Qualified Person / Walloon Brabant / Permanent / Mid Seized company / Salary € 60 - € 75 K
Location: BelgiumSIRE® 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, Biotechnology and Clinical Research organisation, based in Waals-Brabant Belgium.
- Act as Qualified Person Deputy for GMP related activities
- Ensure the release of Investigational Medicinal Products in compliance with applicable regulation
- Ensure contact with Belgian Competent Authorities
- Assist in internal and external Audits
- Review Batch records, CAPA, Change Controls, deviations, ...
- Fluent in French and English
- Excellent communication and intercultural skills
- Team worker and team spirit
- Customer oriented
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
The Company
Interesting global pharmaceutical company dedicated to deliver medicines quickly to patients in need with innovative solutions.Role Description
In this role you will become the QP for the company and act as QP for GMP related activities. You will also help in other QA related activities (CAPA, deviations, ...) and ensuring compliance within the company.Responsibilities
- Establishment of Quality Agreements- Act as Qualified Person Deputy for GMP related activities
- Ensure the release of Investigational Medicinal Products in compliance with applicable regulation
- Ensure contact with Belgian Competent Authorities
- Assist in internal and external Audits
- Review Batch records, CAPA, Change Controls, deviations, ...
Requirements
- Qualified Person (Belgian registration)- Fluent in French and English
- Excellent communication and intercultural skills
- Team worker and team spirit
- Customer oriented
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
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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, Biotechnology and Clinical Research organisation, based in Waals-Brabant Belgium.
- Act as Qualified Person Deputy for GMP related activities
- Ensure the release of Investigational Medicinal Products in compliance with applicable regulation
- Ensure contact with Belgian Competent Authorities
- Assist in internal and external Audits
- Review Batch records, CAPA, Change Controls, deviations, ...
- Fluent in French and English
- Excellent communication and intercultural skills
- Team worker and team spirit
- Customer oriented
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
The Company
Interesting global pharmaceutical company dedicated to deliver medicines quickly to patients in need with innovative solutions.Role Description
In this role you will become the QP for the company and act as QP for GMP related activities. You will also help in other QA related activities (CAPA, deviations, ...) and ensuring compliance within the company.Responsibilities
- Establishment of Quality Agreements- Act as Qualified Person Deputy for GMP related activities
- Ensure the release of Investigational Medicinal Products in compliance with applicable regulation
- Ensure contact with Belgian Competent Authorities
- Assist in internal and external Audits
- Review Batch records, CAPA, Change Controls, deviations, ...
Requirements
- Qualified Person (Belgian registration)- Fluent in French and English
- Excellent communication and intercultural skills
- Team worker and team spirit
- Customer oriented
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Martijn van Nieuwenhovensss.
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