Director Quality Assurance

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:
People Leader

All Job Posting Locations:
Beerse, Antwerp, Belgium

Job Description:

Within Johnson & Johnson Innovative Medicine Supply Chain, we are recruiting a QA Director Commercial Drug Product & Qualified person as member of our Quality management team overseeing Pharmaceutical Drug product manufacturing based in Beerse, Belgium.

J&J Innovative Medicine Supply Chain Beerse serves as Centre of Excellence for the development and manufacturing of Pharmaceutical Drug Products used in treatments that improve the health and lifestyle of people worldwide.

The Supply Chain Quality (SCQ) team supports the Beerse site in its mission as Launch & Grow site and is responsible for the quality oversight and final release of Drug Products guaranteeing reliable supplies in compliance with applicable regulations.

As QA Director you lead a team of QA managers and professionals responsible for the quality oversight and timely release of Drug Products manufactured at the commercial facilities of the Beerse site ensuring compliance with applicable regulations.

You act as QA Point of Contact ensuring quality oversight of the Drug Product production plants, including sterile manufacturing, device assembly & packaging .

You encourage your team and business partners to continuously strengthen the Quality and Compliance Culture at the site.

You act as a leader who provides strategic direction and fosters an environment of innovative thinking.

Under your leadership, you ensure that the GMP activities as manufacturing, packaging, labelling, testing, release, storage, importation and distribution are carried out as required by legislation.

As Qualified Person you keep overall oversight of the global GMP quality systems, enabling compliance with all applicable legislation.

Job Description:

• Lead a team of QA managers and professionals by supporting, coaching and developing team members in reaching quality, business and personal objectives.

As Qualified person you ensure a continuous evaluation of the GMP quality systems used in the different manufacturing areas of operating under ...