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Associate director, regional compliance - europe

Sintra
Hikma Pharmaceuticals
Anunciada dia 6 março
Descrição

Associate Director, Regional Compliance - Europe We're Hiring: Regional Compliance Associate-Director – EuropeLocation: PortugalHikma PharmaceuticalsAt Hikma, we're committed to delivering high‐quality medicines and doing so with integrity, transparency, and strong ethical stewardship. We are now looking for aRegional Compliance Associate-Director – Europeto play a pivotal role in strengthening our Compliance Programme across Portugal and selected European markets.If you're passionate about enabling ethical business, partnering with leaders, and shaping a strong culture of integrity—this role is for you.About the Role Reporting to the Compliance Officer - Europe, you will serve as a strategic business partner supporting commercial, medical, regulatory, supply chain, and corporate teams. You will help ensure our operations meet:EU pharmaceutical regulationsLocal anti‐bribery and anti‐corruption lawsEFPIA Code of PracticeINFARMED requirementsUK governance and internal control expectationsThis is a high-impact role where your expertise directly supports ethical conduct and effective risk mitigation across multiple markets.Key Responsibilities Compliance Programme LeadershipDrive the implementation of the Group Compliance Programme across Portugal and Europe.Tailor global policies to EU and local regulatory needs.Lead risk assessments, compliance reviews, and investigations.Provide trusted guidance to senior business leaders.Anti‐Bribery & Anti‐CorruptionOversee ABC controls aligned with the UK Bribery Act, EU frameworks, and local laws.Review and approve HCP engagements, grants, sponsorships, and third‐party arrangements.Conduct due diligence for distributors and partners.Ensure compliance with promotional rules, EFPIA Code, and transparency reporting.Investigations & WhistleblowingManage local investigations in partnership with Group Compliance and Legal.Promote and oversee confidential reporting channels.Ensure adherence to the EU Whistleblowing Directive and local labour laws.Recommend corrective actions and elevate material matters as needed.Monitoring & TestingExecute risk‐based compliance monitoring and thematic reviews.Validate corrective actions and support audits or inspections.Training & CultureDevelop and deliver training for commercial, supply chain, and leadership teams.Foster a strong speak‐up culture and ethical mindset across the region.Governance & ReportingPrepare regional compliance dashboards and KPIs.Support reporting to the Compliance Officer – Europe, Group Chief Compliance Officer, and Board committees.Qualifications & ExperienceLaw degree (LLB/LLM preferred).Professional compliance certification (ICA, SCCE, etc.) is a plus.8–12 yearsof relevant experience, including5+ years in pharmaceutical compliance .Experience in generics and multi‐country European operations strongly preferred.Exposure to listed or multinational environments is advantageous.Fluency inEnglish and Portugueserequired;Frenchis a plus.Technical SkillsDeep understanding of EU and Portuguese pharma regulations.Expertise in HCP interactions, promotional standards, and third‐party risk management.Familiarity with investigations, risk assessment methodologies, and compliance documentation.Core CompetenciesStrong ethical judgment and independent thinking.Executive presence and credibility with senior stakeholders.Ability to influence without direct authority.Excellent communication and cultural awareness across European markets.Travel Periodic travel across Europe is required to support compliance activities.Ready to Make a Real Impact? At Hikma, you'll help uphold the standards that protect patients, colleagues, and our business. If you're a proactive compliance professional who thrives on purpose‐driven work—we'd love to hear from you.Apply now and help us advance health with integrity.#J-18808-Ljbffr

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