I am looking for a Sr QA Associate for my biotech client from Breda.
We are looking for a detail-oriented colleague, with strong communication skills and the ability to work under pressure. GMP experience is a plus.
Objectives
- To perform QA review and Approval for SAP Master Data and artwork
- To ensure QA systems are maintained, and improved and performance is appropriately monitored
- To establish effective working relationships with the Global Artwork Center, Master Data, SCPM, Site SME and RA department, as well as QA Management
Position Specific Tasks
- Perform review and approval of Master Data-related activities (such as critical value verification and Bill of Materials)
- Perform approval of artwork for medicinal products
- Act as author for operational SOPs and Work Instructions
- QA Review of operational SOPs and Work Instructions
- Participate in QA-related projects as needed
- Assist in various investigations as needed
- Responsible for the preparation of weekly/monthly metrics
- Own and maintain departmental performance boards
Requirements
- MBO or Bachelor’s degree in Life Sciences or related field or the equivalent combination of education and/or experience. Entry-level position for Master's degree in Lifesciences.
- Typically 3 years of related Quality Assurance or manufacturing experience in the pharmaceutical or medical device industry
- Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) and/ or Good Clinical Practice (GCP) knowledge with the ability to interpret and apply in mainly routine cases.
- Fluent in the English language.
- Accurate mindset
If you are interested, please send your CV to f.chauca@panda-int.com today! Let's connect promptly.
Feel free to introduce me to potential candidates. You can also refer a friend and earn €250,- for successful referrals.