Healthcare & Life Sciences - Quality & Regulatory Affairs jobs
28 Matching Jobs
Quality & Regulatory Affairs jobs
- Featured JobNorth HollandPermanent€60.000 - €85.000
Op dit moment zijn we voor RENOLIT Nederland op zoek naar een Regulatory Affairs (RA) Manager die het volledige RA-beleid van de Business Unit MEDICAL, de Business Unit waar RENOLIT Nederland deel van uitmaakt binnen RENOLIT, kan formuleren en implementeren.
AmsterdamPermanent€55.000 - €78.000
- Ervaren Regulatory Affairs Specialist
- Medical Devices/Pharmaceuticals /Chemicals
For an international, fast-growing company in the medical devices industry we are searching for a Regulatory Affairs Specialist EMEA who can act as a strategic business partner to the Quality, Regulatory Affairs and Compliance EMEA team.
KerkradePermanent€50.000 - €72.000
- Regulatory Affairs Strategy and Compliance EMEA
- Medical Devices
The Sr. Quality Engineer collaborates with the quality management team to recommend, design and implement functional process improvements.
KerkradePermanent€65.000 - €92.000
- Quality Engineering
- Continuous Improvement
The Sr. Quality Manager is responsible for implementing continuous improvements and provides vision and leadership for strategic projects.
HoofddorpPermanent€40.000 - €55.000
- Senior Quality Manager
- Quality Compliance, Continuous Improvement
We are exclusively recruiting a Project Management/ Packaging Specialist Pharmaceutical for a one of our top clients. In this position you will be primarily responsible for the creation and updating of the art work & packaging of the products. This will mean a combination of creative work with the legal regulations and planning the whole process.
- International Pharmaceutical Company
- Project Management/ Packaging Specilalist Pharmaceutical
The (Senior) RA Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of the pharmaceutical and medical products in order to control the safety and efficacy of these products. In this position you have to combine scientific, legal and business knowledge to ensure the products meet the required legislation. He/she is responsible for the approval and registration of the products in the (Western) European market.
- Regulatory Affairs
For our client Sanofi Genzyme we are exclusively recruiting a new Project Manager Regulatory Affairs (RA). We are looking for candidates who have a strong analytical mindset with a problem-solving approach. Are you result-driven and do you have good planning and project management skills? Than we might be looking for you!
- Regulatory Affairs
- Project Management
Wij op zoek naar enthousiaste kandidaten met een grote kwaliteitsbeleving en die bij voorkeur ervaring hebben binnen de farmaceutische industrie. Als persoon ben je toe aan je tweede of derde stap binnen kwaliteit en heb je een aanstekelijke passie voor je vak. Je hebt de drive om te verbeteren, je bent proactief en een goede multitasker.
- Quality Assurance
In the position of Quality Systems Manager you act as the company's Quality System Management representative for the Netherlands and provide day to day management and strategic direction to all quality assurance and quality systems compliance activities in support of the company's activities.
AmsterdamTemporary€40.000 - €45.000
- Quality Assurance, Medical Devices
- ISO 13485, FDA, Continuous Improvement
In this position you are Responsible for the development, revision, maintenance and inactivation of the local Stryker site procedures ensuring the alignment with the Corporate Guidelines for Purchasing Controls and Supplier Management. This means you will liaise with other site supplier control and strategic supplier quality divisions and partners to ensure alignment with Company-Wide Supplier strategies. Are you looking for a challenging starting position and a chance to work for a world class Medical Device company, this is you chance.
- Quality, Supplier Control
- Medical Devices