Dottikon
2 quarters ago
Project Manager Quality Assurance (QA Manager) 100% (m/f/d)
- Publication date:05 June 2025
- Workload:100%
- Place of work:Dottikon
Job summary
Dottikon Exclusive Synthesis AG specializes in high-quality chemical products. Join a dynamic team focused on continuous improvement and quality management.
Tasks
- Manage process deviations in a GMP-regulated environment independently.
- Conduct thorough root cause analyses with interdisciplinary teams.
- Monitor and optimize quality processes for compliance with GMP regulations.
Skills
- Degree in chemistry or related sciences; experience in pharmaceutical quality management.
- Strong analytical and pragmatic thinking; flexible and resilient.
- Fluent in German and English, both written and spoken.
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About the job
We manufacture high-quality finishing chemicals, intermediates, and exclusive active ingredients for the world's leading chemical and pharmaceutical industry. As a company with a production site in Dottikon in the canton of Aargau, we specialize in safety-critical reactions and position ourselves as a strategic development and production partner.
Where there is a will, there is a way.
Continuously improving ourselves and our solutions is our top priority. Through attentive quality management, we succeed in responding proactively and quickly to the ever-increasing quality demands of authorities and our customers.
For our quality management, we are looking for a
Project Manager Quality Assurance (m/f/d)
Your Responsibilities
- Independent handling and coordination of process deviations in a GMP-regulated environment
- Conducting thorough root cause analyses in close collaboration with interdisciplinary specialist departments
- Definition and follow-up of corrective and preventive actions (CAPAs)
- Communication and coordination with international customers regarding the investigation, evaluation, and documentation of deviations
- Review and evaluation of manufacturing documents (Batch Record Review)
- Monitoring and optimizing quality-relevant processes to ensure compliance with international GMP guidelines and regulatory requirements
- Participation in the internal audit team as well as support during customer audits and inspections
Your Profile
- University degree in chemistry or a related scientific field
- Interest in production-related issues and troubleshooting
- Professional experience in quality management within the pharmaceutical industry
- Basic knowledge of regulatory requirements (GMP, ICH, FDA, etc.)
- Fluent in German and English (written and spoken)
- Analytical, pragmatic, and flexible mindset as well as enthusiasm and resilience
- Independent, responsible, reliable, and precise working style
Our Environment
- Challenging, dynamic, and performance-oriented company
- Flat hierarchies, open and direct working atmosphere, clear structures
- Individual development opportunities
- Work at the production site
Are you looking for a new challenge? Do you dare to contribute more than you currently can? Are you looking for a strategically sustainable and long-term employer? Then we look forward to receiving your application via the apply button.
More information at www.dottikon.com
Contact
Alessio Patriarca
Personnel Department Clerk
Phone number:+41 56 619 41 67
About the company
Dottikon
Reviews
- Management style3.6
- Salary and benefits3.8
- Career opportunities3.6
- Working atmosphere4.2