Quality Assurance Manager QLP
Location: United KingdomSIRE® 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 and Biotechnology organisation, based in City of London United Kingdom.
Promote GLP compliance, as well as contributing to the development of quality standards in pre-clinical research
Assist in the management of quality assurance audit programmes and maintenance of quality system documents
Support computer system validation activities within the GLP environment.
Perform audits at external subcontractor facilities
Fully conversant in the application and interpretation of international GLP regulations and guidelines.
At least 5 years’ experience working in a Quality Assurance role or GLP environment; previous roles in an analytical laboratory would be advantageous.
Strong interpersonal skills and the ability to develop good working relationships with internal and external colleagues
A systematic approach with a good eye for detail.
Excellent communication and organisational skills. Ability to work independently or as a team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
The Company
We are looking for multiple Quality Assurance Manager QLP for different clients in the greater London are.Role Description
Quality Assurance Manager QLPResponsibilities
Audit of in-house pre-clinical studies conducted within our bio-analytical laboratory to assure compliance with GLP/GCP regulations.Promote GLP compliance, as well as contributing to the development of quality standards in pre-clinical research
Assist in the management of quality assurance audit programmes and maintenance of quality system documents
Support computer system validation activities within the GLP environment.
Perform audits at external subcontractor facilities
Requirements
Higher education in a relevant scientific discipline and/or suitable experience of working in a GxP regulatory/pharmaceutical environment.Fully conversant in the application and interpretation of international GLP regulations and guidelines.
At least 5 years’ experience working in a Quality Assurance role or GLP environment; previous roles in an analytical laboratory would be advantageous.
Strong interpersonal skills and the ability to develop good working relationships with internal and external colleagues
A systematic approach with a good eye for detail.
Excellent communication and organisational skills. Ability to work independently or as a team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
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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 and Biotechnology organisation, based in City of London United Kingdom.
Promote GLP compliance, as well as contributing to the development of quality standards in pre-clinical research
Assist in the management of quality assurance audit programmes and maintenance of quality system documents
Support computer system validation activities within the GLP environment.
Perform audits at external subcontractor facilities
Fully conversant in the application and interpretation of international GLP regulations and guidelines.
At least 5 years’ experience working in a Quality Assurance role or GLP environment; previous roles in an analytical laboratory would be advantageous.
Strong interpersonal skills and the ability to develop good working relationships with internal and external colleagues
A systematic approach with a good eye for detail.
Excellent communication and organisational skills. Ability to work independently or as a team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
The Company
We are looking for multiple Quality Assurance Manager QLP for different clients in the greater London are.Role Description
Quality Assurance Manager QLPResponsibilities
Audit of in-house pre-clinical studies conducted within our bio-analytical laboratory to assure compliance with GLP/GCP regulations.Promote GLP compliance, as well as contributing to the development of quality standards in pre-clinical research
Assist in the management of quality assurance audit programmes and maintenance of quality system documents
Support computer system validation activities within the GLP environment.
Perform audits at external subcontractor facilities
Requirements
Higher education in a relevant scientific discipline and/or suitable experience of working in a GxP regulatory/pharmaceutical environment.Fully conversant in the application and interpretation of international GLP regulations and guidelines.
At least 5 years’ experience working in a Quality Assurance role or GLP environment; previous roles in an analytical laboratory would be advantageous.
Strong interpersonal skills and the ability to develop good working relationships with internal and external colleagues
A systematic approach with a good eye for detail.
Excellent communication and organisational skills. Ability to work independently or as a team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Riko Arends.
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
