Senior Talent Acquisition Specialist at Independent Solution | Hiring for Pharma & Biotech | Expert in Global Sourcing
Mode- Hybrid
Duration- 2 years
We are seeking a highly skilled Computer System Validation (CSV) Engineer to play a pivotal role in delivering complex capital projects supporting next-generation manufacturing operations.
This is a long-term contract opportunity (2 years) within a high-impact digital program, offering outstanding exposure to advanced automation systems, paperless validation, and global regulatory standards.
Role Overview:
You will lead Computer System Validation activities across major capital projects.
You will collaborate with Digital, Automation, IT, and Vendor teams, ensuring systems fully comply with regulatory, data integrity, and GAMP5 standards.
Key Responsibilities:
Act as the CSV Subject Matter Expert (SME) for capital project teams
Develop and maintain Qualification Plans, Test Plans, and validation strategies
Lead the preparation and control of all SDLC validation deliverables, including:
Requirements Specifications
Functional & Design Specifications
Requirements Traceability Matrices (RTM)
Test Specifications & Scripts
Ensure all deliverables comply with global quality and validation standards
Provide FAT oversight and leveraging assessments
Review and approve all SDLC documentation
Partner closely with Digital Data & Quality teams to ensure data integrity compliance
Support project schedules, validation trackers, and documentation control
Work directly with vendors, system integrators, and internal stakeholders
Represent CSV in automation, IT, and project meetings
Experience, Skills & Qualifications:
Mandatory:
Minimum 5 years' experience in CSV within Life Sciences / Pharmaceutical Manufacturing.
Expert knowledge of GAMP5.
Hands-on experience with Emerson Delta V (essential).
Strong experience across SDLC and validation lifecycle.
Proficient in MS Excel, Share Point, Word & Power Point
Degree in Computer Science, Engineering, or equivalent.
Highly Advantageous
Experience with DCS, Siemens PLC/SCADA, OSISoft PI, Werum PAS-X
Previous experience on large capital automation projects
Experience with paperless validation systems (e.g., Kneat)
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Research, Engineering, and Production
Industries: Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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