Radiopharma QA Release Lead (Onsite NL)

Novartis; Netherlands; On-site; EUR 56,000 - 104,000; Full time

Benefits offered by this job

Health insurance

Retirement plans

Wellbeing resources

Global recognition programs

Flexible/hybrid working

Paid parental leave

Job summary

Novartis in Baarle-Nassau, The Netherlands, seeks a Qualified Person to lead batch release, uphold cGMP compliance, and provide QA oversight of site operations and QA systems. The role supports reliable radiopharmaceutical supply and regulatory compliance across EU directives.

Fluent in English and with a strong GMP background are required. The successful candidate will review batch analyses, lead deviations, CAPAs, and change controls, and act as SME during inspections and audits.

Qualifications

• Master's degree in a scientific discipline.
• 3+ years in QA or similar pharmaceutical role.
• Strong GMP knowledge and regulatory familiarity.
• Fluent in English.
• Agile mindset with continuous improvement.

Responsibilities

• Release and approve batch analyses on site.
• Ensure deviations, CAPAs, changes are investigated and managed.
• Provide QA oversight of site operations and QMS activities.
• Interact during inspections and audits as SME.
• Maintain cGMP compliance and timely product release.

Skills

GMP knowledge

Quality Assurance

Agile mindset

English fluency

Education

Master's degree (scientific)

Pharmacy background preferred

Job description

Novartis in Baarle-Nassau, The Netherlands, seeks a Qualified Person to lead batch release, uphold cGMP compliance, and provide QA oversight of site operations and QA systems. The role supports reliable radiopharmaceutical supply and regulatory compliance across EU directives.

Fluent in English and with a strong GMP background are required. The successful candidate will review batch analyses, lead deviations, CAPAs, and change controls, and act as SME during inspections and audits.