Validation Manager

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Lead planning, execution and closure of equipment, process, and computer system validations to meet regulatory and quality expectations.
• Prepare validation plans, protocols, reports, and risk assessments that are clear, inspection-ready and evidence-based.
• Coordinate cross-functional teams (engineering, quality, production, IT) and external vendors to deliver validation deliverables on time.
• Maintain and improve validation lifecycle documentation, change control impact assessments and re-validation strategies.
• Support root cause investigations and corrective/preventive actions when validation deviations occur.
• Train and coach site staff on validation principles, data integrity and inspection readiness.

We are seeking professionals with the following required skills and qualifications to help us achieve our goals

• Bachelor’s degree in Engineering, Pharmacy, Science or a related technical discipline.
• Minimum 5 years’ experience in validation within a regulated manufacturing environment.
• Practical knowledge of equipment, process and/or computerized system validation principles.
• Experience writing and reviewing validation plans, protocols and reports.
• Strong stakeholder management and teamwork skills in cross-functional or matrix settings.
• Fluent English communication skills, both written and verbal.

If you have the following characteristics, it would be a plus:

• Experience with pharmaceutical manufacturing operations in sterile or aseptic environments.
• Familiarity with regulatory expectations for data integrity and computerized system validation (CSV).
• Certification or training in validation, quality, or risk management methodologies.
• Hands-on experience with commissioning and qualification of process equipment or automated systems.
• Experience with project management tools and techniques.
• Prior experience working with external vendors and supplier qualification.

Working arrangement This role is on-site at our Egypt location. You will work closely with site teams and occasional travel to supplier or other sites may be required What we offer You will join a team where your technical expertise directly supports patient safety and product quality. You will get opportunities to stretch your skills, lead important projects, and learn from experienced colleagues. We welcome candidates from different backgrounds and are committed to inclusion. If you are ready to make an impact and grow with us, please apply. We look forward to hearing from you.