Quality Inspector jobs at Cirtec Medical

Job Title: Technician III, Quality Operations At Alcon, we're passionate about enhancing sight and helping people see brilliantly. With more than 25,000 associates, we innovate fearlessly, champion progress, and act swiftly to impact global eye health. We foster an inclusive culture, recognizing your contributions and offering opportunities to grow your career like never before. Together, we make a difference in the lives of our patients and customers. Are you ready to join us? This role is part of Alcon's Quality & Regulatory Affairs function, a team that ensures our products are in compliance with global, local, and internal regulations and meet the strictest standards of quality as we help people see brilliantly. The Technician III, Quality Operations within Receiving and Inspection is primarily responsible for supporting the manufacturing process through performing inspection or quality test of products within the surgical instrumentation and quality organization. This role is responsible for performing all types of quality inspections (including special inspections) to standard AQLs in order to qualify parts into stock locations; examine and identify nonconformance in materials per specifications. The Technical Associate is required to have a higher level of knowledge in the various Receiving and Inspection areas and may be required to train others at times. In this role, a typical day will include: Conduct partial or full First Article Inspections (FAIs) on machined, casting, sheet metal, and plastic components using precision measurement tools such as CMM, optical gaging systems, micrometers, calipers, dial indicators, and height gauges. Inspect incoming materials, purchased parts, assemblies, hardware, and special processes for conformance to engineering specifications. Examine items for defects in materials, workmanship, or damage during transit. Compare received items against purchase orders and specifications to ensure accuracy and completeness. Perform inspections using appropriate sampling plans and standard AQLs. Accurately interpret engineering drawings, with a strong understanding of Geometric Dimensioning and Tolerancing (GD&T). Independently determine appropriate inspection methods for new and complex parts independently. Operate and/or program Coordinate Measuring Machines (CMMs) using PC-DMIS or Calypso software (preferred). Create and maintain detailed, accurate and clear inspection reports. Generate Non-Conformance Reports (NCRs) as needed. Use Microsoft Excel and Office tools for data analysis, reporting, and trend monitoring. Proactively communicate inspection findings and collaborate with engineering, production, and quality teams to resolve issues. Train new or existing associates in Receiving and Inspection procedures. Follow Standardized Work and adhere to safety and quality standards. Promote a continuous improvement culture. Perform physical tasks such as bending, lifting, standing, walking, squatting, and reaching. May be required to operate power jacks, forklifts, pallet jacks, and push carts as needed. WHAT YOU'LL BRING TO ALCON: High School Diploma or equivalent The ability to fluently read, write, understand and communicate in English. Work Location: Onsite Travel Requirements: None Relocation Assistance: No Sponsorship: No PREFERRED SKILLS/QUALIFICATIONS/EXPERIENCE: Experience performing First Article Inspections (FAIs). Proficiency with precision measurement tools including Coordinate Measuring Machines (CMM), Optical gaging systems, Micrometers, calipers, dial indicators, height gauges. Ability to interpret engineering drawings, especially with Geometric Dimensioning and Tolerancing (GD&T). Familiarity with sampling plans and AQL standards. Experience identifying nonconformance in materials. Ability to generate and manage Non-Conformance Reports (NCRs). Skilled in creating and maintaining inspection reports. Knowledge of quality systems and regulatory standards (e.g., cGMP, GDP). Proficiency in Microsoft Excel and other MS Office tools. Experience with CMM programming using PC-DMIS or Calypso (preferred). HOW YOU CAN THRIVE AT ALCON: Join Alcon's mission to provide outstanding, innovative products and solutions to improve sight, improve lives, and grow your career! Collaborate with teammates to share standard processes and findings as work evolves! See your career like never before with focused growth and development opportunities! Alcon provides a robust benefits package including health, life, retirement, flexible time off for exempt associates, PTO for hourly associates, and much more! ATTENTION: Current Alcon Employee/Contingent Worker If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site. Find Jobs for Employees Find Jobs for Contingent Worker Total Rewards Alcon's Total Rewards programs are designed to align to incentives with business goals, encourage the right values and behaviors, and deliver long-term value. The first layer of our rewards program is compensation. We offer a combination of fixed pay and variable pay, which includes short-term incentives, and long-term incentives for eligible population. Our benefits program provides security for life events through life and disability insurance, supports savings for retirement, promotes good health and well-being and supports associates and their families during times of illness. To learn more about Alcon's Corporate Social Responsibility including our Total Rewards, click here Pay Range $26.92 - $40.38 Pay Frequency Hourly Alcon is an Equal Opportunity Employer and participates in E-Verify. Alcon takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status. Alcon is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to *************************** and let us know the nature of your request and your contact information.

Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions. Position Description The Quality Inspector plays a critical role in maintaining the safety, reliability, and compliance of Applied Medical's medical devices following clinical use. This post-market quality inspector position ensures that returned products meet Applied Medical's stringent quality standards while supporting patient safety and continuous product improvement. Working within an ISO 13485 and FDA-regulated environment, the Quality Inspector performs detailed inspections, documentation, and collaboration with cross-functional teams to support ongoing product integrity and regulatory compliance. Key Responsibilities * Inspect and assess returned medical devices to verify condition, cleanliness, and compliance with safety and decontamination standards. * Use calibrated measuring tools to confirm product integrity against specifications. Document findings in Applied Medical's enterprise resource planning (ERP) and electronic quality management system (eQMS) platforms with accuracy and traceability. * Collaborate cross-functionally with the Servicing, Regulatory Affairs, and Customer Relations teams to resolve documentation discrepancies and product concerns. * Maintain compliance with applicable regulatory standards, including 21 CFR Part 820, ISO 9001, and ISO 13485. * Support continuous improvement initiatives by contributing feedback. * Adhere to safety protocols when handling decontaminated or potentially biohazardous materials in accordance with bloodborne pathogen procedures. Success in This Role Looks Like * Conducts accurate and efficient inspections that uphold Applied Medical's quality and safety standards. * Contributes to clear, compliant, and timely documentation that supports post-market surveillance and regulatory reporting. * Demonstrates precision, consistency, and accountability in all inspection and verification activities. * Builds strong working relationships with cross-functional partners to resolve quality issues and improve processes. * Supports Applied Medical's mission of delivering reliable, high-quality devices that advance patient care and clinical outcomes. Position Requirements This position requires the following skills and attributes: * High school diploma or equivalent education. * Minimum of two years of experience in quality assurance or inspection within a regulated manufacturing environment (e.g., medical device, pharmaceutical, or aerospace). * Working knowledge of ISO and FDA regulatory frameworks, including 21 CFR Part 820. * Strong analytical skills with meticulous attention to detail. * Proficiency in ERP and eQMS systems for data entry and documentation (e.g., SAP). * Clear written and verbal communication skills in English. * Ability to lift between fifteen and twenty-five pounds on an occasional to regular basis. * Organizational discipline and the ability to manage time effectively in a fast-paced environment. Preferred The following skills and attributes are preferred: * Experience working in a medical device manufacturing or clinical servicing environment. * Familiarity with bloodborne pathogen protocols, product decontamination, and sterilization processes. * Exposure to continuous improvement methodologies such as Lean or Six Sigma. * Understanding of ISO 13485 quality systems and regulatory documentation practices. Benefits * Competitive compensation range: $18 - 23 / hour (California). * Comprehensive benefits package. * Training and mentorship opportunities. * On-campus wellness activities. * Education reimbursement program. * 401(k) program with discretionary employer match. * Generous vacation accrual and paid holiday schedule. Please note that the compensation range may be based on factors such as relevant education, qualifications, experience. The compensation range may be adjusted in the future, and special discretionary bonus or incentive compensation plans may apply. Our total reward package reflects our commitment to team member growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life. Equal Opportunity Employer Applied Medical is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other basis protected by federal, state or local laws in the locations where Applied Medical operates.

GENERAL INFORMATION Quality Inspector (II, III, or Senior) Department: Quality Assurance Reports to: Quality Engineering Purpose of the Job This Quality Inspector position will report to Quality Engineering. Main responsibilities include performing incoming inspections of materials/parts/products and reviewing and approval of manufacturing batch records and inspection records. This position will require to perform disposition of materials/parts/products. As a Quality Inspector, you will also support Quality Engineering with other Quality Management System (QMS) activities, such as assisting with environmental monitoring and quality metrics. Major Duties and Responsibilities Interpret drawings and specification documents. Perform incoming inspection of materials/components/subassemblies/finished products following standard operating procedures and using standard inspection tools, including the MicroVu and Keyence. Determine inspection sample size based on procedures, specifications, and standards. Help develop inspection methods, including automated inspection programs using the MicroVu and Keyence. Review/approve executed batch records for manufacturing and inspection records in accordance to QMS procedures and Good Documentation Practices. Approve/perform final disposition of materials/components/subassemblies/finished products. Assign and apply expiration dating labels to materials/parts/products, as per specifications/quality procedures. Initiate Non-Conformance Material Reports (NCMRs) and deviations when discrepancies are observed during inspections and record review process. Report discrepancies and issues to QA Engineering and affected function(s). Maintain materials in Quarantine (pending disposition) and MRB (under NCMR and deviations) in order. Maintain accurate records as per Document Control procedures. Support training of IQC personnel. Assist with performing environmental monitoring of Controlled Environment Rooms (CERs), as needed. Support Quality in the collection of quality metrics data. Interact closely with different functions of the organization. Education and/or Job Experience 2-5 years of experience performing inspections and reviews/approvals of manufacturing batch records/inspection records Government Regulated Environment experience such as FDA and ISO 13485 Must have adequate computer experience (knowledge of Microsoft Word, Excel) Experience working in a cGMP environment Skills and Specifications Attention to detail and organizational skills Good interpersonal and communication skills Ability to work as a part of a team and promote a team environment

At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Join a team committed to taking big leaps forward for a global community of healthcare professionals and their patients. Together, let's advance the world of minimally invasive care. Job Description Primary Function of Position: IQC Inspector will be performing dimensional and visual inspections of incoming product parts, assemblies and products to ensure incoming part specifications have been met prior to release to manufacturing and finished goods. IQC Inspector will also inspect R&D parts per Engineer Requests or as First Articles. Essential Job Duties * Perform detailed Documentation Review to ensure all required data and certifications are accurate and present for each lot of parts or assemblies. * Interpret complex mechanical drawings and understand GD&T concepts to inspect parts. * Conduct visual inspection of purchased parts materials and assemblies to ensure it meets the required cosmetic and/or feature details listed in parts' specifications. * Record Inspection results in computer - based software (1Factory). * Use Neptune Software to track inspection times and results. * Create inspection history files and upload to ERP system. * Maintain traceability of component materials as to inspection status * Perform First Article inspections to qualify tooling and new parts. * Perform inspection on parts/fixtures for the PMC (Calibration Group). * Handle materials in accordance with procedures and prevent mix-ups, damage or other adverse effects. * Use company ERP system (Inventory Control) to transact and release materials to for production use. * Physical move materials to released area. * Create Non-conforming reports for parts that fail their incoming specifications. * Communicate inspection results to engineers and others, when requested. * Verify and maintain the accuracy of lot identification and count of materials. * Performs any other projects or duties that may be assigned. * Perform Gage R& R studies requested by engineers and others. Qualifications Required Skills and Experience * Operate standard metrology equipment (caliper, height gauges, micrometer, bore gauges, dial indicators, surface plate, etc.) for open set-up inspection. * Operate and utilize Optical comparators and Vision Systems (Smart Scope, Keyence, or Dynascope) to inspect parts. * Ability to inspect more complex parts using multiple types of inspection tools and equipment. * Requires understanding of SAP or other ERP systems to be able to perform lot transactions is a bonus skill set. * Must be proficient in the Microsoft Office suite of programs. * Must be able to use or understand the use of standard inspection tools, gauges and Optical Comparators. Required Education and Training * High school diploma, A.S. Engineering Degree preferred. * 2-5 years related experience or training; or equivalent combination of education and experience. * Working knowledge of Geometric Dimensioning and Tolerance is required. Working Conditions * Must be able to lift a minimum of 25 lbs. Preferred Skills and Experience * Knowledge of Good Manufacturing Practices * Good organizational skills Compensation and Benefits We provide market-competitive compensation packages, inclusive of base pay, benefits and equity. The target pay range for this position is $63,502/yr to $85,904/yr. Additional Information Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role. Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws. Mandatory Notices U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process). For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee's start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes. We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws. We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target base compensation ranges are listed.

Under minimal supervision, the QC Inspector II oversees quality projects, ensures compliance with Medline SOPs, and maintains product integrity at the distribution center. Responsibilities include investigating and documenting held finished goods, managing holds and releases, completing rework assignments, inspecting raw materials and finished goods using various methods, recording inspection results, providing product disposition, ensuring inventory control, performing final inspections, and ensuring compliance with quality procedures and company policies. Job Description MAJOR RESPONSIBILITIES Apply and remove holds in the system and Q-Tag. Assess and repackage inbound damaged goods. Communicate with divisional partners to determine product disposition. Maintain communication with branch personnel and divisional partners. Operate material handling equipment (e.g., reach truck, order picker) to manage inventory. Assist with item adjustments and other inventory-related tasks. Prioritize and perform recall activities, including stock checks, deviations, relabels, product rework, and pedigree verification. Coordinate project/rework areas and resources. Maintain daily reports of held stock using SAP, Excel, and other systems. Ensure compliance with SOPs and regulations; communicate with management to address non-conformances. Maintain hazardous waste logs and perform weekly audits. Use computer systems for communication, reporting, and tracking project time. Recommend methods to increase efficiency. Ensure shipments are from licensed vendors and maintain electronic logs. Perform in-process and final inspections; complete inspection documentation. Operate test equipment and perform measurements. Identify defects and initiate non-conforming material reports. Communicate effectively with quality assurance and production groups. Verify and approve line start-up and equipment requirements. Participate in continual improvement and customer satisfaction efforts. Read and interpret engineering instructions and other documents. Comply with quality systems, GMP, GDP, OSHA, and company regulations. Review manufacturing/production documents to ensure accuracy. Perform line clearance procedures for product release. Review and approve Engineering Change Notices (ECNs) and substitutions. MINIMUM JOB REQUIREMENTS Education Typically requires High School Diploma or equivalent. Certification / Licensure At least 1 years of quality control experience in a regulated industry setting. Work Experience Knowledge / Skills / Abilities Proficiency in using powered warehouse equipment. Ability to read, write, speak, and understand English. Strong attention to detail, including the ability to read and understand labeling information, discern differences in similar products or packaging, and identify differences in character sequences (e.g., Lot, Expiration, Date of Manufacture). Basic math skills, including addition, subtraction, and fractional to decimal conversions. Basic computer skills, including the ability to generate Non-Conforming Material Reports (NCMRs) or certificates as necessary, and proficiency with Microsoft Office Suite (Outlook, Word, Excel, etc.). Ability to work in hot and cold environments. Capability to sit, walk, or stand for prolonged periods, with frequent twisting and bending. Ability to lift up to 50 lbs. Ability to prioritize quickly in a fast-paced manufacturing environment. Ability to process all relevant details, understand and prioritize their importance, and draw concise conclusions. Basic knowledge of quality regulations such as GMP, GDP, ISO, or 21CFR 820, 210-211. PREFERRED JOB REQUIREMENTS Education Certification / Licensure Work Experience At least 2 years of quality control experience in a regulated industry setting. Knowledge / Skills / Abilities Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization. The anticipated salary range for this position: $23.75 - $33.25 Hourly The actual salary will vary based on applicant's location, education, experience, skills, and abilities. Medline will not pay less than the applicable minimum wage or salary threshold. Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For a more comprehensive list of our benefits please click here. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. We're dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page here. Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws. Medline Industries, LP complies with the Los Angeles County Fair Chance Ordinance for Employees (FCO) and the State of California Fair Chance Act (FCA). In accordance with the FCO and FCA, an applicant's criminal history will not result in automatic disqualification from employment. Qualified applicants with arrest or conviction records will be considered for employment

At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a pioneer and market leader in robotic-assisted surgery, we strive to foster an inclusive and diverse team, committed to making a difference. For more than 25 years, we have worked with hospitals and care teams around the world to help solve some of healthcare's hardest challenges and advance what is possible. Intuitive has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere. We strive to foster an inclusive culture built around diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. Passionate people who want to make a difference drive our culture. Our team members are grounded in integrity, have a strong capacity to learn, the energy to get things done, and bring diverse, real world experiences to help us think in new ways. We actively invest in our team members to support their long-term growth so they can continue to advance our mission and achieve their highest potential. Job Description IQC Inspector will be performing dimensional and visual inspections of purchased parts, assemblies and products to ensure incoming specifications have been met prior to release to manufacturing and finished goods. Document and communicate the results of inspections to engineers and others.This position is based onsite in Sunnyvale, CA, and is expected to transition to the permanent Gilroy, CA facility by December 2025 or early 2026. Essential Job Duties (Specific responsibilities and tasks an individual would be expected to perform in the role. Additional job duties may be determined by functional people manager) * Perform First Article inspections to qualify tooling and new parts. * Operate optical comparator, vision system, and other standard metrology equipment (caliper, height gauges, bore gauges, etc.) for open set-up inspection. * Conduct visual/dimensional inspection of purchased parts materials and assemblies to procedures or specifications and disposition based upon results. * Document inspection results as required. * Maintain traceability of component materials as to inspection status * Handle materials in accordance with procedures and prevent mix-ups, damage or other adverse effects. * Record transactions and move materials to stock locations. * Create Non-conforming reports for parts that fail their incoming specifications. * Communicate inspection results to engineers and others. * Able to verify assembly documentation accuracy, read engineering drawings etc. * Performs any other projects or duties that may be assigned. Qualifications Required Skills and Experience (Specific skills, knowledge, and experience that an individual must possess in order to successfully perform in job) * Operate standard metrology equipment (caliper, height gauges, micrometer, bore gauges, dial indicators, surface plate, etc.) for open set-up inspection. * Interpret mechanical drawings and GD&T * Requires understanding of SAP or other ERP systems to be able to perform lot transactions is a bonus skill set. * Must be proficient in the Microsoft Office suite of programs. Required Education and Training (As applicable - Specific education and training that an individual must possess in order to successfully perform in job) * High school diploma, A.S. Engineering Degree preferred. * 1-3 years related experience or training; or equivalent combination of education and experience. * Requires understanding of SAP or similar ERP systems. Will train, if no experience. Working Conditions (As applicable - Any physical requirements for the job. If not applicable, state "none") * Must be able to lift a minimum of 25 lbs. Preferred Skills and Experience (As applicable - Specific skills, knowledge, and experience that are not required to perform the job, but are desirable to have) * Knowledge of Good Manufacturing Practices * Good organizational skills * Can communicate clearly and concisely. Additional Information Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role. Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws. Mandatory Notices U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process). For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee's start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes. We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws. Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee. We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target compensation ranges are listed.

About Us Hydrafacial is a global category-creating company focused on bringing innovative products to market and delivering beauty health experiences by reinventing our consumer's relationship with their skin, their bodies and their self-confidence. Every person here is a key player in our success. We are firm believers in making the little things count each day so the big things will follow. If this sounds like you, come check us out! This is the perfect opportunity to work with some of the best leaders in the industry while you gain the global and strategic experience to add to your professional toolbox. Job Description: The Quality Control Inspector - Inspection is responsible for performing inspections and testing activities throughout the manufacturing process to ensure compliance with quality standards. This role includes conducting First Article Inspections (FAI), Incoming Quality Control (IQC) In-Process Quality Control (IPQC), and Final Quality Control (FQC) inspections, and maintaining detailed inspection records. The Quality Control Inspector will collaborate with cross-functional teams to address quality and safety issues and contribute to continuous improvement initiatives. This is an on-site position based in Long Beach, CA and requires on-site presence five days a week. This is a full-time role with a schedule of Monday-Friday, 6:00 AM to 02:30 PM or 7:00 AM to -3:30 PM or 08:00 AM to 04:30 PM. What you'll do: Primary Responsibilities: Perform inspection and testing activities during First Article Inspections (FAI), manufacturing processes, and Incoming Quality Control (IQC), In-Process Quality Control (IPQC), and Final Quality Control (FQC) inspections. Generate detailed and accurate inspection data sheets in compliance with current Good Manufacturing Practices (cGMP) and Hydrafacial Quality Management System (QMS) requirements. Properly document inspections, prepare first article documentation, and compile certification packages. Conduct product build documentation reviews and end-item data package reviews. Generate nonconformance reports for discrepancies found during inspection processes. Utilize conventional inspection tools such as calipers, gauges, etc., to ensure precise measurements. Ensure all inspection equipment is qualified and calibrated before use. Interpret engineering drawings and specifications accurately. Conduct visual inspections to identify defects or non-conformities in products. Collect and analyze quality data to identify trends and areas for improvement. Collaborate with cross-functional teams to address quality issues and drive continuous improvement initiatives. Maintain accurate documentation of inspection results and quality records. Participate in continuous improvement initiatives to enhance product quality. Report quality related issues to leads and managers in a timely manner. Adhere to all company safety procedures and perform job functions in a safe and effective manner. Performs other duties as assigned What you need to know: Experience/Skills/Education: Required: High school diploma or equivalent; technical training or certification in quality inspection is a plus. Minimum of 2-3 years of experience in a quality inspection role within a manufacturing environment. Proficiency in using conventional inspection tools such as calipers, micrometers, and gauges. Strong understanding of GDP, cGMP, and QMS requirements. Ability to read and interpret engineering drawings and specifications. Experience with generating nonconformance reports and inspection documentation. Strong analytical and problem-solving skills. Excellent attention to detail and organizational skills. Basic understanding of ERP systems, Micro Office, etc. Ability to work independently, cross train, and collaborate professionally in a team environment. Experience with handling pallet jacks and other various moving equipment. Manufacturing environment with exposure to machinery, equipment, and various temperatures. Requires bending, twisting, heavy lifting, pulling/pushing, standing, sitting, reaching, and walking handling inspection tools for extended periods. Must adhere to all safety guidelines and wear the required personal protective equipment (PPE). Must be able to lift and move 50lbs. Desired: Associate degree or higher in a related field preferred. We mean it when we say you'll LOVE this role. Base Pay : $20.00- $23.00/hour Hydrafacial is proud to be an equal opportunity employer. We prohibit discrimination and harassment of any kind based on race, sex, religion, sexual orientation, national origin, gender identity, gender expression, age, disability, genetic information, pregnancy or any other protected characteristic as outlined by color, federal, state or local laws. We are committed to working with and providing accommodation to applicants with physical and mental disabilities. Hydrafacial does not accept unsolicited assistance or resumes/CVs from third party search firms. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral or CV/resume submitted by a search firm to any employee at our company without a valid written search agreement. If we need additional support, we will be sure to reach out directly to one of our preferred providers. Please no phone calls or emails.

Job Description Under Quality supervision, evaluates materials and products to ensure conformance to drawing requirements, procurement specifications and approved procedures. Evaluations include dimensional, functional, cosmetic and documentation as required per applicable inspection plan. Essential Duties and Responsibilities Perform Quality Control inspections, as required per ATEC procedures Read, understand, and interpret engineering (blueprint) drawings and associated GD&T (Geometric Dimension & Tolerances) Perform mechanical, visual and functional inspection. Utilization of Micro-Vu or similar lighting inspection systems preferred Engage with respective department members to maintain best inspection practices, foster a cooperative work environment, propose improvements when inefficiencies are observed Generate, complete, and maintain quality documentation such as inspection records, non-conformance reports, deviation, and scrap forms Process non-conforming materials following established procedures, able to identify and segregate non-conforming materials, transact as required in the company ERP (SAP) Perform transactions in ERP system, as necessary to release product from Inspection Read and conform to all company policies and procedures Perform documentation evaluations Interface with other departments including, Purchasing, Shipping, Receiving, Manufacturing, and Engineering as well as Supplier representatives Assist auditors during internal audits Other duties as assigned Requirements The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Good communication skills, both verbal and written Strong organization skills and attention to detail Basic math and computer skills required Firm understanding of 21 CFR (Code of Federal Regulations), Part 820, ISO 13485, Good Documentation Practices (GDP) Firm understanding of ASTM (Association of Systems & Test Methods) standards and Heat Treat conditions per ASTM standards Experience in a controlled or regulated environment required Inspection experience with Optical Comparators, Vision Systems, hand tools Education and Experience High School Diploma or equivalent and 2-5 years of experience; experience working in a medical device industry preferred. Familiarity with quality concepts such as visual inspection and defect identification. For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws. Salary Range Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate's qualifications, education, skill set, years of experience, and internal equity. $22.00 to $31.00 Full-Time Hourly Salary.

Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions. Position Description Are you detail-oriented with a passion for maintaining the highest standards of quality in manufacturing? Join Applied Medical as a Quality Control Inspector and play a vital role in ensuring the excellence of our raw materials, components, and finished products. As part of our Quality Assurance team, you'll utilize precision measurement tools, review engineering documentation, and uphold strict compliance with industry standards. Key Responsibilities: * Conduct thorough inspection activities, including receiving, in-process, and final product verification. * Assess raw materials, components, subassemblies, and finished products for adherence to standards, guidelines, and specifications outlined in company procedures. * Interpret engineering drawings, shop order operations, and process controls to ensure accuracy in production. * Inspect products and materials following standard operating procedures and work instructions. * Utilize technical measuring devices to confirm product conformance to defined specifications. * Document and report nonconforming materials, ensuring accurate record-keeping. * Maintain detailed inspection results using data management software. Position Requirements * Forklift certified and/or willingness to learn. * 2+ years of experience working within quality management systems (ISO 9001, ISO 13485, or 21 CFR Part 820). * Ability to read, write, and communicate in English effectively. * Understanding and adherence to Applied Medical's Quality Systems and training guidelines. * Compliance with safety rules and company policies. * Ability to work Monday through Friday 8:00am - 4:30pm. Preferred * Hands-on manufacturing experience, particularly within the medical device industry. Benefits * Competitive compensation range: $18 - 23 / hour (California). * Comprehensive benefits package. * Training and mentorship opportunities. * On-campus wellness activities. * Education reimbursement program. * 401(k) program with discretionary employer match. * Generous vacation accrual and paid holiday schedule. Please note that the compensation range may be adjusted in the future, and bonus and incentive compensation plans may apply. Our total reward package reflects our commitment to employee growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life. All compensation and benefits are subject to plan documents and written agreements. Equal Opportunity Employer Applied Medical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other status protected by federal, state or local laws in the locations where Applied Medical operates.

Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic, and applied market laboratories worldwide with instruments, 8services, consumables, applications, and expertise. Agilent enables customers to gain the answers and insights they seek- so they can do what they do best: improve the world around us. Information about Agilent is available at **************** Essential Responsibilities: This is a 12-hour Variable shift. Performs Micro Array process, which includes, but is not limited to, Writer/synthesis, deprotection, dicing of wafers using standardized tooling, QC Processes/OLS Cleaving documentation and procedures. Performs troubleshooting and verifies that the product conforms to customer specifications. Maintains accurate reports and provides necessary documentation. Helps implement process/product improvements, etc. Additionally, the new hire will be expected to support both Manufacturing Fab and QC operations within 12 months to enhance flexibility and support across functions. This role follows a 12-hour variable shift schedule (5:00 PM - 5:00 AM), working Thursday evening through Sunday morning, with every other Wednesday included in the rotation. The above statements are intended to describe the general nature and level of work being performed by incumbents. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required by all incumbents. Incumbents may perform other duties as assigned in addition to the above. All Agilent employees are expected to: Promote teamwork and cooperative effort. Help train and give guidance to other Agilent employees. Maintain a clean, safe, and unobstructed work area, practice good safety habits, and utilize appropriate safety equipment. Provide customers with the highest quality products and service. Understand and apply appropriate quality improvement and Processes. Qualifications Ability to use basic math applied to the job. Ability to communicate both verbally and in writing. Computer skills on Windows-based applications such as MS Word, Excel, and Outlook. Ability to set up and operate Micro Array Manufacturing machines, preferred. Must be comfortable working around chemicals. May be able to demonstrate the ability to lift materials per entity-specified and approved limits. Desirable: Higher education. Experience Team Leadership. Familiarity with Lab instruments such as LCMS, HPLC, etc., preferred MES, Agile, and SAP experience. Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least September 15, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $30.03 - $46.93/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: NoShift: MorningDuration: No End DateJob Function: Manufacturing

Under Quality supervision, evaluates materials and products to ensure conformance to drawing requirements, procurement specifications and approved procedures. Evaluations include dimensional, functional, cosmetic and documentation as required per applicable inspection plan. Essential Duties and Responsibilities * Perform Quality Control inspections, as required per ATEC procedures * Read, understand, and interpret engineering (blueprint) drawings and associated GD&T (Geometric Dimension & Tolerances) * Perform mechanical, visual and functional inspection. Utilization of Micro-Vu or similar lighting inspection systems preferred * Engage with respective department members to maintain best inspection practices, foster a cooperative work environment, propose improvements when inefficiencies are observed * Generate, complete, and maintain quality documentation such as inspection records, non-conformance reports, deviation, and scrap forms * Process non-conforming materials following established procedures, able to identify and segregate non-conforming materials, transact as required in the company ERP (SAP) * Perform transactions in ERP system, as necessary to release product from Inspection * Read and conform to all company policies and procedures * Perform documentation evaluations * Interface with other departments including, Purchasing, Shipping, Receiving, Manufacturing, and Engineering as well as Supplier representatives * Assist auditors during internal audits * Other duties as assigned

GLAUKOS - QUALITY CONTROL INSPECTOR I - 1st SHIFT (SAN CLEMENTE, CA) How will you make an impact? The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection Receiving inspection of components following procedures, specifications and drawings. Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. Read engineering drawings and interpret geometric dimensioning and tolerancing. Review associated paperwork, complete inspection records using good documentation practices, and release components. Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) Carefully handle and process extremely small components without damaging them. In-Process Inspection Perform Line Clearance for Operations activities Inspect and release labeling Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform inspections on components and assemblies in manufacturing Final Inspection Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. Perform final inspection on finished goods Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing Perform in-house peel testing on sealed packages Maintain sample retain area Other Duties Work with engineering in the design of high quality inspection / metrology fixtures. Support equipment and process validation activities by inspecting process outputs Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance. Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations. Coordinate the monthly environmental monitoring of the cleanrooms. Coordinate quarterly dose audits. How will you get here? High School Diploma required. 0-2 years industry experience. Knowledge, Skills, and Abilities Medical device experience and working knowledge of QSR a must Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable Attention to detail and accuracy a must Must have excellent documentation skills Team player, good written/oral communicator Must be organized and able to coordinate activities with outside vendors #GKOSUS

GLAUKOS - QUALITY CONTROL INSPECTOR I - 1st SHIFT (SAN CLEMENTE, CA) How will you make an impact? The Quality Control Inspector I will be responsible for all aspects of inspection (receiving, in-process and final). In addition, this position will provide QSR support for other QA activities such as calibration, environmental monitoring, product testing, label control, etc. What will you do? Receiving Inspection * Receiving inspection of components following procedures, specifications and drawings. * Utilize a variety of standard metrology equipment, including: Optical comparator, height gauge, master height gauge, CMM, Vision Metrology System (VMS, e.g., Smartscope), calipers, micrometers, surface table, gauge blocks, pin gauges, dial indicators, durometer, measuring microscope, hardness testers, pull force testers, surface roughness testers, etc. * Read engineering drawings and interpret geometric dimensioning and tolerancing. * Review associated paperwork, complete inspection records using good documentation practices, and release components. * Program the Smartscope to run automatic routines for multiple part inspections. (Level 2 and higher) * Write clear and concise procedures for inspection of components, machined tubing, etc. (Level 2 and higher) * Carefully handle and process extremely small components without damaging them. In-Process Inspection * Perform Line Clearance for Operations activities * Inspect and release labeling * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform inspections on components and assemblies in manufacturing Final Inspection * Review device history records for lot release. Ensure all quality records meet good documentation practices in accordance with internal procedures. * Perform final inspection on finished goods * Inspect finished goods for proper labels, packaging, tamper seals and product in accordance with procedures. * Coordinate final inspection activities with outside vendors, i,e, LAL, peel testing * Perform in-house peel testing on sealed packages * Maintain sample retain area Other Duties * Work with engineering in the design of high quality inspection / metrology fixtures. * Support equipment and process validation activities by inspecting process outputs * Conduct periodic compliance audits of manufacturing operations and procedures for cGMP compliance. * Ensures on a daily basis quality records and company practices are compliant with internal procedures and regulations. * Coordinate the monthly environmental monitoring of the cleanrooms. * Coordinate quarterly dose audits. How will you get here? * High School Diploma required. * 0-2 years industry experience. Knowledge, Skills, and Abilities * Medical device experience and working knowledge of QSR a must * Experience working in a clean room and/or performing in-process assembly and manufacturing verification inspections desirable * Attention to detail and accuracy a must * Must have excellent documentation skills * Team player, good written/oral communicator * Must be organized and able to coordinate activities with outside vendors #GKOSUS

Join our mission-driven Quality team as the Sr. Quality Control Inspector at Endologix! WHO WE ARE: Endologix LLC is a California-based global medical device company dedicated to improving patients' lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training-supported by industry-leading clinical evidence. At Endologix, we're driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health. What sets us apart is not just our technology, but our culture. At Endologix, we foster a collaborative, mission-driven environment where every team member plays a vital role in advancing patient care. We value integrity, tenacity, and innovation-and we support our people with the tools, trust, and training they need to grow and continuously learn. If you're passionate about making a meaningful impact in healthcare, you'll find purpose and belonging here. ABOUT THE ROLE: We're looking for a Sr. Quality Control Inspector to join our mission-driven Quality team. In this role, you'll be responsible for performing inspections of components, subassemblies, and finished medical devices to ensure compliance with quality standards and regulatory requirements. This includes conducting quality checks, performance tests, reviewing documentation, and verifying Device History Records (DHR) for product release in accordance with the medical device Quality Management System (QMS). Responsibilities WHAT YOU'LL DO: * Inspect purchased components, tooling, subassemblies, and finished products using defined criteria and standard physical, mechanical, and/or electrical measurements. * Rework or reject subassemblies or finished products as necessary. * Support process and system audits using established procedures as audit standards. * Document inspection and testing results in compliance with Good Documentation Practices (GDP). * Maintain controlled document files and test records accurately and promptly. * Inspect test equipment and fixtures to support maintenance and calibration activities. * Assist in writing and updating inspection procedures, protocols, and checklists. * Evaluate issues and provide initial recommendations for corrective actions or system improvements to the supervisor. * Participate in Non-Conforming Material Report (NCMR) management processes. * Collaborate with production and quality teams to provide feedback on assembly accuracy and compliance. * Review Device History Records and related documentation for adherence to procedures and GDP. * Work within a cleanroom environment following all applicable protocols. * Perform other duties as assigned by supervisor. Qualifications WHAT YOU'LL BRING: Education: * High School Diploma or equivalent required. Experience: * 3-6 years of Quality Control experience, preferably in the medical device industry. Skills/Competencies: * Mechanical aptitude and working knowledge of measurement instruments. * Proficiency in Microsoft Excel and Word. * Ability to read and interpret technical procedures, drawing, specifications, ASTM standards, and medical device regulatory requirements. * Strong written and verbal communication skills for reports, correspondence, and presentations. * Mathematical proficiency in probability, statistical inference, fractions, percentages, ratios, and proportions. * Problem-solving skills with the ability to work in a cross-functional environment and manage multiple priorities. * Experienced in using measuring equipment such as Microscope, CMM, Instron tester, calipers, pin gauge, micrometer, snap gauge etc. HOW YOU'LL SHOW UP: All In: Bring full commitment to everything you do. Support one another, hold yourself accountable, and take ownership of your work. Move with urgency, deliver on your promises, and lead with boldness and passion. Act with Integrity: Prioritize ethics and transparency in every decision. Earn trust by being honest, respectful, and dependable - working diligently to uphold the confidence of your colleagues, customers, and communities. Tenacious: Meet challenges head-on with resilience and resolve. Stay focused, push through obstacles, and consistently look for solutions, not excuses. Pioneering: Challenge the status quo and embrace innovation. Develop new ideas, test bold solutions, and pave the way for others - driving progress through curiosity and creativity. WHAT WE OFFER: At Endologix, we know that great work starts with great people - and people do their best when they feel valued and supported. That's why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You'll be part of a team that's making a real impact on patients' lives. When you join us, you're not just taking a job, you're building a meaningful career with a team that's invested in your success. The compensation package includes: * Hourly rate of $26.44/hr-$30.65/hr * Discretionary bonus * Equity participation as approved by Board of Directors (4-year vesting schedule) * Comprehensive health, dental, and vision insurance plans * Generous PTO and holiday schedule * 401(k) retirement plan with company match Plus: * Employee wellness initiatives and mental health support * Collaborative and inclusive company culture focused on impact and innovation * Opportunities for career growth and internal mobility OUR COMMITMENT TO DIVERSITY AND INCLUSION: Endologix LLC. is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Applied Medical is a new generation medical device company with a proven business model and commitment to innovation fueled by rapid business growth and expansion. Our company has been developing and manufacturing advanced surgical technologies for over 35 years and has earned a strong reputation for excellence in the healthcare field. Our unique business model, combined with our dedication to delivering the highest quality products, enables team members to contribute in a larger capacity than is possible in typical positions. Position Description Do you thrive in a dynamic manufacturing environment where your keen eye for detail can make a significant impact? Join our team at Applied Medical as an In-Process Inspector, where you will play a crucial role in maintaining the integrity and excellence of our production process. As an integral part of our team, you will ensure that our products meet stringent specifications and industry standards at every stage of production. If you are driven by precision and quality and are eager to contribute to a team that values your expertise, we want to hear from you! Key Responsibilities: * Inspection and Quality Assurance: Interpret when parts are non-conforming according to drawings specifications, ensure adherence to Applied Manufacturing QS including SOP's, MI's, QI's, and TM's, maintain good shop order traceability, and meet or exceed production and quality goals. * Technical Competence: Read and understand Engineering drawings such as checking revisions, notes, features (length, diameter-ID/OD, radii, angles, etc.), dimensional tolerances, read and understand shop order operation and router sequence, and input data into the Quality Management (QM) software. * Workplace Safety and Compliance: Work with chemicals such as Isopropyl alcohol and plastic products daily, wear Personal Protective Equipment (PPE) such as gowning, masks, gloves, etc. daily and understand and follow Applied Manufacturing's Quality Systems (QS) and comply with Safety rules and Company policies. * Communication and Collaboration: Communicate effectively with peers, Production Team Leaders, and/or Engineering to resolve discrepancies and errors. Position Requirements * Possess a High school diploma or equivalent. * Familiarity of measurement equipment such as micrometers, calipers, pin gauges, optical comparators, and Nikon Vision Systems or similar tools. * Capable of lifting up to 25 lbs. frequently. * Proficient in reading, writing, and speaking in English. * Excellent hand-eye coordination. * Strong team player with good organizational skills. Preferred * Exceptional focus on precision and accuracy in inspections. * Strong understanding of safety protocols and the importance of following them rigorously. * Previous experience in a manufacturing or quality assurance role is highly desirable. At Applied Medical, your skills and dedication will be valued, and your contributions will make a significant impact. If you are ready to join a forward-thinking company that prioritizes quality, innovation, and employee growth, apply now to become part of our quality assurance team. Together, we'll build a future of excellence! Benefits * Competitive compensation range: $17.50 - $20 /hour (California). * Comprehensive benefits package. * Training and mentorship opportunities. * On-campus wellness activities. * Education reimbursement program. * 401(k) program with discretionary employer match. * Generous vacation accrual and paid holiday schedule. Please note that the compensation range may be based on factors such as relevant education, qualifications, experience. The compensation range may be adjusted in the future, and special discretionary bonus or incentive compensation plans may apply. Our total reward package reflects our commitment to team member growth and well-being, as we invest in your development and offer a range of benefits designed to enhance your career and life. Equal Opportunity Employer Applied Medical is an Equal Employment Opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, political affiliation, race, religious creed, sex (including pregnancy, childbirth, breastfeeding and related medical conditions), or sexual orientation, or any other basis protected by federal, state or local laws in the locations where Applied Medical operates.

Veridiam is a strategic manufacturing partner with over 60 years of experience serving the aerospace, industrial, medical, and nuclear markets. Our roots were formed in the exacting nuclear and aerospace industries, expanded into Medical where we have supplied critical components to a global customer base. We currently provide elegant solutions across a broad range of customers and diverse markets. At Veridiam we recognize that talent is at the forefront of our organization and define who we are in today's industry. POSITION SUMMARY Perform nondestructive testing (NDT) utilizing one of the NDT methods, such as ultrasonic testing (UT), radiography testing (RT), penetrant testing (PT), etc. techniques. Perform tests based on applicable methods. Perform visual and dimensional inspection. Generate inspection and test reports. ESSENTIAL DUTIES AND RESPONSIBILITIES Perform tests to inspect tubing materials, thinner welds, surface flaws, corrosion, wall sizing and thicker forms of welding that may harbor deviations from specifications. Set up equipment to perform non-destructive testing utilizing ultrasonic testing and/or eddy current testing methods on parts, following specified procedures. Examine surface and locate discontinuities in product or metal structure. Perform visual and dimensional inspection of various materials and products including welds. May develop and/or follow work instructions for approved procedures. Prepares and generates reports and/or documentation outlining findings and conclusions. Prepare and generate non-conformance reports in accordance with the Quality Management System specifications. Evaluate test and inspection results against designated standards. May participate in customer and/or quality audits. Ensures instruments and tools are maintained and calibrated according to schedule. Maintain clean and orderly work environment. Demonstrates ability to appear for work on time, follow directions from a supervisor, interact well with co-workers, understand and follow work rules and procedures, comply with company policies and procedures, goals and objectives, and accepts constructive feedback. Other duties as assigned, requested or needed. POSITION REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions. Education and Experience: High school diploma or General Education Development (GED). Minimum two (2) year's related metal material inspection experience or equivalent of education and experience. Prior experience and ultrasonic testing or eddy testing certifications preferred. Knowledge, Skills and Abilities: Knowledge of visual and dimensional inspection methods. Knowledge of and ability to use nondestructive testing methods including ultrasonic and eddy current testing techniques. Knowledge of geometric dimensioning and tolerancing (GD&T). Ability to understand and follow standard operating and safety procedures. Ability to prioritize and handle workflow. Read and comprehend verbal and written instructions. Ability to use basic mathematical equations. Knowledge of and ability to use basic computer functions. Ability to measure and read dimensional tolerance tools and equipment. Ability to view details in close range. The above statements are intended to describe, in broad terms, the general functions and responsibility levels and characteristics of positions assigned to this classification. They should not be viewed as an all-inclusive list of duties and responsibilities. Management has the right to change duties at any time to meet business needs. Veridiam offers competitive wage and excellent benefit package including medical, dental, vision, 401(k) (with company match) and basic life/AD&D. In addition to Paid Time Off, Holidays and career advancement opportunities. Pay Rate: The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience with the industry, education, geographic location, etc. Veridiam, Inc. is an Equal Employment Opportunity (EEO) employer and takes pride in a diverse environment. As an Equal Opportunity Employer, Veridiam will recruit and select applicants for “This position requires access to information which is subject to stringent controls under the International Traffic in Arms Regulations (ITAR) or Export Administration Regulations (EAR). Applicants must be a U.S. citizen or national, U.S. lawful permanent resident, person granted asylee status in the U.S., or person admitted into the U.S. as a refugee.”

Description Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: Join our team as Laboratory Support, Quality Control where your expertise and organizational skills will play a crucial role in maintaining a well-ordered and safe laboratory working environment. This role is perfect for individuals who are detail-oriented and passionate about supporting scientific research through meticulous laboratory upkeep and efficient handling of supplies and waste management. You'll find fulfillment in ensuring that our state-of-the-art lab operates smoothly and is always ready for groundbreaking research. Laboratory maintenance such as cleaning glassware, dusting/wiping bench, restocking of laboratory consumables on shelves, benches, cabinets, and other efforts to support the laboratories. Maintain/organize/distribute stockroom inventories of general supplies needed for use in the laboratory and reorder items as necessary. Record equipment daily readings and function checks of storage units. Clean/monitor/maintain laboratory equipment such as autoclaves, centrifuges, incubators, refrigeration units, cryotanks, fume hoods and water baths. Proper collection and disposal of biohazardous waste, hazardous waste, and recyclable waste in accordance with EHS guidelines. Verify that supplies have been received on time. Perform inventory counts. Prepare and package outgoing shipments via FedEx or World Courier as needed. Prepare buffers/reagents/various solutions for lab personnel and general lab use. Perform duties such as (but not limited to) data entry or manual inventory of lab items, cell lines, etc. Maintain equipment records and daily work logs. Read and comply with necessary SOPs pertaining to the Laboratory Technician position. Perform other duties as assigned. Minimum Qualifications: A Certificate in Biotechnology Lab Assistant or relevant laboratory experience is required for the position. 2+ years of related experience and/or training; or equivalent combination of education and experience. Preferred Qualifications: An understanding of aseptic handling, sterile technique, laboratory etiquette, GDP and GMP is preferred. Position Type/Expected Hours of Work:This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $20.52 to $24.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. Your written and verbal skills are out of this world, and you communicate with clarity and confidence. You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes. Your Role: Join our team as Laboratory Support, Quality Control where your expertise and organizational skills will play a crucial role in maintaining a well-ordered and safe laboratory working environment. This role is perfect for individuals who are detail-oriented and passionate about supporting scientific research through meticulous laboratory upkeep and efficient handling of supplies and waste management. You'll find fulfillment in ensuring that our state-of-the-art lab operates smoothly and is always ready for groundbreaking research. * Laboratory maintenance such as cleaning glassware, dusting/wiping bench, restocking of laboratory consumables on shelves, benches, cabinets, and other efforts to support the laboratories. * Maintain/organize/distribute stockroom inventories of general supplies needed for use in the laboratory and reorder items as necessary. * Record equipment daily readings and function checks of storage units. * Clean/monitor/maintain laboratory equipment such as autoclaves, centrifuges, incubators, refrigeration units, cryotanks, fume hoods and water baths. * Proper collection and disposal of biohazardous waste, hazardous waste, and recyclable waste in accordance with EHS guidelines. * Verify that supplies have been received on time. * Perform inventory counts. * Prepare and package outgoing shipments via FedEx or World Courier as needed. * Prepare buffers/reagents/various solutions for lab personnel and general lab use. * Perform duties such as (but not limited to) data entry or manual inventory of lab items, cell lines, etc. * Maintain equipment records and daily work logs. * Read and comply with necessary SOPs pertaining to the Laboratory Technician position. * Perform other duties as assigned. Minimum Qualifications: * A Certificate in Biotechnology Lab Assistant or relevant laboratory experience is required for the position. * 2+ years of related experience and/or training; or equivalent combination of education and experience. Preferred Qualifications: * An understanding of aseptic handling, sterile technique, laboratory etiquette, GDP and GMP is preferred. Position Type/Expected Hours of Work: This role is a full-time position. Days and hours of work are Monday through Friday, 8:00 a.m. to 5 p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary. Compensation: We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. The compensation range for this role is $20.52 to $24.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. Who you are: * You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way. * Your written and verbal skills are out of this world, and you communicate with clarity and confidence. * You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything. * You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Job DescriptionSalary: $23 - $27 DOE QUALITY CONTROL TECHNICIAN Since 1982, Ampronix develops, distributes, and services medical equipment for use in healthcare facilities across the world. We are a fantastic company to work for! We are looking for an experienced QC Support Technician to join our team at Ampronix, LLC., located in Irvine, CA. Role Ensure all repairs and refurbishments are completed to the highest quality standards. Provide competent and professional technical support and resolution to quality-related problems. Responsibilities Under the guidance of the QC and Service Manager, this position will be responsible for the following duties: Performs initial quality control checks at technician stations when the Service Supervisor is not available Utilize diagnostic equipment to efficiently burn/test all repaired and refurbished units Responsible for the upkeep of the quality control areas and equipment Provide professional and competent technical support to customers, SSSs, and the Sales team as needed Maintain quality procedures by moving finished inventory to assigned locations Compliance with ISO and ESD procedures Investigate and maintain returns and warranties Oversee procedural ISO and ESD compliance amongst the service technician staff Track and incur dispositions of all incoming customer units Oversee and coordinate efforts with Parts Expeditor to finalize units Provide parts expediting duties in the event of the absence of the Parts Expeditor Assure all diagnostic equipment is calibrated and in advance to inform purchasing as to the calibration due dates Provide updates on current repairs to Sales Support Specialists (SSS)/CSRs on customer units Cover for Quality Cosmetic controller during his absences Skills The ability to multi-task The ability to communicate with different departments, management, staff, and our customer base Highly organizational skills Excellent attention to detail Electronic knowledge The ability to expedite and execute quality control procedures in a timely, accurate manner The ability to research and acquire knowledge of current electronic imaging products, video signals, modalities, and any other applicable specifications Understand and communicate technical support to our customers and employees Education / Experience High School graduate or GED equivalent Technical degree or certification, or College Degree and/or a combination of educational work Two (2) years of work experience Physical Requirements Must be able to perform general physical activities by considerable use of your arms and legs and moving your whole body, to lift, balance, walk, stoop, and using hands and arms in handling and moving materials. Must be able to move up to 50 pounds at a time. Benefits Ampronix, LLC., offers an excellent benefits package that includes: Medical Dental Vision Employer pays Life and AD&D Voluntary Life and AD&D, 401(k) Plan and Employer Match Pet Insurance Paid vacation Paid holidays Paid sick time We offer a great work environment with fun activities throughout the year! EEO Statement We are committed to providing equal employment opportunities to all persons regardless of race, color, ancestry, citizenship, national origin, religion, veteran status, disability, genetic characteristic or information, age, gender, sexual orientation, gender identity, marital status, family status, pregnancy, or another legally protected status (collectively, protected statuses). We do not tolerate unlawful discrimination in employment decisions, including recruiting, hiring, compensation, promotion, benefits, discipline, termination, job assignments, or training. As a registered ISO and ESD company seeking dedicated team members, working for the common goal of continuous quality and service. Please go to our website Ampronix.com to learn more about our Company. Thank you and we look forward to hearing from you!