R&D Senior Quality Manager (all gender) | Austria

ALTEN; Österreich; Vor Ort; EUR 38.000 - 51.000; Vollzeit

Benefits dieser Stelle

Talent Management

Work-Life Balance

Green Mobility

Zusammenfassung

ALTEN in Austria is seeking an R&D Senior Quality Manager to oversee quality across complex projects. The role focuses on cGMP compliance, global quality initiatives, and acting as the main QA partner to cross-functional teams.

Requirements include 5+ years in Pharma Quality (or 3+ with a Master’s), strong risk management skills, and fluent English. Attractive permanent, full-time position with competitive salary and mobility benefits.

Qualifikationen

• Bachelor's degree with 5+ years or Master's with 3+ years in Pharma Quality, QA, Development, or Operations.
• Strong knowledge of cGMP regulations, quality systems, and regulatory requirements.
• Experience in quality risk management, deviations, change controls, and CAPA.
• Fluent English communication.

Aufgaben

• Oversight for complex R&D projects and global quality initiatives.
• Be the QA partner for cross-functional stakeholders and project teams.
• Review, approve, and release GMP-relevant documentation.
• Drive quality activities including risk assessments, deviations, change controls, CAPAs, and training.
• Support validation, qualification, and continuous improvement projects.
• Provide expert guidance on cGMP compliance and quality standards.
• Contribute to audits, inspections, and due diligence activities.
• Promote operational excellence and a strong quality culture.

Kenntnisse

Quality oversight

Project management

Stakeholder management

Regulatory compliance

English communication

Ausbildung

Bachelor's degree in Pharma/QA/Development/Operations

Master's degree in Pharma/QA/Development/Operations

Jobbeschreibung

R&D Senior Quality Manager (all gender) | Austria

• Full-time
• Contract Type: Permanent

We are the designers of today for the world of tomorrow.

As one of the world’s leading engineering service providers, we at ALTEN are committed to positively shaping the future of our partners, the careers of our employees and the challenges facing our society and environment.

More than 50,000 employees in 30 countries are already working on innovative solutions in various engineering and IT sectors such as aerospace, renewable energy, medical technology, railway technology and automotive.

YOU

• ensure quality oversight for complex R&D projects and global quality initiatives
• act as the key QA partner for cross-functional stakeholders and project teams
• review, approve, and release GMP-relevant documentation and quality deliverables
• drive quality activities including risk assessments, deviations, change controls, CAPAs, and training initiatives
• support validation, qualification, and continuous improvement projects
• provide expert guidance on cGMP compliance and quality standards
• contribute to audits, inspections, and due diligence activities
• promote operational excellence and a strong quality culture across the organization

YOU

• hold a Bachelor's degree with 5+ years or a Master's degree with 3+ years of experience in Pharma Quality, QA, Development, or Operations
• have strong knowledge of cGMP regulations, quality systems, and regulatory requirements
• bring experience in quality risk management, deviations, change controls, and CAPA processes
• demonstrate strong project management, stakeholder management, and decision-making skills
• possess solid scientific, technical, and compliance knowledge within the pharmaceutical industry
• communicate fluently in English

Nice to have: Experience with validation, analytical development, health authority inspections, and global project environments.

Salary: Starting from €4,000 gross per month, with a clear willingness to offer a higher salary depending on qualifications and professional experience.

We value diversity and therefore welcome all applications, regardless of gender, nationality, ethnic or social background, religion or beliefs, disability, age, sexual orientation, or identity.

Applicants with severe disabilities will be given preferential consideration if equally qualified.

• Talent Management – We support your professional growth and help you develop your career.
• Work-Life Balance – Flexible working hours and the opportunity for mobile working.
• Green Mobility – Benefit from our public transportation subsidy and enjoy discounted commuting.