Pharmaceutical Technology Specialist / Packaging & Assembly, 100% (m/f/d)

Iscador AG is a pharmaceutical company that has taken over the production and worldwide distribution of the leading mistletoe preparation Iscador. Mistletoe therapy has been a proven component of integrative cancer therapy for decades. Our goal is to further expand the use of Iscador in oncology. As a complement to our team in packaging and assembly, we are looking for an experienced individual to join us immediately or by arrangement as

Pharmaceutical Technology Specialist / Packaging & Assembly, 100% (m/f/d)

In this versatile role, you will play a central part in ensuring our technical operational readiness as well as the GMP-compliant packaging and assembly of our medicinal products. You will work closely with various departments and contribute significantly to the quality, efficiency, and further development of our production processes.

Your tasks

• Organization, coordination, and leadership of the packaging and assembly team
• Ensuring timely, quantity-appropriate, and quality-compliant availability of products for shipping
• Capacity and work deployment planning in coordination with Supply Chain Management and Production
• Assessment of disruptions and deviations and initiation of appropriate measures
• Maintenance and upkeep of infrastructure and equipment
• Planning, monitoring, and documentation of maintenance of machines and equipment
• Creation of specifications for technical equipment and production tools
• Management and maintenance of technical documentation
• Creation, review, and updating of standard operating procedures (SOPs)
• Coordination and supervision of external service technicians
• Support in qualification and validation activities and risk analyses
• Ensuring sustainable and efficient spare parts management
• Support with technical questions and process optimizations

Your profile

• Completed technical or scientific education, ideally in the pharmaceutical field
• Experience in the pharmaceutical industry and GMP-regulated areas
• Knowledge in process optimization, quality assurance, and regulatory requirements
• Technical affinity and analytical, structured thinking
• Independent, solution-oriented, and flexible working style
• Organizational skills, proactive time management, and communication
• Teamwork skills, strong communication, and service-oriented demeanor
• Good German and English skills
• Interest in complementary medicine, especially anthroposophic medicine, is an advantage

We offer you a modern working environment with attractive employment conditions in a family atmosphere characterized by flat hierarchies and short decision-making paths. You can expect an exciting and varied field of activity with cross-departmental collaboration, plenty of creative freedom, and interesting development opportunities. Look forward to a dedicated and motivated team that supports you in your work.

Are you ready to take on this challenge with us? Then we look forward to receiving your application in electronic form.

Note for personnel service providers:

For this position, we only consider direct applications.