Quality Assurance Senior Officer
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Before you apply
LocationTripoli, Peloponnese Region, Greece
Work modeon-site
Typefull-time
SenioritySenior
Experience2+ yrs
DepartmentQuality Assurance
Company size501–1,000 people
PostedNov 6, 2026 · 1d ago
Verified live6h ago
At a glanceSummarised by Seekless from the posting.
BSc Degree in Chemical Engineering, Chemistry or Pharmacy
Previous Experience of at least 2 years in Pharmaceutical Industry
Fluent oral and written skills in Greek
Fluent oral and written skills in English
Computer literacy
Self-motivated & results oriented with ability to cope with strict timelines
Ability to deliver on complex project requirements and tasks
Ability to work creatively, analytically with attention to detail
MSc Degree in Quality Management or relevant field
Benefits
Competitive remuneration
Learning and development
Supportive work environment
Responsibilities
Main duties and responsibilities:
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Supports operations and quality control staff to address compliance related concerns
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Contributes to the establishment, maintenance, continuous improvement and effectiveness of the Quality Management System (QMS), ensuring compliance with current Good Manufacturing Practices (cGMP), internal quality standards and applicable regulatory requirement.
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Identify needs for creation or revision written procedures or revision of existing
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Conducts deviation investigations arising from manufacturing and quality processes, maintains associated records, and ensures appropriate communication and distribution of documentation to affected departments and customers, where applicable
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Reviews and evaluates Change Controls related to manufacturing and quality systems, maintains the associated documentation, and ensures appropriate communication to relevant stakeholders and customers
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Implements and monitors the progress of the Corrective and Preventive Action Plan resulting from findings/observations of Audits from customers/ organizations/authorities
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Prepares validation protocols and reports for process validation.
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Coordinates the preparation, maintenance, revision, control, and distribution of Master Production Documents
Requirements
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BSc Degree in Chemical Engineering, Chemistry or Pharmacy. MSc Degree in Quality Management or relevant field will be considered an asset.
•
Previous Experience of at least 2 years in Pharmaceutical Industry
•
Fluent oral and written skills in Greek & English
•
Computer literacy
•
Self-motivated & results oriented with ability to cope with strict timelines
•
Ability to deliver on complex project requirements and tasks
•
Ability to work creatively, analytically with attention to detail
Benefits
The Company offers competitive remuneration, continuous learning and development opportunities, and a friendly and challenging working environment.