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Process Engineer (m/w)
Amaris is an independent and international Consulting Group specialized in Management and Technologies.
Amaris operates in over 45 countries delivering services in Business & Management Consulting, IT/Information Systems, Telecommunications & Networking, Engineering, Pharmaceutical & Biotechnology.
Since 2007, the company has grown exponentially and is committed to building lasting relationships with its clients, delivering innovative solutions from project inception to execution.
Responsible for: - Audit sites’ inspection Plan and reports - Make recommendations - Follow the guidelines regarding norms and regulation
- Pharmaceutical degree or similar - 3-5 years experience within Medical Device industry - Previous experience within quality - Previous experience with audit, regulatory or calibration - Previous experience in sterile environment is a plus - Knowledge of FDA and ISO - Fluent in English and German