Boston Scientific Supervisor Product Complaint 

France, Nouvelle-Aquitaine 

213488981

Francisco Munoz Munoz

Your Responsibilities Include:

• Manage various areas of complaint management including operations related metrics, regulatory reporting, , quality of complaint records, providing feedback to global PMQA for procedure updates, employee training.
• Participate in Product Complaint Trend Analysis Reviews, & Complaint board meetings.
• Leads or is a member of various projects on a global or divisional level as part of the post market quality team.
• Provides expertise in the area of Regulatory Reports and the complaint process as a whole.
• Interaction with other departments related to complaint adverse events including Clinical, Regulatory, Med Safety and Marketing/Sales.
• Liaison between key cross functional teams that work with CMC such as CIS, Medical Safety, Device Tracking.

What We’re Looking For:

• Bachelor or Licentiate’s degree in Chemical, Industrial, Electronic, Biotechnology, Electromechanical Engineering, or related Health Field.
• At least 2-3 years of experience in similar positions.
• English Level desired : 80% - 90%.
• Or an equivalent combination of education and experience.