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Galderma
Galderma
5001 – 10 000 Darbinieki
H1B vīzas sponsorsKonsultācijasSkaistumsVeselības aprūpe
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.
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Vakances uzņēmumā

Global Quality Compliance Manager – EMEAC Audits

Galderma is seeking a Global Quality Compliance Manager to lead inspection readiness and quality audits across EMEAC. The role focuses on risk-based auditing, regulatory preparedness, and strengthening global compliance practices.

PLPolijaHibrīdiPilna slodzeVecākais speciālistsVadošais speciālistsNepieciešamā Valoda: angļuAtbilstība

Apraksts

  • Coordinate regionally managed quality audits across EMEAC, including internal, external, and supplier audits
  • Establish and oversee a sustainable global inspection readiness framework
  • Strengthen regional auditing capabilities, processes, and competencies
  • Track regulatory developments and inspection outcomes to improve audit effectiveness and compliance
  • Own the global inspection readiness playbook, governance model, mock inspection process, and readiness sprint methodology
  • Design and implement a structured, risk-based global mock inspection program
  • Lead inspection readiness sprints ahead of anticipated regulatory inspections
  • Analyze global inspection outcomes and regulatory trends to strengthen regulatory defense capabilities
  • Manage the full lifecycle of internal, supplier, distributor, and third-party audits across EMEAC
  • Administer the global auditor qualification framework
  • Provide audit methodology guidance and systems support to LATAM, US, and JPAC regions
  • Maintain traceability of audit activities, findings, and corrective actions, ensuring timely closure and consistent Good Practices
  • Escalate critical compliance matters, audit findings, regulatory risks, and systemic issues to management
  • Share audit trends, inspection results, and systemic risk insights across regions
  • Guide regional audit leads on inspection readiness standards

Prasības

  • At least 10 years of audit management experience in a pharmaceutical or medical device environment
  • Broad audit experience across regulated cosmetics, medical device, and pharmaceutical operations
  • Fluent English communication skills
  • Additional language skills are advantageous
  • Willingness and ability to work in a hybrid arrangement with three onsite days per week
  • Experience leading internal, external, supplier, distributor, and third-party audits
  • Knowledge of risk-based audit planning, execution, and timely closeout
  • Demonstrated ability to establish and govern inspection readiness frameworks
  • Knowledge of regulatory developments and inspection outcomes
  • Experience with auditor qualification frameworks and Good Practices
  • Ability to manage audit findings, corrective actions, compliance risks, and escalations

Priekšrocības

  • Competitive compensation package with a bonus structure
  • Extended benefits package
  • Hybrid working culture
  • New IT hub environment
  • Career development through global and cross-functional project exposure
  • Meaningful ownership from the start
  • Support to grow professionally and assume accountability
  • Workplace focused on diversity and inclusion

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