We are looking for a "Risk Manager (Medical Devices)" to provide services to a multinational pharmaceutical company

TASKS 🚀: 

• Support the Risk and DQA team in their activities

• Consulting team doing consulting projects.

• Work Closely with the software engineering team to create an excellent cross-functional relationship with the different teams involved

• Cross-functionally manage the quality assurance of digital projects ensuring that deadlines, project plans and quality objectives are met.

• Promote organizational compliance with the quality system, on QMS Software and SDLC framework

• Provide quality oversight during risk, Part 11, Annex 11 and regulatory

SKILLS 🤹:

MUST:

• Strong experience (5+ years) in Quality, including QMS, Design Control, Risk Management, in the area of development, production, planning / quality assurance for Software / In Vitro Diagnostics or Medical Devices

• Experience in setting up and maintaining Quality Management System (QMS) related to Software products, under ISO 13485 and ISO 14971

• Risk management according to ISO 14971

• Advice, guidance and preparation of regulatory documentation prior to commercialization in EU.

• Knowledge of MDR (EU) 2017/745 and/or (EU) IVDR 2017/746 regulations

• Fluent in English. Spanish is highly valued.

PLUS:

• Design and definition of quality systems according to ISO 13485:2016 and/or 21 CFR 820

• Regulatory knowledge for countries outside the European Union and USA (Canada, Japan, ANVISA, etc.), MDSAP. etc.

• Dossiers for application for prior license to operate medical device facilities and USA 510(k).

• Preparation of technical dossier for CE marking.

SCHEDULE 🕘:

• 08/09h -17/18h from Monday to Friday (flexible)

• 100% remote position