Quality & Regulatory Affairs Manager (permanent)
Location: SwitzerlandSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Genf Switzerland.
Our client is a professional Medical Devices organization, based in Switzerland.
Medical Device company specialized in electrical equipment.
ROLE DESCRIPTION
The purpose of the Quality & Regulatory Affairs Manager expert in Medical Devices will be:
Develop, implement and maintain the corporate Quality strategy.
Provide leadership and technical expertise to ensure regulatory compliance, continuous improvement and a high Quality System.
RESPONSIBILITIES
- Establish the Quality and Regulatory goals
- Manage a team (6 people approx.) with different backgrounds (QA, QC, RA, Quality Engineers, Validation)
- Evaluate Quality relate issues: design control, risk management, PMS, product validation...
- Budget responsibility
- Provide hands-on technical expertise
This position is absolutely crucial within the organization.
In this role, you will interact with executive Quality & Regulatory levels within the organization but you will also need to have a hands-on approach towards the team.
REQUIREMENTS
- Technical background
- Strong track record within the Medical Device industry
- Previous experience with Medical Electrical equipment
- Absolute expert in QSR (FDA/CFR regulations, ISO 13485)
- Ability to work under high pressure
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
