Team Leader - Los Angeles, United States - STADA Group

Description

At STADA we pursue our purpose Caring for peoples health as a trusted partner worldwide. Originally founded by pharmacists, we are a leading manufacturer of high-quality pharmaceuticals.

More than 12,300 employees around the globe live our values Integrity, Entrepreneurship, Agility and One STADA to achieve ambitious goals and shape the successful future of STADA.

We know that our talented employees make STADA successful and help us grow and reach new achievements as a company.

Therefore, alongside interesting work in diverse areas, we offer our employees a range of opportunities for professional and personal development as well as a working environment, which enables a healthy work-life balance.

Team Lead (f/m/d) Transfer Technology/Pharmaceutical Industry
Bad Vilbel | Deutschland (DE) | Full-time | Permanent


Your responsibilities:

• Management and organization of a Product Transfers Team
• Planning and coordination of product transfer projects

in terms of time, budget and quality

• Ensuring GMP compliant and timely execution of technology transfers in the context of drug production at internal and external manufacturing sites
• Evaluation of the pharmaceutical-technical and galenic feasibility and regulatory strategy aligment
• Quality assurance in the manufacture and testing of pharmaceutical products
• Ensuring compliance with the legal principles of quality assurance, validation, in-process and final controls
• Review of all documents / GMP documentation required for the transfer
• Analysis of production data using statistical data evaluation to improve manufacturing processes and production output
• Participation in due diligences for product and portfolio acquisitions to assess all pharmaceutical-technical issues relating to the producibility, transferability and quality of the products
• Reporting Project Status to upper Management
• Troubleshooting in order to ensure successful transfer realization and timeline adherence

Your qualification:

• University or college degree in the field of Pharmacy or comparable field
• Work experience (> 5 years) in R&D, Regulatory Affairs, Quality Assurance or Manufacturing
• In-depth knowledge of national pharmaceutical legislation
• Very good knowledge of the EU guidelines for the manufacture, development and approval of pharmaceuticals, food supplements and medical products
• High flexibility, willingness to work and independence through constantly changing and complex issues
• Willingness to travel
• Confident knowledge of all MS Office applications
• Leadership experience is a plus
• Fluent language skills in English (German is a plus)

We are looking for talents with expert knowledge and an entrepreneurial spirit that enjoy working collaboratively in a global team.

We are pleased to get to know you better.

Please use our online portal to submit your application:

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