Qualified Person Delegate - Global Clinical Quality Lead

Johnson & Johnson Co.; Beerse; On-site; EUR 73,000 - 115,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Parental leave

Bereavement leave

Well-being reimbursement

Insurance plans

Job summary

Johnson & Johnson in Belgium seeks a Delegate Qualified Person for the R&DQA-Clinical Supply Quality team. The role covers global clinical supply chains for ATMPs and biotherapeutics, supporting safe, compliant release of clinical materials.

You will build expertise across products, technologies and regulations, collaborating with global partners and leading quality decisions that impact patient supply and trial success.

Qualifications

• Requires university industrial pharmacist degree and EU-certified Qualified Person residing in Belgium.
• At least three years of experience in pharmaceutical supply chain, quality assurance, or related environment.

Responsibilities

• Bring the right experts together with Clinical Supply Chain teams and global quality partners to secure input for timely release and QP certification.
• Influence quality from the start by representing Clinical Supply Quality in cross-functional teams and ensuring quality requirements are built into clinical trial execution.
• Release clinical trial materials and review batch information to keep studies supplied under the Janssen R&D IMP license.

Skills

Business Alignment

Business Savvy

Coaching

Communication

Compliance Management

Continuous Improvement

Fact-Based Decision Making

Human-Centered Design

ISO 9001

Issue Escalation

Problem Solving

Quality Control (QC)

Quality Management Systems (QMS)

Quality Standards

Regulatory Environment

Standard Operating Procedure (SOP)

Education

Industrial Pharmacist degree

EU-certified Qualified Person

Job description

Johnson & Johnson in Belgium seeks a Delegate Qualified Person for the R&DQA-Clinical Supply Quality team. The role covers global clinical supply chains for ATMPs and biotherapeutics, supporting safe, compliant release of clinical materials.

You will build expertise across products, technologies and regulations, collaborating with global partners and leading quality decisions that impact patient supply and trial success.