Validation Specialist - Cayey, Puerto Rico - QRC Group, Inc

Descripción

Validation Specialist to provide support in the manufacturing area with experience in validation of laboratory equipment, methods and processes.

Must have experience with:

• Laboratory Equipment qualification
• Protocols design
• IQ/OQ/PQ execution
• Technical documentation
• Validation activities

• Bachelor of Sciences/Engineering
• Five (5) years of experience in the Medical Devices industry
• ​Bilingual (Spanish/English)

All your information will be kept confidential according to EEO guidelines.