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This role is an individual contributor working cross-functionally to lead and execute validation activities for GxP electronic systems and applications. · ...

The Computer Systems Validation (CSV) Contractor works cross-functionally to lead and execute validation activities for GxP electronic systems and applications. · Author, review and/or approve applicable CSV documentation · Assist Business Owners and Technical Owners during test ...

Lead and oversee multiple quality and validation projects ensuring clear communication of goals timelines and key milestones. Ensure all validation activities and documentation adhere to industry best practices and regulatory requirements. · ...

Seeking a CSV Engineer with hands-on experience in Computer System Validation and Commissioning, Qualification, and Validation (CQV) to support GMP-regulated pharmaceutical or biotech operations. · ...

We are seeking a CSV engineer to join our team for a Windows 11 upgrade. · Lead CSV activities related to the Windows 11 operating system upgrade across GxP-impacted systems and applications. · ...

Piper Companies seeks an CSV Consultant for a contract supporting high-tech automated systems across GMP operations. · Troubleshoot manufacturing equipment controlled by PLC and SCADA systems. · Maintain and support automation lifecycle development. · Author and execute CSV deliv ...

We are recruiting a CSV Lead to join a leading Pharmaceutical company in Belgium.As the CSV Lead you will have the chance to ensure compliance and continuous improvement within GxP environment. · ...

CSV engineer for validation of labelling systems. Net2Source is an employer-of-choice for over 1000 consultants across the globe. · ...

This quality engineer role involves computer system validation (CSV) and reviewing lifecycle documents to ensure alignment with GAMP 5 and data integrity principles. · Review and approve CSV lifecycle documents. · Evaluate system changes through change control. · Support periodic ...

We are seeking Computer System Validation (CSV) Engineers with a strong focus on equipment-level validation. · The role supports validation activities for manufacturing and process control equipment. · ...

The client is looking for a resource to cover UATs, periodic review, and provide a validation summary prior to roll out of the new systems. · ...

We are seeking a CSV Engineer with hands-on experience in Computer System Validation and Commissioning, Qualification, and Validation (CQV) to support GMP-regulated pharmaceutical or biotech operations across multiple sites. · ...

As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. · Provi ...

Job Summary · CSV Engineer to support commissioning and validation activities for a newly built Cell & Gene Therapy R&D and manufacturing facility in Pittsburgh, PA. · The role focuses on reviewing validation deliverables, ensuring compliance with regulatory standards (21 CFR Pa ...

A specialized Medical Device client in Ohio is in immediate need of a Computer System Validation Engineer for a 4-6 month project. · ...

Supporting commissioning activities for a new life sciences manufacturing facility. · Reviewing and executing validation activities for manufacturing and automation systems in a GMP environment. · ...

The CSV Specialist will be responsible for managing and executing all activities related to Computer System Validation (CSV) throughout the full validation lifecycle. · Bachelor's Degree in engineering, Computer Science, or a related scientific discipline. · Minimum of 5 years of ...

The CSV Engineer will play a critical role in ensuring that all computerized systems used in the manufacturing and quality systems of medical devices are validated according to applicable regulations such as FDA 21 CFR Part 11 EU Annex 11 and ISO This role ensures the systems are ...

The CSV Engineer will be responsible for validating Windchill and Product Lifecycle Management (PLM) systems. · Validate Windchill and Product Lifecycle Management (PLM) systems in regulated environments. · Write review execute validation documentation including requirements comp ...

+We are seeking Computer System Validation (CSV) Engineers with a strong focus on equipment-level validation. · +Hands-on experience in equipment CSV · Strong understanding of GxP regulations, FDA 21 CFR Part 11, and validation best practices · ...

A specialized Medical Device client in Ohio needs a Computer System Validation Engineer for 4-6 months project onsite in Cincinnati area. · ...