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BD

Junior Quality and Regulatory Affairs Specialist

BD

. Support the Quality Manager with day-to-day quality activities .

Posted 10/15/2026contractWarsaw • PolandJunior💰 PLN 82,000 - PLN 125,050 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates strong organizational skills and attention to detail while supporting quality management activities, including CAPAs, Nonconformances, and regulatory documentation. Proficient in database management and Microsoft Office applications, with a focus on maintaining accurate quality records and compliance.

Highest-signal resume keywords
Quality Management SupportDatabase ManagementRegulatory DocumentationMicrosoft Office ProficiencyAttention to Detail

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Quality MetricsCAPAsNonconformancesDocument ControlRegulatory CertificatesData ManagementQuality Improvement InitiativesQuality System AdministrationAudit TrackingCompliance Requests
Soft Skills
Organizational SkillsAttention to DetailPositive AttitudeTeam CollaborationTime Management
Industry Keywords
QualityRegulatoryComplianceHealthcareLife SciencesEngineeringAdministrative Processes

About the role

Key responsibilities & impact
  • Support the Quality Manager with day-to-day quality activities
  • Track and follow up on audit actions and quality improvement initiatives
  • Support CAPAs, Nonconformances, and Planned Deviations
  • Assist with quality metrics and reporting
  • Support document updates and document control activities
  • Contribute to customer quality questionnaires and compliance requests
  • Assist with training records and quality system administration
  • Maintain quality records and ensure timely completion of assigned tasks
  • Support continuous improvement initiatives and quality projects
  • Maintain and administer the released product database
  • Keep product records accurate, complete, and up to date
  • Add new products and remove or update obsolete products based on approved changes
  • Upload, replace, and maintain regulatory certificates and supporting documentation
  • Ensure regulatory records reflect the current approval and certification status of products
  • Perform routine reviews and quality checks of database content
  • Resolve data discrepancies and support data-cleanup activities
  • Assist with regulatory documentation and record management
  • Support other entry-level regulatory and administrative activities as needed

Requirements

What you’ll need
  • Good written and spoken English
  • Strong computer skills and confidence working with Microsoft Office applications
  • Excellent attention to detail and organizational skills
  • Ability to manage multiple tasks and prioritize effectively
  • Strong sense of responsibility and ownership
  • Positive attitude and willingness to learn
  • Ability to work both independently and as part of a team
  • Bachelor's degree (completed or in progress) in Life Sciences, Engineering, Healthcare, Business, or a related field (nice to have)
  • Experience working with databases, documentation, or administrative processes (nice to have)
  • Exposure to quality, regulatory, compliance, healthcare, or other regulated environments (nice to have)
  • Knowledge of another European language (nice to have)
  • Fixed-term contract

Benefits

Comp & perks
  • Comprehensive Total Rewards program
  • Reward and recognition opportunities
  • Competitive compensation and benefits programs
  • Face-to-face collaboration supporting learning, progress, and success
  • Learning, growth, and development opportunities