QA Specialist
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-Brabant Netherlands.
Assure agreed validation strategy is properly documented and aligned
Provide support to Plant QA regarding equipment or information system related production issues.
Project team member to develop efficient quality processes and translate them in standard operating procedures;
Perform final review of (technical) change controls, confirming assessments of different stakeholders are complete
At least 5 years of professional experience within a GMP environment;
Relevant experience with equipment and automation validation;
Able to work on a wide variety of projects simultaneously;
Able to work in a changing environment;
Fluent in English.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
The company is one of the major global leaders in the field of biotechnology. Globally, the company provides solutions for patients with all kinds of symptoms.Role Description
In this role you will become part of the quality team with a special focus on validation.Responsibilities
Agree on the validation strategy and provide guidance regarding design, characterization and validationAssure agreed validation strategy is properly documented and aligned
Provide support to Plant QA regarding equipment or information system related production issues.
Project team member to develop efficient quality processes and translate them in standard operating procedures;
Perform final review of (technical) change controls, confirming assessments of different stakeholders are complete
Requirements
Master degree related to the pharmaceutical industry;At least 5 years of professional experience within a GMP environment;
Relevant experience with equipment and automation validation;
Able to work on a wide variety of projects simultaneously;
Able to work in a changing environment;
Fluent in English.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
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