Sr. Officer QA - Fulltime - Amsterdam
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.
Your responsibilities will consists out of developing and implementing Quality Systems and you will also be involved in various projects in order to help the company grow.
Develop and provide training material to all employees.
Ensure accurate and correct use of the QA Systems and SOP’s
Write, review and approve master documents.
Experience in GMP Manufacturing and/or Quality Control
A degree in Biotechnology, Chemistry or equivalent field.
Fluent in English, any other European language is 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
.Role Description
You will be responsible for developing and implementation of various (Electronic) Quality Systems. Simultaneous you will work on a various projects that support the growth of Kiadis for both our corporate and manufacturing sites in various locations.Your responsibilities will consists out of developing and implementing Quality Systems and you will also be involved in various projects in order to help the company grow.
Responsibilities
Perform and initiate internal and external audits.Develop and provide training material to all employees.
Ensure accurate and correct use of the QA Systems and SOP’s
Write, review and approve master documents.
Requirements
Experience in a similar role and international working environmentExperience in GMP Manufacturing and/or Quality Control
A degree in Biotechnology, Chemistry or equivalent field.
Fluent in English, any other European language is 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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