Responsibilities: Validation Specialist for QC Equipment with CSV knowledge (FTIR-Spectrophotometer for ID and Nebula-Endotoxins Equipment) Qualifications: Experience in Lab Equipment with computer systems 3-5 years of experience ...
For Validation support services in the Manufacturing area. WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Science with three (3) years of experience and exposure within the Pharmaceutical or Medical Devices industry. B...
Responsibilities: Develop and implement validation plans, protocols (IQ,OQ ,PQ), and reports for equipment, processes, and systems. Ensure validation activities comply with regulatory requirements, industry standards, and company policie...
For Project Management services WHAT MAKES YOU A FIT: The Technical Part: Bachelor’s Degree in Engineering and seven (7+) years of exposure in Project Management activities within the Medical Device industry. Bilingual (Spanish and En...
The Quality Engineer will be responsible for ensuring that every product produced by a company meets the desired quality standards. The holder of this position will support the implementation of quality initiatives and continuous improvemen...