a MUST Must be local to CA and can attend F2F interview. Qualifications Job Description: Extensive experience with QTP and UFT is a MUST Must be local to CA and can attend F2F interview. Additional Information H1b, US Citizens, GC, EAD and TN Permit. Titles: QA Tester, QA Analyst, Automation Tester, QA Engineer, Test Engineer, QA Test Skills: Testing, QTP, Quick Test Pro, UFT

Job DescriptionSchedule: 8:00 AM to 5:00 PM, Monday through Friday; with flexibility to work evenings, weekends, and holidays, as needed or scheduled Momentum is hiring a Quality Assurance Specialist. The Quality Assurance Specialist is responsible for conducting various quality checks at all programs and providing reports on findings to the Director of Quality and Compliance. Benefits (full-time): Medical/Dental/Vision Insurance Life Assistance Program Flexible Spending Account (FSA) Paid Holidays Paid Vacation/Sick/Bereavement leave Credit Union Benefits and Discounts Retirement Plan (403B) Direct Deposit Quality Assurance Specialist Essential Responsibilities: Manages the scheduling, record keeping, and billing management of required employee certifications. Utilizes mock survey, program review checklist, and monthly safety report tools to conduct assigned quality checks on-site at designated locations. Understands regulations related to ICF/DD-H/N and CCL programs, such as Title 22, Appendix Z, Lanterman Act, etc. Assists with the facilitation of Day One New Employee Orientation, as needed. Reviews various quality control logs at Residential and ADP locations, such as water temp, freezer temp, fridge temp, etc. Provides user support and conducts quarterly audits on various modules Assists with Emergency Preparedness Program (EPP) training, drills, and exercises for each location as assigned. Quality Assurance Specialist Essential Qualifications: High School diploma or equivalent; required AA and/or BA degree in related field, preferred Minimum of two (2) years of experience working in the field of intellectual and developmental disabilities or Human Services field; preferred Must maintain valid and current proof of legal right to drive in California; required Ability to walk, bend, squat, kneel, and lift up to fifty (50) pounds Successfully pass all post offer, pre-employment screening requirements, including criminal background check, physical exam, drug screening, and provide proof of eligibility to work in the United States With 40 programs and service sites spanning several counties, Momentum is the largest nonprofit provider of direct support for individuals with developmental and intellectual disabilities in Southern California. Momentum is an equal opportunity employer and is required to comply with equal opportunity legislation in each jurisdiction in which it operates. Momentum also considers qualified applicants with criminal histories for employment pursuant to California Law and, if applicable, the L.A. Fair Chance Ordinance.

Do you want to play a role in the next generation of technologies improving the planet? We build tiny technologies (MEMS) that empower tomorrow's innovations. Atomica is looking for a wafer technician to fabricate micro machines (MEMS) in our semiconductor type wafer fab in Santa Barbara, CA. You will process wafers through the entire manufacturing line including photolithography, vacuum, electroplating, bonding and wet chemistry equipment. You will work closely with engineers and participate in yield improvement activities. Atomica provides a youthful, interesting and exciting environment with educational and advancement opportunities. Responsibilities: Operate equipment in such areas as photolithography, vacuum, electroplating, bonding and wet chemistry Run lots and perform equipment qualifications under the guidance of the supervisor Work with engineering team to improve processes, reduce processing costs, and improve yield Responsible for monitoring the quality of work and working with the team to constantly improve the quality of the product. Requirements: H.S. education, A.S. degree preferred Wafer handling experience Experience in manufacturing environment, preferably semiconductor manufacturing Ability to consistently follow instructions Basic computer skills including Microsoft office Must be able to work and feel comfortable in a cleanroom Must be able to don PPE Working Hours: 2nd shift: 4:30pm - 3am (M-Th) 3rd shift: 6:30 am - 7 pm (Fri-Sun) 4th shift: 6:30 pm- 6:30am (F-Sun) What Atomica Offers You: Amazing growth and learning opportunities in MEMS Competitive Health, Vision, Dental Insurance 401(k) and Roth 401(k) plan with company match Continuing education opportunities Paid Time Off Flexible Spending Account Catered in-office lunches Compensation: $20 - $30/hr *Atomica encourages applications from candidates at all levels where pay will be based on experience.* Why work with us? Atomica is changing the world. Working at Atomica is truly a one-of-a-kind opportunity to impact groundbreaking technology while living in paradise. Your contributions to our MEMS technology will drive innovation, solve the great problems of our time and directly impact the lives of people across the globe. Life in Santa Barbara: Want to live in paradise? Life in Santa Barbara is just that. Atomica is sandwiched between the beautiful Santa Ynez mountains and the pristine Central California coastline. The weather? Absolutely gorgeous. No more shoveling snow or hiding from tornadoes! Within 5-minutes from the office, you will find rich local culture, world class schools, airport for convenient travel, festivals, and excellent options to wine and dine. We have had employees move from all over the country and say life has never been better! About Atomica: Atomica Corp. unleashes the power of Micro Electro-Mechanical Systems (MEMS) to help solve the great problems of our time. Utilizing a uniquely collaborative approach to development and manufacturing, it partners with innovative companies to deliver breakthrough MEMS-based solutions in cloud computing, autonomous vehicles, cell therapy, molecular diagnostics, genomics, 5G, the Internet of Things (IoT), and more. Atomica is the largest MEMS foundry in the USA, serving customers from its 130,000 ft2 manufacturing campus (including a 30,000 ft2 class 100 cleanroom) in Santa Barbara, California. The company is ISO 9001 certified and ITAR registered. Its extensive experience spans the full spectrum of MEMS, including photonics, sensors, microfluidic biochips, and other micro components.

**Be visionary** Teledyne Technologies Incorporated provides enabling technologies for industrial growth markets that require advanced technology and high reliability. These markets include aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive on making an impact and want the excitement of being on a team that wins. **Job Description** **Position Summary:** This Production Technician will work the second shift allowing us to take full advantage of additional equipment and process capacity. Under supervision of Detector Packaging Manager, provide microelectronics assembly support to packaging operations. This Production Technician will process, build, bond, transfer, cure, test and package a full series of cameras. He or she will learn and function in the exact same manner as the first shift currently does. Work environment is cleanroom / lab. **Primary Duties & Responsibilities:** + Aqueous ultrasonic cleaning operations. + Laser marking, getter welding + Adhesive die bonding + Wirebonding and pull testing + Alignment measurement + Multipart testing + Stereo zoom microscope + Documentation for travelers and WIP tracking + Knowledge of clean room protocol **Job Qualifications:** + Attention to detail + Collaboration and teamwork + Communication skills (oral, written and listening) + Decision-making and problem solving + Initiative and flexibility + Minimum two years' experience in electronics or related field + High school diploma or equivalent **_Applicants must be either a U.S. Citizen, U.S. national, legal permanent resident, asylee, refugee or must be eligible to apply for and obtain the appropriate export control license from the U.S. Departments of State or Commerce._** **Salary Range:** $43,900.00-$58,500.000 **Pay Transparency** The anticipated salary range listed for this role is only an estimate. Actual compensation for successful candidates is carefully determined based on several factors including, but not limited to, location, education/training, work experience, key skills, and type of position. Teledyne and all of our employees are committed to conducting business with the highest ethical standards. We require all employees to comply with all applicable laws, regulations, rules and regulatory orders. Our reputation for honesty, integrity and high ethics is as important to us as our reputation for making innovative sensing solutions. Teledyne 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 characteristic or non-merit based factor made unlawful by federal, state, or local laws. You may not realize it, but Teledyne enables many of the products and services you use every day **.** Teledyne provides enabling technologies to sense, transmit and analyze information for industrial growth markets, including aerospace and defense, factory automation, air and water quality environmental monitoring, electronics design and development, oceanographic research, energy, medical imaging and pharmaceutical research.

Did you know you can make a positive impact on first responder health and safety? Gear Wash is a family-owned Independent Service Provider (ISP) of personal protective equipment (PPE) care and maintenance. We're seeking self-motivated Production & Quality Associates. They will provide production intake and output while using their computer, troubleshooting, physical and detail-oriented skills. Provide both warehouse and quality support through receiving and logging orders, processing, inspecting and testing orders and packaging garment orders for shipping various personal protective equipment (PPE) for firefighters. This job is based out of our Miami, FL location. Additional duties include: Intake, tag, sort and process incoming garment orders Operate laundry machines Drive to deliver gear Accurately enter garment data in internal tracking system Develop strong working knowledge and understanding through referencing and following company procedures, such as laundry and garment inspection and testing, general operations, and cleaning and preparation work procedures Complete work according to company quality standards while achieving company efficiency standards Assist with making pick-ups and deliveries in a company-supplied vehicle Travel to provide additional service for our customers Build working knowledge and demonstrate familiarity of all equipment used for cleaning PPE Provide support as directed to repair department Demonstrate adaptability to learn new skills and follow company procedures. May assist with creating invoices Performs other duties as assigned Work Hours: Monday through Friday: 7:00am - 3:30pm Qualifications: High school diploma, GED or equivalent Previous experience in a warehouse or receiving department, handling warranties, repairs or refurbishments is very helpful Proficient computer skills and ability to learn new software Possess a valid drivers' license with a good driving record Significant troubleshooting skills Possess a high attention to detail and accuracy Strong math skills Ability to occasionally lift and/or move up to 50 pounds due to the nature of handling garments A solution focused mind-set Self-motivated with desire to work hard to meet goals Ability to work carefully and follow safety standards Ability to read and execute instructions and procedures with varying details Ability to work positively in teams as well as possess self-accountability Efficient with prioritizing and multi-tasking, including being productive while handling re-directions and interruptions based upon organizational needs Possess a strong sense of urgency, follow-through and diligence, including meeting deadlines Proficiency to communicate well with all different levels both inside and outside of the organization, including verbal, electronic and written Ability to work in teams as well as possess self-accountability Ability to remain organized with and keep track of multiple sources of information and data Possess strong problem-solving skills, including the ability to deal with problems involving several concrete variables in standardized situations Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards Benefits: Competitive hourly pay Weekly direct deposit pay Health, dental, and vision insurance for you and your family 401k with employer matching PTO (paid time off) starting after 90 days Paid parental leave Life insurance and short-term disability Referral program EAP (employee assistance program) for entire household Steady full-time hours and a set and consistent schedule Attendance incentives Profit sharing bonuses based on company success Local entertainment and event discounts Celebrations (usually involving free food), contests, theme days and parties! Gift for your birthday! Once trained, listen to your own personal devices while working... music, books, podcasts Feel really good about your work and industry, because it's impactful More About Us: We pride ourselves on being a family owned and operated business whose mission is “to serve those who serve”. Our values include fun, integrity, respect, and excellence = FIRE! 40+ years in business Multi award-winning organization Location: 5126 Ralston Street, Ventura, CA 93003 Gear Wash is an equal opportunity employer to all, regardless of age (40 and over), ancestry, color, disability (physical and mental, including HIV and AIDS), genetic information, gender identity and expression, marital status, medical condition, military or veteran status, national origin, race (includes traits historically associated with race, including, but not limited to, hair texture and protective hairstyles), religion (includes religious dress and grooming practices), sex (includes pregnancy, childbirth, breastfeeding, and related medical conditions), sexual orientation, or any other basis protected by law. We are committed to a diverse and inclusive workforce and actively seek to ensure that our hiring and employment practices reflect this commitment. EOE

Employment Type: Contract Business Unit: Drug Product Quality Assurance 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 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: Panel Interview 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.

Details: QA Inspector Client: Leading Motorsports CompanyLocation: Onsite - Santa Clarita, CAStart Date: ASAPHourly Rate: $25 - $45/hour DOE Overview: A premier motorsports company is seeking a detail-oriented QA Inspector to join their team in Santa Clarita, CA. This role is responsible for inspecting components and equipment to ensure compliance with engineering drawings and specifications. Ideal candidates will have a strong background in dimensional inspection, GD&T, and hands-on experience with precision measurement tools. Key Responsibilities: Inspect components and equipment to verify compliance with design specifications Utilize tolerance measurement tools and apply GD&T standards Validate inspection results and document findings Operate and maintain inspection tools including comparators, surface plates, and manual gauges Conduct material analysis and surface roughness evaluations Support inspection planning, reporting, and activity tracking using Microsoft Office and inventory/data management software Apply geometry, trigonometry, and basic machine shop principles to inspection tasks Collaborate with engineering and production teams to resolve quality issues Details: Preferred Skills & Experience: Ability to read blueprints and interpret dimensional tolerancing and GD&T Familiarity with universal inspection tools and manual inspection techniques Knowledge of raw material specifications and machine tool programming Experience with optical scanning systems and CAD/CAM programming Proficiency in Microsoft Word and Excel; experience with inventory or data tracking software is a plus Strong math skills for interpreting and calculating inspection results Experience with CMM software for prismatic parts using scanning probe heads (Calypso highly desirable) Effective verbal and written communication skills Strong organizational and time management abilities Self-motivated, able to work independently and in a team environment Comfortable working under pressure and meeting deadlines High school diploma or equivalent required; technical coursework in machine shop or tooling is a plus Apply now to join a high-performance team in a fast-paced motorsports environment where precision and quality drive success.

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

Job Description The Quality Specialist is responsible for creating, reviewing, and submitting First Article Inspection Reports (FAIRs) in accordance with AS9102 standards. This role ensures all quality documentation complies with customer requirements, internal procedures, and aerospace industry standards. The specialist plays a key role in supporting continuous improvement and maintaining regulatory compliance throughout the manufacturing process. Key Responsibilities: Prepare and submit FAIRs per AS9102 requirements Review manufacturing and inspection documentation for accuracy and completeness Maintain quality records, certifications, and traceability documentation Collaborate with engineering, production, and quality teams to gather necessary data Support internal and external audits by organizing and providing required documentation Ensure compliance with customer specifications, drawings, and quality requirements Participate in root cause analysis and corrective actions when quality issues arise Qualifications: 2+ years of experience in quality assurance or documentation within aerospace or a similar regulated industry Proficient in AS9102 standards and FAIR preparation Strong attention to detail and organizational skills Experience with quality management systems (QMS) and documentation control Familiarity with aerospace specifications and manufacturing processes Proficient in Microsoft Office and inspection software (e.g., Net-Inspect, CMM reports) Preferred: Knowledge of ISO 9001/AS9100 standards Experience working with defense or aerospace OEMs or Tier 1 suppliers