Senior Automation CSV Engineer

Biopharma Careers; Leiden; Remote; EUR 54,000 - 85,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave (min 12 weeks)

Well-being programs

Job summary

Johnson & Johnson Leiden seeks a Senior Automation CSV Engineer to lead validation across the full system lifecycle for automation, digital, and GMP-relevant systems. You will define risk-based validation strategies, implement DI-aligned CSV workflows, and coach engineers while coordinating with cross-functional teams.

The role starts with a 12-month contract with intent to convert to permanent, working closely with Engineering, Quality, Manufacturing, IT, and project teams to meet regulatory

Qualifications

• Bachelor's or master's degree in Engineering, Automation, Computer Science, Information Technology, Life Sciences, or related discipline.
• 5+ years in a GMP-regulated pharmaceutical/biotechnology environment with hands-on CSV work.
• Strong knowledge of cGMP, GAMP 5, DI expectations, ALCOA+, EU GMP Annex 11, and 21 CFR Part 11.

Responsibilities

• Lead CSV and qualification across the full system lifecycle, from implementation to retirement.
• Define risk-based validation strategies in line with GAMP 5 and develop, review, and approve validation deliverables.
• Integrate Data Integrity standards into CSV workflows and deliverables with the Data Integrity Lead.
• Support lifecycle governance for automation systems, including OT cybersecurity and patching under change control.
• Coach validation engineers and act as a main contact for inspections and regulatory interactions.

Skills

Analytical reasoning

Cross-functional collaboration

Project management

Problem solving

Education

Bachelor's or Master's degree in Engineering

Tools

DeltaV

PLC

SCADA

MES

Job description

# Senior Automation CSV EngineerLeiden, Netherlands Full timeManufacturing & CMC SeniorNotify me about similar jobsView Full Job & Apply at Johnson & JohnsonJohnson & Johnson is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.## About this opportunityAt Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com .As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.**Job Function:**Supply Chain Engineering**Job Sub Function:**Automation Engineering**Job Category:**Scientific/Technology**All Job Posting Locations:**Leiden, South Holland, Netherlands**Job Description:**We offer an initial 12-month contract with the intention to convert to a permanent contract.**About Innovative Medicine**Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.Learn more at https://www.jnj.com/innovative-medicine**We are searching for the best talent for Computerized System Validation (CSV) Execution Lead.****Purpose:** The CSV Execution Lead leads validation and qualification activities for automation, digital, and GMP-relevant systems across capital projects and day-to-day operations. The scope covers modernized and legacy manufacturing equipment, laboratory equipment, utilities, facilities, infrastructure, and computerized systems. The work spans new implementations, upgrades, re-qualifications, lifecycle changes, periodic reviews, and inspection preparation.As the Automation SME for CSV, this person plans, coordinates, and delivers validation work. They also coach validation engineers and act as a core or extended team member on projects. The role works closely with Engineering, Quality, Manufacturing, C&Q, IT, and project teams. Together, they make sure systems are delivered and maintained in line with company standards, regulatory requirements, and industry best practice.**You will be responsible for:**Leading CSV and qualification across the full system lifecycle, from implementation and upgrades through periodic review and retirement.Defining risk-based validation strategies in line with GAMP 5, and developing, reviewing, and approving validation deliverables.Integrating Data Integrity (DI) standards into CSV workflows, templates, and deliverables in partnership with the Data Integrity Lead, including supporting remediation of legacy systems.Supporting lifecycle governance for automation systems, including the system inventory, configuration management, periodic reviews, and OT cybersecurity and patching under change control.Leading change impact assessments, deviation investigations, and CAPAs for validated systems.Keeping validation documentation inspection-ready, and acting as a main contact for validation topics during regulatory and third-party inspections.Managing CSV scope, estimates, resources, and workload across projects, and maintaining the CSV work catalogue to drive standardization.Partnering cross-functionally and coaching validation engineers on CSV and compliance, in line with the Johnson & Johnson Credo and Leadership Imperatives.**Qualifications / Requirements:**Required:Bachelor's or Master's degree in Engineering, Automation, Computer Science, Information Technology, Life Sciences, or a related discipline.5+ years of experience in a GMP-regulated pharmaceutical, biotechnology, or medical device environment, including hands-on qualification and CSV work.Strong knowledge of cGMP, validation lifecycle principles, GAMP 5, DI expectations, ALCOA+, EU GMP Annex 11, and 21 CFR Part 11.Experience with GMP-relevant manufacturing, laboratory, or facility systems such as DeltaV, PLC, SCADA, and MES, including their interfaces, electronic records, and data flows.Proven ability to develop, review, and approve qualification and validation documentation, including user requirements, risk assessments, protocols, reports, traceability, deviations, CAPAs, and change controls.Proven ability to lead validation work across several projects at once and to coordinate cross-functional stakeholders and external suppliers.Strong analytical, risk-based, problem-solving, and root cause analysis skills, with the ability to make sound and defensible decisions.Excellent communication, technical writing, and stakeholder management skills in a cross-functional, international environment, including engaging with leadership and inspectors.Experience coaching, mentoring, and developing technical team members.Strong organizational, planning, and prioritization skills, with the ability to manage competing demands while meeting compliance and delivery commitments.Fluent written and spoken English.Preferred:Experience supporting audits and regulatory inspections.Knowledge of OT cybersecurity practices, such as ISA/IEC 62443.**Required Skills:****Preferred Skills:**Analytical Reasoning, Artificial Intelligence (AI), Controls Compliance, Cross-Functional Collaboration, Industry Analysis, Innovation, Lean Supply Chain Management, Machine Learning (ML), Project Management, Prototyping, Robotic Automation, Science, Technology, Engineering, and Math (STEM) Application, Scope Management, Systems Development, Technologically Savvy, Testing**The anticipated base pay range for this position is:**€53.500,00 - €85.445,00**Benefits:**In addition to base pay, we offer the following benefits\\*: an annual bonus with set target (% of pay) depending on pay grade / location, where the actual amount is based on the employees’ and companies’ performance of the previous calendar year, or sales commissions. Moreover, we offer vacation days, parental leave for a minimum of 12 weeks, bereavement leave, caregiver leave, volunteer leave, well-being reimbursement, programs for financial, physical and mental health. We also offer service anniversary and recognition awards, and subject to the terms of their respective plans, employees - and in some location’s eligible dependents - can participate in several insurance plans. For more information, visit Employee benefits | Supporting well-being & career growth | Johnson & Johnson Careers.\\*This is for informative purposes only. Amounts and actual benefits may vary by location and are subject to change.