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Octapharma

Group Expert - QC Innovation for Operations

Octapharma

. Drive and coordinate innovation and improvement projects within Group QC .

Posted 10/9/2026contractVienna • AustriaMid-LevelSenior💰 €4,356 per monthWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in analytical method development, validation, and transfer within a GMP-regulated environment, while effectively managing stakeholder communication and project coordination across global teams.

Highest-signal resume keywords
Analytical Method DevelopmentMethod ValidationGMP ComplianceStakeholder ManagementProject Coordination

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Analytical ChemistryBiochemistryChemistryMethod TransferRisk AssessmentSOP DevelopmentQuality Documentation
Soft Skills
Strong CommunicationCollaborationIndependent Work
Industry Keywords
GMP-Regulated EnvironmentQuality ControlProject ManagementCross-Functional TeamsGlobal Organisation

About the role

Key responsibilities & impact
  • Drive and coordinate innovation and improvement projects within Group QC
  • Act as the key link between project teams, analytical experts, Group QC Method Validation and local QC organisations
  • Coordinate and follow up analytical method development, validation and transfer activities across development and technology transfer projects
  • Represent Group QC in cross-functional project teams and provide quality control expertise
  • Prepare and present analytical method status assessments, analytical risk assessments and project updates to stakeholders
  • Drive GMP-related activities including risk assessments, change controls, SOPs and other quality documentation
  • Support development of new pipeline products, optimization of licensed products, technology transfers and continuous development of Octapharma's global Quality Control organisation

Requirements

What you’ll need
  • Master's degree or Ph.D. in Chemistry, Biochemistry, Analytical Chemistry or a related scientific discipline
  • Experience with analytical methods and method validation in a GMP-regulated environment
  • Strong communication and stakeholder management skills, with the ability to collaborate effectively across functions and sites
  • Experience of coordinating projects and driving activities to completion
  • Ability to work independently and navigate a global organisation with multiple stakeholders
  • Fluency in German and English

Benefits

Comp & perks
  • Company restaurant & meal subsidy
  • Training & further education
  • Health promotion
  • Parking spaces and good public transport connections
  • Company and team events