QA Consultant
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 organisation, based in Netherlands.
Advice on supplier audits
Work on backlog deviation
Provide Lean Quality Control
Provide Quality Efficiency by design
Proven background in a Manufacturing/Production or Product development environment.
Experience working with quality and reliability tools and templates
Perform by a unique end-to-end approach combining technology, usage and verification & validation
Familiar with relevant regulations and standards (e.g. EU MDD, FDA, ISO 13485, IEC 62302)
Good knowledge of management structure (ISO certified) providing continuous and effective support and training programmes, pooling and sharing knowledge and experience, as well as industry-specific best practices and benchmarks is an absolute plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
The company is a global market leader in providing consultancy in several industries and it its the companies sole mission to bring innovation in a every changing market.Role Description
In this role we are looking for someone who is a real team player and is highly ambitious to take a next step. It is important that you are able to able to adapt in new environments, where you creative mindset will prove to be necessary.Responsibilities
Perform regulatory inspection preparation & remediationAdvice on supplier audits
Work on backlog deviation
Provide Lean Quality Control
Provide Quality Efficiency by design
Requirements
Bachelor or University degree in (Bio)Medical Engineering, Electrical Engineering, or equivalentProven background in a Manufacturing/Production or Product development environment.
Experience working with quality and reliability tools and templates
Perform by a unique end-to-end approach combining technology, usage and verification & validation
Familiar with relevant regulations and standards (e.g. EU MDD, FDA, ISO 13485, IEC 62302)
Good knowledge of management structure (ISO certified) providing continuous and effective support and training programmes, pooling and sharing knowledge and experience, as well as industry-specific best practices and benchmarks is an absolute plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
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Job Description
SIRE® 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 organisation, based in Netherlands.
Advice on supplier audits
Work on backlog deviation
Provide Lean Quality Control
Provide Quality Efficiency by design
Proven background in a Manufacturing/Production or Product development environment.
Experience working with quality and reliability tools and templates
Perform by a unique end-to-end approach combining technology, usage and verification & validation
Familiar with relevant regulations and standards (e.g. EU MDD, FDA, ISO 13485, IEC 62302)
Good knowledge of management structure (ISO certified) providing continuous and effective support and training programmes, pooling and sharing knowledge and experience, as well as industry-specific best practices and benchmarks is an absolute plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
The company is a global market leader in providing consultancy in several industries and it its the companies sole mission to bring innovation in a every changing market.Role Description
In this role we are looking for someone who is a real team player and is highly ambitious to take a next step. It is important that you are able to able to adapt in new environments, where you creative mindset will prove to be necessary.Responsibilities
Perform regulatory inspection preparation & remediationAdvice on supplier audits
Work on backlog deviation
Provide Lean Quality Control
Provide Quality Efficiency by design
Requirements
Bachelor or University degree in (Bio)Medical Engineering, Electrical Engineering, or equivalentProven background in a Manufacturing/Production or Product development environment.
Experience working with quality and reliability tools and templates
Perform by a unique end-to-end approach combining technology, usage and verification & validation
Familiar with relevant regulations and standards (e.g. EU MDD, FDA, ISO 13485, IEC 62302)
Good knowledge of management structure (ISO certified) providing continuous and effective support and training programmes, pooling and sharing knowledge and experience, as well as industry-specific best practices and benchmarks is an absolute plus
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
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 / Production Audit
