Senior QA Associate: GMP, Master Data & Artwork Review

Panda International; Breda; Sur place; EUR 60 000 - 75 000; Plein temps

Résumé du poste

Panda International in Breda, the Netherlands, seeks a detail-oriented QA professional to support GMP-compliant master data and artwork processes. You will review and approve SAP master data, ensure QA systems are maintained, and collaborate with the Global Artwork Center, Master Data, and site SMEs.

Key responsibilities include approving BOMs and artwork for medicinal products, authoring SOPs and work instructions, and preparing weekly and monthly performance metrics.

Qualifications

• Bachelor's degree in Life Sciences or related field, or equivalent experience.
• Typically, three years of QA or manufacturing experience in the pharmaceutical or medical device industry.
• Knowledge of GMP, GDP, and GCP with ability to interpret and apply requirements.
• Fluency in English, written and spoken.
• Strong attention to detail and accuracy.

Responsabilités

• Review and approve Master Data-related activities, including critical value verification and BOMs.
• Approve artwork for medicinal products.
• Act as an author of operational SOPs and Work Instructions.
• Perform QA reviews of operational SOPs and Work Instructions.
• Prepare weekly and monthly performance metrics.
• Own and maintain departmental performance boards.
• Participate in QA-related projects as required.
• Assist with investigations as needed.
• Establish effective working relationships with stakeholders outside the immediate area of expertise.

Connaissances

Attention to detail

Communication skills

Policy adherence

Pressure management

Formation

Bachelor's in Life Sciences

Outils

SAP Master Data

Description du poste

Panda International in Breda, the Netherlands, seeks a detail-oriented QA professional to support GMP-compliant master data and artwork processes. You will review and approve SAP master data, ensure QA systems are maintained, and collaborate with the Global Artwork Center, Master Data, and site SMEs.

Key responsibilities include approving BOMs and artwork for medicinal products, authoring SOPs and work instructions, and preparing weekly and monthly performance metrics.