Senior Associate QA – Master Data & Artwork Compliance, Breda, Noord-Brabant

Company:
Our client is a leading pharmaceutical organization dedicated to the development and manufacturing of high-quality medicinal products. They are committed to maintaining the highest standards in quality, compliance, and operational excellence to ensure patient safety worldwide.

Job Description:
We are seeking a detail-oriented and quality-focused QA professional to support Operational Life Cycle Management activities within a GMP-regulated environment. The successful candidate will be responsible for reviewing and approving SAP Master Data, Bill of Materials (BOMs), commercial artwork, and operational documentation while ensuring compliance with internal quality standards and regulatory requirements.
This role requires strong attention to detail, the ability to remain focused on operational verification activities, and effective communication with cross-functional stakeholders. Both junior and experienced candidates are encouraged to apply.

Responsibilities:
• Review and approve SAP Master Data activities, including critical value verification and Bill of Materials (BOM) checks.
• Perform QA approval of commercial artwork for medicinal products.
• Ensure QA systems are maintained, monitored, and continuously improved.
• Collaborate with Global Artwork teams, Master Data teams, Supply Chain, Site SMEs, Regulatory Affairs, and QA Management.
• Author, review, and maintain operational SOPs and Work Instructions.
• Participate in QA-related projects and support continuous improvement initiatives.
• Assist with minor deviations, investigations, and data integrity related activities.
• Support compliance within a regulated GMP environment through accurate verification and documentation activities.
• Provide guidance and support within the QA team when required.

Requirements:
• Bachelor’s or Master’s degree in Life Sciences, Biology, Biotechnology, Pharmacy, Pharmaceutical Sciences, or a related scientific field.
• Open to MSc graduates without experience as well as candidates with relevant QA or manufacturing experience within pharmaceutical, biotech, or medical device industries.
• Knowledge of GMP, GDP, and/or GCP regulations and the ability to apply them in routine operational activities.
• Experience with SAP Master Data, artwork management, BOMs, SOPs, or documentation processes is considered an advantage.
• Strong communication skills and stakeholder management abilities.
• Excellent attention to detail with an accurate and meticulous working style.
• Comfortable working under pressure and performing repetitive verification tasks with consistent focus.
• Fluent in English.

Other Information:
• Initial contract duration of 1 year with possible extension and long-term potential.
• Hybrid working model with a minimum of 2 onsite working days per week.
• Collaborative international QA team environment.
If you are interested and want to apply, please submit your application via the apply button below and contact me.

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