Validation Supervisor | Process and Equipment Qualification للعمل في مهندس الجزائر

Role Summary

We are seeking a Validation Supervisor to define and oversee validation plans for processes, services, IT applications, and equipment qualification, ensuring compliance and quality standards are met across all operations.

Responsibilities

• Develop and implement validation plans for manufacturing processes, services, and computer systems.
• Coordinate and control the execution of equipment qualification and process validation activities.
• Ensure all validation activities comply with regulatory requirements and company quality policies.
• Review and approve validation documentation, including protocols and reports.
• Collaborate with cross-functional teams to support continuous improvement initiatives.

Qualifications

• Bachelor's degree in engineering, life sciences, or a related technical field.
• Minimum 5 years of experience in validation within a regulated industry (pharmaceutical, medical device, or biotechnology preferred).
• Strong knowledge of risk assessment and validation lifecycle methodologies.
• Excellent documentation and communication skills in French and English.
• Proven ability to lead validation projects and manage multiple priorities.

Skills

• Validation planning and execution
• Equipment qualification (IQ, OQ, PQ)
• Process validation and computer system validation
• Regulatory compliance (cGMP, ISO, etc.)
• Quality management and deviation investigation