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ALTEN

Senior Quality Manager – R&D

ALTEN

. Ensure quality oversight for complex R&D projects and global quality initiatives .

Posted 9/17/2026full-timeRemote • AustriaSenior💰 €4,000 per monthWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in cGMP compliance, quality risk management, and project management within the pharmaceutical industry, ensuring quality oversight and operational excellence across R&D projects and global initiatives.

Highest-signal resume keywords
CGMP ComplianceQuality Risk ManagementProject ManagementStakeholder ManagementCAPA Processes

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Quality SystemsRegulatory RequirementsDeviations ManagementChange ControlsValidationAnalytical DevelopmentContinuous ImprovementTraining InitiativesAuditsInspections
Soft Skills
Decision-MakingCollaboration
Industry Keywords
Pharmaceutical IndustryGMP-Relevant DocumentationQuality DeliverablesOperational ExcellenceQuality Culture

About the role

Key responsibilities & impact
  • 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

Requirements

What you’ll need
  • Bachelor's degree with 5+ years of experience or Master's degree with 3+ years of experience 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 processes
  • Strong project management, stakeholder management, and decision-making skills
  • Solid scientific, technical, and compliance knowledge within the pharmaceutical industry
  • Fluent in English
  • Nice to have: Experience with validation, analytical development, health authority inspections, and global project environments

Benefits

Comp & perks
  • 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.