Pilot Plant Compliance Expert

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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 https://www.jnj.com

Job Function:
Quality

Job Sub Function:
Business Process Quality

Job Category:
Professional

All Job Posting Locations:
Beerse, Antwerp, Belgium

Job Description:

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

Join the Global Pharmaceutical Product Development and Supply (PPDS) organization within the Therapeutics Development and Supply (TDS) team at Johnson & Johnson.

Based in Beerse, Antwerp, Belgium, our development centers span the US, Asia, and Europe, driving the creation of cutting-edge pharmaceutical dosage forms.

Your Role
As a Pilot Plant Compliance Expert you will be a key player in our Pharmaceutical Supply and Engineering Sciences (PSES) organization.

You will ensure that our organization consistently operates in line with the GMP regulations and internal policies for safety and quality. 
You will take process ownership of specific elements of our Compliance Framework and you will act as the bridge between complex regulatory requirements and practical business operations, translating rules into clear, workable guidelines.

With your expertise and communication skills, you foster a culture of integrity, accountability, and compliance awareness across our organization. 
In this role, you will collaborate within a dynamic, multi-disciplinary team of project and compliance engineers, technology leads, operations partners and QA experts.

You’ll take ownership in upgrading and optimizing our drug product technology and manufacturing processes in our state-of-the art drug product Pilot Plant, whilst being exposed to every facet of our business.

From engineering and operations to quality and compliance, you’ll be at the heart of it all.

The variety of challenges and the breadth of interaction across departments and teams make this an exciting and impactful position. 
As a key player of our organization, you will help shape the future of drug product development and clinical manufacturing.

Your responsibilities will include:



* Be the expert and process owner: Develop, implement and monitor GMP compliance policies, processes and inte...