Our dynamic team in the heart of picturesque Penzberg sets new standards in the development of pioneering medical solutions. We offer ambitious talents the opportunity to contribute and develop their expertise in the position of Specialist (m/f/d) for deviations and CAPAs.
Here's what we offer
1. Attractive salary and long-term job security through group affiliation
2. Up to 30 days vacation per year
3. Contribution to company pension scheme after end of probationary period
4. Extensive social benefits, including Christmas and vacation bonuses
5. Reimbursement of travel expenses
6. Generally an open-ended employment contract
7. Good chances of being taken on by our business partners
8. Tailored further training opportunities and free language courses
9. A wide range of employee benefits
Your tasks
- Responsibility for the creation and processing of deviations and CAPAs
- Participation in local and global initiatives and continuous improvement projects (CIP)
- Creation, monitoring and reporting of relevant key performance indicators (KPIs)
- Working closely with internal and external stakeholders to ensure compliance standards according to GMP
- Development and implementation of strategic initiatives to improve compliance according to GMP Pharma EU
- Management and coordination of projects for risk minimization and process optimization
- Training and advising employees in the area of deviation and CAPA management
Your profile
Must Have:
- Degree in pharmacy, chemistry, biotechnology, engineering or training in a related field with professional experience
- Professional experience in the creation and processing of deviations and CAPAs
- Production and process knowledge and experience of working in a pharmaceutical production environment highly desirable
- Analytical thinking and excellent problem solving skills
- Strong communication and teamwork skills
- High resilience and the ability to stay on top of things even in stressful situations
- Fluency in written and spoken German
Nice to Have:
- extended professional experience in the GMP environment
- Experience in risk and change management is a plus
- advanced knowledge of English
- PhD is possible, but not a must (laboratory work)