Aptar is an equal opportunities employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief.
Your new employer:
- Aptar Pharma is part of AptarGroup, Inc., a global leader in drug and consumer product dosing, dispensing and protection technologies. Aptar serves a number of attractive end markets including pharmaceutical, beauty, food, beverage, personal care and home care.
- 14.000 employees - 57 locations - 20 countries
- Our location: Radolfzell & Eigeltingen
- Founded 1947
- More than 950 employees
- Continuously growing company
- Aptar - more crisis-proof than other employers
- Production for pharmaceutical industry customers with more than 500 million innovative dosing systems p.a.
- Quality representative and active member in global operations/manufacturing projects: You will play a key role in product transfer projects, customer and development projects at international sites.
- Quality champion for compliance with QM standards (ISO 13485 and 15378): You will ensure the application of these standards in all projects and establish cooperation between the quality units of the sites.
- Partner with international customers in the pharma industry: You understand the quality and regulatory framework for our customers' products and provide valuable quality support.
- Contributing to design control and control strategy of our products: You support design control and control strategy for our products.
- Career development opportunity: This position offers you the chance to develop your skills and to explore your next career step – whether as a leader or an expert.
- Degree in engineering or natural sciences
- High level of quality and technical understanding
- Leadership and proactive mindset
- Communication and team orientation: You are communicative, team-oriented, and open-minded with interdisciplinary interests, always looking for constructive solutions.
- Experience in GMP regulated areas: You are experienced in the GMP regulated medical device and/or pharmaceutical industry or suppliers.
- International project management experience
- Business fluency in English and German
- Professional development and career planning
- Flexible working time and 30 vacation days
- Employee profit-sharing
- Special financial benefits including employee health and fitness program, employee discounts, retirement provisions, canteen meals
- Employee events
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