Senior Quality System 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 Pharmaceutical organisation, based in Netherlands.
The QA Officer is responsible for reporting and improvements of the systems order to maintain the highest standards by continuously making suggestions for improvement of processes and policies.
Issue as part of QA monthly report the Quality KPIs, overview of internal and external audits
Scheduling CAPAs and Change request forms, act as QA lead in cooperation with the other departments for a timely closure
Arrange approval / signing of controlled documents associated with KPIs, supplier qualification or Validation and Qualification packages.
Prepare the following overview for the Quality Review Board Monthly KPI, Supplier Qualification overview, overview of internal and external audits.
Manage paper and electronic copies of controlled KPIs, supplier qualification package and Qualification & Validation protocols
Support for the QA officers, QC department and Manufacturing department
Review and approval of validation protocols and reports (equipment, analytical methods, utilities, re-qualification validations).
A masters degree in Life Sciences or a different related field
Fluency 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 Seppe Verhoeven.
The Company
.Role Description
The Quality Assurance Officer for quality systems is responsible for the smooth running of the systemsThe QA Officer is responsible for reporting and improvements of the systems order to maintain the highest standards by continuously making suggestions for improvement of processes and policies.
Responsibilities
Issue, monitor and maintain the quality KPI systemsIssue as part of QA monthly report the Quality KPIs, overview of internal and external audits
Scheduling CAPAs and Change request forms, act as QA lead in cooperation with the other departments for a timely closure
Arrange approval / signing of controlled documents associated with KPIs, supplier qualification or Validation and Qualification packages.
Prepare the following overview for the Quality Review Board Monthly KPI, Supplier Qualification overview, overview of internal and external audits.
Manage paper and electronic copies of controlled KPIs, supplier qualification package and Qualification & Validation protocols
Support for the QA officers, QC department and Manufacturing department
Review and approval of validation protocols and reports (equipment, analytical methods, utilities, re-qualification validations).
Requirements
3-5 years of relevant experience within a similar roleA masters degree in Life Sciences or a different related field
Fluency 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 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 Pharmaceutical organisation, based in Netherlands.
The QA Officer is responsible for reporting and improvements of the systems order to maintain the highest standards by continuously making suggestions for improvement of processes and policies.
Issue as part of QA monthly report the Quality KPIs, overview of internal and external audits
Scheduling CAPAs and Change request forms, act as QA lead in cooperation with the other departments for a timely closure
Arrange approval / signing of controlled documents associated with KPIs, supplier qualification or Validation and Qualification packages.
Prepare the following overview for the Quality Review Board Monthly KPI, Supplier Qualification overview, overview of internal and external audits.
Manage paper and electronic copies of controlled KPIs, supplier qualification package and Qualification & Validation protocols
Support for the QA officers, QC department and Manufacturing department
Review and approval of validation protocols and reports (equipment, analytical methods, utilities, re-qualification validations).
A masters degree in Life Sciences or a different related field
Fluency 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 Seppe Verhoeven.
The Company
.Role Description
The Quality Assurance Officer for quality systems is responsible for the smooth running of the systemsThe QA Officer is responsible for reporting and improvements of the systems order to maintain the highest standards by continuously making suggestions for improvement of processes and policies.
Responsibilities
Issue, monitor and maintain the quality KPI systemsIssue as part of QA monthly report the Quality KPIs, overview of internal and external audits
Scheduling CAPAs and Change request forms, act as QA lead in cooperation with the other departments for a timely closure
Arrange approval / signing of controlled documents associated with KPIs, supplier qualification or Validation and Qualification packages.
Prepare the following overview for the Quality Review Board Monthly KPI, Supplier Qualification overview, overview of internal and external audits.
Manage paper and electronic copies of controlled KPIs, supplier qualification package and Qualification & Validation protocols
Support for the QA officers, QC department and Manufacturing department
Review and approval of validation protocols and reports (equipment, analytical methods, utilities, re-qualification validations).
Requirements
3-5 years of relevant experience within a similar roleA masters degree in Life Sciences or a different related field
Fluency 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 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
