Quality Control Associate II, Controls

Capricor Therapeutics; San Diego (CA); On-site; USD 75,000 - 87,000; Full time

Job summary

A biotechnology company in San Diego is seeking a laboratory professional to support quality control (QC) analytical assays. The ideal candidate will have a Bachelor's in Biological Sciences and at least 2 years of experience in laboratory environments. Responsibilities include executing assays, maintaining control materials, and documenting laboratory work in compliance with GMP. The position offers a salary range of $75,000 - $87,000 annually, reflecting the company's commitment to advancing medical science and innovative therapies.

Qualifications

• 2+ years of laboratory experience in GMP-regulated environments.
• Hands-on experience performing analytical assays.
• Ability to communicate findings clearly.

Responsibilities

• Generate and maintain control materials for QC analytical assays.
• Execute analytical assays to support control evaluation.
• Document all laboratory work in GMP-compliant systems.

Skills

Laboratory experience

Analytical assays such as ELISA or PCR/qPCR

Data analysis

Time management skills

Strong organizational skills

Education

Bachelor’s degree in Biological Sciences or related discipline

Tools

Analytical instrumentation

Job description

Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.

Responsibilities

• Generate, prepare, and maintain positive and negative control materials used in QC analytical assays.
• Support the qualification and characterization of control materials to ensure suitability for routine QC testing.
• Execute analytical assays to support control evaluation, assay troubleshooting, and assay optimization studies.
• Perform laboratory activities related to control generation, characterization, and assay performance evaluation.
• Maintain inventory, traceability, and documentation of assay control materials used across QC testing programs.
• Analyze experimental data, summarize results, and document findings in accordance with GMP and data integrity requirements.
• Document all laboratory work in GMP-compliant systems including laboratory notebooks, controlled forms, and electronic records.
• Support preparation and maintenance of technical documentation including study protocols, reports, SOP updates, and control qualification records.
• Assist with investigations related to assay performance including deviations, OOS/OOT events, and atypical assay results.
• Collaborate with QC scientists and cross-functional teams including Analytical Development, Process Development, Manufacturing, and Quality to support assay readiness and continuous improvement initiatives.
• Manage multiple laboratory assignments and testing priorities to meet project timelines and QC operational needs.
• Perform additional QC duties as assigned.

Required Qualifications (Must‑Haves)

• Bachelor’s degree in Biological Sciences, Biochemistry, Molecular Biology, or a related discipline.
• 2+ years of laboratory experience in biotechnology, pharmaceutical, or GMP-regulated environments.
• Hands-on experience performing analytical assays such as ELISA, PCR/qPCR, flow cytometry, or other biochemical or cell-based assays.
• Experience preparing or maintaining assay controls or reference materials.
• Strong laboratory documentation practices and familiarity with GMP and data integrity expectations.
• Ability to analyze data and communicate findings clearly.
• Ability to work independently and manage multiple assignments in a laboratory environment.
• Strong organizational and time management skills.

Preferred Qualifications (Nice-to-Haves)

• Experience supporting analytical studies related to assay performance or assay optimization.
• Experience working with mammalian cell culture or cell-based assays.
• Experience supporting method qualification or assay performance monitoring activities.
• Experience supporting deviations, investigations, or technical reports in regulated environments.
• Experience working with cell therapy, biologics, or exosome-based products.

Work Environment & Physical Requirements

• Laboratory-based role requiring routine bench work.
• Work involves analytical instrumentation, laboratory documentation, and computer-based data analysis.
• Ability to lift up to 20 pounds.
• Occasional participation in cross-functional meetings and technical discussions.

$75,000 - $87,000 a year

Why Capricor?

Capricor Therapeutics, a trailblazer in cell and exosome therapy, is dedicated to redefining standards of care with innovative treatments rooted in scientific excellence. Guided by integrity and a passion for patient-centered impact, our team is shaping a brighter future for healthcare. Join us and contribute to a mission-driven group that’s transforming lives with every breakthrough.

Come Work With Us!

At Capricor, you’ll thrive in a collaborative environment that nurtures your professional growth and innovation. Join a dedicated team fueled by a passion for advancing medical science and transforming patient lives through our cutting-edge therapies.

Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by an official Capricor email address which is @capricor.com. Capricor will never ask potential employees to send a check or money to the Company for any reason.

Notice to Recruiting Agencies

Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.