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Posted 7 days ago

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

Österreich, AustriaRemoteFull-time

AI Summary

R&D Senior Quality Manager at Alten in Austria, responsible for quality oversight of complex R&D projects, GMP documentation review and release, risk assessments, deviations, CAPAs, validation, and cGMP compliance across cross-functional teams.

About this role

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

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

Qualifications

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.

Any questions?

Feel free to contact me: Maja Kujundzic (Mobile: +43 699 10979556).

Additional Information

  • 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.

Skills

Analytical DevelopmentAuditCAPACGMPChange ControlsContinuous ImprovementDeviationsDue DiligenceGMPHealth Authority InspectionsOperational ExcellenceProject ManagementQualificationQuality Risk ManagementQuality SystemsRegulatory RequirementsStakeholder ManagementValidation

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