Process Development Scientist

Capricor; San Diego (CA); On-site; USD 90,000 - 120,000; Full time

Job summary

Capricor is seeking a Process Development Scientist to enhance biomanufacturing processes for cell and exosome therapies. This role requires leading cross-functional projects, mentoring junior scientists, and optimizing production techniques.

The ideal candidate will have a Ph.D. or MS with extensive experience in cell biology, particularly in large scale adherent cell culture. Join Capricor to contribute to transformative therapies for rare diseases and be part of a mission-driven team dedicated to patient impact.

Qualifications

• Ph.D. required with 2+ years or MS with 7+ years of experience.
• Hands-on experience in large scale adherent cell culture.
• Experience in designing closed systems for automated processes.

Responsibilities

• Lead development of biomanufacturing processes to enhance product yield.
• Design and execute scientific research projects.
• Mentor junior team members in project priorities and expertise.
• Collaborate with teams to translate research into validated processes.

Skills

Aseptic techniques

Mammalian cell and tissue culture

Managing junior scientists

Collaborating with cross-functional teams

Designing closed systems

Excellent communication skills

Education

Ph.D. in Cell Biology, Biotechnology, or Bioengineering

MS in Cell Biology, Biotechnology, or Bioengineering

Tools

Automated cell processing 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.

The Process Development Scientist at Capricor will lead development of biomanufacturing processes to enhance product yield, quality, and cost‑efficiency with a focus on closed system processes and scale‑up. This role is responsible for driving process improvements, evaluating new technologies, mentoring junior team members, and collaborating with cross‑functional teams to translate discoveries into validated processes.

Responsibilities

• Lead development and optimization of closed‑system cell culture processes with a focus on adherent cell production.
• Design, execution, and interpretation of complex scientific research projects.
• Develop processes to address manufacturing challenges and advance product development.
• Lead and mentor a small project team providing guidance on priorities and technical expertise to ensure deadlines are met.
• Manage scientific aspects of cross‑functional teams, ensuring alignment with organizational goals.
• Contribute to intellectual property, publications, patents, and present findings at internal meetings as needed.
• Collaborate with MSAT, manufacturing, quality and regulatory teams to translate research into actionable plans.
• Perform other duties as assigned to support process development objectives.

Qualifications

• Ph.D. in Cell Biology, Biotechnology, Bioengineering, or a related field with 2+ years of relevant experience or MS in Cell Biology, Biotechnology, Bioengineering, or a related field with 7+ years of relevant experience.
• Hands on experience in aseptic techniques including mammalian cell and tissue culture with a focus on large scale adherent cell culture.
• Demonstrated experience designing closed systems and using automated cell processing instrumentation.
• Experience managing junior scientists and collaborating with cross‑functional teams.
• Excellent communication and interpersonal skills with the ability to work collaboratively within a team environment.
• Previous experience authoring or reviewing CMC sections of regulatory submissions preferred.
• Familiarity with regulatory requirements for cell therapy products.

Physical or Workplace Requirements

• Primarily laboratory‑based, may require time in GMP spaces to aid technology transfers and troubleshooting.
• Requires prolonged periods of computer use for data analysis, documentation, and reporting.
• May involve lifting laboratory materials or equipment up to 50 pounds.
• Ability to navigate laboratory and GMP environments for experiments and coordination.

Why Capricor?

Capricor Therapeutics is advancing cell and exosome-based therapies with a focus on serious diseases where patients and families need new treatment options. Our work is grounded in scientific rigor, collaboration, and a shared commitment to moving meaningful therapies forward. Joining Capricor means being part of a mission‑driven team working at the intersection of innovation, execution, and patient impact.

Come Work With Us

At Capricor, you’ll join a collaborative environment where employees are encouraged to contribute, grow, and help build the systems, science, and operations needed to support our next stage of growth. We value people who are thoughtful, accountable, hands‑on, and motivated by work that can make a real difference.