QA Release Lead – Device Assembly & Parenteral

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

Job summary

Johnson & Johnson Innovative Medicine in Beerse, Belgium, seeks a QA Release Responsible for Device Assembly & Parenteral Packaging. You will join the Quality organization to ensure products meet quality and regulatory standards in a fast-paced pharmaceutical manufacturing environment.

The role requires 2–5 years of pharma experience, fluency in Dutch and English, and strong GMP knowledge to support investigations, releases, and audits.

Qualifications

• University degree in Pharmaceutical, Chemical, Biological Sciences, Engineering, or related field.
• 2–5 years of experience in the pharmaceutical industry.
• Familiarity with GMP requirements and manufacturing environments.
• Fluent Dutch and English in a bilingual setting.
• Strong analytical and problem-solving skills with attention to detail.

Responsibilities

• Release incoming half-finished products and assembled/finished products on time.
• Review investigations, deviations, CAPAs, Change Controls, and trend reports.
• Provide QA expertise during investigations and issue resolution activities.
• Ensure GMP compliance and marketing authorizations.
• Act as QA spokesperson during Health Authority inspections, audits and customer audits.
• Perform check rounds and periodic witnessing of processes.
• Maintain relationships with Business and Quality partners as QA contact.
• Review GMP documentation for quality oversight of operations.
• Represent QA on projects and ensure alignment with quality requirements.
• Escalate events impacting patient safety or product quality.

Skills

Fluent Dutch

Fluent English

GMP knowledge

Quality Assurance

Pharma industry experience

Education

University degree in Pharmaceutical, Chemical, Biological Sciences, Engineering, or related field

Job description

Johnson & Johnson Innovative Medicine in Beerse, Belgium, seeks a QA Release Responsible for Device Assembly & Parenteral Packaging. You will join the Quality organization to ensure products meet quality and regulatory standards in a fast-paced pharmaceutical manufacturing environment.

The role requires 2–5 years of pharma experience, fluency in Dutch and English, and strong GMP knowledge to support investigations, releases, and audits.