CSV Automation Lead – GMP Systems (12-Month Contract)

7266-Janssen Biologics B.V. Legal Entity; Amsterdam; On-site; EUR 54,000 - 85,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Well-being reimbursement

Insurance plans

Awards program

Job summary

Johnson & Johnson is seeking an Automation CSV Lead to drive validation across capital projects and daily operations, ensuring compliance with GAMP 5, DI, and industry standards. You will coach engineers and collaborate with engineering, quality, IT, and project teams to deliver validated, inspection-ready systems.

The role focuses on risk-based validation, lifecycle governance, and cross-functional execution within a GMP environment, starting with a 12-month contract and aiming for permanent

Qualifications

• 5+ years of experience in a GMP-regulated pharmaceutical, biotechnology, or medical device environment, including hands-on qualification and CSV work.

Responsibilities

• Lead CSV and qualification across the full system lifecycle from implementation and upgrades to periodic review and retirement.

Skills

Analytical reasoning

AI

Machine Learning

Cross‑Functional collaboration

Project management

Robotic Automation

Systems Development

Testing

Education

Bachelor's or Master's degree in Engineering, Automation, Computer Science, Information Technology, Life Sciences, or related discipline

Tools

DeltaV

PLC

SCADA

MES

Job description

Johnson & Johnson is seeking an Automation CSV Lead to drive validation across capital projects and daily operations, ensuring compliance with GAMP 5, DI, and industry standards. You will coach engineers and collaborate with engineering, quality, IT, and project teams to deliver validated, inspection-ready systems.

The role focuses on risk-based validation, lifecycle governance, and cross-functional execution within a GMP environment, starting with a 12-month contract and aiming for permanent