Quality consultant
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 Noord-Holland Netherlands.
They are a Dutch company focussed on sterilisation products, devices and packaging materials. They are on the international market and are looking for support in the Quality Assurance due to unforeseen fallout of the current manager.
ROLE DESCRIPTION
Your role will be focused on the Quality Management Systems and performing internal and external audits. The company is looking for someone who can fully take over all tasks but focussed on the current deadlines that are coming regarding ISO 13485 and the upcoming audits and reviews. You will work together with the current team to ensure a complaint system and company concerning all requirements and regulations.
RESPONSIBILITIES
As the consultant and substitute of the manager it is your task to guide and supervise the team and company through all reviews, audits and other challenges that the company will face. You will at first focus on upcoming dead lines and non-conformities. After these priorities you and the team will focus on implementing improvements and maintaining/ensuring compliancy to requirements that the company has to meet for next deadlines. The length of the project is unknown but is expected be for at least three months.
REQUIREMENTS
At least 5 years experience within QA Medical Devices
Highly experienced with audits
Proven experience of at least 1 year leading/supervising/managing
Knowledge and understanding of ISO 13485 and MDR is a big plus
Fluent in English
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.
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 Noord-Holland Netherlands.
They are a Dutch company focussed on sterilisation products, devices and packaging materials. They are on the international market and are looking for support in the Quality Assurance due to unforeseen fallout of the current manager.
ROLE DESCRIPTION
Your role will be focused on the Quality Management Systems and performing internal and external audits. The company is looking for someone who can fully take over all tasks but focussed on the current deadlines that are coming regarding ISO 13485 and the upcoming audits and reviews. You will work together with the current team to ensure a complaint system and company concerning all requirements and regulations.
RESPONSIBILITIES
As the consultant and substitute of the manager it is your task to guide and supervise the team and company through all reviews, audits and other challenges that the company will face. You will at first focus on upcoming dead lines and non-conformities. After these priorities you and the team will focus on implementing improvements and maintaining/ensuring compliancy to requirements that the company has to meet for next deadlines. The length of the project is unknown but is expected be for at least three months.
REQUIREMENTS
At least 5 years experience within QA Medical Devices
Highly experienced with audits
Proven experience of at least 1 year leading/supervising/managing
Knowledge and understanding of ISO 13485 and MDR is a big plus
Fluent in English
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.
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
