367 days ago on sire-search.com

Senior Project Manager Quality Assurance

SIRE Life Sciences

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 Please refer to JobSuchmaschine in your application

Senior Project Manager Quality Assurance

SIRE 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!


Our client is a professional Medical Devices organization, based in Switzerland.

The company is one of the leading manufacturers of interventional cardiology devices. They are currently growing rapidly and for this reason, would like to hire new people for the quality department.


In this role, you will be one of the Senior Project Managers for Quality Assurance for all interventional cardiology products. You will be overseeing several projects regarding the companies vascular products, making sure that all requirements, both for ISO 13485 and FDA 21 CFR 820, are being met. You will manage Corrective Actions and Preventive Actions (CAPAs) and lead teams of various departments, business units and nationalities.


- Leading of the operational quality activities (planning, budgeting, and responsibility)
- Supplier control and audit
- Using of Lean and Sigma for quality operations
- Leadership and coaching of teams
- Management of international teams located in several plants worldwide
- Take part in audits for Notified Bodies and FDA
- Managing of CAPAs


- 4-5 years of experience with Class III Medical Devices in quality assurance
- Fluent in German
- Fluent in English
- Degree in Engineering, Materials or Life Sciences
- MBA would be a big plus
- PMP Certificate

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Matthias Kunkel.