QA Manager Projects
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 Reading United Kingdom.
- Contribute to the review and evaluation on corporate Quality management system. GMP-guidance in collaboration with other Quality Management functions, assuring implementation in due time:
- Collaborate at to the new version based on the new requirements
- Contribute to the final communication within Quality Management
- Ensure that adequate level of knowledge & competence is given to the rest of the Quality Management organisation for new GSOP and external regulations
- Assist major transfer activities involving several sites including analytical and technical activities derived as well as stakeholders interactions
- At least 5 years experience in pharmaceutical quality assurance/management or equivalent experience
- Skilled in achieving results and managing others to achieve corporate, site, and departmental objectives
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
Our client is a global Pharmaceutical company in BerkshireRole Description
QA Manager ProjectsResponsibilities
- Support and follow up global projects in the area of Quality Management in order to guarantee timely and harmonised implementation of new quality and regulatory initiatives. E.g. PDE, ICH Q3D, data integrity- Contribute to the review and evaluation on corporate Quality management system. GMP-guidance in collaboration with other Quality Management functions, assuring implementation in due time:
- Collaborate at to the new version based on the new requirements
- Contribute to the final communication within Quality Management
- Ensure that adequate level of knowledge & competence is given to the rest of the Quality Management organisation for new GSOP and external regulations
- Assist major transfer activities involving several sites including analytical and technical activities derived as well as stakeholders interactions
Requirements
- Master degree in the life sciences or pharmacy- At least 5 years experience in pharmaceutical quality assurance/management or equivalent experience
- Skilled in achieving results and managing others to achieve corporate, site, and departmental objectives
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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