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Ferring Pharmaceuticals

Develops peptide hormone-based medicines and therapies

Manager Distribution Compliance

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeLisbon, PortugalNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree in Business, Supply Chain, Life Sciences, Engineering, Finance or a related field is required; a master's degree or MBA is advantageous.
  • At least 5 years of relevant experience in supply chain, distribution compliance, commercial operations, transformation or program management.
  • Experience in pharmaceuticals, healthcare, medical devices or another highly regulated industry.
  • Experience with global or regional organizations, GDP-compliant distribution and cross-functional transformation initiatives.
  • Knowledge of GDP and pharmaceutical distribution regulations, distribution and lane risk management, program and project management, business-process design, change management and distributor governance.
  • Data analysis, KPI reporting and strong proficiency in Excel and PowerPoint.
  • Strategic thinking with strong execution focus; stakeholder management and influence without direct authority; clear communication and presentation; sound judgement, problem solving and decision making; cross-cultural collaboration and relationship building; resilience and adaptability in complex environments.

Responsibilities

  • Lead the preparation, review and lifecycle management of Lane Risk Assessments for Marketing & Sales affiliates using Validaide or equivalent tools.
  • Assess temperature-controlled and ambient distribution routes, climatic exposure and operating environments in line with GDP, quality and regulatory requirements.
  • Partner with Supply Chain, Quality, Logistics and Commercial teams to define, implement and monitor risk-mitigation measures.
  • Develop, revise and continuously improve SOPs, work instructions, guidelines and policies covering distribution compliance.
  • Coordinate stakeholder review and approval, maintain controlled documentation and promote global process harmonization.
  • Develop and deliver training on lane risk assessments, temperature management and related procedures; support onboarding, audits and inspections.
  • Act as back-up administrator for the Learning Management System, including curricula, assignments, completion monitoring, metrics, issue resolution and audit-ready records.
  • Manage budgets, forecasts and expenditure reporting for cold chain compliance and customs operations, identifying compliant cost-optimization opportunities.
  • Coordinate with Procurement, Logistics, Finance and Supply Chain; create and manage purchase orders in Coupa and support timely invoice processing.
  • Support design and execution of go-to-market model changes, including transitions to new operating models.
  • Maintain integrated roadmaps, milestones, KPIs, governance, dashboards, risks, dependencies and mitigation plans.
  • Coordinate workstreams across Commercial, Supply Chain, Quality, Regulatory, Trade Compliance, Finance, Tax and Legal.
  • Support market-readiness assessments, transition planning, distributor governance and future-state roles and decision rights.
  • Support global serialization compliance, governance documentation, training, issue escalation, data-integrity monitoring and KPI reporting.
  • Support investigation and documentation of suspected product events and coordinate responses to alerts from internal stakeholders, trading partners, regulators and healthcare channels.
  • Participate in root-cause analysis, CAPA activities, trend monitoring and risk assessments covering counterfeiting, diversion, theft and unauthorized distribution.

Desired Qualifications

  • Exposure to market transitions, risk assessments, quality systems, SOPs and training administration.
  • Experience with Validaide or similar lane-risk tools, Coupa or equivalent procurement systems, and Learning Management Systems.
  • Working knowledge of serialization, product security and suspect-event management.
  • A master's degree or MBA is an advantage.

About the Company

Ferring Pharmaceuticals

Develops peptide hormone-based medicines and therapies

Ferring Pharmaceuticals develops medicines that use the body's own peptide hormones, focusing on specialties such as reproductive health, gastroenterology, and urology. Its products range from hormone-based therapies to newer gene-based treatments, such as Adstiladrin for bladder cancer. The company achieves its solutions through research-driven development and manufacturing, including synthetic production of peptide hormones (historically oxytocin and vasopressin) and ongoing expansion of production and clinical programs. Ferring differentiates itself by remaining privately held to pursue a long-term research vision, growing through organic expansion and strategic acquisitions while maintaining a global footprint (over 100 countries, 7,000+ employees). Its goal is to advance therapies that leverage the body's biology to treat diseases more effectively, supported by a sustained investment in R&D and manufacturing, with a future focus on bioengineered and gene-based approaches.

Company size
5,001-10,000
Company stage
Debt Financing
Total funding
$302.5M
Headquarters
Saint-Prex, Switzerland
Founded
1950

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