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Validation Engineer
San Francisco, CA

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Katalyst Healthcares and Lifesciences

CSV Engineer

Pay: Not specified
Posted: 5 days ago
Location: San Francisco, CA (Onsite)
Last Updated: 1 day ago
Hours: Full-Time
Expires: 11/5/2026
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Job Description

Roles & Responsibilities:
Develop and implement validation strategies for computer systems and software applications. Create and maintain validation documentation, including Validation Plans, Protocols (IQ/OQ/PQ), and Validation Reports. Perform risk assessments to identify potential issues and ensure compliance with regulatory requirements. Collaborate with cross-functional teams, including IT, Quality Assurance, and Operations, to ensure successful validation of systems. Conduct validation testing and review test results to ensure systems meet specified requirements. Provide training and support to staff on validation processes and procedures. Stay up-to-date with industry trends and regulatory changes to ensure ongoing compliance. Participate in audits and inspections by regulatory agencies. Execute Validation Project Plans (VPPs) for manufacturing GxP systems such as, Client, EMS, & PCS. Support the execution of VPPs to qualify systems for GMP Manufacturing Equipment in accordance with Software Development Lifecycle (SDLC) procedures as per GAMP5 industry standards ssist site Automation groups in configuring I/O and executing CSV protocol requirements. Independently perform CSV lifecycle deliverables, including but not limited to, Functional Requirements Specification (FRS), Configuration Specification (CS), Electronic Records and Electronic Signatures (ERES), Risk Assessment (RA), Data Integrity (DI)
Assessment, IQ/OQ/PQ, & Summary Report Requirements:
Bachelor's degree in Computer Science, Engineering, or a related field. Minimum of 2-5 years of experience in computer system validation or a related field. Strong knowledge of regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GAMP 5). Experience with validation of various types of systems, including ERP, LIMS, and MES. Excellent documentation and technical writing skills. Strong analytical and problem-solving abilities. bility to work independently and as part of a team. Excellent communication and interpersonal skills.
Preferred:
Certification in Computer System Validation or related areas. Experience with cloud-based systems and software validation, experience with Blue Mountain RAM. 3+ years of work experience with Computer System Validation. 3+ years of Biotechnology Research experience.