Research Associate III

Join Capricor Therapeutics as a Quality Control Associate III specializing in Sample Management. In this vital role, you will ensure the integrity and quality of sample management processes that support our innovative therapies. You will collaborate with cross-functional teams to uphold the highest standards of quality in our laboratory operations.

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 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.

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.

About Capricor Therapeutics Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company focused on developing 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’s StealthX™ exosome platform supports new approaches in targeted delivery systems and vaccinology, with a mission to advance science and deliver new treatments for patients and families facing serious conditions. Role Overview: Quality Control Scientist, Analytical Controls This role is based in San Diego (SD1). The Quality Control Scientist, Analytical Controls, develops, qualifies, and manages analytical control materials for QC assays. The scientist will generate and maintain both positive and negative controls, design and execute analytical studies, and troubleshoot or improve analytical methods used in QC testing. Key Responsibilities Develop and qualify analytical control materials for use in QC assays. Manage the lifecycle of control materials, including ongoing maintenance and documentation. Design and conduct analytical studies to support QC operations. Troubleshoot and refine analytical methodologies as needed for QC testing. Ensure reliability, reproducibility, and regulatory compliance of QC assays. Provide scientific guidance on assay control strategies. Collaborate with teams in Quality Control, Analytical Development, Process Development, Manufacturing, and Quality to support analytical readiness for Capricor’s therapeutic programs. Collaboration This position works closely with multiple teams to ensure analytical controls meet the needs of Capricor’s research and manufacturing efforts. The scientist will contribute expertise to cross-functional projects and help maintain high standards for QC laboratory performance.

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.

We are seeking a detail-oriented and analytical Quality Control Chemist to join our dynamic team in San Diego. In this role, you will be responsible for performing a variety of quality control tests and analyses to ensure that our products meet the highest standards of quality and compliance. You will work closely with other departments to develop and implement quality control protocols and contribute to continuous improvement efforts.

At BioAgilytix, we are dedicated to advancing the field of science and its transformative effects on our world. Our team of skilled scientists and industry professionals provides customized services that facilitate breakthroughs in new medicine through our top-tier bioanalytical services. We are unwavering in our commitment to our clients, focusing on solutions and adhering to deadlines. As we continue to expand, we offer a dynamic, fast-paced, and enjoyable workplace where no day is the same. With opportunities to engage with a diverse range of clients and drug modalities, you have the potential for rapid career growth. You will tackle various challenges while playing a pivotal role in delivering life-changing and life-saving therapies to those in need.In this on-site role in San Diego, the Sample Management Technician will be responsible for the GxP-compliant handling of incoming samples and reference materials.

Join our dynamic team at Turner Townsend as a Quality Assurance/Quality Control Inspector specializing in federal projects. In this role, you will be responsible for ensuring that all aspects of construction comply with established standards and regulations. Your keen eye for detail and commitment to quality will contribute significantly to the success of our projects.

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.

Join our dynamic team at Integrated Resources, Inc. as a Quality Control Biochemist. This role is essential in ensuring the quality and safety of our biochemical products. You will engage in rigorous testing and analysis, contributing to the development of innovative solutions in the biotech industry.

Join our team at Capricor Therapeutics as an Analytical Quality Control Specialist, where you will play a crucial role in ensuring the highest quality standards for our innovative therapeutics. You will engage in analytical testing, data analysis, and quality assessments, contributing to our mission of developing breakthrough treatments. We are looking for a detail-oriented individual who excels in a collaborative environment and is passionate about quality assurance in the pharmaceutical industry.

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.

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.

Role Overview Saalex Solutions, Inc. is hiring a Network Control Technician III in San Diego, California. This position focuses on supporting and managing network operations to ensure smooth and reliable connectivity. What You Will Do Monitor and maintain network systems to support daily operations Troubleshoot issues related to network connectivity and performance Apply knowledge of network protocols to resolve technical problems Collaborate with team members to implement network changes and upgrades What We Look For Hands-on experience working with network systems Strong understanding of network protocols Ability to identify and resolve network issues efficiently

The Quality Operations Manager plays a pivotal role in facilitating the transition from outdated paper-based processes to a robust and compliant Electronic Quality Management System (eQMS). This position is essential for ensuring that the Quality System effectively supports all phases of drug development, including nonclinical and clinical development, regulatory submissions (IND, NDA/BLA), commercialization, and product lifecycle management.The Quality Operations Manager is tasked with maintaining compliance with relevant GxP requirements (GLP, GCP, GMP), FDA regulations, global standards, and industry best practices. This role also emphasizes readiness for inspections, regulatory submissions, vendor oversight, and the promotion of a quality-centric culture throughout the organization.Key Responsibilities:eQMS Transition:Evaluate current paper-based procedures and devise a comprehensive plan for transitioning to electronic workflows.Ensure data integrity, compliance with Part 11 where necessary, and proper system validation.Facilitate the integration of GxP processes across all functional areas into a cohesive, risk-based framework.Quality System Management:Develop, implement, and uphold procedures for document control, training management, handling deviations and nonconformances, CAPA, change control, risk management, audit management, and complaint handling (if applicable).Coordinate and deliver training on GxP procedures.Support for External Quality Operations: If applicable.Inspection Readiness & Regulatory Interface:Lead inspection readiness initiatives across the organization.Manage regulatory agency inspections (e.g., FDA, EMA, and other global authorities).Oversee the timely and effective development and implementation of CAPAs in response to regulatory findings.Cross-Functional Leadership:Collaborate with Clinical, Regulatory, CMC, Nonclinical, IT, and Commercial teams.Provide training and foster a culture of quality across the organization.Act as a quality advisor to senior leadership.

Join the culinary team at Addison by William Bradley as a Cook III, where your passion for cooking and commitment to excellence will contribute to an unforgettable dining experience. In this role, you will work alongside talented chefs, preparing exquisite dishes while ensuring the highest standards of quality and presentation.

Join our dynamic team at Accor Hotels as an Amaya Cook III, where your culinary expertise will shine! As part of our professional kitchen staff, you will be responsible for preparing a variety of dishes, ensuring high-quality food standards, and contributing to an exceptional dining experience for our guests. This role is perfect for passionate individuals who thrive in a fast-paced environment and are eager to enhance their culinary skills.