Technical Writer

Summary

Join RQM+, a leading MedTech service provider, as a Technical Writer specializing in Medical Devices. You will create and maintain documentation for an ISO 13485 Quality Management System, collaborating with stakeholders to ensure accuracy and compliance. This role involves writing manuals, guides, and SOPs, updating existing documentation, and working with subject matter experts. You will ensure documentation meets industry standards and legal requirements, contributing to process improvement within the QA department. RQM+ offers a rewarding work environment with an industry-leading compensation package and a focus on work-life balance.

Requirements

• Bachelor’s degree in a related field
• 3-7 years of experience
• Strong writing skills
• Ability to communicate quickly and clearly (written and verbal)
• Attention to detail
• Ability to write quality plans and procedures
• Ability to balance quality compliance with business needs
• Ability to work cross-functionally in a matrix organization
• Strong understanding of quality system management

Responsibilities

• Create documentation: Write manuals, guides, and standard operating procedures (SOPs) that explain technical processes
• Update documentation: Keep documentation up to date to reflect changes in processes and procedures
• Prepare quality documentation and reports by collecting, analyzing, and summarizing information and trends
• Work with subject matter experts, management, and employees to ensure documentation is accurate and meets needs
• Ensure compliance: Make sure documentation meets industry standards, legal requirements, and guidelines
• Improve processes: Work with the QA department to improve quality across deliverables

Preferred Qualifications

• Technical or engineering degree
• Medical Device experience
• Knowledge of ISO 13485

Benefits

• Industry leading compensation package
• Focus on work life balance
• Ongoing learning and development