Senior Quality & Regulatory Manager/ Deputy Head of Quality Management
Your area of responsibility
Support for local and global QM projects and active implementation of projects at the locations, e.g. introduction of quality tools, process harmonization, etc.
Responsibility for regulatory monitoring and support for new product registrations and updating dossiers with local authorities (e.g. US DMF)
Conducting risk analyses and evaluating compliance requirements for suppliers
Actively deputizing for the Head of Quality Management in day-to-day business and projects
Carrying out validations and risk analyses (FMEAs)
Maintenance of the QMS and support with customer and authority audits
Your profile
Completed scientific or technical studies with specialist further training in quality management
At least 5 years of experience in quality management in a manufacturing company in the fields of medical technology, pharmaceuticals or food production
Experience in the field of regulatory affairs / approvals of medical devices
Good knowledge of CAQ tools and experience in project management
Business fluent in German and English
You are characterized by a high degree of initiative and a structured, organized and conscientious way of working.
Your advantages
Progressive employment conditions, with flexitime regulations, above-average pension fund and other benefits
Modern office space with very good transport connections
A good team atmosphere and short decision-making processes
Our customer
Perlen Packaging is a dynamic, innovative and committed company that develops, produces and coats films for blister packaging worldwide. The processes, systems, products and environment are geared to the needs of the pharmaceutical industry. With sites in Switzerland, Germany, the USA, China and Brazil, Perlen Packaging is one of the global market leaders. The quality team is being expanded to further develop and maintain the global QM system under ISO 9001 and 15378.
Work location Perlen
