The Medical Writer II collaborates in the development and execution of clinical, scientific, and regulatory documents for global regulatory agencies. This involves collaboration with internal and external partners to support technical, medical and clinical writing outputs for Clinical and Regulatory business needs in accordance with the relevant and evolving international standards as well as LABORIE standard operating procedures. This person will write a variety of documents for distinct audiences including Post-Market Surveillance (PMS) plans, PMS reports, Periodic Safety Update Reports (PSURs) and Proactive PMS study protocols, and will contribute to Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up Reports (PMCFERs). About the Role: • Perform on-line external vigilance reviews and compare results to the Risk Management File. • Critically appraise, analyze, and summarize internal and external data in support of the PMS requirements for geographies such as the EU, Health Canada, UK, etc. • Search out, review, write and maintain records of PMS data pertaining to the safety and effectiveness of Laborie devices. • Assist in ensuring all PMS requirements are met for device registrations and maintenance while working with other LABORIE team members. • Work cross functionally to develop, compile and report proactive PMS activities and integrate reporting into PMCFERs and PSURs. • Undertake various projects and tasks as assigned. What you Bring: • Bachelor's degree in a scientific field or in writing/composition discipline and 5+ years' experience writing PSURs. Experience with Medical Writing required. • Working knowledge of medical device clinical and PMS regulations, standards and guidelines (ISO, MEDDEV, MDR, IVDR, FDA CFR, UKCA, Health Canada) and experience conducting focused analysis of internal and external complaint data • Demonstrated ability to manage project timelines, including ability to adapt to shifting priorities and competing demands while maintaining strong attention to detail • Strong computer skills, proficiency with MS Office and ability to work both independently and collaboratively in a team setting • Excellent English verbal, written and presentation skills with great attention to detail • Experience working in the medical device industry preferred • Project Management experience preferred

• Paid time off and paid volunteer time
• Medical, Dental, Vision
• Pension Plan
• Parental Leave and Adoption Services
• Health and Wellness Programs and Events