Senior QA Analyst – GMP & Validation Leader

Johnson & Johnson Co.; Netherlands; Presencial; EUR 64 000 - 103 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Annual bonus

Vacation days

Parental leave

Bereavement leave

Caregiver leave

Volunteer leave

Well-being reimbursement

Health programs

Resumo da oferta

Johnson & Johnson is seeking a Senior QA Analyst – Technical QA to join our Quality Assurance team in Leiden, Netherlands. You will oversee qualification and validation lifecycles for equipment, systems, and facilities within pilot plant and QC labs, ensuring GMP compliance and a strong quality mindset across functions.

You will review validation deliverables, support CAPA activities, and collaborate with Manufacturing, Facilities, Engineering, Validation, QC and IT to implement compliant GMP

Qualificações

• Experience in QA oversight for qualification/validation lifecycles.
• Strong understanding of GMP requirements and quality systems.
• Ability to lead investigations, CAPA, change controls and risk assessments.

Responsabilidades

• Provide QA oversight for qualification, validation lifecycle of equipment, systems and facilities.
• Review and approve validation deliverables (IQ/OQ/PQ) and reports.
• Ensure GMP compliance through QA support of events, investigations and CAPA.
• Serve as QA representative on cross-functional teams and drive site-wide quality initiatives.
• Collaborate with Manufacturing, Facilities, Engineering, QC and IT to implement compliant GMP systems.
• Support audit readiness and regulatory inspections; identify process improvements.

Conhecimentos

Quality Assurance

Regulatory Compliance

Risk Assessment

CAPA

GMP

Validation

Cross-functional Collaboration

Descrição da oferta de emprego

Johnson & Johnson is seeking a Senior QA Analyst – Technical QA to join our Quality Assurance team in Leiden, Netherlands. You will oversee qualification and validation lifecycles for equipment, systems, and facilities within pilot plant and QC labs, ensuring GMP compliance and a strong quality mindset across functions.

You will review validation deliverables, support CAPA activities, and collaborate with Manufacturing, Facilities, Engineering, Validation, QC and IT to implement compliant GMP