Description
Currently, I am recruiting for one of my most prestigious clients, based in the Benelux area. They're amongst the top leaders in their niche industry, specializing in medical devices within the diagnosis and therapy market. Now that their products are focussing more and more on biographic and biometric traits, they have grown even more over the last year, since this has opened so many new markets for them. With their substantial growth and continuous innovation and product development, they are now urgently looking for a QA Engineer who can guide this company through an upcoming new project in terms of Quality Assurance.
About the company
Founded over 15 years ago, this prestigious international organization headquartered in the Benelux has customers around the globe and employs over 300 people.
For all their clients, their technology is mission-critical and has to comply with the highest performance and security standards. That's why, in order to achieve optimal quality and innovative outcomes, they are only looking to hire bright, passionate, forward-thinking professionals, who would work well in an open, non-hierarchical company culture focused on quality and customer success.
Key responsibilities
*You will be working closely together with the R&D team
*Point of contact for a number of project groups
*You will be guarding the process- and product quality and look for further process optimisation
*Execute risk analysis and FMEAs
*Setting up and executing Corrective and Preventive Actions (CAPAs)
*Point of contact for other Quality specialists within/and external suppliers
The ideal profile for this QA Engineer would look like this:
*2+ years experience in a QA role, preferably within Medical Devices (ISO13485 and ISO9001)
*Strong knowledge of international quality guidelines
*BA or MA degree in a relevant field is a big plus
*Fluent in English, Dutch and/or French is a big plus
Key competences
*Excellent communicator and presenter;
*Good organizational skills;
*Independent thinker with a keen eye for detail
Interested?
Candidates whom are interested or want to learn more about the role or position, can send an e-mail with their CV (in word-format) to Christiaan de Wit at (see below)
Key search terms: Biotechnology, Pharmaceutical, Medical Devices, Food Science, Cosmetic, Clinical Research Organisations, HSE, Chemical, R&D, Medical Writing & Communication, Medical Affairs, Regulatory Projects, PhD, Master, Bachelor, Freelance, Interim, zzp, contract, project, temporary, QA, Quality Assurance, Quality Assurance Manager, Quality Assurance Officer, ISO, GMP, QC, Quality Control, Quality Control Manager, QP, Qualified Person, Qualified Personnel, RA, Regulatory Affairs, Regulatory Affairs Manager, Regulatory Affairs Officer
Disclaimer: Amoria Bond operates as an employment agency and employment business. No terminology in this advert is intended to discriminate on the grounds of age or experience, and we confirm that we are happy to accept applications from persons of any age or experience for this role.