CSV Engineer

Posted 18 Days Ago
Be an Early Applicant
Haarlem, NLD
In-Office
Mid level
Consulting • Automation
The Role
Provides Computer System Validation leadership for pharmaceutical capital projects. Develops, reviews, and approves validation, qualification, SDLC, testing, and requirements documentation; coordinates with Automation, IT, Quality, Engineering, vendors, and system integrators; ensures GAMP5, GMP, data integrity, and regulatory compliance; supports FAT, audits, inspections, project planning, stakeholder communication, validation execution, and project closeout.
Summary Generated by Built In
Engagement Summary
    • Objective: Provide Computer System Validation (CSV) leadership and support for capital projects, ensuring all automated and computerized systems are implemented, qualified, and validated in compliance with quality standards, GAMP5, SDLC methodology, and applicable regulatory requirements.
    • Engagement Type: Time-and-materials
Scope and Core Responsibilities

·         Serve as the Computer System Validation (CSV) Subject Matter Expert (SME) for capital projects.

·          Provide a standardized CSV approach across projects in alignment with the CSV Lead's validation strategy.

·          Work closely with Automation, IT, Quality, Engineering, and teams responsible for system delivery and implementation.

·         Collaborate with vendors, suppliers, and system integrators to ensure compliance with validation and quality requirements.

·          Develop and maintain Qualification Plans, Validation Plans, and Test Plans aligned with project Commissioning & Qualification (C&Q) strategies.

·          Develop, review, and approve Software Development Lifecycle (SDLC) deliverables, including:

ü  Requirements Specifications

ü  Functional Specifications

ü  Design Specifications

ü  Requirements Traceability Matrices (RTM)

ü  Code Review Documentation

ü  Test Specifications and Test Scripts

ü  Validation Summary Reports

ü  Other qualification and validation documentation as required

 

·          Ensure all CSV deliverables comply with quality procedures, GAMP5 guidance, SDLC requirements, and applicable regulatory standards.

·         Partner with Digital Data & Quality (DDQ) teams to ensure all data integrity and compliance requirements are addressed.

·          Review vendor documentation and validation packages to confirm compliance with standards and leveraging requirements.

·         Provide Factory Acceptance Testing (FAT) oversight and perform validation leveraging assessments.

·         Support project teams with CSV guidance, document generation, review, and execution activities.

·         Participate in project planning activities and provide input into realistic project schedules and validation trackers.

·         Represent the CSV function at project, automation, IT, quality, and stakeholder meetings.

·         Facilitate communication between project stakeholders regarding validation strategy, documentation, testing, and compliance requirements.

·         Support regulatory inspections, audits, and quality reviews as required.

Deliverables

·         Computer System Validation Plans (CSV Plans)

·         Qualification Plans and Test Plans

·         Requirements Specifications (URS/RS)

·         Functional Specifications (FS)

·         Design Specifications (DS)

·         Requirements Traceability Matrices (RTM)

·         Code Review Documentation

·         Test Specifications and Test Scripts

·         Validation Summary Reports

·         FAT Oversight Documentation and Leveraging Assessments

·         Vendor Compliance Review Reports

·         SDLC Templates and Validation Documentation Standards

·         Qualification and Validation Execution Records

·         Validation Schedules and Document Trackers

·         Risk Assessments and Compliance Assessments

·         Audit and Inspection Support Documentation

·         Project Status Reports and Stakeholder Updates

·          Final Validation Approval and Project Closeout Documentation

 

Required Qualifications and Competencies

·          Bachelor's Degree in Computer Science, Engineering, Automation, Information Technology, or related discipline.

·         Minimum 3 years of Computer System Validation experience within Life Sciences or Pharmaceutical Manufacturing.

·         Expert knowledge of GAMP5 validation methodology.

·         Strong understanding of SDLC processes and validation lifecycle requirements.

·         Experience developing and executing validation documentation within GMP-regulated environments.

·         Demonstrated experience reviewing and approving validation deliverables.

·         Experience working with vendors and system integrators on regulated projects.

·         Strong stakeholder management, communication, and technical writing skills.

·          Ability to operate effectively within cross-functional project teams.



Skills Required

  • Bachelor's degree in Computer Science, Engineering, Automation, Information Technology, or a related discipline
  • Minimum 3 years of Computer System Validation experience within Life Sciences or pharmaceutical manufacturing
  • Expert knowledge of GAMP5 validation methodology
  • Strong understanding of SDLC processes and validation lifecycle requirements
  • Experience developing and executing validation documentation within GMP-regulated environments
  • Experience reviewing and approving validation deliverables
  • Experience working with vendors and system integrators on regulated projects
  • Strong stakeholder management, communication, and technical writing skills
  • Ability to operate effectively within cross-functional project teams
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The Company
HQ: Plymouth Meeting, PA
72 Employees
Year Founded: 2005

What We Do

Horizon Controls Group: A global leader in automation consulting, enabling both clients and employees to live on the forefront of evolving technology. Horizon Controls Group is a modern, global technology company, specializing in automation consulting, engineering, and training. Founded on the belief that our people are the difference​, we have grown entirely from customer references and successive projects. Our people and their established reputation are our most valued assets. This belief has created a great place to work, enabling us to attract the very best and to give our customers confidence in our superior solutions. Our business is comprised of excellence at every level. We employ a pro-active and comprehensive approach to projects -- asking the right questions, analyzing client needs, and engineering a skilled solution. We are committed to understanding the entire spectrum of your automation challenges and to developing uniquely tailored innovative solutions. Our decision to be vendor-independent enables us to offer tailored solutions and represent your needs free of any conflict of interest. We are aligned exclusively with our customers'​ goals and system requirements, enabling us to provide maximum value. Ultimately, the ability to harvest maximum value from new systems is dependent on the quality and training of your people. Just as we expect and ensure absolute expertise in our people, we work with you to ensure your team is trained to the specific needs of your organization and remain at the forefront of industry trends. We are a global company operating in the United States from our headquarters in Blue Bell, PA and offices in Indiana, Massachusetts, North Carolina, and California and from Cork in Ireland. This is Horizon Controls Group’s official company LinkedIn page.

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