Spezialist für Qualitätsprojekte

Job Description

The main goal of our Production & Delivery department is to act as the most reliable manufacturer and supplier of biopharmaceuticals worldwide. We operate a global production network in close collaboration with our internal production facilities, external contractors, suppliers, and partners to deliver high-quality products to customers and patients reliably and on time.

Our quality assurance ensures that all materials and substances in our products are manufactured, processed, tested, packaged, stored, and delivered in compliance with our strict quality standards and regulatory requirements. By closely working together with our internal production sites and collaborating with external manufacturers and suppliers, we establish a global production network dedicated to supplying customers and patients worldwide with products that meet high-quality standards.

With our new production site in Krems an der Donau, we aim to be a provider of innovative vaccines and immunotherapies for the protection and treatment of livestock and pets. Expanding our biotechnological facilities, our company aims to become a significant employer in Lower Austria, offering attractive career opportunities in various roles within a modern and secure working environment.

For this location in Krems, we are looking for a

Quality Projects Specialist (m/f/d)

temporary until

Responsibilities:

• Coordination, planning, and execution of project activities;
• Coordinating with various local and global teams;
• Point of contact for quality-related questions related to ongoing and future transfer activities
• Review and approval of documents related to method or process transfers.
• Participation in Coreteam meetings as a representative of Quality Krems
• Support and execution of quality master data updates (SAP, LIMS...);
• Review of quality system records such as change controls, CAPAs, or deviations;
• Creation and revision of Standard Operating Procedures (SOPs) and other quality assurance documents;
• Responsibility for personal and immediate environment's safety
• Compliance with all safety regulations and immediate reporting of defects to superiors

Requirements:

• Completed degree in natural sciences, engineering, or pharmaceutical studies (Bachelor's or equivalent)
• Very good German and English language skills (fluent in speaking and writing)
• Excellent knowledge of Office programs
• Work experience in the GMP area
• Transfer experience is advantageous
• Good knowledge of quality systems and related electronic systems (Reliance, E-documentation systems, LIMS, Supplier Transparency...) is advantageous
• Good organizational, communication, and team skills
• Quick comprehension and resilience
• Ability to manage multiple topics simultaneously
• High sense of responsibility for assigned tasks

What we offer:

• Unique opportunity to contribute to the development of a modern 'State-of-the-Art' production facility
• Exciting and challenging work in a new, growing organization
• Varied tasks in an internationally operating company
• Collaboration in a professional, ambitious, and highly motivated team and a supportive positive work environment
• Good education and training opportunities
• Flexible working hours and attractive social benefits
• Paid parental leave for mothers and fathers for 12 weeks

The collective bargaining minimum salary for this position is EUR 48,600 gross per year. Depending on the successful candidate's qualifications and work experience, willingness to pay above this amount is given.

We are proud to be a company that builds on the values of its diverse, talented, and dedicated employees. The fastest way to drive innovative developments forward is to bring together different ideas in an integrative environment. We encourage our colleagues to discuss their ideas objectively and tackle problems together. We see ourselves as an equal opportunity employer and are committed to promoting inclusive, diverse workplaces.