QA Systems Associate (0.5 FTE)
QA Systems Associate (0.5 FTE)
The Role:
- Act as Business Administrator and coordinate all aspects of the full operation of Merus eQMS including:
- Document Management
- Learning Management System (including study specific training)
- QMS (Change Control, Deviation handling, CAPA, Complaints, Supplier Management, Audit & Inspection)
- Manage GxP documents and ensure training is assigned appropriately
- Foster a quality mindset around Good Documentation Practices
- Collaborate with all GxP departments to provide customer service, analyze system incidents, and introduce system optimization
- Contribute to continuous development of Merus’ Quality Management System to address changing needs of Merus
- Compile, monitor and trend Merus quality indicators for weekly, monthly, and quarterly Quality Reviews
- Participate in and prepare for (internal) audits and inspections as SME.
Your Profile:
Your Profile
We are looking for a highly organized and detail-oriented individual with experience with Document Management Systems. The ideal candidate will have a background in document control and quality management processes. It is a big plus if you have had any experience participating in audits and inspections. Effective communication skills, ability to collaborate and a proactive approach to continuous improvement are essential.
- Degree in Biosciences or related field
- Minimum of 2-3 years relevant GMP work experience within biotechnology/ pharmaceutical /medical device industry, in a manufacturing or quality environment.
- Experience with MS Office (Word, Excel in particular)
- Proficient in an eDMS/LMS system, experience as business administrator is a plus.
- Knowledge of GMP; working knowledge of GCP, GDP
- Fluency in English (written and verbal)
Why Merus?
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