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Senior Associate QA | Breda

LocationBreda, Netherlands
Business SectorBiotechnology
Contact nameDaria Finikova
Contact email
Job ref27194
Published1 day ago

IMPORTANT INFO:
We are looking for a detail-oriented colleague, with strong communication skills and the ability to work under pressure. GMP experience is a plus.

Expectations/scope/complexity
Objectives:
• To perform QA review and Approval for SAP Master Data and artwork
• To ensure QA systems are maintained, improved and performance is appropriately monitored
• To establish effective working relationships with the Global Artwork Center, Master Data, SCPM, Site SME’s 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 SOP’s and Work Instructions
• QA Review of operational SOP’s and Work Instructions
• Participate in QA related projects as needed
• Assist in various investigations as needed

Minimum Requirements
o Education level: BSc degree with relevant working experience, or this position is also a good entry-level position for a Master degree in Lifesciences
o Preferred, but not required: previous experience in GMP/pharma
• 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 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 English language.
• Accurate mindset

Interested? Send your CV to Daria at d.finikova@panda-int.com or call +31202044502