QA Release Lead – Device Assembly & Parenteral Packaging

7555-Janssen Pharmaceutica NV Legal Entity; Geel; On-site; EUR 73,000 - 115,000; Full time

Benefits offered by this job

Annual bonus

Vacation days

Healthcare benefits

Job summary

Johnson & Johnson Innovative Medicine in Beerse, Belgium is seeking a QA Release Responsible for Device Assembly & Parenteral Packaging to join the Quality organization. You will oversee batch release, investigations, and GMP compliance, partnering with Operations and cross-functional teams.

You will contribute to inspection readiness and support quality documentation, acting as a QA spokesperson during Health Authority inspections and audits. Fluency in Dutch and English is required.

Qualifications

• Education: University degree in Pharmaceutical, Chemical, Biological Sciences, Engineering, or related field.
• Experience: 2–5 years in pharmaceutical industry.
• Familiarity with GMP and pharmaceutical manufacturing environments.
• Fluent Dutch and English, both spoken and written.

Responsibilities

• Releasing incoming half-finished and finished products in a timely manner.
• Reviewing investigations, deviations, CAPAs, Change Controls, and trend reports.
• Providing QA oversight during investigations and issue resolution.
• Ensuring GMP compliance and marketing authorizations.
• Acting as Quality spokesperson during inspections and audits.
• Supporting quality oversight of operational activities through GMP documentation.

Skills

GMP knowledge

Quality Assurance

Dutch language

English language

Investigation skills

CAPA / Change Control

Education

University degree in Pharmaceutical/Science

Job description

Johnson & Johnson Innovative Medicine in Beerse, Belgium is seeking a QA Release Responsible for Device Assembly & Parenteral Packaging to join the Quality organization. You will oversee batch release, investigations, and GMP compliance, partnering with Operations and cross-functional teams.

You will contribute to inspection readiness and support quality documentation, acting as a QA spokesperson during Health Authority inspections and audits. Fluency in Dutch and English is required.