Boston Scientific Senior Compliance Specialist - & EMEA Proctor Bureau 

France, Ile-de-France 

430977265

France-Voisins le Bretonneux

Governance and strategy

• Represent Boston Scientific in local trade associations (e.g., SNITEM) to ensure alignment with evolving industry codes and regulations

• Chair the local compliance committee in France, driving effective governance and timely decision-making

• Lead the annual risk assessment process by partnering with the Country Leadership Team to identify and prioritize key compliance risks

• Drive the strategy and execution of Annual Country Compliance Plans, aligning initiatives with risk assessments and compliance objectives

• Track progress of key initiatives, report on compliance KPIs, and escalate material risks as appropriate

Culture and partnership development

• Partner closely with the Country Leadership Team in France to embed compliance into commercial and operational strategies

• Act as a visible compliance ambassador and business partner, fostering a speak-up culture and ethical decision-making

• Design and deliver engaging compliance training and communication programs tailored to various levels of the organization

• Collaborate cross-functionally with Legal, Commercial Divisions, HR, Finance, and other stakeholders to ensure proactive, solution-oriented compliance

• Represent France in regional and global compliance forums to share local insights and ensure alignment across business units

Operational support

• Serve as the primary point of contact for review and approval of HCP/HCO interactions in France and the EMEA Proctor Bureau

• Ensure documentation, due diligence, and approvals are compliant with internal controls, SOPs, and MedTech/local codes

• Provide expert-level advice on complex compliance scenarios, including high-risk and non-standard cases

• Deliver timely, pragmatic guidance on both local and international compliance policies (e.g., MedTech Europe Code, Anti-Gift Law)

• Monitor and drive continuous improvement of compliance systems, workflows, and internal controls

• Mentor and support junior compliance professionals and business partners to build internal compliance capabilities

Required qualifications:

• Minimum of 7 years' experience in compliance, legal, or a related field, preferably within the medical device, pharmaceutical, or healthcare sector

• Deep understanding of local and international healthcare compliance regulations, including MedTech Europe Code and Anti-Gift Law

• Proven ability to lead cross-functional initiatives and influence senior stakeholders

• Strong analytical, problem-solving, and decision-making skills

• Excellent communication skills in both English and French

• Familiarity with compliance systems and tools used in multinational organizations
• Previous experience supporting operational compliance activities or anti-bribery/anti-corruption audit activities across EMEA