Quality Assurance Manager Freelance
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 Gelderland Netherlands.
- Manage quality systems and judge quality aspects
- Participate in audits
- Handling of deviations and CAPA’s in the systems
- Lead QA improvement projects, the QMS and cGMP-compliance intern and extern
- Coordinate, describe, document, research the processes
- At least 5 years of QA experience within the pharmaceutical industry
- Audits & self-inspection
- Experience with QMS, GMP
- Knowledge of Medical devices and/or medicines
- Fluent in English and Dutch
The Company
They have a production in sterile medical products in the area of biomaterials and medicines. They focus on quality and knowledge to deliver their part in making life a better quality for humans. You will work in a dynamic and growing organization.Role Description
As a Quality Assurance manager at our client you will be responsible for the management at the QA department. You will ensure intern QMS is in line with regulatory. You will follow GMP-guidelines and ISO 9001/ ISO 13485. To fulfil your responsibilities there are a few main tasks which you will find below.Responsibilities
Building the strategy and goals of the QA department. Lead, coach and develop the employees within your department.- Manage quality systems and judge quality aspects
- Participate in audits
- Handling of deviations and CAPA’s in the systems
- Lead QA improvement projects, the QMS and cGMP-compliance intern and extern
- Coordinate, describe, document, research the processes
Requirements
- BSc., MSc.- At least 5 years of QA experience within the pharmaceutical industry
- Audits & self-inspection
- Experience with QMS, GMP
- Knowledge of Medical devices and/or medicines
- Fluent in English and Dutch
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
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 Gelderland Netherlands.
- Manage quality systems and judge quality aspects
- Participate in audits
- Handling of deviations and CAPA’s in the systems
- Lead QA improvement projects, the QMS and cGMP-compliance intern and extern
- Coordinate, describe, document, research the processes
- At least 5 years of QA experience within the pharmaceutical industry
- Audits & self-inspection
- Experience with QMS, GMP
- Knowledge of Medical devices and/or medicines
- Fluent in English and Dutch
The Company
They have a production in sterile medical products in the area of biomaterials and medicines. They focus on quality and knowledge to deliver their part in making life a better quality for humans. You will work in a dynamic and growing organization.Role Description
As a Quality Assurance manager at our client you will be responsible for the management at the QA department. You will ensure intern QMS is in line with regulatory. You will follow GMP-guidelines and ISO 9001/ ISO 13485. To fulfil your responsibilities there are a few main tasks which you will find below.Responsibilities
Building the strategy and goals of the QA department. Lead, coach and develop the employees within your department.- Manage quality systems and judge quality aspects
- Participate in audits
- Handling of deviations and CAPA’s in the systems
- Lead QA improvement projects, the QMS and cGMP-compliance intern and extern
- Coordinate, describe, document, research the processes
Requirements
- BSc., MSc.- At least 5 years of QA experience within the pharmaceutical industry
- Audits & self-inspection
- Experience with QMS, GMP
- Knowledge of Medical devices and/or medicines
- Fluent in English and Dutch
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 Medicine / Medical service
