Our partner, a leading European pharmaceutical manufacturer, is looking for a Quality Assurance Manager to join their expanding operations in Hungary.
In this key role, the QA Manager will be responsible for overseeing GMP compliance and Quality Systems related to chemical production and development. The position plays a strategic role in managing quality operations, audits, and continuous improvement in a highly regulated manufacturing environment.
Key Responsibilities:
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Leading and supervising the QA team supporting chemical and biotech production and development
-
Managing GMP-based Quality Management Systems and documentation control
-
Driving audit readiness, handling internal and external audits and inspections
-
Defining KPIs and initiating improvement actions
-
Handling deviations, CAPAs, change control, and risk management
-
Supporting qualification/validation, supplier audits, and regulatory compliance activities
-
Overseeing training systems, quality agreements, and QA-related metrics and reports
Requirements:
-
University degree in chemistry, chemical engineering or related life sciences
-
5+ years of QA/QC experience in pharmaceutical manufacturing
-
Minimum 1 year in a leadership role
-
Deep knowledge of GMP, quality systems and regulatory requirements
-
Fluency in English and Hungarian
-
Experience with audit preparation, change management and documentation systems
What’s offered:
-
Diverse technologies and opportunity for professional development
-
Regulated, modern pharmaceutical manufacturing environment
-
Competitive salary and benefits package (cafeteria, private healthcare, gym access, pension fund, annual health screening, and more)
-
Independent role with space for process improvement and innovation
Our partner, a leading European pharmaceutical manufacturer, is looking for a Quality Assurance Manager to join their expanding operations in Hungary.
In this key role, the QA Manager will be responsible for overseeing GMP compliance and Quality Systems related to chemical production and development. The position plays a strategic role in managing quality operations, audits, and continuous improvement in a highly regulated manufacturing environment.
Key Responsibilities:
-
Leading and supervising the QA team supporting chemical and biotech production and development
-
Managing GMP-based Quality Management Systems and documentation control
-
Driving audit readiness, handling internal and external audits and inspections
-
Defining KPIs and initiating improvement actions
-
Handling deviations, CAPAs, change control, and risk management
-
Supporting qualification/validation, supplier audits, and regulatory compliance activities
-
Overseeing training systems, quality agreements, and QA-related metrics and reports
Requirements:
-
University degree in chemistry, chemical engineering or related life sciences
-
5+ years of QA/QC experience in pharmaceutical manufacturing
-
Minimum 1 year in a leadership role
-
Deep knowledge of GMP, quality systems and regulatory requirements
-
Fluency in English and Hungarian
-
Experience with audit preparation, change management and documentation systems
What’s offered:
-
Diverse technologies and opportunity for professional development
-
Regulated, modern pharmaceutical manufacturing environment
-
Competitive salary and benefits package (cafeteria, private healthcare, gym access, pension fund, annual health screening, and more)
-
Independent role with space for process improvement and innovation