The Medical Devices industry is fundamental to a developing world of innovation within the Healthcare sector. We understand how the impact of regulatory change, funding and advancements in technology affect talent acquisition for our clients.
In an industry where talent is in short supply, our focus is on building global candidate communities that are unique to SciPro. Through offering our clients access to these communities, we are able to deliver talent that positively impacts across the Medical Device Life Cycle.
Our specialism includes roles within:
Responsible for the management of verification and validation tasks Involvement in the generation, reviewing, editing and reviewing of various protocols, FMEAs, test plans and summary reports Responsible for the generating, reviewing, editing and approving of SOPs, CAPAs and other appli... Read More
Senior Quality Assurance & Regulatory Affairs Manager What does this position offer to you? ● Competitive remuneration package - €70K - €80K ● Work for the top company in their field ● Fast-paced, intellectually intense, service-oriented environment ● Diverse training and possibilities ... Read More