QA Officer - Amsterdam - Dutch not necessary
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 organisation, based in Noord-Holland Netherlands.
Review master documents and batch documentation
Perform audits
Write, review and approve applicable controlled documentation
Perform initiation, review and assessment of deviations, change control requests, CAPA’s, OOS and other QMS input.
Manage QA related aspects of projects
Develop training material and train personnel
A background in biotechnology
You are result-oriented, a team player with integrity and tenacity.
Fluency in English, other languages are a plus.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Greg Silberstein.
The Company
They focus on the bio pharmaceutical industry the mission of developing treatments against several forms of cancer.Role Description
As a QA Officer you will be performing all day to day QA activities in an independent and pro-active manner.Responsibilities
Ensure correct use of QA systems, SOP’s and Procedures within Kiadis PharmaReview master documents and batch documentation
Perform audits
Write, review and approve applicable controlled documentation
Perform initiation, review and assessment of deviations, change control requests, CAPA’s, OOS and other QMS input.
Manage QA related aspects of projects
Develop training material and train personnel
Requirements
Minimum of 3 years experience in a GMP environment within a similar roleA background in biotechnology
You are result-oriented, a team player with integrity and tenacity.
Fluency in English, other languages are a plus.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Greg Silberstein.
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