Quality Control Technician

We are seeking a highly motivated and detail-oriented Quality Control Technician to join our team. In this role, you will be responsible for ensuring the quality and safety of our products through rigorous testing and inspection processes. Your keen eye for detail and dedication to quality will contribute significantly to our commitment to excellence.

Join our dynamic team at SGS as a Quality Assurance Engineer in Irvine, California. In this pivotal role, you will be responsible for ensuring the highest quality standards in our inspection and field testing services. You will collaborate with cross-functional teams to develop and implement testing strategies that enhance product integrity and customer satisfaction.

At Anduril Industries, we are revolutionizing defense technology to enhance the capabilities of the U.S. and allied militaries through state-of-the-art innovations. Our mission is to integrate the expertise and technologies from the most forward-thinking companies of the 21st century into military systems, fundamentally changing how they are designed, manufactured, and deployed. Our advanced systems are driven by Lattice OS, an AI-enhanced operating system that transforms vast data streams into a dynamic 3D command and control environment. In a world of heightened strategic competition, Anduril is dedicated to delivering pioneering autonomy, AI, computer vision, sensor fusion, and networking solutions to military operations in months instead of years.We invite you to join our team as a Quality Engineering Specialist for our Sentry program. This role requires a dedicated professional responsible for monitoring, inspecting, and implementing corrective measures to enhance final product quality, ensuring adherence to established standards. The ideal candidate will be a highly motivated team player eager to thrive in a fast-paced environment.

Join AbbVie, a global biopharmaceutical company, as a Senior Quality Engineer specializing in Combo Product External Quality. In this pivotal role, you will ensure the highest standards of product quality, collaborating with cross-functional teams to maintain compliance and uphold our commitment to patient safety.

Hello, and thank you for your interest in the Quality Compliance Manager II position at itcss! We encourage you to review the details below. If this role aligns with your career aspirations, please discuss with your current manager and HR business partner to see if your qualifications match. If all goes well, we invite you to apply, and our Talent Acquisition team will reach out for an interview to learn more about you.- Your Human Resources TeamAbout the Role:The Quality Compliance Manager II plays a crucial role in supporting the Product Quality Complaint program, ensuring all complaints are addressed in compliance with Good Manufacturing Practices (GMPs) and health authority regulations. This position will also support Annual Product Reviews and assist in various Quality Management System (QMS) areas as needed, such as audits, inspections, change control, document control, and corrective action and preventive action (CAPA).Key Responsibilities:Manage the product complaint program throughout its lifecycle, including:Initiating Product Complaint InvestigationsCollaborating with Call Center staff for complaint intakeFollowing up with complainants as neededParticipating in Weekly Product Complaint MeetingsDrafting response letters to complainantsReviewing and closing Product Complaint investigationsContributing data to Annual Product ReviewsPreparing monthly metrics and management presentationsSupporting regulatory inspections or partner audits as necessaryAuthoring, revising, or approving controlled documentsStay abreast of regulatory changes and proactively adjust systems and procedures to ensure compliance with company policies and regulations.Monitor and escalate product complaints appropriately, including expedited complaints.Foster strong relationships, cooperation, and alignment with internal Quality partners.Compile Annual Product Reviews, ensuring timely data submission from collaborating departments.Assist with product recalls or field alerts as needed.

Become part of a pioneering team where your contributions extend beyond the stars! At Terran Orbital, your role is not just a position – you are a crucial element in driving our mission ahead. As leaders in satellite manufacturing and aerospace innovation, we break barriers daily to provide transformative solutions that enhance our nation’s defense and commercial initiatives. We are a distinct, rapidly growing, and trusted team committed to the swift and efficient design, construction, launch, and operation of cutting-edge satellites for advanced mission constellations. If you are motivated by purpose, inspired by challenges, and eager to make a significant impact on the universe, you will discover a welcoming environment and limitless opportunities for growth here. Together, let us redefine what is achievable in orbit and beyond!Terran Orbital is seeking a skilled Senior Supplier Quality Engineer to join our vibrant team. Reporting to the Director of Quality, the Senior Supplier Quality Engineer will oversee supplier programs for manufacturing and other operational processes, ensuring adherence to quality programs that meet customer and regulatory standards.

Greetings, and thank you for your interest in the Manager II, Quality Assurance (Commercial) position at Tarsus Pharmaceuticals! If you believe this role aligns with your career aspirations, please engage with your current manager and HR Business Partner to discuss your qualifications. If all aligns, we encourage you to apply, and our Talent Acquisition team will reach out for an interview to learn more about you.- Your Human Resources TeamIn this role, reporting to the Associate Director of Quality Assurance, you will play a pivotal role in managing the review and processing of manufacturing Deviations and Laboratory Out of Specification (OOS) cases, as well as overseeing manufacturing-related Change Controls within Tarsus’ Quality Management System (QMS). Your responsibilities will also include authoring Annual Product Reviews, analyzing and trending analytical data, approving Certificates of Analysis, and conducting thorough reviews of manufacturing batch records and product disposition.Key Responsibilities:Approve Vendor Change ControlsAssess vendor documentation such as Master Batch Records and Master Packaging RecordsReview SpecificationsEvaluate and approve Deviations and OOS casesAnalyze and trend data for quality assuranceWrite Annual Product ReviewsDraft and revise relevant Quality Assurance ProceduresReview new proposed master manufacturing records and related process validation protocolsReview and approve Test Record Review Forms and Certificates of AnalysisOversee the review and approval of executed manufacturing and packaging batch recordsComplete Batch Record Review Forms for batch dispositionFinalize Product Disposition Forms and Certificates of ComplianceEngage in internal operations discussionsParticipate in meetings and discussions with Tarsus' manufacturing partners and testing laboratoriesAttributes for Success:Preferred Bachelor's Degree with over 8 years of experience in the Pharmaceutical IndustryMinimum of 5 years in Pharmaceutical Quality AssuranceMeticulous attention to detailProficient technical abilities across various platformsStrong knowledge of Microsoft Office, including charts and graphsASQ Certification is preferred

About the Role:The Quality Compliance Manager II plays a vital role in overseeing the Product Quality Complaint program, ensuring that all complaints are managed in strict adherence to Good Manufacturing Practices (GMPs) and the expectations of health authorities. This position will also contribute to the Annual Product Reviews and support various Quality Management System (QMS) areas as needed, such as audits, inspections, change control, document control, and corrective actions.Key Responsibilities:Manage the entire product complaint process from initiation to resolution, including:Initiating Product Complaint InvestigationsCollaborating with Call Center staff for complaint intakeDirectly following up with complainants when necessaryParticipating in weekly product complaint meetingsDrafting response letters for complainantsReviewing and closing product complaint investigationsContributing complaint data to Annual Product ReviewsPreparing monthly metrics and management review presentationsAssisting with regulatory inspections and audits, as requiredAuthoring and revising controlled documentsStay abreast of the regulatory landscape to proactively enhance systems and procedures for effective complaint management.Ensure proper monitoring and escalation of product complaints, including those requiring expedited attention.Foster effective collaboration and alignment within the Quality team and across internal partners.Compile and ensure timely delivery of data for Annual Product Reviews, including:Coordinating with contributing departmentsPreparing necessary product complaint metricsDelivering the final report on scheduleAssist with recalls or field alerts as necessary.Conduct mock recalls and support other Quality Management Systems, including Document Control, Change Control, and CAPA.Perform any additional duties assigned by department management.

As a pivotal member of our Quality Assurance team, the Manager II, Quality Assurance will report directly to the Associate Director of Quality Assurance. This crucial role entails the meticulous review and management of manufacturing deviations and laboratory out-of-specification (OOS) reports, along with the assessment of manufacturing-related change controls in alignment with Tarsus’ Quality Management System (QMS). The Manager II will also take charge of authoring Annual Product Reviews, interpreting and trending analytical data, approving Certificates of Analysis, reviewing manufacturing batch records, and determining product disposition.Key Responsibilities:Evaluate and authorize vendor change controls.Scrutinize vendor documents such as Master Batch Records and Master Packaging Records.Review product specifications for compliance.Assess and approve deviations and OOS reports.Conduct data analysis and trend evaluations.Author Annual Product Reviews to ensure product integrity.Revise and author Quality Assurance Procedures as necessary.Examine new master manufacturing records and process validation protocols.Review and approve test records and Certificates of Analysis.Evaluate executed manufacturing and packaging batch records.Complete batch record review forms for product disposition.Finalize product disposition forms and Certificates of Compliance.Engage in internal operations discussions.Collaborate with Tarsus’ manufacturing partners and testing laboratories.

About the Role As a pivotal member of the Clinical Quality Assurance team, reporting directly to the Director of Clinical Quality Assurance, the Manager II will spearhead clinical quality support and the management of our comprehensive supplier qualification programs encompassing Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Pharmacovigilance Practice (GVP). The ideal candidate will play a crucial role in ensuring inspection readiness across the organization, providing training and guidance to maintain compliance with the latest ICH GCP E6 standards and relevant regulations. Key Responsibilities: Deliver daily clinical quality support and training to uphold adherence to regulatory requirements, company policies, and procedures. Oversee internal and supplier audits related to GCP/GLP/GVP, including the management of the audit schedule within the Quality Management System (QMS). Conduct supplier audits and prepare comprehensive reports as necessary. Compile responses to audits and assess evidence of implementation. Assist in the development and execution of quality systems and processes within the Clinical Quality domain. Review and approve QMS records for completeness and compliance with SOPs and regulations. Support the development of remediation plans and monitor the resolution of quality issues. Contribute to the review of Clinical Quality Management Plans (CQMPs) for clinical trials and vendor performance. Manage and enhance clinical training curricula. Support the creation of tracking tools for reporting quality metrics. Conduct and review Risk Assessments as required. Collaborate closely with Quality Management to ensure compliance with all applicable guidelines and SOPs. Act as a resource for Clinical Development, Operations, and Quality teams.

Thank you for your interest in the Manager II, Clinical Quality Assurance position at itcss! We encourage you to explore the details below. If you believe this role aligns with your career aspirations, please discuss with your current manager and HR business partner to assess your qualifications. Should everything align, we invite you to apply, and our Talent Acquisition team will reach out to you for an interview. We look forward to getting to know you!- Your Human Resources TeamAbout the RoleAs the Manager II of Clinical Quality Assurance, reporting to the Director of Clinical Quality Assurance, you will play a pivotal role in overseeing clinical quality support and the management of the Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Pharmacovigilance Practice (GVP) supplier qualification program.The ideal candidate will be instrumental in preparing the company for inspections, providing training, and ensuring compliance with current ICH GCP E6 guidance and relevant regulations.Key Responsibilities:Deliver daily clinical quality support and training to ensure compliance with regulatory requirements and internal policies.Manage GCP/GLP/GVP internal and supplier audits, including maintaining the qualification program's audit schedule within the Quality Management System (QMS).Conduct supplier audits and prepare reports as necessary.Compile audit responses and evaluate implementation evidence.Assist in the development of quality systems and processes in the Clinical Quality domain.Review and approve QMS records (deviations, CAPAs, change controls, etc.) for completeness and adherence to SOPs and regulations.Support remediation and corrective action plans, ensuring resolution of quality issues.Assist in reviewing Clinical Quality Management Plans (CQMPs) for trials and vendor performance.Manage clinical training curricula and assist in creating tools to track quality metrics.Support risk assessments and conduct periodic reviews of clinical trial systems (e.g., CTMS, TMF).Collaborate with Quality Management to maintain compliance with various standards.

We are seeking a highly skilled and innovative Lead Flight Control Systems CLAW Engineer to join our dynamic team at dev2. In this role, you will lead the design, development, and implementation of advanced flight control systems, ensuring the highest standards of safety and performance.Your expertise will contribute to cutting-edge projects that push the boundaries of aerospace technology. You will collaborate closely with cross-functional teams, guiding junior engineers and providing insights that drive project success.

About Balt Balt is dedicated to transforming the lives of over 150,000 patients by 2026. Our Journey As a trailblazer in the medical device industry for 45 years, Balt has partnered with healthcare professionals and institutions to innovate cutting-edge medical devices. Our products are utilized by medical experts globally, with 13 offices across 11 countries and expanding. Since introducing one of the first neurovascular intervention devices in 1977, Balt has developed the world’s most extensive portfolio of medical devices for stroke care. As the leading global neurovascular platform, we are now venturing into the peripheral vascular sector with our innovative solutions. We take pride in our mission, our passionate team, and the remarkable work we do together to empower physicians in saving lives. Why Join Balt? Be part of a mission-driven team that finds meaning in their work, with a strong sense of pride. Experience a collaborative team environment guided by our core mission, vision, and values. Enjoy recognition, respect, and a multicultural community that contributes to our collective success. We prioritize the well-being of our employees, regardless of location. Ready to become part of our story? We invite you to join us! Opportunity Overview – Senior Quality Engineer The Senior Quality Engineer will play a crucial role in enhancing production quality, facilitating the transfer of neurovascular products to production, and managing supplier quality initiatives. This position requires close collaboration with production teams and suppliers, with moderate support from other engineers and management to achieve objectives. The engineer will be responsible for driving continuous improvements in manufacturing and supplier quality processes through technical and innovative solutions for neurovascular medical devices that save lives.

Become a key player in a team that reaches for the stars! At Terran Orbital, you play an essential role in our mission. As pioneers in satellite manufacturing and aerospace innovation, we continually break barriers to deliver cutting-edge solutions that support our nation’s defense and commercial endeavors. We are a fast-growing, trusted team committed to the rapid and efficient design, construction, launch, and operation of state-of-the-art satellites for advanced mission constellations. If you are motivated by purpose, inspired by challenges, and eager to make your mark on the universe, you’ll find endless opportunities for growth here. Let’s redefine possibilities in orbit and beyond together!We are currently seeking an experienced Inventory Controller to become part of our dynamic team. Reporting directly to the Logistics Manager, the Inventory Controller will be tasked with organizing and maintaining our inventory system while constantly seeking opportunities to enhance the efficiency of our inventory management processes. This role involves supporting the receiving and logging of parts into inventory, managing the disbursement of parts, assisting with hardware production kitting, and overseeing kitting support personnel. Additionally, the Inventory Controller will provide accurate inventory data to accounting for external audits.This position will operate on our Weekday Shift from Monday to Thursday, 6:00 AM – 4:30 PM.

Join our dynamic team at AbbVie as an Associate Director of Quality Assurance. In this pivotal role, you will oversee quality assurance operations, ensuring that our products meet the highest standards of quality and compliance. You will lead a team in the development and implementation of quality systems and processes, driving continuous improvement initiatives that align with our organizational goals.Your expertise will be crucial in managing audits, regulatory inspections, and ensuring adherence to industry regulations. If you are a proactive leader with a passion for quality and compliance, we encourage you to apply and be a part of our commitment to delivering exceptional healthcare solutions.

Rivian and Volkswagen Group Technologies combines expertise from two major automotive companies to drive progress in electric vehicle technology. The partnership develops advanced operating systems, zonal controllers, and cloud connectivity solutions designed specifically for electric vehicles. The team aims to raise standards for software-defined vehicles, focusing on integration, intelligence, and sustainability in mobility. Role overview The Controls Engineer - State Estimation works on the design, analysis, and testing of real-time state estimation algorithms for electric vehicles. This role is part of a group tackling complex technical challenges unique to EVs. Adapting to changing priorities and solving difficult engineering problems are valued in this environment. Location This position is based in Irvine, California.

Join Artech Information Systems LLC as a Data Quality Assurance Analyst and play a crucial role in ensuring the integrity and accuracy of our data systems. In this dynamic position, you will work closely with cross-functional teams to develop and implement quality assurance protocols, identify data inconsistencies, and enhance data management processes.Your analytical skills and attention to detail will be vital in monitoring data quality metrics, documenting findings, and driving continuous improvement initiatives.

Position OverviewJoin field.ai as the Director of Export Control and Technology Compliance, where you will play a pivotal role in establishing and leading our compliance framework for defense-adjacent and commercial technology initiatives. In this dynamic position, you will be responsible for the classification, protection, and access management of technical data, software, and systems in alignment with U.S. export regulations and government contract stipulations. This hands-on role requires strategic acumen and operational execution, collaborating closely with leadership across Engineering, IT, Legal, Human Resources, and Program teams to facilitate swift development while upholding rigorous compliance standards.

Field AI is at the forefront of revolutionizing robot interactions with the physical world. Our mission is to develop risk-aware, dependable, and field-ready AI systems that tackle the most intricate challenges in robotics, thereby unleashing the full potential of embodied intelligence. Unlike traditional data-driven methods or solely transformer-based designs, we are pioneering a novel direction, featuring globally deployed solutions that yield tangible results and continuously enhance models through practical field applications.

Join AbbVie as a Senior Quality Engineer specializing in Risk Management, where your expertise will enhance our commitment to delivering high-quality products. In this role, you'll be responsible for assessing and managing risks associated with product quality, ensuring compliance with regulatory standards, and driving continuous improvement initiatives. Collaborate with cross-functional teams to identify potential quality issues and implement effective solutions.