Quality engineer jobs in Poway, CA

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. The Qnity Carlsbad Site is seeking a Quality Manager at our manufacturing site in Carlsbad, CA. This role includes managing the quality systems at the site. This Site is part of DuPont's Electronics and Industrial Division. Electronics and Industrial is comprised of a number of high growth, global businesses, supplying a broad array of materials to multiple consumer electronics and industrial sectors. The Quality Manager is responsible for managing the objectives and performance of the Quality organization and Quality Management System. The Quality Manager is responsible for assuring product quality within our manufacturing plant by providing leadership and direction to maintain and improve our quality management systems. Intent/Value Enhances the front-line knowledge and accountability for quality, Promote a customer-focused culture and Drive customer centricity efforts across North America Sites Critical Success Factors: * This is a key role to ensure that the business and unit quality programs are effectively implemented and maintained. * The job requires out of the box thinking, strong interpersonal skill across all functions and levels, constructive gate-keeping skills, sound technical skills (product and technology of quality management), as well as strong corporate core competencies in collaborating for superior results, leading courageously, delivering innovative solutions, and generating customer value. * Ability to align customer, quality, and business requirements into goals, objectives, and strategies and effectively communicate these requirements across multiple sites. * Ability to build trust and create strong relationships across unit level and global teams both cross-culturally and cross-functionally. Responsibilities: * Develop, implement, and maintain the unit quality programs which align to the Quality Management System Strategy. * Assist in the development of business level goals & objectives, critical operating tasks (COTs), customer and product improvement plans, then ensure these initiatives are adopted as plant / unit level objectives and ensure yearly COTs are aligned with individual plant level quality team. * Lead and direct the activities of the quality staff, manage / supervisor team of quality engineers, laboratory specialist, and quality management system coordinators. * Lead risk management activities at all phases of the product life cycle. * Ensure that product returns and non-conforming product processes are appropriately managed to prevent unintended use, including disposition. * Monitor the effectiveness of the quality management system and communicate to site leadership all improvement opportunities through our management review process. * Generate and use quality data (customer complaints, plant metrics etc.) to enable cross functional partners to drive product quality improvements. * Participate in management of change reviews that potentially impact product quality (specification, train qualifications, plant equipment / systems, analytical testing, etc.). * Ensure plant operating discipline system, procedures and guidelines meet quality system and customer requirements, as appropriate. * Identify and lead improvement opportunities as determined through data analysis, customer audits, Six Sigma projects, and other quality-related programs. * Lead / champion product quality problem solving efforts (corrective action, preventive action, root cause investigation process, including customer feedback, etc.). * Establish and manage the plant quality system Internal Audit program in conjunction with unit strategies. * Oversee and support the audits of plants, labs, terminals, warehouses, contract manufacturers, distributors, suppliers, customers, etc. to ensure customer needs are met. Leverage findings and drive all corrective action and continual improvement. * Participate in the review of unit and cross functional projects having a potential impact on product quality and Quality Management Systems. * Ensure quality system tools are validated throughout the unit quality architecture. * Work with Global Quality, Product Stewardship and Regulatory leaders to standardize Quality Assurance program to ensure North American Sites adhere to established protocols, risk assessments, audits, training & competency, corrective actions and records, and controls. * Implement systems to comply with ISO-9001:2015 and AS9100 standards. Required Qualifications: * Bachelor's degree in science or engineering discipline * Minimum of 7 years relevant experience in Quality Assurance, Quality Engineering, Industrial or Manufacturing * A proven track record of success in implementing and maintaining quality systems in regulated markets. * Experience implementing quality management systems compliant with ISO9001:2015 International Standard and AS9100 Aerospace Standards. * Excellent spoken and written communication skills. * Excellent MS Office Skill (Excel, Word, PowerPoint) * Six Sigma certification is preferred. * Internal Audit experience/certification preferred. ~20% travel required As required by a federal contract or subcontract, only U.S. citizens will be hired for this position. Join our Talent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a **maker of possible** with us. **Job Summary:** The Quality Manager will lead and oversee all aspects of execution of the Quality Management System (QMS), including Risk Management for the Alaris System. This role is responsible for ensuring compliance with regulatory requirements, company policies, and industry standards, driving continuous improvement initiatives, and maintaining a culture of quality throughout the organization. **Job Responsibilities:** _QMS Leadership and Management:_ + Develop, implement, and maintain the Quality Management System (QMS) in accordance with ISO 13485, 21 CFR Part 820 (QSR), and other applicable global regulations and standards. + Lead and manage a team of quality professionals, providing guidance, coaching, and performance feedback. _Quality Improvement and Risk Management:_ + Drive continuous improvement initiatives through data analysis, root cause investigation, and implementation of effective CAPAs. + Facilitate risk management activities, including FMEAs and risk assessments, throughout the product lifecycle. + Oversee non-conformance and deviation management processes. + Promote a strong quality culture through training, communication, and engagement across all departments. **Job Qualifications:** _Education:_ + Bachelor's degree in Engineering, Life Sciences, or a related field. Master's degree preferred. _Experience:_ + Minimum of 5 years of experience in Quality Assurance within the medical device industry. + Minimum of 3 years of experience in a leadership role, preferred. + In-depth knowledge and practical experience with ISO 13485, 21 CFR Part 820 (QSR), MDR, and other relevant global medical device regulations. + Proven experience in managing and developing quality teams. + Demonstrated success in leading regulatory audits (e.g., FDA, Notified Body). _Skills:_ + Strong analytical and problem-solving skills with a data-driven approach. + Excellent written and verbal communication skills, with the ability to effectively interact with all levels of the organization and external stakeholders. + Proficient in quality tools and methodologies (e.g., Lean, Six Sigma, FMEA, Root Cause Analysis). + Strong leadership and interpersonal skills, with the ability to influence and motivate others. + Proficiency in Microsoft Office Suite and QMS software. **Certifications (Preferred):** + ASQ Certified Quality Manager (CQM), Certified Quality Engineer (CQE), or equivalent. At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. **Why Join Us?** A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . **Primary Work Location** USA CA - San Diego Bldg A&B **Additional Locations** **Work Shift** At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You (********************************************* . Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. **Salary Range Information** $126,600.00 - $208,900.00 USD Annual Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

SOMACIS, Inc. - Global Printed Circuit Board Manufacturer for 50+ Years SOMACIS, Inc. is a global leader in high-performance printed circuit board manufacturing, serving aerospace, avionics, military, commercial, and medical industries. With more than fifty years of experience, SOMACIS is recognized for quality, innovation, and strong customer partnerships. Position Summary The Quality Manager ensures SOMACIS delivers products that meet industry and customer quality standards. This role leads the company's QMS (Quality Management System), oversees internal and external audits, manages corrective and preventive actions, strengthens process control, and drives continuous improvement initiatives. Duties and Responsibilities • Maintain and continually improve the facility's Quality Management System in compliance with ISO 9001, AS9100, MIL-PRF-31032, and customer-specified requirements. • Serve as the AS9100 Management Representative for customer and accreditation audits. • Develop and maintain internal audit programs, corrective and preventive action processes, and management review activities. • Establish, monitor, and analyze process capability metrics, including Statistical Process Control, yield, scrap, and rework. • Ensure adherence to workmanship standards such as IPC-6012 and IPC-A-600. • Review and approve First Article Inspections in accordance with AS9102, along with qualification samples and process validations. • Act as the primary contact for customer quality issues, including complaints, corrective actions, and return investigations. • Oversee root cause analysis and corrective actions using structured tools such as 8D, 5-Why, and fishbone analysis. • Support customer audits, technical reviews, and onsite visits. • Manage and develop a quality team across three shifts, including engineers, supervisors, and inspectors. • Provide training and guidance on quality procedures, inspection methods, documentation requirements, and industry standards. • Participate in company knowledge advancement and continuous learning programs. • Support SOMACIS global operations as needed. • Foster a proactive quality culture across departments. • Qualify and monitor key suppliers, including raw materials such as copper-clad laminates, prepregs, chemicals, and epoxy pastes. • Oversee supplier audit activities and supplier performance review programs. • Ensure incoming materials are thoroughly inspected and meet all specification and quality requirements. • Collaborate with internal teams to drive process improvements, reduce defects, and enhance product reliability. • Complete assigned tasks and corrective actions to closure. • Maintain a safe, organized, and compliant work environment. Export Compliance Responsibilities • Comply with ITAR, EAR, and OFAC requirements. • Reinforce export compliance expectations throughout the organization. • Follow foreign-visitor procedures, including Visitor Authorization Letters. • Support export compliance personnel during audits, training sessions, and reviews. Managerial Responsibilities • Allocate resources to meet quality, production, customer, and audit objectives. • Recommend and implement departmental process and policy improvements. • Manage schedules, workflow, and performance expectations; may assist with budgeting. • Evaluate complex technical or operational issues and provide guidance to supervisors, engineers, and cross-functional teams. • Collaborate frequently with internal leadership, customers, suppliers, and external partners. • Lead continuous improvement initiatives across functional areas. Travel and Work Requirements • Travel to customer and supplier locations as needed. • Ability to work extended hours based on business requirements. Required Knowledge, Skills, and Abilities • Strong teamwork, communication, and leadership skills. • Ability to solve complex technical problems using structured methods such as 8D and root cause and corrective action. • Advanced analytical and computer skills, including proficiency with Microsoft Excel and Microsoft Access. • Ability to read and interpret blueprints, specifications, and technical documentation. • Ability to manage multiple priorities with accuracy, urgency, and professionalism. Education and Experience • Bachelor's degree in a quality-related field or equivalent experience. • Experience in printed circuit board manufacturing strongly preferred. • Knowledge of IPC and ISO requirements. • Quality Engineer or Quality Manager certification through ASQ preferred. • Six Sigma Black Belt training is a plus. Benefits • Medical, dental, and vision insurance • 401(k) retirement program • Company-paid life and accidental death and dismemberment insurance • Voluntary life, long-term disability, accident, hospital indemnity, and critical illness coverage • Health savings account option • Paid time off program • Employee referral program • Education reimbursement program • Six company holidays, three floating holidays, and incentive days Eligibility Requirement Applicants must be United States citizens, permanent residents, asylees, or refugees in accordance with federal export control regulations. Equal Employment Opportunity Statement SOMACIS is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Note: Job descriptions aim to provide accurate overviews of roles without exhaustive detail. They serve as reference points for fair pay considerations.

**Are you looking to power the next leap in the exciting world of advanced electronics?** Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. The **Qnity** Carlsbad Site is seeking a **Quality Manager** at our manufacturing site in Carlsbad, CA. This role includes managing the quality systems at the site. This Site is part of DuPont's Electronics and Industrial Division. Electronics and Industrial is comprised of a number of high growth, global businesses, supplying a broad array of materials to multiple consumer electronics and industrial sectors. The Quality Manager is responsible for managing the objectives and performance of the Quality organization and Quality Management System. The Quality Manager is responsible for assuring product quality within our manufacturing plant by providing leadership and direction to maintain and improve our quality management systems. **Intent/Value** Enhances the front-line knowledge and accountability for quality, Promote a customer-focused culture and Drive customer centricity efforts across North America Sites **Critical Success Factors:** + This is a key role to ensure that the business and unit quality programs are effectively implemented and maintained. + The job requires out of the box thinking, strong interpersonal skill across all functions and levels, constructive gate-keeping skills, sound technical skills (product and technology of quality management), as well as strong corporate core competencies in collaborating for superior results, leading courageously, delivering innovative solutions, and generating customer value. + Ability to align customer, quality, and business requirements into goals, objectives, and strategies and effectively communicate these requirements across multiple sites. + Ability to build trust and create strong relationships across unit level and global teams both cross-culturally and cross-functionally. **Responsibilities:** + Develop, implement, and maintain the unit quality programs which align to the Quality Management System Strategy. + Assist in the development of business level goals & objectives, critical operating tasks (COTs), customer and product improvement plans, then ensure these initiatives are adopted as plant / unit level objectives and ensure yearly COTs are aligned with individual plant level quality team. + Lead and direct the activities of the quality staff, manage / supervisor team of quality engineers, laboratory specialist, and quality management system coordinators. + Lead risk management activities at all phases of the product life cycle. + Ensure that product returns and non-conforming product processes are appropriately managed to prevent unintended use, including disposition. + Monitor the effectiveness of the quality management system and communicate to site leadership all improvement opportunities through our management review process. + Generate and use quality data (customer complaints, plant metrics etc.) to enable cross functional partners to drive product quality improvements. + Participate in management of change reviews that potentially impact product quality (specification, train qualifications, plant equipment / systems, analytical testing, etc.). + Ensure plant operating discipline system, procedures and guidelines meet quality system and customer requirements, as appropriate. + Identify and lead improvement opportunities as determined through data analysis, customer audits, Six Sigma projects, and other quality-related programs. + Lead / champion product quality problem solving efforts (corrective action, preventive action, root cause investigation process, including customer feedback, etc.). + Establish and manage the plant quality system Internal Audit program in conjunction with unit strategies. + Oversee and support the audits of plants, labs, terminals, warehouses, contract manufacturers, distributors, suppliers, customers, etc. to ensure customer needs are met. Leverage findings and drive all corrective action and continual improvement. + Participate in the review of unit and cross functional projects having a potential impact on product quality and Quality Management Systems. + Ensure quality system tools are validated throughout the unit quality architecture. + Work with Global Quality, Product Stewardship and Regulatory leaders to standardize Quality Assurance program to ensure North American Sites adhere to established protocols, risk assessments, audits, training & competency, corrective actions and records, and controls. + Implement systems to comply with ISO-9001:2015 and AS9100 standards. **Required Qualifications:** + Bachelor's degree in science or engineering discipline + Minimum of 7 years relevant experience in Quality Assurance, Quality Engineering, Industrial or Manufacturing + A proven track record of success in implementing and maintaining quality systems in regulated markets. + Experience implementing quality management systems compliant with ISO9001:2015 International Standard and AS9100 Aerospace Standards. + Excellent spoken and written communication skills. + Excellent MS Office Skill (Excel, Word, PowerPoint) + Six Sigma certification is preferred. + Internal Audit experience/certification preferred. ~20% travel required As required by a federal contract or subcontract, only U.S. citizens will be hired for this position. Join our Talent Community (*************************************************************** to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information (**************************************************** . Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** . The Pay range for this role is $102,900.00 - $161,700.00 Annual **How Base Pay is Determined:** Qnity has job leveling frameworks that help organize roles based on progressive levels of responsibility, proficiency and qualifications. Each role has an associated pay range (or an established pay rate for some roles) based on the competitive market in each country where we operate. Each individual's pay is based on a variety of factors, including their role and the associated pay range for that role, their geographic location (i.e., country, state, metropolitan area), as well as their skills, experience, education and certifications, and performance.

The Quality Control Manager is responsible for developing and maintaining Quality QC systems for the Analytical department. Achieves organizational objectives through the coordinated achievements of subordinate staff. Establishes departmental goals and objectives and functions with autonomy. Manages the accountability and stewardship of human, financial, and often physical resources in compliance with departmental and organizational goals and objectives. Ensures subordinate supervisors and professionals adhere to defined internal controls. Manages systems and procedures to protect departmental assets. Demonstrated experience in leadership and a history of developing a culture of teamwork, collaboration, and ability to advance group goals to meet company objectives. Job Responsibilities 1. Achieves organizational objectives through the coordinated achievements of subordinate staff. Establishes departmental goals and objectives and functions with autonomy. Manages the accountability and stewardship of human, financial, and often physical resources in compliance with departmental and organizational goals and objectives. 2. • Ensures subordinate supervisors and professionals adhere to defined internal controls. Manages systems and procedures to protect departmental assets. Responsible for developing a culture of teamwork, collaboration, and ability to advance group goals to meet company objectives. 3. • Responsible for optimization and operation of the quality control laboratory in a biopharmaceutical manufacturing setting, including all related infrastructure, documentation, equipment validation and analyst training. Develops, implements, and maintains quality control systems in accordance with cGMP requirements. Manages all aspects of Quality Control, in support of and in full compliance with established cGMP and company requirements. 4. • Develop staff to improve individual and departmental performance. Department oversight of manufacturing support testing for multiple projects and related stability studies. 5. • Oversight of assay verification, qualification, validation, and tech transfer activities. Verification of maintenance, calibration, and qualification of laboratory equipment. Assist in troubleshooting equipment malfunctions, assay system suitability failures, assay deviations, CAPAs, and out of specifications investigations. Coordinate instrument preventive maintenance and validation activities. 6. • Author and review Quality Control Standard Operating Procedures (SOPs), Assay Qualification Reports, and Stability Protocols Qualifications: Experience in the development and establishment of operations of QC laboratories in a GMP regulated environment. In -depth experience related to method development, optimization, validation, and tech transfers. Demonstrated ability to manage a team and work independently on projects, and review project data and provide summary analysis reports based upon the data. Ability to provide support for regulatory and client audits, as well as interact with clients. A profound understanding of analytical instrument principals and application of advance instrumentation analysis for pharmaceutical and biologic products which could include HPLC (MWD, DAD, ELSD, RID detection), UV/Vis Spectroscopy, qPCR, Capillary Electrophoresis, MS, Genetic Analyzer, Place Readers, Gel Imagers, etc. Familiarity with analytical testing procedures: AGE, qPCR/dPCR, HPLC (IEX, RP, SEC), Sequencing, Plate Based Assays (BCA, Kanamycin). Strong knowledge of pharmacopeia (USP/EP) and regulatory requirements for the industry (ICH, GDP, cGMP and quality systems including OOS investigations, deviations and CAPAs). Sets stretch goals and links them to strategic outcomes and business deliverables. Strong leadership and motivational capabilities. Exercises sound judgment within defined procedures and policies to determine appropriate action. Strong scientific, analytical, and problem -solving skills as well as sound judgment, to identify problems and leads efforts to resolve them. Ability to be self -motivated, proactive, accountable, and flexible. Ability to work well under pressure, handle multiple tasks/projects and meet deadlines. High attention to detail, highly organized, and excellent documentation skills. Strong communication skills, both written and verbal in the English language, and outstanding interpersonal skills are essential job requirements. Accountable for the work performed, productive within the company, provide open communication, and exemplify effective teamwork skills. Knowledgeable using Microsoft Office as well as developing any documentation and creating tables for laboratory inventory and data entry. RequirementsRequired Education and Experience: Bachelor of Science Degree in the Biological Sciences, Bioengineering or Chemistry with a combination of education and experience performing biochemistry, molecular biology, microbiology, and chemistry. Master's degree preferred. A minimum of 8+ years of experience performing quality control activities in the pharmaceutical and biotech industry under GMP guidelines, with a demonstrated expertise in multiple disciplines, assays, fields. A minimum of 5+ years of GMP operations experience in the manufacture of for drugs substances / drug products. A minimum of 3+ years supervisory experience. Percentage of Travel: 5% BenefitsDental, Medical, Vision and 401K

TekPro Engineering is looking to hire a Quality Manager with direct experience within Aerospace Manufacturing. This position offers very competitive salary rates, full benefits, long term job security, and future career growth! Inquire immediately if interested, as this position will not be available for long! Qualifications: Minimum of 10+ years of previous management or quality engineering experience in aerospace. Must have experience in coordinating, monitoring, maintaining, and evaluating the company's QC programs. Must have experience working with AS9100 & AS13100. Must be physically able to lift lbs. and mentally capable of performing the job demands as listed above. Six Sigma experience is a PLUS. Contact Information: Nico Conwi - Hiring Manager Email: **********************

Job Description We are looking for an experienced Quality Manager to ensure that our products and services meet all necessary requirements before they reach the consumer. The Quality Manager, or Quality Assurance Manager, will inspect the final product to make sure it has been built with compliance to legal standards and meets customer expectations. A great quality manager is thorough and observant with an eye for detail. They must fully understand the requirements for the product or service and have a sense of responsibility towards our potential and existing customers as well as the competition. The goal is to help preserve our reputation by ensuring that our products and services are capable to drive sustainable growth. Position: Quality Manager Location: San Diego(Onsite) Salary: $100,000- $130,000 Responsibilities Understand customer needs and requirements to develop effective quality control processes Devise and review specifications for products or processes Set requirements for raw material or intermediate products for suppliers and monitor their compliance Ensure adherence to health and safety guidelines as well as legal obligations Supervise inspectors, technicians and other staff and provide guidance and feedback Oversee all product development procedures to identify deviations from quality standards Inspect final output and compare properties to requirements Approve the right products or reject defectives Keep accurate documentation and perform statistical analysis Solicit feedback from customers to assess whether their requirements are met Submit detailed reports to appropriate executives Implement, manage, and improve the company's quality management system, with a primary focus on IVD products and equipment. Conduct internal audits, compile audit reports, perform problem analysis, propose improvement initiatives, and monitor the implementation of corrective and preventive actions (CAPA). Lead and participate in internal audits and management reviews of the company's quality system as a key member of the quality department. Manage the documentation of the company's quality management system, ensuring compliance with relevant standards and regulations. Oversee the quality management system for IVD equipment, ensuring compliance with applicable regulations and standards. Perform statistical analysis of IVD equipment quality data, prepare reports, and develop corrective and preventive measures as needed. Update company documents in accordance with new or revised quality standards, laws, and regulations. Establish collaborative relationships with key opinion leaders and certification bodies to ensure alignment with industry best practices and regulatory requirements. Requirements Minimum Bachelor's degree in Science or related field. ISO 13485:2016 lead auditor certification preferred. Thorough knowledge of US FDA 21 CFR 820 Quality System Regulation and ISO 13485:2016 standards. Strong understanding of quality management principles and practices in the medical device industry. Excellent communication and interpersonal skills. Ability to work collaboratively in a team environment. Demonstrated problem-solving and analytical skills. Attention to detail and strong organizational skills. Minimum 10 Years experience in Medical devices, Quality Management , Regulatory compliance and ISO standards Benefits Medical Insurance Plan Retirement Plan Paid Time Off Training & Development We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access certain necessary systems. Security Clearance: None/Not Required Collins Aerospace is seeking a Quality Inspector for our Chula Vista, CA location. In this role, you will perform detailed inspections of aircraft parts, sub-assemblies, and installations to ensure compliance with engineering and quality standards. The position involves operating penetrant testing equipment, conducting dimensional and functional inspections, documenting findings, and supporting the repair and verification of aircraft engines, components, and assemblies. If you have a strong eye for detail, experience in precision inspection, and a passion for aerospace quality, we encourage you to apply! This position is based on-site at our Chula Vista, CA facility and will be part of the IAM Local 755 What You Will Do: * Work 2nd shift hours (2:30pm - 11pm) Monday -Friday. * Work 1st shift hours for training purposes Monday - Friday (6:30am-3pm) * Perform detailed inspections of aircraft parts, assemblies, and installations to ensure conformance with engineering drawings, specifications, and quality standards. * Conduct first article, in-process, and final inspections, including visual, dimensional, and penetrant testing. * Inspect returned and repaired components in accordance with FAA and company requirements, issuing return-to-service documentation as needed. * Verify configuration, workmanship, and tooling accuracy using blueprints, gages, and precision measurement instruments. * Perform receiving inspections to validate incoming materials and documentation for compliance. * Inspect processed, painted, and fabricated parts for finish quality, dimensional accuracy, and structural integrity. * Set up and operate inspection tools and equipment, including optical and mechanical measurement systems. * Maintain accurate inspection records and documentation in compliance with quality and EH&S procedures. * Support quality improvement initiatives by identifying nonconformances and recommending corrective actions. * Collaborate with production, engineering, and quality teams to resolve inspection findings and ensure product conformity. * Maintain a clean, organized work environment and represent Collins Aerospace during audits or customer visits as required. * Performs all other duties as assigned Qualifications You Must Have: * Typically, an HS Diploma with relevant Quality experience is required. What We Offer * Medical, dental, and vision insurance * 2 weeks (10 days) vacation for newly hired employees * Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option * Tuition reimbursement program * Student Loan Repayment Program * Life insurance and disability coverage * Optional coverages you can buy pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection * Ovia Health, fertility, and family planning * Adoption Assistance * Autism Benefit * Employee Assistance Plan, including up to 10 free counseling sessions * Healthy You Incentives, wellness rewards program * Doctor on Demand, virtual doctor visits * Bright Horizons, child, and elder care services * Teladoc Medical Experts, second opinion program Our Advanced Structures team leverages advanced materials and additive manufacturing to develop complex interior and exterior solutions. These solutions ensure structural integrity of the aircraft, help aircraft take off and land, stay trim in the air, move forward, carry cargo and conduct rescues. We delight our customers with superior products and best-in-class service. Our global team is committed to continuous improvement - we work hard to make our solutions lighter-weight, stronger and more technically advanced, so that plane travel can be safer, more affordable and more sustainable in the years to come. We are looking for the best and brightest to fly and land with us! Please ensure the role type (defined below) is appropriate for your needs before applying to this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again. Apply now and be part of the team that's redefining aerospace, every day The pay range for this role is $24.40 - $52.13; however, RTX considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. At Collins, the paths we pave together lead to limitless possibilities. And the bonds we form - with our customers and with each other -- propel us all higher, again and again. Apply now and be part of the team that's redefining aerospace, every day. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access certain necessary systems. Security Clearance: None/Not Required Collins Aerospace is seeking a Quality Inspector for our Chula Vista, CA location. In this role, you will perform detailed inspections of aircraft parts, sub-assemblies, and installations to ensure compliance with engineering and quality standards. The position involves operating penetrant testing equipment, conducting dimensional and functional inspections, documenting findings, and supporting the repair and verification of aircraft engines, components, and assemblies. If you have a strong eye for detail, experience in precision inspection, and a passion for aerospace quality, we encourage you to apply! This position is based on-site at our Chula Vista, CA facility and will be part of the IAM Local 755 What You Will Do: Work 2nd shift hours (2:30pm - 11pm) Monday -Friday. Work 1st shift hours for training purposes Monday - Friday (6:30am-3pm) Perform detailed inspections of aircraft parts, assemblies, and installations to ensure conformance with engineering drawings, specifications, and quality standards. Conduct first article, in-process, and final inspections, including visual, dimensional, and penetrant testing. Inspect returned and repaired components in accordance with FAA and company requirements, issuing return-to-service documentation as needed. Verify configuration, workmanship, and tooling accuracy using blueprints, gages, and precision measurement instruments. Perform receiving inspections to validate incoming materials and documentation for compliance. Inspect processed, painted, and fabricated parts for finish quality, dimensional accuracy, and structural integrity. Set up and operate inspection tools and equipment, including optical and mechanical measurement systems. Maintain accurate inspection records and documentation in compliance with quality and EH&S procedures. Support quality improvement initiatives by identifying nonconformances and recommending corrective actions. Collaborate with production, engineering, and quality teams to resolve inspection findings and ensure product conformity. Maintain a clean, organized work environment and represent Collins Aerospace during audits or customer visits as required. Performs all other duties as assigned Qualifications You Must Have: Typically, an HS Diploma with relevant Quality experience is required. What We Offer Medical, dental, and vision insurance 2 weeks (10 days) vacation for newly hired employees Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option Tuition reimbursement program Student Loan Repayment Program Life insurance and disability coverage Optional coverages you can buy pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection Ovia Health, fertility, and family planning Adoption Assistance Autism Benefit Employee Assistance Plan, including up to 10 free counseling sessions Healthy You Incentives, wellness rewards program Doctor on Demand, virtual doctor visits Bright Horizons, child, and elder care services Teladoc Medical Experts, second opinion program Our Advanced Structures team leverages advanced materials and additive manufacturing to develop complex interior and exterior solutions. These solutions ensure structural integrity of the aircraft, help aircraft take off and land, stay trim in the air, move forward, carry cargo and conduct rescues. We delight our customers with superior products and best-in-class service. Our global team is committed to continuous improvement - we work hard to make our solutions lighter-weight, stronger and more technically advanced, so that plane travel can be safer, more affordable and more sustainable in the years to come. We are looking for the best and brightest to fly and land with us! Please ensure the role type (defined below) is appropriate for your needs before applying to this role. Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again. Apply now and be part of the team that's redefining aerospace, every day The pay range for this role is $24.40 - $52.13; however, RTX considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. At Collins, the paths we pave together lead to limitless possibilities. And the bonds we form - with our customers and with each other -- propel us all higher, again and again. Apply now and be part of the team that's redefining aerospace, every day. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

The primary responsibility of the Quality Systems Specialist is to support the Quality Assurance System by providing training, coaching, leading improvement efforts and driving change while working closely with leaders and associates. General Responsibilities: Improving processes monitor processes and inspect goods and services to ensure reliability and minimize errors and defects. Track, document, and report quality levels and communicate quality information to the organization. Work with process owners to identify trends in data related to the processes. Help drive and sustain a continuous improvement culture. Identify and incorporate lean best practices where needed into the organization. Quality Systems Assist in the development and maintenance of the Quality Management System (QMS). Provide oversight for the design, implementation, and continuous improvement of quality programs, systems, processes, and procedures to ensure compliance with internal policies and external standards. Ensure that the performance and quality of services consistently meet or exceed established guidelines and regulatory requirements. Develop, review, and adjust quality standards, procedures, and checklists. Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to ensure compliance. Leads internal audits and inspection preparation, resolution of audit and inspection findings and liaises with auditing groups and inspectors through all stages of the audits. Assist process owners with recommendation to correct identified negative trends. Assist with document control and revision requirements. Train employees on quality standards and provide support to quality assurance team members. Miscellaneous Perform other duties as requested by the Quality Assurance Director. Conduct and/or facilitate Corrective and Preventative Action (CAPA) internally and externally with customers and suppliers. Prepares reports and/or necessary documentation (e.g. CAPA) and provides to applicable stakeholders, both internal and external Plan, execute, and oversee the inspection and testing of products to ensure they meet specifications and deliverables. Your profile Skills, Knowledge, Abilities High school diploma or equivalent. Training in Lean tools (5S, Kaizen, Six Sigma). Training in ISO9001 and 17025 Ability to use basic math to solve problems and analyze data. Capable of interpreting documents and instructions. Good organizational skills. Good facilitation skills. Good knowledge of the functionality of all Mensor products. Must have a solid understanding of pressure technology and terminology. General PC and computer skills.

North County San Diego, CA Direct Hire. 32\-36\/hr. Onsite. Talentry is looking for a Quality Systems Associate who will facilitate and implement quality standards in compliance with FDA, ISO, cGMP, and other regulations - as well as company policy. This Specialist will ensure that our client is able to produce and sell the best scientific product used by many biotech and pharmaceutical companies. The right person for this role will assist in the configuration and implementation of a Quality Management System company\-wide. This also requires delivery of appropriate employee training on regulatory and quality standards, SOPs, etc. He or she will participate in audits, investigate and document quality events such as NCRs, CAPAs, change control, etc.) This QSS II will assist in the implementation of the eQMS and maintain\/modify as appropriate. Requirements BS in Science 3\-5 years of experience working in a cGXP\/ISO environment. Prior experience in a quality related role. Proven attention to detail and excellent documentation skills. Ability to work onsite in North County San Diego. Benefits 32\-36\/hour+ benefits, bonus, etc. "}}],"is Mobile":false,"iframe":"true","job Type":"Full time","apply Name":"Apply Now","zsoid":"642499540","FontFamily":"Verdana, Geneva, sans\-serif","job OtherDetails":[{"field Label":"Industry","uitype":2,"value":"Pharma\/Biotech\/Clinical Research"},{"field Label":"Work Experience","uitype":2,"value":"1\-3 years"},{"field Label":"Salary","uitype":1,"value":"35\-36\/hr"},{"field Label":"City","uitype":1,"value":"Oceanside"},{"field Label":"State\/Province","uitype":1,"value":"California"},{"field Label":"Zip\/Postal Code","uitype":1,"value":"92058"}],"header Name":"Quality Systems Specialist II","widget Id":"**********00072311","is JobBoard":"false","user Id":"**********00143030","attach Arr":[],"custom Template":"3","is CandidateLoginEnabled":true,"job Id":"**********08798005","FontSize":"12","google IndexUrl":"https:\/\/talentry.zohorecruit.com\/recruit\/ViewJob.na?digest=VtjcLgysU8341@TlI@93cIcM.CnF6I3amBfM32t8GZk\-&embedsource=Google","location":"Oceanside","embedsource":"CareerSite","indeed CallBackUrl":"https:\/\/recruit.zoho.com\/recruit\/JBApplyAuth.do","logo Id":"kpa3g78fecd22d77c4a778b704382770fc045"}

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. We're looking for people who put their innovation work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. What YOU WILL EXPERIENCE IN THIS POSITION: Provide quality assurance support and lead root cause problem solving activities that are aligned to improve internal and external quality levels, supporting overall customer satisfaction of our products. This position is a development track to a quality engineering position, by providing structured involvement with quality engineering responsibilities. * Lead problem solving activities for both product and manufacturing processes, with assistance from Quality Engineer * Perform process validations, in-process inspections, and monitoring, analyzing the quality of manufacturing processes and products * Provide support to design, manufacturing, and quality engineering functions for data collection, analysis, product review, and process capabilities * Understand, adhere to, and develop processes compliant with the Quality Management Systems (QMS) objectives, as well as train other personnel to adhere to QMS standards * Disposition NCR product and assign appropriate resolution * Provide formal documented FAI reports suitable for customer or internal use as required * Determine and use appropriate measuring tools and equipment to verify dimensional and functional requirements * Effectively communicate with appropriate areas as needed, (Operations, Supply, Manufacturing Engineering, Design, Quality, Customer Service, Production Planning, Logistics, etc.) * Lead and/or assist in supporting the activities that maintain the calibration status of inspection, test, and measurement equipment * Perform other related duties as assigned You have: Academics: * High school diploma or GED * American Welding Society (AWS) Certification as Certified Welding Inspector (optional) * Ability to read blueprints. GD&T knowledge is a plus. Previous experience in or with: * 2+ years working in the quality/manufacturing field * Ability to use measurement tools and techniques - strongly preferred * Strong knowledge and understanding of charting and process control methods preferred * Experience with Quality Management Systems (QMS) preferred Skills: * Strong written, verbal, and interpersonal communication skills * Attention to detail and ability to prioritize tasks is key to being successful in this role * Must be able to interpret order requirements, drawings, and draw conclusions * Ability to use precision measuring equipment (e.g., calipers, micrometer, paint mill gauges, etc.) * Skilled in identifying root causes of routine problems/issues and the ability to develop recommendations for resolution * Ability to interpret and apply Quality Systems / ISO procedures and documentation * Comfortable using computer systems and software including MS Office Applications Abilities to meet the physical and environmental demands: * Lift up to 50lbs * Stand and walk frequently * Operate hand tools * Work primarily indoors where there is frequently noise of 85 dB and occasional exposure to chemical hazards (solvents) WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees Pay Transparency nVent's pay scale is based on the expected range of base pay for this job and the employee's work location. Employee pay within this range will be based on a combination of factors including knowledge, skills, abilities, experience, education, and performance. Where federal, state, or local minimum wage requirements exist, employee pay will comply. Compensation Range: $23.90 - $44.40 Per Hour Depending on the position offered, employee may be eligible for other forms of compensation, such as annual incentives. Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for eligible full-time employees that includes: * Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. * A 401(k) retirement plan and an employee stock purchase plan - both include a company match. * Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

Your Work Shapes the World at Caterpillar Inc. When you join Caterpillar, you're joining a global team who cares not just about the work we do - but also about each other. We are the makers, problem solvers, and future world builders who are creating stronger, more sustainable communities. We don't just talk about progress and innovation here - we make it happen, with our customers, where we work and live. Together, we are building a better world, so we can all enjoy living in it. Job Summary: Join our dynamic team as an Entry Level Supplier Technical Engineer, where you'll play a critical role in ensuring the timely availability of purchased materials to support customer needs and operational efficiency. This is an excellent opportunity to gain hands-on experience in supply chain and vendor management within a fast-paced, collaborative environment. Key Responsibilities: Leadership in resolution of quality problems associated with the purchased materials and engineering issues. Responsible for concept drawing, communication of concept with supplier, design/drawing review and acceptance, Windchill activities (drawing finalized), perform functions in BAAN ERP, tooling management, Q Notes, etc. Acts as a technical liaison between external suppliers and internal customers through various methods, including supplier site visits. The supplier technical engineer will participate in and may lead projects on cross-functional teams utilizing 6 Sigma tools. At the senior level, projects will increase in complexity and value to Solar's strategic objectives. Participates in the development of supplier quality metrics and the monthly gathering and distribution of measurements. Reviews, analyzes, and reports supplier quality performance data and trends. Is the focal point for SARN (Supplier Advanced Reject Notices) and RN (Reject Notices) resolution. Initiates root cause analysis and implements supplier corrective and preventative action plans. Participates in continuous process improvement and warranty cost recovery related to supplier quality, including recovery of line stop and rework charge analysis. Collaborate with sourcing specialist, buyer, supplier development engineer, and material scheduler to improve supplier cost, quality, and throughput. Develop and maintain thorough knowledge of technological developments and trends for guidance of commodity teams in advancement of design, quality, and manufacturing. Provides input into the supplier selection process as a technical subject matter expert. Participates on survey teams; collaborates with sourcing specialists and buyers in supplier qualification, selection, and ongoing evaluation. Coordinates with engineering personnel on matters regarding Concurrent Product and Process Development (CPPD), New Product Introduction (NPI), Continuous Process Improvement (CPI) teams; prove design to production, configuration management, deviations, supplier designs, specification approvals and meeting cost reduction goals. Participate in design and process Failure Modes and Effects Analysis (FMEA). Leads the PPAP (Production Part Approval Process) and develops the FAPITP (First Article Production Inspection Test Plan) with initial input from Design Engineering. Identifies and provides input to the Buyer for the purchase of supplier tooling. Qualifications: Bachelor's degree in supply chain, engineering, business, or a related field. Overall GPA of at least 2.8 on a 4.0 scale. 0-2 years of relevant experience related to this field (internships or academic projects are a plus) Strong analytical and problem-solving skills. Effective communication and collaboration abilities. Interest in process improvement and vendor relationship management. Core Competencies: Analytical Thinking Apply structured analysis to identify root causes and develop effective solutions. Decision Making & Critical Thinking Use data-driven judgment to evaluate risks and make informed decisions. Business Process Improvement Support initiatives to streamline operations and reduce waste. Effective Communication Deliver clear, concise feedback and interpret information accurately across teams. Problem Solving Diagnose issues and propose actionable resolutions using proven tools and techniques. Matrix Management Collaborate across departments and functions to balance priorities and drive results. Vendor/Supplier Management Build strong relationships with external providers to ensure quality and timeliness. Procurement Support purchasing activities using established systems and procedures. Why Join Us? Be part of a team that values innovation, collaboration, and continuous improvement. Gain exposure to cross-functional operations and global supply chain strategies. Grow your career with mentorship and development opportunities. Compensation & Benefits Base salary for this role ranges from $92,500, to $118,000. Actual salary will be based on experience. #2026ETposting This position requires working onsite five days a week.Relocation is available for this position.Visa Sponsorship is not available for this position. This employer is not currently hiring foreign national applicants that require or will require sponsorship tied to a specific employer, such as, H, L, TN, F, J, E, O. As a global company, Caterpillar offers many job opportunities outside of the U.S which can be found through our employment website at **************************** Posting Dates: September 10, 2025 - December 31, 2025 Any offer of employment is conditioned upon the successful completion of a drug screen. Caterpillar is an Equal Opportunity Employer, Including Veterans and Individuals with Disabilities. Qualified applicants of any age are encouraged to apply. Not ready to apply? Join our Talent Community.

Primary contact for engineering support of In-Process Inspectors. Support production efforts and process improvements (trend analysis, process validation, SPC). Coordinate In-Process MRB acitvities. Support Quality Systems (perform audits, SOP improvement, training, CAPA investigations). Ensure from the Quality prospective the transfer of new products from R&D to Production. Support Statistical Techniques and SPC interpretation. Present PPR and Management Review. 0-1 years of industry experience in ISO-9001 environment, preferably medical device. Bachelor of Science or higher degree in ME, IE or equivalent. BS degree required in either engineering or a related scientific field. This will be for a line support engineer

5th Axis is the world leader in automated production, manufacturing, and machining. We are a turn-key solution provider with a focus on product development, milling, turning, assembly, plating, Are you a creative thinker who loves turning ideas into reality? Ready to tackle exciting challenges and design the future? Join our team of forward-thinkers and shape groundbreaking solutions in an environment that rewards your expertise and passion! Are you a creative thinker who loves turning ideas into reality? Ready to tackle exciting challenges and design the future? Join our team of forward-thinkers and shape groundbreaking solutions in an environment that rewards your expertise and passion! As an Automation Maintenance and Quality Technician, you will play a crucial role in ensuring the efficient operation of our automation systems, maintaining high-quality production standards, and contributing to the overall success of our manufacturing processes. What You Will Do: Perform routine maintenance tasks on CNC machines and automation systems. Clean and maintain the robot, including emptying chips, cleaning, and replacing coolant as needed. Ensure that all equipment is in proper working condition for continuous production. Monitor production processes and make necessary adjustments to maintain efficiency and quality. Perform routine quality checks to ensure parts are within tolerance. Inspect finished parts using micrometers, calipers, and other precision measuring tools. Compare finished parts to blueprints to ensure they meet specified standards. Document and report any deviations or quality issues. Unload and reload materials in the robot to facilitate continuous production. Safely handle and transport materials as required. Maintain detailed records of maintenance activities, production data, and quality control checks. Report any equipment malfunctions, maintenance needs, or quality concerns to the supervisor. Assist with material management as needed Adherence to safety protocols and practices Perform other duties as assigned. Do you have: High school diploma or equivalent; technical certification or degree in a related field is a plus. Proven experience operating CNC machines for at least 2 years. Proficiency in using micrometers, calipers, and other precision measuring tools. Strong blueprint reading skills and the ability to interpret technical drawings. Attention to detail and a commitment to maintaining high-quality standards. Knowledge of robotics and automation technology is advantageous. Excellent problem-solving and troubleshooting skills. Strong communication skills and the ability to work effectively within a team. Basic computer skills for data entry and equipment control. Adherence to safety protocols and practices. Able to use proper tools such as calipers, gauge, pins and micrometers. Knowledgeable using test indicators. Ability to understand setup sheets. Basic knowledge of programs. Basic knowledge of G&M codes. Basic tooling knowledge. Ability to maintain a safe and clean working environment while adhering to company policies, quality policies, and industry standards. Detail oriented, organized, and able to demonstrate a high sense of urgency. What We Offer: Training and room to grow We pay 100% of our employees' costs toward medical, and dental. Company sponsored life and disability Insurance 401K with up to 4% matching Paid holidays Generous Paid Time Off accrual Pleasant non-corporate environment Fun team bonding events Are You Ready to Join Us? Hyper-growth means hyper opportunities for everyone on our team! At our company, we believe in growing talent from within, providing clear paths for advancement across all roles. Over 90% of our managers and countless others in key positions were promoted internally. If you're ready to grow with us, join our team and discover where your potential can lead! 5th Axis believes that everyone can make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. If you require an accommodation to complete the application or the interview process, please contact *******************

Kennedy Jenks is seeking a Drinking Water Process Engineer to provide technical expertise and support for drinking water treatment projects. The ideal candidate will have experience in drinking water treatment technologies and regulations, with a strong interest in continuing to develop their skills in water treatment. This role offers opportunities to work alongside experienced engineers and support clients on a variety of water quality and treatment projects. Key Responsibilities: Provide technical support for drinking water treatment projects, including treatment process evaluation, process selection, and operations optimization. Assist in preliminary engineering studies and feasibility assessments for municipal drinking water treatment systems. Support project teams with design and technical contributions, including developing process flow diagrams and design criteria for water treatment facilities. Collaborate with client service managers by contributing technical insights during project meetings and presentations. Participate in research and process improvements related to water quality and treatment technologies. Provide input on water treatment facility performance evaluations and assist in operations optimization. Stay engaged in water-focused professional organizations and present technical material at conferences. Qualifications: Bachelor's or Master's degree in civil / environmental engineering, or related scientific discipline required. 7+ years of experience in drinking water treatment engineering Practical professional engineer (PE) license or ability to obtain licensure within one year of hire. License in one or multiple states (CA, CO, FL, HI, OR, TX, VA, WA) preferred. Strong familiarity with drinking water treatment regulations and technologies. Ability to work as part of a project team, supporting senior staff and contributing to technical deliverables. Strong communication skills and ability to convey technical information clearly to colleagues and clients. Kennedy Jenks supports a healthy work-life balance and utilizes a hybrid model of home and office work, with a minimum of two days per week in the office. This approach empowers our people to thrive, collaborate, and achieve their full potential. The salary range for this position is anticipated to be $110,000 to $140,000, and may vary based upon education, experience, qualifications, licensure/certifications and geographic location. This position is eligible for performance and incentive compensation. #LI-Hybrid

Established in 1991, Collabera is one of the fastest growing end-to-end information technology services and solutions companies globally. As a half a billion dollar IT company, Collabera's client-centric business model, commitment to service excellence and Global Delivery Model enables its global 2000 and leading mid-market clients to deliver successfully in an increasingly competitive marketplace. With over 8200 IT professionals globally, Collabera provides value-added onsite, offsite and offshore technology services and solutions to premier corporations. Over the past few years, Collabera has been awarded numerous accolades and Industry recognitions including. • Collabera awarded Best Staffing Company to work for in 2012 by SIA. (hyperlink here) • Collabera listed in GS 100 - recognized for excellence and maturity • Collabera named among the Top 500 Diversity Owned Businesses • Collabera listed in GS 100 & ranked among top 10 service providers • Collabera was ranked: • 32 in the Top 100 Large Businesses in the U.S • 18 in Top 500 Diversity Owned Businesses in the U.S • 3 in the Top 100 Diversity Owned Businesses in New Jersey • 3 in the Top 100 Privately-held Businesses in New Jersey • 66th on FinTech 100 • 35th among top private companies in New Jersey *********************************************** Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance. Job Description Exercise knowledge of technical skills and understanding of the business objectives, manufacturing operations and dynamics of the companys environment to take an effective and proactive leadership role in a specific technical manufacturing discipline. Set direction for, lead, and take ownership of complex manufacturing engineering technical tasks that may have multiple inter-coordinating elements. Expectation that the individual will be able both to anticipate and identify key issues and make recommendations for resolution where precedent may not exist and creative thinking is required. Resolution may involve the application of new methods and approaches and may require the consideration of impact with other system components. Interaction with peers and mentors on the individuals projects is generally in the context of peer review to confirm the rationale for task approach direction as well as peer review of verification/validation activities. Qualifications Bachelor Engineering Curriculum trains students in skills required to perform assignments. The individual will typically have had a minimum 2-5 years experience in an engineering discipline or advanced education to achieve the level of skill. Additional Information All your information will be kept confidential according to EEO guidelines.

Discover a career with real meaning. One that offers the opportunity to showcase your talents, achieve measurable success and gain immense satisfaction by enabling healthier lives everywhere, every day. The San Diego Campus is the center of our Diagnostics Solutions Division. With the focus on Molecular Diagnostics, most products produced are utilized onboard innovative and fully automated sample-to-result instrument systems. The consumables required for patient testing are integral to our business. The business growth projections and new product development projects provide unique opportunities to enable our Purpose, Passion, and Promise to empower global health advancements. Our Manufacturing Operations department is looking for an experienced Manufacturing Engineer responsible for providing engineering support in the areas of injection molded consumables, services including evaluation, purchase, installation, and qualification of new manufacturing equipment. This is a fully onsite role based in San Diego, CA. Essential Duties and Responsibilities Provide technical guidance and interface with injection molding vendors Provide technical input on consumable parts drawings and mold drawings Manage qualifying and changes in raw materials, vendors and perform investigations for non-conformance events Provides general engineering services and support Manage the design, acquisition, installation and commission of mechanical/electrical equipment, systems and parts to support manufacturing Perform process transfers from Engineering to Manufacturing including processes and equipment training Provides technical engineering support for repairing, troubleshooting and modifying equipment and systems Supports equipment mechanics Create and/or modifies equipment maintenance procedures Manage outside vendor's with installation, qualification and sustaining support of equipment and processes Writing and reviewing operating procedures, documents and reports Performs equipment, process and product performance testing Provides QS validation input and support for new equipment and process validations Writing and executing Installation, Operation, and Performance Qualification Validations; including writing final reports Reviews and approves calibration datasheets Core Competencies required: In-depth knowledge of injection molding process for high volume consumable plastics Familiarity with cGMP regulations and guidelines related to plastics in the pharmaceutical or biotechnology industry. Working knowledge of microprocessor controls, utility distribution systems and process engineering Biotech / Medical Device / Pharmaceutical industry experience Thorough knowledge of manufacturing automation systems and best design practice Experience with PLC/SCADA systems used for water system control and monitoring. Experience generating and updating FMEAs Proficient with GD&T and technical drawings Excellent problem-solving, analytical, and troubleshooting skills. Strong technical writing and communication skills. Ability to work independently and as part of a multidisciplinary team. High proficiency with Microsoft Suite High proficiency with statistical analysis techniques Working knowledge of manufacturing automation systems and design practices Working knowledge of cGMP, GAMP, ISO 13485, and FDA 21 CFR, Part 820 Identifies problems, solves them, acts decisively, and shows good judgment Plans and organizes work efficiently to manage time wisely. Prioritizes tasks within a dynamic and fast-paced working environment Exhibits a high level of energy and is self-motivated to sustain ambitious work Continuously seeks new knowledge and rapidly assimilates it into the organization Required Qualifications and Experience BS degree in Chemical Engineering, Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or related Engineering discipline with 6 -8 years of related industry experience Certified Water Technologist (CWT) preferred but not required Lean Manufacturing and/or Six-Sigma Certification preferred but not required Certified Quality Engineering Certification preferred but not required The annualized base salary range for this role is $98,500 to $154,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs, and market demand. Why Hologic? We are committed to making Hologic the company where top talent comes to grow. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. We offer a competitive salary and annual bonus scheme, and one of our Talent Partners would be happy to discuss this in more detail with you. If you have the right skills and experience, apply today! #LI-RF1 #Mid-level Agency and Third Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

CRB is a leading provider of sustainable engineering, architecture, construction and consulting solutions to the global life sciences and food and beverage industries. Our more than 1,100 employees provide best-in-class solutions that drive success and positive change for our clients, our people and our communities. CRB is a privately held company with a rich history of serving clients throughout the world, consistently striving for the highest standard of technical knowledge, creativity and execution. Job Description We are seeking a skilled and experienced Process Engineer III/ IV with deep expertise in small molecule manufacturing to join our engineering consulting team. This role combines technical leadership with strategic client engagement, supporting process design, scale-up, optimization, and regulatory compliance across a variety of pharmaceutical and chemical industry projects. The Process Engineer III will lead the design and execution of process scopes-such as unit operations, systems, or facility areas-on small to medium-sized projects. You will manage scope, budget, and schedule, while maintaining clear communication with clients and internal teams. This role also includes mentoring junior staff, contributing to high-quality deliverables, and supporting capital project planning and regulatory alignment. This position can be based near any CRB location Key Responsibilities * Lead and support client projects focused on small molecule API process development, scale-up, and manufacturing optimization. * Conduct site assessments, gap analyses, and provide recommendations for process improvements and compliance. * Develop process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), and mass/energy balances. * Translate client requirements into actionable design scope and document decisions, open issues, and action items. * Identify and escalate scope changes or design deviations to project leadership. * Collaborate with cross-functional teams including architecture, mechanical, electrical, and construction. * Prepare technical reports, proposals, and presentations for internal and client stakeholders. * Support capital project planning including feasibility studies, equipment selection, and facility design. * Ensure alignment with industry standards including cGMP, FDA, EMA, and ICH guidelines. * Participate in advanced project activities such as: * Technical bid tabulations * Vendor package management * Factory acceptance testing * Risk assessments (e.g., HAZOP, HACCP) * 3D model reviews and coordination * Sequence of operations and functional specification reviews * Mentor junior engineers and design staff. * Lead system design programming and planning with support from senior engineers. * Participate in cross-discipline squad checks and drive overall project quality. Qualifications Minimum Qualifications * Bachelor's or Master's degree in Chemical Engineering or a related discipline (ABET-accredited). * Minimum of 5 years of experience in small molecule process engineering, preferably in a consulting or client-facing role. * Strong understanding of chemical synthesis, purification, and formulation processes. * Experience in design firm or operating company settings within a related industry. * Strong written and verbal communication skills. * Intermediate experience with applicable industry and regulatory guidance and building codes. * Advanced technical knowledge and experience with small molecule API manufacturing equipment and utility systems, such as chemical reactors, filters, centrifuges, dryers, vacuum pumps, scrubbers, purified water, process compressed gases, and engineered heat transfer fluid systems. * Experience designing and implementing engineering controls for containment of highly potent APIs. * Experience with cGMP practices within regulated industries (FDA, EMA, JP, etc.). Preferred Qualifications * EIT or PE certification. * Experience coordinating and managing design within project teams and with external partners. * Familiarity with commissioning, startup, qualification, and troubleshooting of process systems. * Experience with regulatory environments and validation documentation. * Prior experience in engineering consulting or client services. * Familiarity with process safety, risk assessments, and HAZOP studies. * Demonstrated experience leading a small team of process engineers on complex engineering design projects. The pay range for a candidate selected for this position who is based in San Diego is typically $120,125 to $175,000 annually. The base salary range represents the low and high end of the salary range for this position. The selected candidate's actual pay will be based on various factors, including but not limited to work location, qualifications, and relevant experience. In addition, CRB offers a total rewards package that includes comprehensive insurance coverage as well as the opportunity to participate in one or more annual incentive programs based on company and individual performance. Additional Information All your information will be kept confidential according to EEO guidelines. CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening. CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails. CRB offers a complete and competitive benefit package designed to meet individual and family needs. If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.