Job Title: Manufacturing Project Specialist
The role will focus on supporting compliance with medical device regulations, validation of equipment and processes, change control processes, and project execution in a fast-paced manufacturing environment.
Key Responsibilities:
1. Regulatory Compliance: Ensure adherence to medical device regulations (ISO 13485, FDA) in manufacturing processes.
2. Validation: Lead and execute validation activities (IQ/OQ/PQ) for equipment, processes, and systems.
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