Wie möchten Sie sich registrieren?
Wie möchten Sie sich anmelden?


Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.
As a Group Lead Expert - Good Distribution Practice (GDP), you will play a key role in ensuring GDP compliance across Octapharmas global operations. You will drive the qualification and oversight of distributors, strengthen quality standards throughout the distribution network and collaborate with international stakeholders to ensure the safe and compliant distribution of our life-saving medicines.
The position will be filled in Vienna (Austria), Springe (Germany), Stockholm (Sweden) or Lingolsheim (France).
Join us in shaping our vision of providing new health solutions advancing human life.
Ensure GDP compliance across Octapharmas global distribution network
Manage the qualification and oversight of distributors and subsidiaries, including audits and quality agreements
Drive quality initiatives and continuous improvement across the organisation
Oversee transportation processes, approve validation activities and 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 and support the harmonisation of the Pharmaceutical Quality System
Develop and deliver training and review and approve corporate quality documentation
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 and 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
You will thrive in this role if you enjoy taking ownership, translating regulatory requirements into practical solutions and collaborating across international teams to ensure the safe and compliant distribution of life-saving medicines.
The minimum gross salary according to the collective agreement (chemical industry) is EUR 4,355.55 based on 38 hours per week (full-time). As we strive to offer a salary that reflects your individual profile and qualifications, there is a willingness to pay above the minimum salary.
We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion.
Do you have any questions? Then get in touch with your contact person.
Larissa Amling
Octapharma Pharmazeutika Produktionsges.m.b.H.
Oberlaaer Straße 235, 1100 Wien
Visit our website Octapharma Career and follow us daily on LinkedIn.