Quality Systems Associate II

Join Capricor Therapeutics as a Quality Systems Associate II, where you'll play a vital role in ensuring the integrity and compliance of our quality systems. This position offers the opportunity to work alongside a talented team committed to advancing innovative therapeutic solutions.

Join iambic therapeutics as the Director of Quality Systems and Compliance, a pivotal role in shaping our Quality Management System (QMS) to support our innovative clinical development programs and expanding pipeline. This leadership position collaborates with various departments including Regulatory, Medical, Clinical, R&D, and Technology to ensure our quality systems foster innovation, uphold compliance, and maintain readiness for inspections across both U.S. and international clinical initiatives.This position is based in our San Diego headquarters or can be performed remotely within the United States.KEY RESPONSIBILITIESSpearhead the design, implementation, and continuous improvement of the Quality Management System (QMS).Develop policies, procedures, and governance frameworks governing essential quality processes, including document control, change management, deviations, CAPA, training, and risk management.Serve as a strategic quality partner to Regulatory, Medical, Clinical Operations, R&D, and CMC teams.Create and execute a quality roadmap that translates regulatory and quality requirements into scalable operational models, aligned with current compliance needs and future organizational growth.Collaborate with Regulatory and Clinical teams to ensure quality systems effectively support global clinical trial programs, ensuring alignment across regions.Proactively identify and mitigate compliance risks through data-driven monitoring and governance.Establish key quality metrics and dashboards to track system health, compliance trends, and opportunities for continuous improvement.Cultivate a culture of accountability, transparency, and quality ownership throughout the organization.Oversee quality interactions with health authorities, internal audits, and third-party audits as necessary.Ensure inspection readiness for U.S. and global clinical programs through established quality systems, governance, and cross-functional collaboration.QUALIFICATIONSEducation & Experience:Bachelor’s degree in chemistry, biology, engineering, or a related health science.Experience:A minimum of 10 years of progressive experience in Quality Systems, Compliance, and/or Quality leadership within a regulated industry.

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.

About Capricor Therapeutics Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company focused on cell and exosome-based therapies for rare diseases. The company’s lead product, Deramiocel (CAP-1002), is in late-stage development for Duchenne muscular dystrophy. Capricor is also advancing its StealthX™ exosome platform to pursue innovations in targeted delivery and vaccinology. Role Overview: Quality Control Associate II, Controls This position is based in San Diego (SD1). The Quality Control Associate II, Controls, supports the development, qualification, and ongoing management of analytical control materials used in quality control assays. The role ensures QC assays remain reliable and consistent by generating, characterizing, and maintaining both positive and negative controls. What You Will Do Generate and maintain analytical control materials, including positive and negative controls for QC assays. Conduct analytical studies to evaluate assay performance. Assist with troubleshooting and optimizing analytical methods used in quality control testing. Collaborate with QC scientists and cross-functional teams to monitor assay performance and support continuous improvement of analytical methods across Capricor’s therapeutic programs. Impact This role is central to maintaining the accuracy and consistency of QC assays, directly supporting Capricor’s mission to deliver new therapies to patients and families affected by rare diseases.

Join our dynamic team as a Scientist II, where you will leverage your expertise to drive innovation and contribute to cutting-edge research projects. You will work collaboratively with a team of professionals in a stimulating environment that fosters growth and creativity.

Join Capricor Therapeutics, Inc. as a Quality Control Associate II/III, Analytical and contribute to the development of innovative therapies. In this role, you will play a crucial part in ensuring the quality and reliability of our analytical laboratory results.

Position Overview:Join our dynamic team as a Quality Control Associate I, where you will engage in both routine and non-routine analysis of incoming products. Utilizing a variety of advanced analyzers and instruments, you will play a key role in supporting the release, characterization, and stability testing of raw materials, production intermediates, and final products.

About the Role Saalex Solutions, Inc. is seeking a System Administrator II for its IT team in San Diego, California. This position focuses on supporting and maintaining computing systems to keep them secure, reliable, and performing well for users across the organization. What You Will Do Maintain and support company computing systems Troubleshoot technical issues alongside IT colleagues Implement new technologies as needed Enhance and improve existing infrastructure Apply critical thinking to solve system management challenges Who Succeeds in This Role Brings hands-on experience with system administration Works well with other IT professionals Approaches problems methodically and proactively Communicates clearly and collaborates effectively This position is based in San Diego, California, United States.

About the Role Saalex Solutions, Inc. is hiring a Systems Engineer II in San Diego, California. This role focuses on designing, implementing, and maintaining complex systems. The position involves working with advanced technologies and collaborating closely with a skilled team to support technical projects.

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.

AECOM is seeking a dedicated and detail-oriented Special Systems Inspector to join our team in San Diego, California. In this role, you will play a critical part in ensuring the quality and compliance of specialized systems within various projects. Your expertise will contribute to the successful execution of our projects and the overall satisfaction of our clients.As a Special Systems Inspector, you will be responsible for conducting thorough inspections, documenting findings, and collaborating with project teams to resolve any issues. Your role is crucial in maintaining our high standards and delivering exceptional results.

We are seeking a dedicated and detail-oriented Research Associate II to join our dynamic team in San Diego. In this role, you will be responsible for conducting research, analyzing data, and contributing to the development of innovative solutions. You will work collaboratively with senior researchers and other team members to support ongoing projects and initiatives.

Capricor Therapeutics (NASDAQ: CAPR) is an innovative biotechnology company committed to pioneering groundbreaking cell and exosome-based therapies aimed at treating rare diseases. Our flagship product, Deramiocel (CAP-1002), is a cutting-edge cell therapy currently in late-stage development for Duchenne muscular dystrophy. Additionally, we leverage our proprietary StealthX™ exosome platform to explore novel avenues in targeted delivery and vaccinology. Each of our initiatives reflects a steadfast dedication to advancing scientific boundaries and delivering transformative treatments to patients and families in dire need.The MSAT Associate II plays a critical role in supporting cGMP manufacturing operations through the development of technical documentation, management of investigations, and addressing process-oriented scientific challenges. This position calls for a deep understanding of cell therapy or biologics manufacturing, coupled with proven analytical skills, the ability to manage quality events, and the capacity to provide real-time support for production activities.As a Subject Matter Expert (SME) in this role, you will be integral to various manufacturing processes, including technology transfers, continuous improvement efforts, deviation investigations, and the creation and revision of controlled documents. You will collaborate closely with teams in Manufacturing, Quality Assurance (QA), Process Development, and Supplier Quality to ensure compliant, efficient, and thoroughly documented operations.

Join AbbVie as a Scientist II specializing in In Vitro Pharmacology. In this pivotal role, you will collaborate with a dynamic team of scientists to drive innovative research that advances our understanding of pharmacological compounds. Your expertise will contribute to the development of groundbreaking therapies aimed at improving patient outcomes.

About Us At DLH Corporation, we are committed to enhancing national security and health readiness for federal programs through cutting-edge research and development, systems engineering, and digital transformation. Our dedicated team of professionals applies their expertise in public health, performance evaluation, and health operations to tackle complex challenges faced by both military and civilian clients. By harnessing advanced technologies such as artificial intelligence, data analytics, and simulation, we are able to devise innovative solutions that improve the lives of millions. With over 2,400 employees, our mission is clear: "Your Mission is Our Passion." Role Overview As a Mechanical Engineer II, you will take on a pivotal role in the research, development, design, manufacturing, and testing of mechanical devices and systems. You will work on a variety of power-producing machines, including electric generators and combustion engines, as well as power-using machines like refrigeration units and industrial equipment. Proficiency in Computer-Aided Design (CAD) and Computer-Aided Manufacturing (CAM) is essential for developing precise 2D drawings and 3D models, enabling you to bring innovative designs to fruition and optimize existing systems.

AECOM is hiring an IT Specialist II in San Diego, focusing on Project Management Information Systems (PMIS). This role centers on supporting and improving software platforms that help project teams deliver results efficiently. Key responsibilities Maintain and support PMIS platforms used throughout various projects Find ways to streamline workflows and enhance system performance Work closely with colleagues to address technical issues and implement effective solutions Apply technical expertise to keep projects running smoothly Who succeeds in this role Problem-solvers who enjoy collaboration People who contribute new ideas to technical challenges Those motivated by technology and eager to see their work have an impact This position offers the chance to use IT and project management systems expertise to help shape the success of project outcomes at AECOM.

Capricor Therapeutics (NASDAQ: CAPR) is an innovative biotechnology firm dedicated to pioneering transformative therapies utilizing cell and exosome technology for rare diseases. Our flagship product, Deramiocel (CAP-1002), is in advanced stages of development aimed at treating Duchenne muscular dystrophy. We are also leveraging our proprietary StealthX™ exosome platform to explore new avenues in targeted delivery and vaccinology. Each of our programs underscores our commitment to advancing scientific boundaries and providing life-altering treatments to patients and their families in need.The Quality Control Associate specializing in Environmental Monitoring (EM) is crucial for ensuring optimal environmental conditions necessary for GMP manufacturing. This role involves conducting routine and specialized sampling, analyzing data trends, meticulously documenting results, and ensuring that controlled areas adhere to both regulatory and internal quality standards. As a member of the QC EM team, you will engage in hands-on monitoring of air quality, surfaces, personnel, and testing of water systems and utilities to uphold facility integrity. You will be responsible for maintaining precise, real-time documentation and aiding in investigations of any environmental deviations or anomalies. Collaborating closely with QC, QA, and Production teams, this position ensures that manufacturing and testing environments consistently uphold quality standards to support the production of high-caliber therapeutic products.

Join Our Dynamic Team!At DSI Systems, we leverage over 40 years of expertise in sales enablement and tailored business solutions, providing unparalleled value that drives success for our clients and partners. We are actively seeking enthusiastic individuals who are ready to leave their mark in the realms of sales and customer service. Our vibrant and fulfilling workplace offers a platform for you to grow alongside us and make a meaningful contribution.Position OverviewThe Retail Support Specialist (RSS) is pivotal in delivering direct, hands-on assistance to AT&T customers within bustling national retail settings. In this role, you will directly interact with customers and retail partners to address account issues, billing inquiries, device assistance, and service-related concerns, often in high-pressure, fast-paced environments. To succeed, you must possess excellent communication skills, emotional fortitude, a knack for technology, and the ability to maintain composure, accuracy, and professionalism amidst the dynamic nature of retail.Key Responsibilities:Customer SupportDeliver professional, friendly, and solution-oriented support to AT&T customers in national retail locations.Handle inquiries regarding billing, account modifications, plan adjustments, device troubleshooting, and service issues.Diagnose and resolve wireless device issues, network challenges, and feature functionality queries.Thrive in high-volume retail settings, upholding focus, professionalism, and service excellence during peak times and escalated situations.Retail Partner SupportServe as the AT&T subject-matter expert for retail staff and third-party labor partners.Act as the primary AT&T representative for these partners, leading in-store support for retail escalations.Engage proactively with store management to address customer concerns, enhancing partnership alignment and ensuring a top-tier customer experience.Work Environment & Schedule Expectations:This role is conducted in a retail environment and necessitates standing, walking, and engaging with customers on the sales floor for up to 8 hours daily.Willingness to work flexible hours, including evenings, weekends, and holidays, based on business needs.Comfort in busy, customer-facing environments requiring frequent interaction and problem-solving.Operational Excellence:Effectively navigate multiple systems while interacting with customers in real-time.Thoroughly document all interactions with precision.Adhere to company policies, compliance mandates, and privacy standards.Achieve or surpass performance metrics, including quality, efficiency, and customer satisfaction ratings.Execute and maintain approved planograms for mobile devices and signage.

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.

About UsAt DLH Corporation, we are committed to enhancing health outcomes and national security through innovative solutions in research, systems engineering, and digital transformation. Our dedicated team of over 2,400 professionals is passionate about addressing the complex challenges faced by our federal clients, utilizing cutting-edge technologies such as artificial intelligence, data analytics, and cloud solutions. We pride ourselves on our unique blend of governmental expertise, proven methodologies, and a steadfast commitment to innovation, which enables us to positively impact millions of lives.OverviewAs an Engineer II, you will leverage scientific and mathematical principles to research and develop cost-effective solutions for technical challenges. This role serves as a vital link between societal needs and commercial applications, encompassing the design of products and machinery, enhancing methods for resource extraction and processing, and innovating materials for improved performance. You will assess the environmental and societal impacts of your designs while being involved in testing, production, and quality assurance processes. The Engineer II role within C5ISR involves the development and technical support of Command, Control, Communications, Computers, Intelligence, Surveillance, and Reconnaissance (C5ISR) systems, contributing to national security operations.