CSV Engineer II
About The Position
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.
Requirements
- Bachelorâs 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.
Nice To Haves
- Relevant certifications (e.g., Certified Validation Professional) preferred.
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
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
101-250 employees
