Freelance QA Design Control
Location: NetherlandsSIRE 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 Netherlands.
A medical device company, based in the Netherlands with multiple sites.
ROLE DESCRIPTION
In one of the project teams they are looking for a Quality Assurance expert who is familiar with the Design Controls according to the regulations of the FDA CFR820.30 or the MDD/ISO13485. You will be operating in a multifunctional team including disciplines as R&D, legal, sales and marketing. From the beginning you are involved with the New Product Development and the Quality Assurance of the product for a longer period of time as from November 2016. You will be defining the Quality aspect within this development process
RESPONSIBILITIES
- Quality Assurance of New Product Design
- Applying Design Control to the New Product (design input/output, verification, validation)
- Keeping track of timeline with deadlines
- Make sure the level of Quality meets or exceeds the clients standards
REQUIREMENTS
- 3 to 5 years of experience in Quality Assurance (preferably in Medical Devices)
- Knowledge of Design Controls essentials of regulations FDA and MDD
- Able to commit yourself to a project for 1,5 year
- Handson experience
- Knowledge of Quality Management Systems
- Can do attitude
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.
Job Description
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!
THE COMPANY
Our client is a professional Medical Devices organization, based in Netherlands.
A medical device company, based in the Netherlands with multiple sites.
ROLE DESCRIPTION
In one of the project teams they are looking for a Quality Assurance expert who is familiar with the Design Controls according to the regulations of the FDA CFR820.30 or the MDD/ISO13485. You will be operating in a multifunctional team including disciplines as R&D, legal, sales and marketing. From the beginning you are involved with the New Product Development and the Quality Assurance of the product for a longer period of time as from November 2016. You will be defining the Quality aspect within this development process
RESPONSIBILITIES
- Quality Assurance of New Product Design
- Applying Design Control to the New Product (design input/output, verification, validation)
- Keeping track of timeline with deadlines
- Make sure the level of Quality meets or exceeds the clients standards
REQUIREMENTS
- 3 to 5 years of experience in Quality Assurance (preferably in Medical Devices)
- Knowledge of Design Controls essentials of regulations FDA and MDD
- Able to commit yourself to a project for 1,5 year
- Handson experience
- Knowledge of Quality Management Systems
- Can do attitude
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control
