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:
Supply Chain Engineering
Job Sub Function:
Quality Engineering
Job Category:
Scientific/Technology
All Job Posting Locations:
Geel, Antwerp, Belgium
Job Description:
About Innovative Medicine
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
We are searching for the best talent for a Quality Engineer – QA Quality Excellence within a QA dept in Geel, Belgium.
Within the Innovative Medicine Supply Chain, a member of Johnson & Johnson's Family of Companies, we are recruiting a Staff Quality Engineer (M/F/X). You will be a member of our quality engineering team, ensuring quality and compliance oversight of systems and data related to manufacturing of Small Molecule Active Pharmaceutical Ingredients (SM-API) and Drug Product Intermediates at the Innovative Medicine Supply Chain site in Geel, Belgium. You will be part of an enthusiastic team that has a strong quality focus on technology, qualification/validation, automation, and continuous improvement. Employees are very valuable to our organization and development is a daily responsibility. Through on the job training, e-learning, implementation of various projects and programs we ensure personal growth by focusing on your talents. We offer you a contract of indefinite duration with an attractive salary package including extra-legal benefits such as meal vouchers, additional pension plan and hospitalization insurance.
Innovative Medicine Supply Chain Geel serves as Centre of Excellence for the development and manufacturing of SM-APIs and DP Intermediates used in treatments that improve the health and lifestyle of people worldwide. Innovative Medicine Supply Chain Quality (IMSCQ) supports the Geel site in its mission as Launch & Grow site and is responsible for the quality oversight and final release of SM-APIs and DP Intermediates guaranteeing reliable supplies in compliance with applicable regulations.
As Staff Quality Engineer, you act as Subject Matter Expert ensuring Quality and Compliance governance on GMP data and systems.
The responsibilities and the impact YOU will have:
- Ensure adequate Quality and Compliance governance of GMP systems and data.
- Taking on the QA Key User role for IT systems such as MES and SAP.
- Be the QA contact for innovation projects regarding digitalization and automation.
- Maintain a current knowledge of international laws, guidelines and new evolutions related to Data Integrity and general GMP through courses, conferences, seminars, internal and external benchmarking and literature studies.
- Prepare for and be spokesperson in audits and inspections.
- Perform and follow up on internal and external audits to accomplish regulatory compliance.
- Cooperate with IT, engineering, operations and other teams for the introduction of new systems and processes.
- To give advice and support for the preparation of Data Integrity related activities and ensure Data Integrity governance. Be a member of multi-functional teams to realize cross-departmental objectives.
We would love to hear from YOU, if you have the following essential requirements:
- Master scientific degree or equivalent experience.
- 4 - 6 years’ experience in pharmaceutical or chemical industry.
- Knowledge of cGMP compliance (21 CFR Parts 211; EU Directive 2003/94/EC and annex 11/15; ICH Q7, GAMP, Data Integrity Guidelines…)
- Knowledge of IT and equipment systems and the related data flows.
- Strong ownership and quality attitude. You are able to deliver on commitment timelines.
- Strong analytical thinking skills and able to work in a flexible way under time pressure.
- Ability to make risk-based decisions. Understands the business implications regarding quality positions and decisions.
- You work accurately and proactively across organizational boundaries as One Team.
- Fluent in verbal and written communication in English and Dutch and are able to connect with diverse partners.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
This is what awaits YOU at J&J:
This is an opportunity to work with a ground-breaking biomedicine operation and to be a member of a Johnson & Johnson company, with an excellent record in employee continuous professional development and business improvement.
We are passionate about our work; we play vital roles across a range of professional disciplines, and care deeply about our customers and communities. At Johnson & Johnson, our culture enables dynamic and impactful careers.
Whether you’re one of the people who already work here, or you’re considering joining the team, we offer:
- An opportunity to be part of a global market leader.
- A dynamic and inspiring working environment.
- Opportunities to work on challenging projects and assignments.
- Possibilities for further personal and professional development/education
- Excellent benefits.
Required Skills:
Preferred Skills:
Coaching, Consistency, Controls Compliance, Critical Thinking, Data Savvy, Engineering, Financial Competence, Good Automated Manufacturing Practice (GAMP), ISO 9001, Lean Supply Chain Management, Leverages Information, Process Improvements, Quality Control (QC), Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy
