Analytical Development Scientist - Cell Therapy

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.

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.

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.

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.

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.

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 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.

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.

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 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 AbbVie as a Senior Scientist II in Analytical Development, where your expertise will contribute to innovative solutions in biopharmaceuticals. You will collaborate with a dynamic team, leveraging your analytical skills to drive research and development efforts. This role is pivotal in advancing our mission to improve patient outcomes through groundbreaking therapies.

JOB SUMMARYiambic therapeutics is on the lookout for a talented and motivated Analytical/Bioanalytical Scientist specializing in chromatography-based purification to enhance our drug discovery initiatives. The chosen candidate will be instrumental in facilitating high-throughput purification and assay workflows, supporting a weekly design-make-test-analysis cycle driven by our proprietary AI-based drug discovery engine. The ideal individual will possess extensive expertise in chromatographic purification, particularly in SFC and/or LC purification of small molecules, along with demonstrated skills in instrument troubleshooting, workflow optimization, and a solid understanding of ADME/DMPK assay design and execution.KEY RESPONSIBILITIESAct as the authority in chromatography-based purification, leveraging significant experience in SFC and LC purification of small molecules within a drug discovery context.Create, implement, and refine purification workflows, including preparative chromatography methods, fraction collection strategies, and post-purification data integration.Design and sustain automated purification workflows to enhance throughput, reproducibility, and sample quality.Work collaboratively with medicinal chemistry, purification, and DMPK teams to supply high-quality purified compounds, aiding in lead optimization and screening.Provide direct support, preventive maintenance, and troubleshooting for LC, LC/MS, and SFC instruments to reduce downtime and ensure continuous lab operations.Engage with vendors and automation partners for service, upgrades, installations, and workflow integration.Potentially assist with ADME/DMPK and physicochemical assays, contributing to method development, troubleshooting, and execution as required.Document purification workflows, maintenance activities, and troubleshooting in line with laboratory best practices.QUALIFICATIONSPossession of an advanced degree (M.S. or Ph.D.) in Analytical Chemistry, Chemistry, Chemical Engineering, or a related discipline; or equivalent industry experience.A minimum of a Ph.D. with 2 years of relevant experience OR an M.S. with 6 years of relevant experience.Extensive hands-on experience with chromatography-based purification, particularly SFC and/or LC purification of small molecules.Strong proficiency in operating, maintaining, and troubleshooting chromatography and mass spectrometry instruments.

Join AbbVie as a Principal Research Scientist II in our Analytical Development team, where you will play a pivotal role in advancing our therapeutic solutions. Your expertise will be crucial in developing and validating analytical methods, ensuring our products meet the highest standards of quality and efficacy.This position offers a unique opportunity to collaborate with cross-functional teams, driving innovation and excellence in our research initiatives. If you are passionate about scientific discovery and eager to contribute to impactful projects, we invite you to apply.

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.

Role Overview Saalex Solutions, Inc. is seeking a Network Control Technician II in San Diego, California. This position focuses on maintaining and managing network operations to keep communication systems reliable and efficient. What You Will Do Monitor and support daily network operations Troubleshoot network issues as they arise Work with a team of IT professionals to resolve problems and improve performance Implement solutions that strengthen operational capabilities

Join PM2CM, Inc., a premier professional services firm specializing in Program and Project Management, Construction Management, and Project Controls services throughout the design and construction phases. Our expertise lies in Project Controls, which encompasses Scheduling, Cost Controls, Document Management, Budget Tracking and Monitoring, Estimating, Risk Analysis, Claims Avoidance, Mitigation, Change Management, and Earned Value Management.This role is based in Pomona, California, with a hybrid work arrangement (Tuesdays and Wednesdays in the office/field).The Project Controls Estimator I will play a crucial role in consolidating project scope and cost for initiatives ranging from approximately $25 million to over $1 billion. This position ensures compliance with governance processes and assists Project Managers in obtaining executive approvals throughout the project lifecycle. The Estimator will be a subject matter expert on project estimation methodologies, including risk and contingency applications. Collaborate with Project Management, Engineering, Finance, Legal, Regulatory, and other stakeholders to plan, schedule, and manage the scope and cost aggregation process at each stage gate. Analyze cost estimates to ensure alignment with historical benchmarks and investigate discrepancies with estimators from functional groups. Manage documentation related to stage gate updates and regulatory submissions. Conduct peer reviews of project aggregations while working independently. Develop cost estimates for new Transmission & Distribution Substations, Substation Rebuilds/Expansions, Major Equipment Replacements, Protection Upgrades/SA3, and new Customer Substations. Prepare scope take-offs based on Design Specifications, Meeting Minutes/Scope of Work, and Electrical & Civil drawings. Estimate material and labor costs following industry standards for direct and indirect costs, utilizing Cost Estimating Tools such as SCMT and InEight. Engage cross-functional stakeholders to review cost estimates and secure necessary approvals. Perform detailed variance analysis of cost estimates throughout the project lifecycle and update estimates based on scope, cost, and schedule change requests.

Join our dynamic team as a Cost Control Analyst II at CRB Builders, LLC, where your analytical skills and attention to detail will play a crucial role in managing financial oversight across diverse projects. You will be responsible for developing and maintaining project labor and expense plans, utilizing advanced accounting and project management systems to forecast costs, and ensuring precise billing and financial reporting. The ideal candidate will partner closely with project teams to uphold cost control policies and enhance financial performance.Key ResponsibilitiesFormulate and oversee project labor and expense plans.Execute cost forecasting utilizing accounting and project management tools.Accurately process project and client billings in a timely manner.Conduct thorough financial reviews of assigned projects.Engage regularly with the cost control team, Project Directors/Managers, and field staff to reinforce financial procedures and ensure compliance with internal policies.