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Octapharma

Group Lead Expert – Good Distribution Practice

Octapharma

. Ensure GDP compliance across Octapharma's global distribution network .

Posted 10/23/2026full-timeVienna • AustriaSenior💰 €4,356 per monthWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Good Distribution Practice (GDP) compliance and pharmaceutical quality assurance, with a strong focus on regulatory requirements and quality initiatives. Proven ability to manage audits, develop training, and lead cross-functional projects in an international environment.

Highest-signal resume keywords
Good Distribution Practice (GDP)Pharmaceutical Quality AssuranceLead Auditor TrainingProject ManagementRegulatory Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
GDP ComplianceQuality AuditingRegulatory KnowledgeQuality Documentation ReviewTraining Development
Soft Skills
Excellent CommunicationStakeholder Management
Certifications & Qualifications
Lead Auditor Certification
Industry Keywords
Pharmaceutical Quality SystemCFR Parts 3 and 4EU MDR Annex 1Quality AgreementsContinuous Improvement

About the role

Key responsibilities & impact
  • Ensure GDP compliance across Octapharma's global distribution network
  • Manage qualification and oversight of distributors and subsidiaries, including audits and quality agreements
  • Drive quality initiatives and continuous improvement across the organisation
  • Oversee transportation processes and approve validation activities
  • Collaborate with local GDP Officers
  • Monitor regulatory developments and translate requirements into corporate standards and procedures
  • Lead the corporate GDP Forum to promote knowledge sharing and alignment across sites
  • Represent Group Quality Assurance in cross-functional supply chain projects
  • Support harmonisation of the Pharmaceutical Quality System
  • Develop and deliver training
  • Review and approve corporate quality documentation

Requirements

What you’ll need
  • University degree in Pharmacy, Chemistry, Chemical Engineering or a related scientific discipline
  • At least 5 years of experience in GDP and pharmaceutical quality activities
  • At least 3 years of GDP auditing experience
  • Documented lead auditor training
  • In-depth knowledge of GDP regulations, including requirements for combination products (CFR Parts 3 and 4, EU MDR Annex 1)
  • Strong project management skills and experience driving initiatives across multiple sites
  • Excellent communication and stakeholder management skills in an international environment

Benefits

Comp & perks
  • Attractive salary and benefits package
  • Internal and external employee and leadership trainings
  • Trainee programs
  • Digital solutions
  • Meaningful work producing life-saving medicines
  • High level of influence and opportunity to make a difference
  • Work with skilled and fun colleagues in a relatively informal organization
  • Long-term perspective for employees and relationships