QA Release Lead – Device Assembly & Parenteral

Johnson & Johnson Innovative Medicine; Beerse; On-site; EUR 73,000 - 115,000; Full time

Job summary

Johnson & Johnson Innovative Medicine is seeking a QA Release Responsible for Device Assembly and Parenteral Packaging at the Beerse, Belgium site. The role ensures product quality, supports GMP activities, and oversees batch release while partnering with Operations, Quality and cross‑functional teams in a bilingual (Dutch/English) environment.

The candidate will review investigations, deviations, CAPAs and change controls, ensure regulatory alignment, and act as a Quality spokesperson during

Qualifications

• University degree in Pharmaceutical, Chemical, Biological Sciences, Engineering
• 2–5 years of experience in the pharmaceutical industry
• Fluent Dutch and English, both spoken and written
• Familiarity with GMP requirements and pharmaceutical manufacturing environments

Responsibilities

• Release incoming half-finished and finished products in a timely manner
• Support investigations, deviations, CAPAs, Change Controls, and trend reports
• Provide quality and compliance expertise during investigations and issue resolution
• Ensure compliance with GMP requirements and marketing authorizations
• Act as Quality spokesperson during inspections, audits
• Maintain relationships with Business and Quality partners
• Review GMP documentation for quality oversight
• Represent Quality on projects and ensure regulatory alignment

Skills

Quality GMP

Fluent Dutch

Fluent English

Risk-based decisions

Analytical skills

Cross-functional collaboration

Quality-focused

Communication

Education

University degree in Pharmaceutical, Chemical, Biological Sciences, Engineering

Tools

GMP documentation tools

Job description

Johnson & Johnson Innovative Medicine is seeking a QA Release Responsible for Device Assembly and Parenteral Packaging at the Beerse, Belgium site. The role ensures product quality, supports GMP activities, and oversees batch release while partnering with Operations, Quality and cross‑functional teams in a bilingual (Dutch/English) environment.

The candidate will review investigations, deviations, CAPAs and change controls, ensure regulatory alignment, and act as a Quality spokesperson during