CSV Engineer II
Company: Capricor Therapeutics
Location: San Diego
Posted on: February 13, 2026
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Job Description:
Job Description 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. We are seeking a
meticulous and detail-oriented CSV (Computer System Validation)
Engineer to join our dynamic team. The CSV Engineer will be
responsible for ensuring that computerized systems used in the
biopharma industry comply with regulatory requirements. This
includes developing and executing validation protocols, documenting
processes, acting as the business system owner, and providing
technical expertise to ensure systems operate effectively and meet
industry standards. Responsibilities: Lead Data Process Flow
Mapping activities to ensure all GMP systems are compliant with 21
CFR Part 11 regulations in preparation for BLA and PLI. Ensure
Computer System Operation and Administration SOPs are developed for
all applicable GMP systems in preparation for PLI. Lead and assist
in Packaging and Label Validation activities. Develop and execute
validation protocols (IQ, OQ, PQ) for computerized systems to
ensure compliance with regulatory requirements (e.g., FDA, GMP).
Perform risk assessments and impact analyses related to system
changes or updates. Collaborate with cross-functional teams to
define user requirements and specifications for computer systems.
Write and review technical documentation, including validation
plans, test scripts, and summary reports. Conduct testing and
document results to ensure systems meet functional and performance
requirements. Provide technical support and guidance to project
teams throughout the system lifecycle. Stay informed about industry
trends and regulatory changes to ensure compliance. Participate in
audits and inspections, responding to findings and implementing
corrective actions as needed. Support continuous improvement
initiatives related to CSV processes and procedures. Other
responsibilities as assigned related to computer system validation
Requirements: Bachelor’s degree in Computer Science, Engineering,
or a related field. Prove experience (2 years) in CSV within a
regulated industry (pharmaceuticals, medical devices, etc.).
In-depth knowledge of FDA regulations (21 CFR Part 11, Part
210/211) and GMP guidelines. Strong understanding of validation
principles, methodologies, and best practices. Experience with
validation tools and documentation systems (e.g., Document
Management Systems, LIMS). Excellent analytical and problem-solving
skills, with keen attention to detail. Effective communication
skills, both verbal and written, with the ability to convey
technical information clearly. Ability to work both independently
and collaboratively in a team environment. Relevant certifications
(e.g., Certified Validation Professional) preferred. 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. Please note that 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. Additionally, 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.
Keywords: Capricor Therapeutics, Costa Mesa , CSV Engineer II, Engineering , San Diego, California