What are the responsibilities and job description for the Process Development Associate 2/3 position at Capricor Inc?
About Capricor Therapeutics
Capricor Therapeutics, Inc. (NASDAQ: CAPR) is a cutting-edge biotech company based in San Diego, CA, focused on the discovery and development of novel cell and exosome-based therapeutics for the treatment and prevention of various diseases and disorders. Our lead product candidate, allogeneic Cardiosphere-Derived Cells (CDCs), known as deramiocel, is under investigation as a treatment for Duchenne muscular dystrophy and COVID-19. We are also advancing our exosome platform technology for several indications, including a novel COVID-19 vaccination approach. Capricor offers exciting opportunities and invites qualified professionals to join our expanding team. We offer competitive compensation and benefits packages.
Position Overview: Process Development Associate
The Process Development Associate will play a key role in advancing Capricor’s biomanufacturing efforts by evaluating, improving, and scaling processes for therapeutic production. This position focuses on optimizing product yield, reducing costs, and ensuring scalability—from small experimental batches to large-scale manufacturing—while maintaining quality and efficiency. Reporting to the Process Development Director or Associate Scientist, the associate will collaborate with cross-functional teams to support the production of cell -based therapeutics, troubleshoot challenges, and implement innovative solutions. This role is ideal for a hands-on, detail-oriented professional eager to contribute to cutting-edge biotech advancements.
Responsibilities:
• Evaluate and improve biomanufacturing processes to enhance product yield and reduce overall production costs.
• Scale up cell and tissue culture processes for larger batches of materials and work on small batches as needed, adapting techniques to meet increasing production demands.
• Evaluate impact of new equipment and processes on production yield and potency.
• Assist in characterization of product for identity, purity and potency to ensure quality standards are met.
• Troubleshoot and resolve problems associated with different phases of full-scale biomanufacturing production.
• Participate in researching, developing, and implementing new methods and technologies to improve production processes.
• Collaborate with team members to document findings, maintain accurate records, and support process development goals.
Requirements:
Education: Bachelor’s degree in a scientific discipline (e.g., biology, biotechnology, or related field) required
Experience: Minimum of 2-4 years (or 0-2 with a Master’s degree) in a research laboratory, process development, or biomanufacturing environment.
Technical Expertise: Proven skills in cell and tissue culture, with experience troubleshooting biomanufacturing challenges. Tissue dissection experience preferred but not required.
Process Improvement: Demonstrated ability to evaluate and enhance biomanufacturing processes, improving yield or reducing costs.
Aseptic Handling: Familiarity with aseptic processes and maintaining contamination-free environments.
Equipment Maintenance: Hands-on experience assisting with production equipment upkeep and basic operational troubleshooting.
Assay Development: Practical knowledge of flow cytometry, RNA isolation, qRT-PCR and other basic molecular biology techniques .
Closed System (Preferred): Experience with closed systems for biomanufacturing in a process development setting is a plus.
Collaboration: Ability to work effectively with cross-functional teams to support process development goals.
Work Arrangement: Onsite role in San Diego, CA, with occasional flexibility based on project needs.
Work Environment and Physical Demands:
• Professional lab and office environment.
• Ability to stand or sit for extended periods while working with lab equipment or computers.
• May require occasional lifting of materials or equipment up to 50 pounds.
• Ability to work in a laboratory environment adhering to safety and contamination protocols.
Why Capricor?
Capricor Therapeutics is an industry leader in cell and exosome therapy, pushing boundaries to create innovative treatments that raise the standard of care. Grounded in integrity and driven by science, our team is committed to making a meaningful impact through patient-centered innovation. Join us and be part of a team that’s changing lives—help us shape the future of healthcare.
Compensation (USD):
• Salary Range: Competitive, based on experience and education level.
• Comprehensive benefits package, including health insurance, retirement plans, and opportunities for professional development.
Come work with us!
At Capricor, we offer a collaborative work environment that supports your professional growth. Join a passionate team committed to transforming the lives of patients and pushing the boundaries of medical science.
