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:
QualityJob Sub Function:
Customer/Commercial QualityJob Category:
ProfessionalAll Job Posting Locations:
Issy-les-Moulineaux, France, Lyon, Rhone, FranceJob Description:
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/
J&J MedTech, Commercial Quality department, is recruiting for a Spécialiste Qualité reporting to the Commercial Quality Supervisor and to be based in Issy-les-Moulineaux or Lyon (France).
The Spécialiste Qualité effectively partners and collaborates in delivering the future of healthcare and performs quality support duties including complaint handling, internal auditing, general quality compliance duties. Provides support for special quality projects.
Principal Duties and Responsibilities
- Complaint handling, vigilance reporting and FSCA activities
- Assist in internal auditing
- Assist in maintaining local QM Systems
- Take part in project teams when needed
Education and / or Experience
- Universities/Bachelor degree or equivalent
- 2+ years’ experience in regulated healthcare industry
- Basic understanding of QM-Systems and local/European Medical Device regulations
Other Skills and Abilities
- Ability to work effectively with minimal supervision
- Must be able to handle multiple and competing priorities
- Must be proactive in assessing work load
- Experience with MS-Office based applications
- Experience with IT Tools and data management
- Strong organizational and planning skills needed
- Adapts to changing priorities
- Must be committed to teamwork
- Able to identify and resolve regulatory/compliance problems of diverse scope in consultation with supervisor
- Good verbal and written communication skills (French and English)
