CSV Engineer: GMP Validation & Compliance

Katalyst CRO; Woburn (MA); Presencial; USD 90.000 - 130.000; Jornada completa

Descripción de la vacante

Katalyst CRO is seeking a Computer System Validation (CSV) Engineer with experience in CSV within a GMP-regulated pharmaceutical or biotechnology environment. The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance.

Develop, execute, and maintain CSV documentation and validation protocols for QC laboratory systems

Formación

• Bachelor's degree in engineering, CS, life sciences, pharmacy, or biotech.
• Experience in CSV within GMP pharma/biotech environment.
• Strong knowledge of GAMP 5 and 21 CFR Part 11.
• Hands-on validation of QC laboratory and manufacturing systems.
• Excellent writing, communication and problem-solving skills.

Responsabilidades

• Develop, execute, and maintain CSV documentation and validation protocols for QC laboratory systems and manufacturing systems.
• Support the complete validation lifecycle: URS, IQ, OQ, PQ, risk assessments, and validation reports.
• Perform risk assessments to identify and mitigate validation and compliance risks.
• Ensure compliance with GAMP 5, 21 CFR Part 11, GMP, and internal quality standards.
• Review validation documentation for accuracy, completeness, and regulatory compliance.
• Collaborate with QA, Manufacturing, Engineering, and IT teams to support validation activities and system implementations.
• Provide validation support for QC laboratory systems and manufacturing equipment throughout their lifecycle.
• Assist with change control, deviation investigations, and periodic reviews related to validated systems.
• Maintain accurate validation records and ensure documentation is audit ready.
• Support internal and external regulatory inspections by providing validation documentation and technical expertise.

Conocimientos

CSV lifecycle understanding

Technical writing

Regulatory compliance

Cross-functional collaboration

Risk assessment

Educación

Bachelor's degree in engineering or related field

Herramientas

URS/IQ/OQ/PQ templates

Validation protocols

Descripción del empleo

Katalyst CRO is seeking a Computer System Validation (CSV) Engineer with experience in CSV within a GMP-regulated pharmaceutical or biotechnology environment. The ideal candidate will have expertise in GAMP 5, 21 CFR Part 11, validation lifecycle documentation, and QC laboratory or manufacturing systems validation, while collaborating with cross-functional teams to ensure regulatory compliance.

Develop, execute, and maintain CSV documentation and validation protocols for QC laboratory systems