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Stellenbeschreibung

STADA Arzneimittel GmbH
What You Can Expect

• You ensure development deliverables for our Biosimilar / Specialty programs are completed in time, at agreed costs and carefully balancing benefits & risks
• You manage cross-functional alignment and decision-making
• You provide scientific and technical expertise, e.g. in regulatory, tech, transfer etc.
• You are responsible for comprehensive project documentation, tracking and reporting
• You manage joint decision-making as well as of potential escalation in case of non-agreement
• You review all kinds of documents such as analytical and manufacturing documents
• You closely collaborate between individual Project Management as well as Regulatory team members to allow for best practice sharing and lessons learned
• You contribute to department initiatives such as training and soft skill development

Who We Are Looking For

• You have a university degree in life sciences, e.g., Biologist/Biochemist, or comparable (master's degree)
• You have a minimum of 8 years of working experience in the life science sector
• You have expertise in the development and manufacture of biotechnology-derived medicinal products, ideally in biosimilar projects
• You have professional experience and / or educational background in project management
• You are professional in the use of MS Office
• You have strong communication skills, proactive team worker, high sense of responsibility and urgency, problem-solving skills
• You have the willingness to collaborate in internal as well as in inter-company cross-functional teams
• You are fluent in English, another language is a plus