CQV Engineer

Your responsibilities:

• Validation activities: Facilities, Utilities, Validation Life Cycle,
• Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
• The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
• Prepare validation documents. Execution of IQ/OQ and PQ for equipment, systems and utilities.
• Write reports of completed validation activities.
• Quality Systems activities including Document Management system, Change Control, Non-Conformities, and CAPA?s.
• Writing and/or revising procedures applicable to the Engineering activities.
• Support the Engineering group to prepare the validation, requalification, and maintenance program.

Your background:

• Bachelor in Science or Technical field.
• Advanced Level Pharma Industry 5-10 years.
• Excellent technical writing skills and the ability to document all work in a thorough, accurate and timely manner.
• Excellent written and oral communication skills and the ability to work interdepartmentally in an effective manner to carry out daily duties.