The role involves assisting in the development of new products or improvements while ensuring compliance with quality systems and regulations
Job Summary
The role involves assisting in the development of new products or improvements while ensuring compliance with quality systems and regulations.
Candidates will be responsible for managing design history files to guarantee product safety, effectiveness, and adherence to legal standards.
The position requires close collaboration with product technology, quality, and regulatory affairs departments to support technical transfers and validation.
Matching Summary
The role involves assisting in the development of new products or improvements while ensuring compliance with quality systems and regulations.
Skills & Requirements
Must-have
Biomedical or pharmaceutical background
English proficiency level CET-4 or higher
Proficiency in Microsoft Office suite
Knowledge of quality systems and regulations
Experience with design control documentation
Nice-to-have
Strong coordination and communication skills
Ability to handle temporary tasks from management
Collaborative approach with cross-functional teams