QA Manager
Location: NetherlandsSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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 organisation, based in Limburg Netherlands.
• Manage QA and operation team
• Implement and document improvement changes in QA
• Liaise with relevant teams and serve as single point of contact
• Manage Quality related activities regarding inspections and audits
• Coordinate Post Market Surveillance activities and processes
• Manage CAPA and A3 processes to stimulate improvements
• At least 3 to 5 years working experience within QA Medical Devices
• Working experience and QA understanding of Medical Pouches
• Hygiene management
• Communicative and able to teach and train
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Evertsen.
The Company
They are a global manufacturer and distributor of Medical Device packaging en pouches. Due to their growth they are now looking for a QA Manager to solely focus on the Quality of the Cleanroom and Medical Pouches in their production site.Role Description
You will fulfil a central role in the organisation to catch up on the quality standards that are required and cleanroom standards in the production site. The new QA Manager will communicate closely with relevant (ranging from sales to production) teams internationally to achieve the required standards and documentation. You will guide and manage a small QA team of two and will be working closely and hands-on with your colleagues.Responsibilities
• Achieve required ISO 13485:2016 standards• Manage QA and operation team
• Implement and document improvement changes in QA
• Liaise with relevant teams and serve as single point of contact
• Manage Quality related activities regarding inspections and audits
• Coordinate Post Market Surveillance activities and processes
• Manage CAPA and A3 processes to stimulate improvements
Requirements
• Experience with QA ISO 13485 and ISO11607• At least 3 to 5 years working experience within QA Medical Devices
• Working experience and QA understanding of Medical Pouches
• Hygiene management
• Communicative and able to teach and train
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Jeroen Evertsen.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
