Senior Group QA Lead – GMP & Global Quality

Octapharma-Plasma; Wien; Vor Ort; EUR 80.000 - 120.000; Vollzeit

Benefits dieser Stelle

Salary & benefits

Career development

Zusammenfassung

Octapharma is seeking a Group Lead Expert for Pharmaceutical Quality System to guide GMP compliance across multiple sites in Europe. The role focuses on leading QA initiatives, harmonising quality processes, and driving global procedures in a senior capacity.

The candidate will oversee regulatory changes, coordinate audits, and manage cross-site quality programs while traveling 5–10 times per year within Europe. A deep GMP background and leadership experience are essential.

Qualifikationen

• 10+ years of QA experience in pharmaceutical manufacturing and GMP quality systems across Europe and the US.
• Proven experience leading cross-site quality initiatives and harmonising processes.
• Strong stakeholder management and ability to drive collaboration across sites and teams.

Aufgaben

• Act as Group Subject Matter Expert for GMP regulations and guidelines, advising Octapharma sites on GMP topics.
• Monitor evolving GMP regulations, assess impact and communicate changes through Quality Bulletins.
• Lead the development and harmonisation of the Pharmaceutical Quality System, including global procedures and templates.
• Participate in and support intersite audits of manufacturing and packaging sites.
• Coordinate Group Quality activities, including annual mock recalls and alignment with local QA teams.

Kenntnisse

GMP regulations

Quality systems

Cross-site leadership

Stakeholder management

CAPA & deviations

Ausbildung

University degree in Chemistry, Chemical Engineering, Pharmacy

Jobbeschreibung

Octapharma is seeking a Group Lead Expert for Pharmaceutical Quality System to guide GMP compliance across multiple sites in Europe. The role focuses on leading QA initiatives, harmonising quality processes, and driving global procedures in a senior capacity.

The candidate will oversee regulatory changes, coordinate audits, and manage cross-site quality programs while traveling 5–10 times per year within Europe. A deep GMP background and leadership experience are essential.