QA Associate - Delegate Qualified Person (Belgium)

Johnson & Johnson Co.; Geel; On-site; EUR 60,000 - 96,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being reimbursement

Job summary

Johnson & Johnson in Belgium seeks a Quality Assurance Associate – Delegate Qualified Person to support release of clinical trial materials and ensure GMP/GDP compliance across global clinical supply chains. You will gain experience in QA, regulatory inspections, and QP responsibilities in a dynamic environment.

Proven ability to work with cross-functional teams, coupled with a university-level QA/Pharma background and EU QP status in Belgium, will help you contribute to timely, compliant

Qualifications

• Requires EU-certified Qualified Person residing in Belgium.
• Experience in pharmaceutical quality assurance or related environment is an advantage.
• Willingness to learn, take responsibility and apply quality requirements to decisions.

Responsibilities

• Connect with Clinical Supply Chain teams and global quality partners to gather information for release and QP certification.
• Support quality from the start by working with cross-functional teams and ensuring quality requirements in trial execution.
• Release of clinical trial materials by reviewing batch information and performing release activities.
• Progress toward broader Delegate QP responsibilities with experience.
• Apply GMP, GDP and trial requirements; guide operating teams accordingly.
• Assist with investigations of deviations, CAPAs, and risk mitigation with guidance from colleagues.
• Support audits and inspections readiness and maintain documentation.

Skills

Quality Assurance

Quality Standards

Data Analysis

Problem Solving

Compliance Management

Quality Management Systems

Internal Controls

Education

Industrial Pharmacist degree

Job description

Johnson & Johnson in Belgium seeks a Quality Assurance Associate – Delegate Qualified Person to support release of clinical trial materials and ensure GMP/GDP compliance across global clinical supply chains. You will gain experience in QA, regulatory inspections, and QP responsibilities in a dynamic environment.

Proven ability to work with cross-functional teams, coupled with a university-level QA/Pharma background and EU QP status in Belgium, will help you contribute to timely, compliant