Galderma
Galderma
Galderma ir globāls dermatoloģijas uzņēmums, kas darbojas injicējamās estētikas, dermatoloģiskās ādas kopšanas un terapeitiskās dermatoloģijas jomā. Tā produktu portfelī apvienotas klīniskās zināšanas un augstas kvalitātes produkti, kas izstrādāti dažādām ādas vajadzībām, savukārt starptautiskās komandas un partnerības atbalsta jaunu risinājumu izstrādi un nodrošināšanu. Galderma darbu vada mērķis attīstīt dermatoloģiju ikvienam ādas stāstam, vienlaikus pievēršot uzmanību atbildīgai uzņēmējdarbībai un ilgtspējai.

Global Quality Compliance Manager, EMEAC Audits

Lead Galderma’s global quality compliance and inspection readiness activities for dermatology operations. Coordinate EMEAC audits, regulatory preparation, and compliance capability development across regions.

Apraksts

  • Coordinate regionally managed quality audits across EMEAC, covering internal, external, and supplier engagements
  • Establish and oversee a durable global framework for regulatory inspection readiness
  • Strengthen regional audit capabilities, resources, and professional competencies
  • Track regulatory developments and evaluate inspection results
  • Create and maintain the global inspection readiness playbook
  • Develop and implement a structured, risk-based global mock inspection program
  • Direct inspection readiness sprints ahead of expected regulatory inspections
  • Assess worldwide inspection outcomes and regulatory developments to improve compliance defense capabilities
  • Manage the complete delivery of internal, supplier, distributor, and third-party audits across EMEAC
  • Implement and manage the global auditor qualification framework
  • Offer audit methodology expertise and systems support to LATAM, US, and JPAC teams
  • Maintain complete traceability for audit activities, findings, and corrective actions
  • Raise significant regulatory compliance concerns, audit findings, risks, and systemic issues with management
  • Distribute audit trends, inspection results, and systemic risk analysis across regions
  • Guide regional audit leads on functional standards for inspection readiness

Prasības

  • At least 10 years of audit management experience in the pharmaceutical or medical device sector
  • Extensive audit experience across regulated areas relevant to cosmetics, medical devices, and pharmaceuticals
  • Professional fluency in English
  • Additional language skills are advantageous

Priekšrocības

  • Competitive compensation package that includes a bonus structure
  • Comprehensive extended benefits package
  • Hybrid working environment
  • New IT hub facilities
  • Opportunities for professional growth and development
  • Involvement in global, cross-functional initiatives
  • Access to international career opportunities
  • Meaningful ownership from the start
  • Support to develop professionally and assume greater accountability

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