Principal Software Engineer at Tendo | San Diego

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 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.

Brain Corporation is seeking a Principal Software Engineer, Cloud, to help shape the next generation of cloud-based solutions. This position is based in San Diego, CA. Role overview This role focuses on designing, developing, and implementing software systems that support and enhance Brain Corporation's product offerings. The Principal Software Engineer will draw on deep technical experience to create solutions that improve the performance, scalability, and reliability of the company’s cloud infrastructure. Collaboration and mentorship Working closely with cross-functional teams, the Principal Software Engineer will participate in code reviews and mentor junior engineers. Collaboration is central to this position, ensuring that technical standards are met and knowledge is shared across the team. Impact Contributions in this role have a direct effect on the quality and robustness of Brain Corporation’s cloud systems, supporting the company’s ongoing innovation in cloud technology.

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.

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

Join the team at Systems Technology Research (STR) as a Principal Software Reverse Engineer, where your expertise in research and analysis of vulnerabilities in cyber-physical systems will be valued. This position is part of a dynamic, multidisciplinary team focused on pioneering technologies that significantly impact national security. You will play a crucial role at the intersection of computing and real-world physical systems. We cherish the unique skills and diverse perspectives each employee brings, which are vital for delivering innovative solutions to our clients.Note: This position requires on-site work and an Active Top Secret (TS) Clearance.Key Responsibilities:Conduct reverse engineering of complex software or firmware, including Windows/Linux binaries and embedded firmware on unconventional architectures.Create and utilize automated reverse engineering and binary analysis tools to analyze protocols, interfaces, and functionalities of target systems.Develop cutting-edge cybersecurity solutions.Lead cross-disciplinary teams to address complex challenges across various technologies.Engage in vulnerability weaponization, exploit development, and mitigation strategies for a diverse range of targets.Perform technical marketing to existing and prospective clients.Contribute to the development of technical proposals through idea generation, writing, and editing.Document, showcase, and present research findings.Tackle real-world challenges that enhance national security.

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.

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.

Join Radiant Infosystems Ltd as an Embedded Software Test Engineer, where you'll play a crucial role in ensuring the quality and functionality of our innovative software solutions. You will collaborate with a dynamic team of engineers to develop and execute testing strategies for embedded systems, helping to deliver high-quality products to our customers.

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.

We seek an innovative and passionate Senior Principal Software Engineer to lead the development of transformative healthcare software aimed at significantly enhancing the experiences of patients, clinicians, and caregivers. In this pivotal role, you will guide a talented team through the crucial early stages of product development while also contributing your own coding expertise and expanding your skill set.The ideal candidate boasts extensive full stack experience in crafting SaaS and/or Cloud Native solutions tailored for the regulated healthcare industry. You will possess significant knowledge in advanced technologies, including distributed microservice architecture, Go, Ent, gRPC, Twirp, and AWS services such as EventBridge and Aurora. Your ability to share insights and mentor developing team members will be essential for our growth.As a Senior Principal Software Engineer, you will thrive in an Agile, collaborative setting alongside product managers, designers, external partners, and fellow engineers, all working together to create high-quality, consumer-focused products from the ground up.About TendoJoin a mission-driven team making a real difference!At Tendo, we are rapidly expanding, fostering a culture that empowers teams and individuals to excel. Our commitment to a team-oriented environment has earned us recognition as one of Forbes’ Top Startup Employers for both 2024 and 2025. Guided by an experienced leadership team, we uphold our values and continuously seek motivated individuals from diverse backgrounds to enhance the care journey for all stakeholders by developing intuitive, user-friendly software.If you are excited to work with cutting-edge technologies and want to be part of a growing team that is reshaping the healthcare landscape, we invite you to apply today!

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.

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.

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.

Join Shield AI as a Principal Engineer in Mission Systems where you will play a pivotal role in designing and implementing advanced technology solutions. In this position, you will lead engineering efforts, collaborate with cross-functional teams, and contribute to the development of cutting-edge systems that enhance mission effectiveness. If you are passionate about technology and driven to make an impact, we want to hear from you!