Quality Assurance/Quality Control Inspector - Federal Projects

Join 360 IT Professionals as an Automation Quality Assurance Engineer (SDET) in San Diego, where you'll play a crucial role in enhancing software quality through automated testing. We are seeking a detail-oriented and proactive individual to develop and implement automated tests that ensure the functionality and performance of our software products.

Join 360IT Professionals as a Senior Automation QA Engineer / SDET in beautiful San Diego, California. We are seeking an innovative and detail-oriented individual who is passionate about quality and automation testing. In this role, you will be responsible for designing, developing, and implementing robust automated testing frameworks for our software products, ensuring the highest quality standards are met.

At Veracyte, we provide thrilling career prospects for individuals eager to join a groundbreaking team dedicated to revolutionizing cancer care for patients worldwide. Being part of Veracyte allows our team members to create a significant impact on the lives of patients, while also fostering personal and professional growth within a mission-driven environment. This embodies what we refer to as the Veracyte way – a collaborative approach guided by our core values, ensuring clinicians have the insights necessary to assist patients in making life-altering decisions.Our Values:We Seek A Better Way: We innovate with courage, learn from our challenges, and remain resilient in our mission to transform cancer care.We Make It Happen: We act swiftly, uphold quality, and infuse enjoyment into our dedicated efforts.We Are Stronger Together: We collaborate transparently, seek understanding, and celebrate our achievements.We Care Deeply: We embrace our diversity, uphold integrity, and support one another.The Position:We are in search of a highly skilled and team-oriented Principal Test Engineer to spearhead the testing processes for applications at Veracyte. This role is critical in our endeavor to expand and develop innovative diagnostic solutions aimed at enhancing patient outcomes and reducing healthcare costs.The Principal Test Engineer is a senior, hands-on quality leader responsible for defining, executing, and continuously refining the software testing strategy within Veracyte's regulated environment. This position guarantees that all software products adhere to relevant quality, safety, and compliance standards while facilitating streamlined delivery processes. The Principal Test Engineer will serve as a subject-matter expert in verification and validation (V&V), test automation, risk-based testing, and regulatory compliance, offering technical guidance to junior testers and working closely with engineering, product, and quality teams.

Join Eurofins Scientific as a Quality Assurance Manager in San Diego, where you will play a crucial role in ensuring the highest standards of quality and compliance in our laboratory operations. In this dynamic position, you will lead a dedicated team, develop and implement quality assurance programs, and foster an environment of continuous improvement.

The Quality Assurance Manager is responsible for overseeing the quality control processes and ensuring that all project deliverables meet established standards and client expectations. This role involves developing and implementing quality assurance strategies, conducting audits, and collaborating with project teams to address quality-related issues.

Capricor Therapeutics (NASDAQ: CAPR) is a pioneering biotechnology firm committed to the development of groundbreaking cell and exosome-based therapies aimed at addressing rare diseases. Our flagship innovation, Deramiocel (CAP-1002), is currently in late-stage development for Duchenne muscular dystrophy. Additionally, we leverage our proprietary StealthX™ exosome platform to explore new avenues in targeted delivery systems and vaccinology. Each initiative exemplifies our dedication to expanding the frontiers of science and providing transformative treatments to patients and families in urgent need.The Senior Director of Quality Assurance and Quality Systems will spearhead strategic and operational oversight of all quality initiatives supporting Capricor’s clinical-stage and advancing commercial-stage operations. This role holds comprehensive responsibility for the architecture, implementation, and ongoing enhancement of the Quality Management System (QMS), ensuring adherence to regulatory standards, inspection readiness, and robust quality governance throughout development, manufacturing (including cell therapy production), and the prospective commercialization of Deramiocel and StealthX™-based programs.In this critical position, the Senior Director will collaborate closely with executive leadership, Regulatory Affairs, CMC, Clinical, Manufacturing, and other cross-functional teams to facilitate late-stage development, BLA submissions and responses (including managing all quality-related aspects of the Deramiocel pathway), ensuring commercial readiness, and promoting scalable growth while fostering a proactive, risk-based quality culture throughout the organization.

Ensure adherence to all relevant local and international pharmaceutical regulations.Lead Quality Chemistry, Manufacturing, and Controls (CMC) operations, overseeing batch disposition, manufacturing, packaging, labeling, and testing to guarantee product integrity and timely material release.Provide decisive leadership to enhance quality-related processes including batch disposition, investigations, analytical data reviews, supply chain management, and risk assessment.Act as the primary contact for complex and high-stakes quality challenges and resolutions.Proactively assess and manage quality risks throughout the product lifecycle, recommending and implementing effective mitigation strategies.Collaborate closely with ORIC's technical operations team, Contract Manufacturing Organizations (CMOs), contract testing labs, and distribution centers to ensure rigorous quality reviews of all process and analytical data, supporting informed program decisions.Work synergistically with Regulatory Affairs to facilitate timely and precise submission reviews.Engage actively with clinical program teams, contributing to clinical development meetings to ensure ongoing quality support.Design and implement performance-driven quality metrics and trend analyses to foster continuous improvement.Conduct and present Annual Product Reviews for advanced-stage programs.Lead, mentor, and cultivate a high-performing Quality team, scaling effectively to support transitions from clinical to commercial phases.Serve as Chair or a key member of various governance committees, including ORIC’s Stability Review Board, Material Review Board, and Change Review Board.Represent ORIC Quality in discussions with CDMOs, regulatory authorities, and strategic leadership meetings as required.Exhibit a high degree of adaptability in fast-paced environments, adjusting strategies and priorities according to evolving business needs, technologies, and stakeholder expectations.Develop new functional Standard Operating Procedures (SOPs), policies, and plans for late-phase and commercial readiness as required.

Join our dynamic team at Integrated Resources, Inc. as a Quality Assurance Specialist focused on the pharmaceutical industry. In this role, you will play a crucial part in ensuring the highest quality standards in the development and manufacturing of pharmaceutical products. Your expertise will help maintain compliance with regulatory requirements and enhance product safety and effectiveness.

Oric Pharmaceuticals is seeking a Director of Clinical Quality Assurance to lead our quality assurance efforts. This pivotal role will involve developing and implementing robust quality systems that comply with regulatory standards. As a key player in our clinical operations, you will ensure the integrity of our clinical trials and contribute to the overall success of our drug development programs.

Brain Corporation is seeking a Software Development Engineer in Test II in San Diego, CA. This position centers on building and maintaining automated tests for software products. Collaboration with development teams is a key part of the role, with a focus on identifying and resolving defects to maintain high standards of quality and reliability. Role overview This engineer will design and implement automated test suites, helping to catch issues early in the development cycle. The work involves close communication with software developers to improve testing processes and support product stability. What you will do Create and maintain automated tests for software projects Work with development teams to find and fix defects Suggest and implement improvements to testing workflows

As the Quality Assurance Manager for Good Clinical Practice (GCP) at Sobi, you will play a pivotal role in ensuring the highest standards of quality oversight, assurance, and design within the GCP/GCLP domains. Your responsibilities will include:Overseeing quality assurance and design activities related to GCP/GCLP.Providing guidance and support on GCP/GCLP and GPP-related activities throughout Sobi, including audits, inspections, and risk assessments associated with BLA/NDA/IND/CTA submissions globally.Facilitating the collection of data necessary for the audit program risk assessment.Supporting clinical study-related quality activities across Sobi.Ensuring the qualification of global and local ESP in GCP regulated areas according to Sobi procedures.Collaborating with relevant stakeholders across the Sobi organization.Key Responsibilities:Manage the GCP audit process to ensure excellence throughout the audit lifecycle.Assess and approve GCP deviations and related CAPAs from a quality perspective.Prepare regular status reports on audits, trending deviations, and CAPAs to uphold quality oversight.Contribute to GCP audit risk assessments according to SOPs.Actively engage with cross-functional teams on GxP and Quality requirements, ensuring proper qualification of GCP service providers.Serve as the QA representative during GCP inspections and promote a continuous quality mindset across Sobi.Develop and review GCP QA-related processes under the global framework.

Join our dynamic team at StemXpert as a Quality Assurance Specialist! In this full-time role, you will play a critical part in ensuring the highest standards of quality in our products. Your keen eye for detail and commitment to excellence will help us maintain our reputation for delivering outstanding solutions to our clients. You will collaborate with cross-functional teams to identify areas for improvement and implement effective testing procedures. If you are passionate about quality assurance and eager to contribute to innovative projects, we would love to hear from you!

Position Title: Quality Assurance Analyst Studio/Department: Quality Assurance Employee Type: Full Time Location: San Diego, CA/Remote (Daybreak Approved Remote Locations: CA, WA, TX, NY) Salary Range: $14.00 - $17.00 per hour, pay may vary based on location. The Quality Assurance Analyst plays a pivotal role in testing various elements of Magic the Gathering Online within the QA Department. Responsibilities include: Developing and implementing test plans for upcoming Card Content and Feature releases Collaborating with fellow analysts and developers to ensure comprehensive testing Validating changes across multiple environments Identifying and testing edge cases beyond expected functionality Championing the player experience by providing qualitative feedback Prioritizing assigned tasks within the QA team Qualifications: Proficient in QA methodologies and best practices Excellent written and verbal communication skills Proactive in raising visibility on issues Minimum of 1 year experience in quality assurance Understanding of Magic the Gathering rules and gameplay A passion for gaming and Quality Assurance is a plus Ability to foster inter-team collaboration to enhance game quality for players Company Culture: Innovative Ownership: Empowering ownership and encouraging creativity We believe in learning from both successes and failures, embracing new ideas, and teaching one another. Our commitment to smart work and passionate craftsmanship drives our team forward. Empathy: Understanding perspectives of team members and players alike We value emotional intelligence, positive behavior, and candid communication, fostering an environment of respect and appreciation. Collaboration: Focusing on the best idea rather than individual recognition We thrive on teamwork, believing that great ideas can originate from anyone.

Join our dynamic team at 360 IT Professionals as a Software Development Engineer in Test (SDET). We are seeking a skilled individual with expertise in Selenium automation and Java to enhance our testing frameworks and contribute to our software quality assurance efforts. This is a fantastic opportunity for local candidates in San Diego who are eager to make an impact in a growing tech environment.

Join our team as a Quality Assurance Associate, where you'll play a crucial role in ensuring the functionality and reliability of our innovative hiring software. This position involves meticulous testing within Lever's testing environment, which is pivotal for continuous improvement and enhancement of our products.At Lever, we have redefined the talent acquisition landscape, partnering with industry leaders such as Netflix, Shopify, and Cirque du Soleil. Our commitment to fostering a people-first culture and investing in our employees has earned us accolades as one of the best workplaces in the U.S. We are excited to expand our team with dedicated individuals who are passionate about quality and excellence.

Brain Corporation, based in the vibrant city of San Diego, California, is a pioneering AI company dedicated to revolutionizing the robotics industry. Our mission is to develop autonomous technologies that enhance efficiency in real-world applications. With our advanced robotic and AI solutions, we assist retailers in ensuring optimal product placement, pricing, and cleanliness in their stores. Through the BrainOS® Robotics Platform, we empower the world's largest fleet of Autonomous Mobile Robots (AMRs), currently exceeding 30,000 units, to deliver efficient automated solutions for commercial floor cleaning and inventory management. Backed by esteemed investors including the SoftBank Vision Fund, Clearbridge, and Qualcomm Ventures, we are at the forefront of innovation.Position Overview:The Software Development Engineer in Test II (SDET II) is an integral part of our engineering team, focusing on the design, development, and enhancement of automated systems that validate our cutting-edge software applications and services. Collaborating closely with product developers, the SDET II is responsible for creating test automation frameworks, validation tools, and quality insights to ensure reliable software releases across various platforms including web applications, cloud services, and mobile systems.Moving beyond traditional QA roles, the SDET II actively contributes to coding, automation, and tooling efforts alongside development teams, ensuring that our systems are designed to be testable, observable, and scalable throughout the software development lifecycle.This role involves direct contributions to engineering tasks while working collaboratively with product, development, and quality assurance teams to deliver superior software solutions.

Capricor Therapeutics (NASDAQ: CAPR) is an innovative biotechnology firm committed to pioneering cell and exosome-based therapies aimed at treating rare diseases. Our flagship product, Deramiocel (CAP-1002), is currently in late-stage development for Duchenne muscular dystrophy. Additionally, we are leveraging our unique StealthX™ exosome platform to explore new avenues in targeted drug delivery and vaccine development. Every initiative at Capricor embodies our dedication to advancing scientific boundaries and providing transformative therapies for patients and their families.We are looking for a dedicated Quality Assurance Associate II to enhance our team. This pivotal role focuses on scaling our clinical production activities while ensuring adherence to cGMP and regulatory standards. The ideal candidate will assist in batch record reviews, deviation investigations, label issuance, and the management of controlled documents across GLP/GCP/GMP systems. We seek an individual who is detail-oriented, organized, and driven to achieve quality excellence in a dynamic environment.

We are seeking a meticulous Quality Control Reviewer to join our dynamic team in San Diego. In this vital role, you will ensure that all products meet our quality standards and regulatory compliance before they reach our clients. Your keen eye for detail and analytical skills will help us maintain our commitment to excellence.

Join ServiceNow as a Staff Network Development Engineer specializing in Cloud Network Automation. In this role, you will be at the forefront of innovative cloud solutions, driving the automation of network services to enhance our platform’s capabilities. You will collaborate with cross-functional teams to design, implement, and optimize robust network solutions that meet the needs of our clients.