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QA Release Responsible (DAP)

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Quality

Job Sub Function:
Quality Assurance

Job Category:
Professional

All Job Posting Locations:
Beerse, Antwerp, Belgium

Job Description:
We are searching for the best talent for a QA Release Responsible - Device Assembly & Parenteral Packaging.

Purpose

We are looking for a QA Release Responsible to join the Quality organization at Johnson & Johnson Innovative Medicine in Beerse, Belgium.

Do you enjoy working in a dynamic pharmaceutical manufacturing environment while helping ensure products meet the highest quality and compliance standards?

The Quality Department supports all GMP activities related to manufacturing, packaging, labeling, testing, release, and distribution of products manufactured on the Belgium campus.

In this role, you will provide Quality Assurance support for Device Assembly and Parenteral Packaging operations, including batch release activities, quality oversight of manufacturing processes, investigation management, and inspection readiness activities.

You will work closely with Operations, Quality, and cross-functional partners to help ensure compliance with GMP requirements, marketing authorizations, and internal quality standards.

You will be responsible for

In this role, you will provide Quality oversight for Device Assembly and Parenteral Packaging activities and support day-to-day quality operations within the area.

Key responsibilities include:


* Releasing incoming half-finished products and assembled/finished products in a timely manner


* Reviewing and supporting investigations, deviations, CAPAs, Change Controls, and trend reports to help ensure issues are appropriately assessed and addressed


* Providing Quality and compliance expertise during investigations and issue resolution activities


* Ensuring compliance with applicable GMP requirements and marketing authorizations


* Acting as a Quality spokesperson during Health Authority inspections, internal audits, and customer audits


* Performing check rounds and periodic witnessing of operational processes


* Establishing and maintaining effective working relationships with Business and Quality partners...




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