Manager Clinical Trial Supply

Granzer Pharmaceutical Services GmbH was founded in 2022 as a spin-off of Granzer Regulatory Consulting & Services GmbH. We are a Pharmaceutical Service Provider and Consultancy for the Development, Manufacturing and Quality Assurance of Medicinal Products. Our focus is the EU Import, Storage, Distribution and EU-Release of Investigational Medicinal Products, supporting the Clinical Trials of our Clients.

For our team in Munich, we are looking for a

Manager Clinical Trial Supply

Responsibilities

• Compile the release documentation for clients’ clinical trials, including the PSF
• Perform clinical distribution activities
• Align with external CMOs and logistics providers
• Provide advice to our clients on their clinical trial supply chains
• Provide advice to our clients on regulatory requirements
• Support our clients in vendor selection and qualification activities
• Support the import processes for client IMP
• Support project management
• Support the maintenance of our GMP storage
• Support the Continuous Improvement of our Pharmaceutical Quality System
• Support inspections by authorities, client audits and self-inspections

Qualifications

• Academic degree as a pharmacist or in a Life Science related field, or degree as pharmaceutical-technical assistant (PTA)
• At least 5 years of experience in the pharmaceutical industry with relevant experience for the position
• Excellent knowledge of GxP regulations in Europe and US
• Willingness for occasional on-call duty
• Willingness to travel occasionally (e.g. meetings with clients or CDMO)
• Strong team work ethic and sound organizational skills for functioning with a high degree of independence on projects with minimal supervision
• Flexible working style and willingness for continuous education
• Knowledge of IT applications such as Microsoft Office and SAP
• Fluency in German and English

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