On-Site QA Ops: Batch Release & GMP Compliance

Novartis; Noord-Brabant; On-site; EUR 50,000 - 70,000; Full time

Job summary

Novartis is looking for a Quality Assurance Operations Specialist in Noord-Brabant, Netherlands. The role involves providing QA support for GMP related activities, focusing on the batch release process and ensuring regulatory compliance.

The ideal candidate will have a scientific education (MBO/HBO level) and solid knowledge of quality systems. Tasks include document reviews, quality support for operations, and managing deviations. Fluency in English is required. Join us to contribute to an inclusive work environment while maintaining the highest quality standards.

Qualifications

• Solid understanding of GMP regulatory requirements.
• Experience with quality issues and management.
• Good communication skills in English.

Responsibilities

• Prepare and perform QA review of batch release documents.
• Provide on-site quality support for operations.
• Manage document lifecycle and ensure proper archiving.
• Release starting materials and conduct inspections.
• Approve quality documentation and support deviation management.
• Contribute to audits and inspections preparation.

Skills

Knowledge of quality system (GMP)

Organizational skills

Attention to detail

Sense of urgency

Teamwork

Fluent in English

Education

MBO/HBO level in a scientific field

Job description

Novartis is looking for a Quality Assurance Operations Specialist in Noord-Brabant, Netherlands. The role involves providing QA support for GMP related activities, focusing on the batch release process and ensuring regulatory compliance.

The ideal candidate will have a scientific education (MBO/HBO level) and solid knowledge of quality systems. Tasks include document reviews, quality support for operations, and managing deviations. Fluency in English is required. Join us to contribute to an inclusive work environment while maintaining the highest quality standards.