Senior QA Associate

Senior QA Associate

Position Summary
We are looking for a detail-oriented Senior Associate QA with strong communication skills and the ability to perform effectively under pressure. The ideal candidate will support Quality Assurance activities related to SAP Master Data and artwork management, ensuring compliance within a regulated environment. Experience in GMP is considered a strong advantage.

Key Responsibilities

• Perform QA review and approval of SAP Master Data, including critical value verification and Bill of Materials
• Review and approve artwork for medicinal products in accordance with regulatory requirements
• Maintain and improve QA systems, ensuring performance is effectively monitored
• Participate in QA-related projects and continuous improvement initiatives
• Support investigations, including data integrity and quality-related issues
• Collaborate with internal stakeholders such as Global Artwork Center, Master Data teams, SCPM, Site SMEs, RA department, and QA Management
• Ensure compliance with applicable regulatory standards and internal procedures

Problem Solving & Responsibilities

• Analyze and resolve issues of moderate complexity within QA processes
• Identify, evaluate, and resolve data integrity risks
• Interpret and apply established procedures, standards, and regulatory frameworks

Autonomy & Contribution

• Work under general direction aligned with departmental objectives
• Independently manage tasks, priorities, and timelines within assigned projects
• Contribute to team deliverables and project milestones
• Act as a subject matter resource and provide guidance or training to colleagues
• Build effective working relationships across cross-functional teams

Requirements

• Bachelor's degree (BSc) in Life Sciences or related field, or equivalent experience
• This role is also suitable as an entry-level position for candidates with a Master's degree in Life Sciences
• Typically around 3 years of experience in Quality Assurance or manufacturing within the pharmaceutical or medical device industry
• Knowledge of GMP, GDP and/or GCP, with the ability to apply these in routine scenarios
• Strong attention to detail and structured working approach
• Good communication skills and ability to collaborate across teams
• Fluent in English

Preferred

• Prior experience working in a GMP-regulated environment

Let op: vacaturefraude

Helaas komt vacaturefraude steeds vaker voor. We waarschuwen je voor mogelijke misleiding:
* Wij zullen nooit via WhatsApp of in een videogesprek vragen om jouw persoonlijke gegevens (zoals een kopie van je ID, bankgegevens of BSN).
* Twijfel je over de echtheid van een vacature of contactpersoon? Neem dan altijd rechtstreeks contact met ons op via de officiële contactgegevens op onze website.

Important: job fraud

Unfortunately, job fraud is becoming more common. Beware of such scams:
* We will never ask for personal information (such as a copy of your ID, bank details, or social security number) via WhatsApp or during a video call.
* If you're unsure whether a vacancy or contact person is legitimate, please reach out to us directly using the official contact details on our website.