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Boehringer Ingelheim

QC Compliance Officer

Boehringer Ingelheim

. Coordinate validation activities for QC laboratory equipment and computerized systems .

Posted 10/8/2026full-timeKoropi • GreeceJuniorMid-LevelWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in Quality Control processes, including validation activities and compliance with GMP/cGMP requirements. Proficient in analytical laboratory equipment and Data Integrity practices, with strong communication and organizational skills to support cross-functional collaboration.

Highest-signal resume keywords
Quality Control Laboratory ExperienceGMP/cGMP ComplianceData Integrity PrinciplesAnalytical Laboratory Equipment KnowledgeValidation Activities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Validation ActivitiesAnalytical Laboratory EquipmentGMP/cGMP RequirementsData Integrity PrinciplesQC Documentation PreparationChange Control ManagementTroubleshooting ActivitiesCompliance Record ReviewQC Process ImprovementLaboratory Equipment Coordination
Soft Skills
Organizational SkillsCommunication SkillsProblem-Solving SkillsCollaborative Mindset
Tools & Technologies
Computerized Quality SystemsLaboratory Software
Industry Keywords
Quality ControlCGMP ComplianceQC DocumentationAudit ReadinessCross-Functional Teams

About the role

Key responsibilities & impact
  • Coordinate validation activities for QC laboratory equipment and computerized systems
  • Support implementation and continuous improvement of Data Integrity practices within the QC laboratory
  • Prepare, issue, and review QC documentation, SOPs, change controls, and compliance records
  • Support investigations, deviations, and troubleshooting activities
  • Provide guidance to QC analysts on validation and compliance topics
  • Contribute to audit readiness and continuous improvement of QC compliance
  • Work closely with QC colleagues and cross-functional teams to ensure laboratory equipment, documentation, and processes comply with cGMP requirements and company policies
  • Report to the QC Compliance Coordinator

Requirements

What you’ll need
  • University degree in Chemistry, Pharmacy, Biology, Food Technology or another relevant discipline
  • At least 2 years of experience in a Quality Control laboratory
  • Fluency in Greek and good command of English
  • Strong knowledge of analytical laboratory equipment and instrumentation
  • Experience in validation activities considered an advantage
  • Good understanding of GMP/cGMP requirements and Data Integrity principles
  • Ability to apply GMP/cGMP and Data Integrity principles in a laboratory environment
  • Confidence working with software and computerized quality systems
  • IT or technology-related background considered a strong advantage
  • Strong organizational, communication, and problem-solving skills
  • Collaborative mindset and ability to work effectively across teams

Benefits

Comp & perks
  • Premium access to Headspace
  • Ongoing support and initiatives related to ways of working to help employees stay healthy and improve physical, emotional, mental, and spiritual well-being
  • Customized development plan based on role and aspirations
  • Access to international development opportunities
  • Languages and training programs
  • Annual bonus
  • Participation in company life insurance
  • Private healthcare program
  • Extra benefits
  • Fun and diverse working environment
  • Flexibility to work from home based on mutual agreement and business needs