Quality Control Inspector jobs at Orchid Orthopedic Solutions - 114 jobs

ABOUT US The Oregon City, OR site was established in 1973 and joined the Orchid team in 2012. Our 80,000 square foot facility employs approximately 300 team members. We specialize in hip and knee joint implants that enable our customers to live a longer active life. We are a full-service plant, meaning our team can manufacture medical implants from start to finish in-house. A career with Orchid provides growth opportunities, a great benefits package including performance bonuses, insurance, 401(k) with company match, and paid time off. For more information, please visit ********************* SHIFT ORE - Shift 1 ($0) (United States of America - Oregon) A BRIEF OVERVIEW The QC Inspector, Visual, Orchid Oregon, performs tasks to visually inspect machined and machined & polished parts to ensure compliance to customer acceptance criteria in accordance with established policies and procedures. The QC Inspector, Visual, Orchid Oregon reports to the Quality Control Supervisor. WHAT YOU WILL DO Ensure compliance to Orchid requirements in inspection and record keeping. Collect inspection data and report results. Maintain accurate documentation at all times during the manufacturing and inspection process per Good Manufacturing Practices. Perform complete Device History Record review including inspection documentation Ensure all raw materials received meet specifications. Perform testing and inspection at various stages of production, including visual and dimensional inspection Ensure customer specifications and other applicable internal external requirements are followed. Use handheld inspection tools for measurement purposes, such as micrometers, calipers, height gages, optical comparator, gage blocks, and dial indicators. Conduct physical inspection of product with gauging such as: Thread gages, plug gages, pin gages, functional gages. Perform visual and/or cosmetic inspection of product following applicable procedure(s) using appropriate light sources. Monitor equipment to ensure proper operation and escalate any equipment-related issues. Communicate potential nonconforming situations to Quality Engineering and Quality Management. Demonstrate an understanding of basic manufacturing concepts and processes. Quarantine non-conforming or potential non-conforming parts or materials. Work modified schedules to support production requirements as necessary. Complete First Article Inspections as well as receiving, in-process, and final and packaging inspections against customer requirements with minimal supervision Train inspection personnel. Inspect customer-returned parts Under guidance, perform first piece inspections to support production and perform internal manufactured first articles. Advocate for the health and safety of self, co-workers, customers, and the community. Support quality and compliance by adhering to all procedures, work instructions, and forms per the Quality Management Systems (QMS). Complete all required training. Visually inspect machined and polished parts Confirm discrepancies using appropriate tools including, but not limited to calipers, pin gages, measuring instruments and surface profilometers as required Route non-conforming product for rework operations to ensure compliance of customer acceptance criteria Accurately document inspection results Communicate nonconformance's and work with Quality to drive corrective actions Complete proper documentation as required including, but not limited to, process routing card, salvage router, scrap tags, dimensional reports, etc. EDUCATION QUALIFICATIONS High School Or Equivalent (Required) EXPERIENCE QUALIFICATIONS No previous work experience required Experience in a Scientific Field (Preferred) Experience in Quality Inspection and Lean Manufacturing (Preferred) LICENSES AND CERTIFICATIONS Any Technical Trade School (Preferred) Any American Society for Quality (Preferred) KNOWLEDGE & SKILLS THAT ENABLE SUCCESS Mathematical Ability - Working Experience Data Entry - Working Experience Computer Knowledge - Working Experience Communication - Working Experience Collaboration - Working Experience Handwriting - Working Experience Accuracy and Attention to Detail - Working Experience Quality Inspection Metrology Tools - Working Experience Information Processing - Working Experience Blueprint Reading - Working Experience GD&T - Working Experience Visual Quality Assurance - Working Experience Layout Inspection - Working Experience Time management - Working Experience Problem Solving - Working Experience PHYSICAL DEMANDS Must be able to remain in a stationary position - Frequently Must be able to move about the inside of the building - Occasionally Must be able to move equipment around the building - Occasionally Must be able to position oneself and move under/around/over equipment - Occasionally Must be able to handle/adjust/inspect/position various items and equipment - Constantly Must be able to communicate and exchange information with others - Frequently Must be able to perform tasks that require repetitive handling/adjusting/inspecting/positioning of items and equipment - Constantly Must be able to distinguish and detect information such as writing and defects - Constantly Must be able to move equipment - Occasionally WORKING CONDITIONS Noise - Occasionally WHAT WE OFFER Opportunity to work in a growing company Ability to help people live a longer, more active life Comprehensive benefit package Ability to work in an organization that values: Integrity First: We do the right thing Teamwork: We are one Orchid Results: Our results matter ADDITIONAL REQUIREMENTS Candidates offered employment may be required to submit to a pre-employment background check and pre-employment drug-screening based on position requirements Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time Candidates must be able to provide proof of eligibility to work in the United States through eVerify At Orchid, we fully support a diverse and inclusive workplace and we are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, religion, sex, sexual orientation, gender identity, national origin, hair type, age, status as a protected veteran, or disability. Orchid Orthopedic Solutions only pays fees for solicited presentations of job seekers submitted through our preferred vendor job board by recruiters, employment agencies, or other parties.

A leading biotechnology firm located in California is seeking a Director of Quality Assurance to oversee product quality and establish specifications for clinical and commercial products. The role requires extensive experience in analytical chemistry and regulatory compliance, along with strong leadership skills in a complex matrix environment. This is a full-time on-site position offering the opportunity to lead strategic quality initiatives. #J-18808-Ljbffr

A leading biopharmaceutical company in California is seeking a Senior Director for Global Supplier Quality. The successful candidate will lead a team of Quality Professionals, ensuring compliance with GMP standards while managing supplier quality initiatives. This role requires extensive experience in biopharmaceutical management, exceptional leadership skills, and a strong understanding of regulatory requirements. Candidates should have a solid educational background in science and proven leadership experience in complex organizations. Competitive salary & benefits are offered. #J-18808-Ljbffr

The primary responsibility for this position is to establish phase appropriate product specifications for Gilead's clinical and commercial products. In addition, this position is responsible for end to end product quality strategy and serves as the QA main point of contact on the PDM Product Strategy Team(s). The position holds a scientific and technical understanding of drug development and commercialization and able to provide effective quality oversight and feedback for their assigned program(s) by liaising between the Product Strategy Team, Manufacturing, and Analytical functions, Supply Chain, RA CMC, and the wider PDM Quality organization. Job Functions Expert in analytical control systems, assuring network-wide harmonization of control systems by proactive lifecycle management, technical leadership and ownership. Provide technical oversight of product specification setting and justification based on scientific approach. Deep understanding of analytical methods (development, validation, transfer, and monitoring) and product (process development, CQA analysis, stability, comparability, etc). Ability to evaluate Global product filing strategies with core PDM Team for implementation. Provide timely support for health authority interactions on the product, authorship/review (as needed) relevant health authority information requests for in-process controls, process development (comparability), method validation, specifications, reference standard, and stability sections of regulatory submissions. Build internal knowledge and capabilities on product control strategies. Proactively share expertise with other functional groups to generate alignment and improvement opportunities. Accountable for end-to-end quality compliance of the assigned product/program, which include but not limited to providing strategic leadership and direction for quality and compliance activities and owns the overall product risk log. Serve as the primary Quality representative in the PDM meeting. Lead Product Quality Teams (PQT) supporting the product/program, and ensure visibility and communication of strategy, key project timelines and CMC milestones. Monitor and review cross-functional process and product data to identify trends to ensure significant quality and compliance risks are identified, mitigated and, if necessary, escalated in a timely manner. Review and approve the strategy for change control(s) impacting the product/program lifecycle. Provide technical oversight of Major and/or Critical Deviations, CAPAs, Biological Product Deviation and Complaints. Contribute to Review Regulatory Submissions (IND, IMPD, BLA, NDA, MAA), and assist with regulatory communications as needed (e.g. responses to agency information requests, the Notified Body Option). Provide oversight for changes to drug substance and drug product CMC details. Accountable for PAI/PLI readiness and supports Gilead PAI/PLI inspection preparation efforts and post-PAI/PLI follow up as a Subject Matter Expert with Quality representatives at CXO(s) and Gilead Sites. Support drug substance and drug product technology transfer, and new product launches. Participate in drafting commercial Annual Product Quality Review (APQR) and review/approve Gilead and CMO APQRs for commercial products. Accountable for medical device/ combination product quality compliance: engage/liaise with medical device product engineering, development, and quality teams. Facilitate Analytical Strategy (stability strategy, specifications, Critical Quality Attributes). Perform work that requires independent decision making and the exercise of independent judgment. Serve as the delegate for direct manager, as needed, for meeting and decision making. Knowledge, Experience and Skills Well verse in technical requirements for product control systems. Strong knowledge and practical experience in analytical chemistry, including separation science, wet chemistry, physicochemical characterization or related areas. Strong experience in the assessment of technical data and scientific information is required in order to provide technical reviews for documents and regulatory submissions. In-depth understanding and application of GMP principles, concepts, best practices, and standards in the US and internationally. Demonstrated ability to develop and improve complex concepts, techniques, and standards and new applications based on quality principles. In-depth knowledge in Global requirements/standards for product registration and life-cycle management of product quality. Extensive knowledge and experience in technology validation/transfer of Drug Substance and Drug Product. Skilled at managing multiple projects and timelines and to facilitate meetings. In-depth understanding and execution of Quality Risk Management. Ability to track and follow up on actions. Excellent in verbal, written and interpersonal communication skills. Ability to work in a team-oriented approach to address complex issues in a scientifically sound and compliant way. Ability to lead and influence a matrix-based cross-functional team. Critical and strategic thinking skills and ability to provide pragmatic, risk-based, and phase appropriate guidance and decision-making even when quality and compliance requirements are not well-defined. Extensive knowledge and experience in technology validation/transfer of Drug Substance and Drug Product. Basic Qualifications 12+ years of relevant experience and a Bachelor's degree in science or related fields. OR 10+ years of relevant experience and a science degree MS OR 8+ years PhD Preferred Qualifications Prior Quality leadership and technical management experience in development and/or commercial programs. 15+ years of relevant experience and a Bachelor's degree in science or related fields; or 10+ years of relevant experience and an advanced science degree such as MS, PharmD, PhD or an advanced business degree such as an MBA. Demonstrated experience and knowledge in quality assurance in a highly regulated manufacturing environment. Direct experience with regulatory health authority submissions (e.g. IND, NDA, BLA, MAA) and/or inspections. Broad experience across several including process validation, drug development experience, packaging/labeling and understanding of Parenteral, Oral Solid Dosage, and Biologics. Job Requisition ID R0047720 Full Time/Part Time Full-Time Job Level Director Remote Type Onsite Required #J-18808-Ljbffr

The QC Inspector I will play a vital role in ensuring the quality and safety of products in either manufacturing or distribution environments. Responsible for inspecting materials, components, and/or finished products to ensure they meet established quality standards. This role involves conducting visual and measurement tests, documenting findings, and reporting any defects or discrepancies. This role will work closely with production or distribution teams to identify and resolve quality issues, contributing to the overall improvement of processes. Job Description Shift: 1st shift, starting at 6am daily MAJOR RESPONSIBILITIES Perform inspections on incoming materials, in-process items, and/or finished products. Document inspection results and maintain accurate records. Use measurement tools and equipment to test and verify product dimensions and specifications. Identify and report defects, deviations, and non-conformities. Collaborate with respective production or distribution teams to address quality issues, implement corrective actions, or determine disposition of product. Assist in the development and implementation of quality control procedures and standards. Participate in continuous improvement initiatives to enhance product quality and efficiency. Assess inbound damaged finished goods and repackage. Support various tasks including inventory stock checks, recall stock verifications, handling deviations, relabeling, product rework, pedigree verification, and other assigned projects. May be required to operate powered material handling equipment. Read and interpret instructions, blueprints, and other documents. Comply with Standard Operating Procedures (SOPs), Quality Systems, OSHA guidelines, and Medline's rules and regulations. REQUIREMENTS: Education: High School Diploma EXPERIENCE: Experience within Quality Control environment, preferably in manufacturing. Working knowledge of Microsoft Office tools. 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: $18.50 - $26.75 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.

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. 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: $19.75 - $27.75 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.

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.

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.

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 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 currently onsite in Sunnyvale, CA, with an anticipated transition to the permanent Gilroy, CA facility in or after April 2026. Essential Job Duties * 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 * 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 * 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 * Must be able to lift a minimum of 25 lbs. Preferred Skills and Experience * Knowledge of Good Manufacturing Practices * Good organizational skills * Can communicate clearly and concisely. Compensation and Benefits We provide market-competitive compensation packages, inclusive of base pay, benefits and equity. The target pay range for this position is $52,790/yr to $71,406/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.

The anticipated salary range for candidates who will work in San Diego, CA is $72,000 to $90,000 annually. 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 years of experience within the job, type and years of experience within the blood banking industry, education, etc. Job Summary Under minimal supervision of management, Medical Laboratory Scientists perform manufacturing processes in a highly regulated environment-from receipt of unprocessed apheresis platelets, through maintaining accurate records of finished components in preparation to distribute to available inventory. The QC lab CLSs test products across the three stages of production (before, in-process, and final) and review the data to ensure the high quality and maximum efficacy of blood components. Responsibilities Perform essential laboratory responsibilities according to established procedures. Support the SDBB safety, GMP and Quality Plan. Adheres to GMP guidelines. Safely operate laboratory equipment in accordance with established SOPs. Obtain samples for product QC testing and further manufacturing. Perform donor and product quality control evaluations. Perform sterility testing on apheresis platelets and operate Bact/ALERT instrument. Perform pathogen reduction process using illuminator instrument. Operate Hematology analyzer to manufacture platelets using large volume delayed sampling and pathogen reduction methods. Perform pH analysis using pH Meters Perform residual WBC testing using Fluorescence Microscopy method. Perform routine equipment QC and maintenance. Evaluate, gather data, trend, and assess results. Assist in training new personnel and other staff members. Assist in laboratory paperwork documenting information accurately and completely in a timely manner. Complete all tests required for each product. Initiate and participate in the investigations and assess any potential impact on product quality. Conduct retesting of product as needed to support quality investigations. Participate in research projects. Participate in department meetings and educational programs. Review and approve quality control on products, reagents, and various test kits. Receive / Review, Upload and Commit IDM test results. Provide support for the donor notification/look-back process. Perform Iso titration on platelet components. Communicate with production personnel and Quality Assurance department. Assist with validations, special projects, and new process developments. Monitor supply inventory levels and assist with material ordering. Understand and adhere to the policies and standards as developed as part of the San Diego Blood Bank Compliance Program. Perform other related duties as assigned or requested. Working Environment Normal laboratory environment with biohazard precautions. May be exposed to blood or bodily fluids that may be capable of transmitting diseases. May be exposed to chemicals that may be hazardous. May be called on to work or attend meetings at other than routinely scheduled hours. Physical Requirements Must be able to stand or sit long hours. Must be able to work on a computer 4 - 8 hours a day. Must be able to communicate clearly. May be required to lift to 40 pounds. Equipment Used General office equipment (computer, printer, fax, copy machine). Various software systems (Blood Establishment Computer System, Quality Management System). Laboratory equipment, including, but not limited to: Centrifuges. Heat sealers. Scales. Refrigerators/incubators. Sterile Connection Devices. BacT/ALERT 3D analyzer. Hematology cell counter. Illuminators. ADAM rWBC analyzer. pH Meter. Qualifications Education: MLS/MT (ASCP)cm or equivalent experience. CA Clinical Laboratory Scientist (CLS)- Generalist. Experience: Laboratory experience preferred but not required. Understanding of technical aspects of lab department, blood banking concepts, hematology, microbiology, serology, and flow cytometry. Skills: Organized and able to efficiently prioritize and handle multiple tasks at one time to provide a productive workflow. Professional communication both written and oral, which is clear and precise. Provide direct and constant supervision over unlicensed laboratory personnel. Must be detail oriented, well organized and display good time management skills. Ability to perform under pressure and work under stressful situations. Interpersonal skills to establish and maintain professional relationships. The San Diego Blood Bank is an Equal Opportunity Employer. EOE/Minority/Female/Disability/Vets The above statements are intended to describe the general nature and level of work being performed. This job description is not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified.

Join our mission-driven Quality team as the 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 forward-thinking, mission-driven environment where every team member plays a vital role in advancing patient care. Our values guide how we operate: we prioritize patient outcomes, act with integrity, stay curious and innovative, move boldly in pursuit of excellence, and collaborate across teams and with physicians to achieve exceptional results. As for our people? We empower them with the tools, trust, and continuous learning they need to grow. If you're passionate about making a meaningful difference in healthcare, you'll find purpose and belonging here. ABOUT THE ROLE: We're looking for a 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: * Perform audits, inspections, configuration checks, and functional testing to ensure product quality and compliance with established procedures. * Review and verify lot history records for completeness, accuracy, and adherence to SOPs; investigate records related to customer experience reports. * Inspect subassemblies, finished products, purchased components, and tools using defined criteria and standard mechanical, and/or electrical measurements. * Conduct product rework on subassemblies or finished goods as required. * Accurately document inspection and testing results in compliance with Good Documentation Practices (GDP). * Review Device History Records (DHR) for compliance with established procedures and GDP requirements. * Identify issues and provide initial recommendations for corrective actions or process improvements to supervisors. * Perform product testing to ensure conformance to quality standards. * Work within a cleanroom environment, following all applicable protocols and safety requirements. * Perform temperature and particle count monitoring; manage ERP (QAD) and MES application transactions; handle multiple tasks efficiently in a fast-paced manufacturing environment. * Perform other duties as assigned by the supervisor. * Demonstrate punctuality, reliability, and a strong work ethic. Qualifications WHAT YOU'LL BRING: Education: * High School Diploma or equivalent required. Experience: * 1-5 years of Quality Control experience, preferably in the medical device industry. Skills/Competencies: * Ability to understand and follow technical procedures, work instructions, and basic specifications related to the inspection of products and components. * Skill in identifying relevant information in technical drawings and documents and reporting any discrepancies to the supervisor. * Familiarity with applicable quality standards and willingness to learn about specific regulations under supervision * Mechanical aptitude and working knowledge of measurement instruments. * Strong written and verbal communication skills for reports, correspondence, and presentations. * Mathematical proficiency in fractions, percentages, ratios, and proportions. * Problem-solving skills with the ability to work in a cross-functional environment and manage multiple priorities. 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 $24.03/hr-$29.44/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 HOW WE LEAD WITH OUR CORE VALUES: * Patient Outcomes Drive Us: We improve lives with every advancement we deliver. * Integrity Defines Us: We do what's right, stay transparent, prioritize quality, and own our actions. * Innovation Advances Us: We stay curious, adaptable, and push boundaries. * Boldness Propels Us: We take smart risks and are unafraid in our pursuit of excellence. * Collaboration Unites Us: We partner across teams and with physicians to drive exceptional results. OUR COMMITMENT TO EQUAL OPPORTUNITY & VETERAN INCLUSION: Endologix LLC is an Equal Opportunity and Affirmative Action 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. As a federal contractor, Endologix LLC is committed to taking affirmative action to recruit, employ, and advance in employment qualified individuals with disabilities and protected veterans.

The Bed Control Coordinator insures the effective and efficient utilization of acute and long-term care beds, and hospital resources as well as insuring proper registration procedures are followed. This position acts as a liaison between physician, department managers, patients and external agencies concerning the admitting process and is responsible for maintaining the confidentiality of all patient information. Responsibilities POSITION SPECIFIC DUTIES (other duties may be assigned) Assumes responsibility for position responsibilities outlined in the Registrar job description. Maintains the hospital census and reconciliation with nursing units. Calculate observation hours and enter on the account. Reports direct admissions to the nursing supervisor who determines medical necessity and appropriate level of care; coordinates effective patient flow to insure internal and external customer satisfaction; informs physicians of patient arrival times; coordinates admissions with nursing units, ambulances and external entities. Evaluates patient financial status at admission and/or referring to the Patient Financial Advisor as appropriate. Secures and releases patient valuables at admission and discharge. Prepares all surgery and/or GI packets for the following day securing patient orders, insurance verifications and patient notification of possible out of pockets. Completes additional projects as requested by Supervisor or Director. Takes initiative and performs as self-starter in daily activities. Qualifications QUALIFICATIONS/JOB REQUIREMENTS: EXPERIENCE: One year of patient registration experience in an acute facility. More years of experience may be required if hired in a registration area that demands more experience. Work in a physician's office may be substituted for an acute hospital setting if duties are similar. OTHER SKILLS, ABILITIES & KNOWLEDGE: Understands the registration process, managed care/capitation, Medi‑Cal, Medicare regulations, Medical Terminology, HIPAA, ABN, and EMTALA regulations Works effectively with the public, physicians, and staff Provides quality customer service including enhancing patient satisfaction while possessing the ability to work in a high volume production‑oriented and structured environment

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.

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.

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

Under minimal supervision of management, Medical Laboratory Scientists perform manufacturing processes in a highly regulated environment-from receipt of unprocessed apheresis platelets, through maintaining accurate records of finished components in preparation to distribute to available inventory. The QC lab CLSs test products across the three stages of production (before, in-process, and final) and review the data to ensure the high quality and maximum efficacy of blood components.

Under minimal supervision of management, Medical Laboratory Scientists perform manufacturing processes in a highly regulated environment-from receipt of unprocessed apheresis platelets, through maintaining accurate records of finished components in preparation to distribute to available inventory. The QC lab CLSs test products across the three stages of production (before, in-process, and final) and review the data to ensure the high quality and maximum efficacy of blood components.

Performs non-destructive testing on products using fluorescent penetrant inspection as required to conform to customer and/or national standards, by performing the following duties. The role requires the above to be accomplished within Tecomet's principles of continuous improvement, customer driven innovation and a win first culture, while meeting company financial and other performance metrics. **Principle Responsibilities** + Performs inspection procedures following customers' specifications. + Determines acceptability of product based on results of testing. + Interprets results, and determines probable cause of defects. + Performs daily system checks. + Documents and publishes results of FPI testing. + Read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. + Write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of the organization. + Add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. And compute rate, ratio, and percent and to draw and interpret bar graphs. + Apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. And deal with problems involving several concrete variables in standardized situations. + Maintain confidentiality. + Work well under pressure and to remain flexible to changing schedules and demands. + Additional duties as requested by management. **Qualification Requirements** **Credentials/Experience:** + 2 years related experience and/or training preferred **Experience/Educational/Training Preferred:** + High school diploma or general education degree (GED) + SNTC Level I or II preferred + NAS 410 Level I or II preferred **Knowledge, Skills, and Abilities:** + Excellent communication and interpersonal skills + Ability to work independently and exercise judgment + Working knowledge of fluorescent penetrant inspection equipment **Other Requirements** **Work Environment** The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. **Physical Requirements** While performing the duties of this job, the employee could be required to stand. The employee could frequently be required to walk; use hand to finger, handle, or feel; reach with hands and arms and talk or hear. The employee could be required to sit; climb or balance and stoop, kneel, crouch, or crawl. The employee could occasionally lift and or move up to 50 pounds.Specific vision abilities required by the job could include close vision, distance vision, peripheral vision, and ability to adjust focus. **Travel Requirements** N/A **Americans with Disabilities Act (ADA):** Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. _The statements herein are intended to describe the general nature and level of work being performed by employees and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the Company._ **Pay Range** $20.00 - $26.10 / hour **Pay Transparency** In order to support the Fair Compensation Strategy by the US Govt., HR Dept., clients are required to adhere to "Pay Transparency Law"; in the impacted states; that have mandated the employers to list the salary ranges in Job advertisements or postings for job opportunities and Job promotions.

- AUTHORIZED INSPECTOR Bureau Veritas is looking for a hardworking, observant, and mechanically inclined inspector for the metal fabrication and pressure vessel industry. This role is ideal for individuals who are self-motivated and prefer to work independently. Excellent pay and benefits, plus opportunity for a long-term career. WE PROVIDE TRAINING. Key Responsibilities Performs ASME and National Board shop and field inspection services at assigned clients, including review and verification of code required activities, implementation and applicability of the manufacturers written quality control system, and witnessing of all required tests. Monitors client quality control system for compliance with relevant codes and requirements. Documents all inspection activities per established policies. Ensures compliance with applicable sections of the ASME Code, the National Board Inspection Code, and Jurisdictional requirements for the construction and repair of boilers and pressure vessels. Acquires and maintains knowledge of the applicable sections of the ASME code, the National Board code, and the Jurisdiction. Continually enhances knowledge through self-study, internal training, and approved courses. Required Education and/or Experience Must have 4 years of demonstrated experience in nuclear reactors or the boiler and pressure vessel industry, such as design, welding, fabrication, operation, repair, inspection, nondestructive examination, or quality control system oversight. A STEM BS or AS degree, CWI, or technical certificate may be substituted for 2 years of experience. Must have a high school diploma Must complete a 2-week preparatory training course provided by Bureau Veritas on ASME Sections I, IV, V, VIII, IX, and B31.1. Must be able to obtain a National Board Authorized Inspector Commission with "R" Endorsement. Obtaining this commission requires attendance at a 72-hour course and a 32-hour course provided by the National Board, passing (2) exams administered by the National Board, and 80- hours of on-the-job training with another Commissioned Inspector. OR Must have a National Board Authorized Inspector Commission with "R" Endorsement. Competencies Ability to read, write, speak clearly and informatively, use a computer, and perform basic arithmetic. Ability to understand and interpret the boiler and pressure vessel codes. Ability to interact with clients. Ability to apply industry knowledge, technical skill, and sound business practice to decision making. Ability to adhere to established company policies, directives, and procedures, and to ensure accurate and timely reporting and submission of results for assigned activities.