Automation Specialist: QC Lab Systems & Compliance

Biopharma Careers; Leiden; Remote; EUR 45,000 - 71,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave (12 weeks)

Well-being reimbursement

Health insurance

Job summary

Johnson & Johnson Innovative Medicine seeks an Automation Specialist to support QC laboratories, lead automation projects, and maintain computerized systems ensuring data integrity and GMP compliance. You will drive LEAN improvements across the team and collaborate with multiple departments to ensure product quality.

The role requires a strong background in life sciences, GMP, and software validation, with good English and Dutch language skills preferred. Leiden-based, full-time position.

Qualifications

• Bachelor’s degree in Life Sciences or equivalent with strong GMP knowledge.
• Experience with validated computerized systems in a GxP environment is required.
• 2+ years in pharma QA/QC or automation roles is preferred.

Responsibilities

• Lead the technical implementation of new laboratory systems with cross-functional teams.
• Create and maintain installation, validation, and maintenance procedures.
• Provide timely support and troubleshoot issues involving computerized systems.
• Ensure compliance with 21 CFR Part 11 requirements for all systems.
• Drive investigations into non-conformances involving systems and materials.
• Coordinate corrections and preventive actions with follow-up validation.

Skills

Analytical Reasoning

Data Analysis

Compliance Management

Continuous Improvement

Quality Control (QC)

Quality Standards

ISO 9001

Lab Automation

Education

Bachelor’s degree (HBO) in Life Sciences or equivalent

Tools

Computerized system validation tools

Job description

Johnson & Johnson Innovative Medicine seeks an Automation Specialist to support QC laboratories, lead automation projects, and maintain computerized systems ensuring data integrity and GMP compliance. You will drive LEAN improvements across the team and collaborate with multiple departments to ensure product quality.

The role requires a strong background in life sciences, GMP, and software validation, with good English and Dutch language skills preferred. Leiden-based, full-time position.