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.
Large pharmaceutical company with a strong distribution site in The Netherlands.
ROLE DESCRIPTION
The Quality Assurance Officer will support with correct maintenance of the Quality Management System within a (GDP) distribution environment.
The main activities associated to this role are the correct coordination between departments.
As the first point of contact, you will identify and collect the potential deviation and non-conformances that might occur.
The QA Officer will support the investigation of CAPAs and deviations and will help with root cause analysis.
Writing reports is also an important part of the work load.
Additionally, you will be responsible for implementing preventive, corrective actions and improvements.
Extra information:
- Type of contract: It begins with 1 year contract (payroll) and then it becomes a permanent role
- Full-time
- On-site
RESPONSIBILITIES
Main responsibilities:
- Compliance of GMP/GDP
- Coordination between departments (increase the communications)
- Documentation review
- Investigation of deviations, CAPAs (escalate to Sr. QAO/ QAM when needed)
- Change control
- Release of raw materials
- Support customer complaints
- Coordination with warehouse, order & handling
- Batch record review
- Internal audit support
- Review, write and work with SOPs (QA and production)
REQUIREMENTS
- Bachelor degree in a scientific environment (preferred)
- Previous experience in a Quality role
- Strong knowledge on GMP and GDP guidelines
- Good experience with document management system
- Familiar with experience with Trackwise/LIMS/SAP/ERP.
- Proficient level of English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
