Qualified Person Freelance
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 Biotechnology and Pharmaceutical organization, based in Zuid-Holland Netherlands.
Our client is a Pharmaceutical company in Zuid Holland
ROLE DESCRIPTION
- In this role you will be QP and part of the QA team
- You will receive QP training and take part in QA activities
- You are responsible for maintaining and improving a cGMP compliant QMS
- Ensure Quality of BioTechnical Pharmaceutical products
- Legally responsible for release of materials, DS, DP and final products
RESPONSIBILITIES
- Document Management
- Change Control
- Deviations
- Inspection Management
- Training of Employees
- Review of Batch records
- Release of products
- Auditing of suppliers
- Writing of SOPs
- Responsible for Periodic Quality Reports
REQUIREMENTS
- Degree in Pharmacy (preferred), BioChemistry or related
- Experience in highly regulated environment (GMP or GDP or GLP or GVP or GCP or ISO13485)
- Experience in Pharmaceutical Production environment or Quality Control/Assurance
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.
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 Biotechnology and Pharmaceutical organization, based in Zuid-Holland Netherlands.
Our client is a Pharmaceutical company in Zuid Holland
ROLE DESCRIPTION
- In this role you will be QP and part of the QA team
- You will receive QP training and take part in QA activities
- You are responsible for maintaining and improving a cGMP compliant QMS
- Ensure Quality of BioTechnical Pharmaceutical products
- Legally responsible for release of materials, DS, DP and final products
RESPONSIBILITIES
- Document Management
- Change Control
- Deviations
- Inspection Management
- Training of Employees
- Review of Batch records
- Release of products
- Auditing of suppliers
- Writing of SOPs
- Responsible for Periodic Quality Reports
REQUIREMENTS
- Degree in Pharmacy (preferred), BioChemistry or related
- Experience in highly regulated environment (GMP or GDP or GLP or GVP or GCP or ISO13485)
- Experience in Pharmaceutical Production environment or Quality Control/Assurance
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Daniel Woudenberg.
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
