Validation Manager
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Before you apply
LocationAthens, Attica, Greece
Work modeon-site
Typefull-time
SenioritySenior
Experience6+ yrs
DepartmentQuality Assurance
Company size501–1,000 people
PostedAug 24, 2026 · 2mo ago
Verified live3d ago
At a glanceSummarised by Seekless from the posting.
Bachelor's degree in Life Sciences or Engineering field
Minimum 6 years of experience in pharmaceutical manufacturing, validation, engineering, technical operations, or quality assurance within a regulated environment
Proven experience in qualification and validation of pharmaceutical facilities, utilities, production equipment, and computerized systems
Strong knowledge of validation lifecycle activities including DQ, IQ, OQ, PQ, requalification, and calibration programs
Good understanding of EU GMP, Annex 1, FDA regulations, 21 CFR Part 11, and Data Integrity requirements
Demonstrated experience leading teams or coordinating multidisciplinary project activities
Strong project management, planning, and stakeholder management skills
Excellent communication skills in both Greek and English
Ability to manage multiple priorities in a fast-paced manufacturing and project environment
Strong analytical thinking, problem-solving mindset, and ability to drive decisions through collaboration and influence
MSc degree
Experience supporting commissioning, startup, expansion, or greenfield pharmaceutical projects
Skills
Validation
cGMP
FDA
EU GMP
21 CFR Part 11
Data Integrity
Benefits
Competitive remuneration
Learning and development
Friendly working environment
Challenging working environment
About the role
At DEMO SA, one of the world’s largest pharmaceutical manufacturers in injectable facilities, we are looking for a talented candidate for the position of Validation Manager for New Facilities Department. The position reports to the Senior Validation Manager and is based in Kryoneri.
Responsibilities
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Lead and coordinate Validation activities for new pharmaceutical manufacturing facilities, utilities, equipment, and computerized systems.
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Ensure qualification and validation activities are executed in compliance with cGMP, FDA, EU GMP, and internal quality requirements.
•
Review and approve validation documentation, including Validation Master Plans (VMP), User Requirement Specifications, risk assessments, qualification protocols (IQ/OQ/PQ), and validation reports.
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Collaborate closely with Engineering, Projects, Production, Maintenance, Automation, and Quality teams during the design, construction, commissioning, qualification, and startup phases of new facilities.
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Ensure the validated state of facilities, equipment, utilities, and computerized systems throughout their lifecycle.
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Monitor and maintain validation and calibration programs for critical systems and equipment.
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Review and support investigations, deviations, CAPAs, change controls, and requalification activities related to validation processes.
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Participate in regulatory inspections, customer audits, and internal audits, providing validation expertise and support.
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Lead, coach, and develop Validation team members while promoting a culture of quality, compliance, and continuous improvement.
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Support cross-functional projects related to facility expansions, equipment installations, technology transfers, and process improvements.
Requirements
•
Bachelor’s degree in Life Sciences or Engineering field. An MSc degree will be considered an asset.
•
Minimum 6 years of experience in pharmaceutical manufacturing, validation, engineering, technical operations, or quality assurance within a regulated environment.
•
Proven experience in qualification and validation of pharmaceutical facilities, utilities, production equipment, and computerized systems.
•
Experience supporting commissioning, startup, expansion, or greenfield pharmaceutical projects will be considered a strong advantage.
•
Strong knowledge of validation lifecycle activities including DQ, IQ, OQ, PQ, requalification, and calibration programs.
•
Good understanding of EU GMP, Annex 1, FDA regulations, 21 CFR Part 11, and Data Integrity requirements.
•
Demonstrated experience leading teams or coordinating multidisciplinary project activities.
•
Strong project management, planning, and stakeholder management skills.
•
Excellent communication skills in both Greek and English.
•
Ability to manage multiple priorities in a fast-paced manufacturing and project environment.
•
Strong analytical thinking, problem-solving mindset, and ability to drive decisions through collaboration and influence.
Benefits
The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.