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Benefits dieser Stelle
Flexible working hours
Option to work from home
Individual career opportunities
Attractive benefits and health programs
Lunch and REKA vouchers
Zusammenfassung
A leading engineering firm in Switzerland is seeking a specialist for qualification and validation of pharmaceutical processes. The role involves coordinating project activities, preparing documentation, and supporting team leadership. Ideal candidates have a degree in relevant fields, 3-5 years of experience in the pharmaceutical industry, and are fluent in German and English. A flexible working environment and individual career opportunities are offered.
Qualifikationen
3 to 5 years of professional experience in the pharmaceutical industry.
Experience with ISO 13485 and 21 CFR 820 regulations.
Willingness to travel within Switzerland.
Aufgaben
Coordinate project-specific qualification and validation activities.
Support preparation of qualification and validation documentation.
Conduct risk analyses and support team leadership.
Kenntnisse
GMP compliance
Strong communication skills
Customer orientation
Independent working style
Fluent in German
Fluent in English
Ausbildung
Degree in pharmaceutical engineering or related field
Jobbeschreibung
A leading engineering firm in Switzerland is seeking a specialist for qualification and validation of pharmaceutical processes. The role involves coordinating project activities, preparing documentation, and supporting team leadership. Ideal candidates have a degree in relevant fields, 3-5 years of experience in the pharmaceutical industry, and are fluent in German and English. A flexible working environment and individual career opportunities are offered.
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