Quality assurance officer
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands.
They are a dynamic, global organization fully dedicated to providing laboratory services to support all phases of clinical trials. They are focused on the best science, technology and people.
ROLE DESCRIPTION
As Quality Assurance Officer you will act as QA coordinator within the organization, you will perform quality assessments on the operational processes and advise on improvements towards the departments. Are you willing to show your analytical skills? And you are an organizational talent, continue to perform effectively under pressure and know how to monitor progress? Then this is the job for you!
RESPONSIBILITIES
You will be responsible for making plans, execute and report audits according to the audit timetable and applicable procedures for the organization and suppliers. Next to that you will monitor the progress, appropriateness and correct implementation of corrective measures. You will also be responsible for the following:
- You prepare, review and improve QA procedures;
- You review and approve procedures of other departments within the organization;
- You provide quality-enhance training on your own initiative and on request;
- You will be a contact person for quality questions from the organization;
- You maintain current knowledge of standard requirements according to GLP, GCP, GMP, CAP, ISO17025 and ISO 15189 guidelines related to the business process;
REQUIREMENTS
- A Bachelor or Master degree in Life Science or a Quality oriented education;
- Confident en dare to engage in the discussion with the management;
- Work experience with or strong affinity with quality systems set up according to GLP and GMP;
- You are able to increase the quality consciousness of employees by your persuasiveness;
- Work experience in the field of ISO / IEC 17025 and 15189 is a pré;
- You have an excellent command of English, spoken and written;
- Customer and quality, team spirit and integrity are very important competencies.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
