United States onlyRQM+ is the leading MedTech solutions partner, accelerating the product lifecycle from innovation to patient impact. While manufacturers create medical technology, we apply our end-to-end expertise to propel products from concept through market entry and ongoing post-market support.
Our tailored solutions bring unmatched regulatory and quality expertise, FDA-recognized laboratory and materials science, comprehensive clinical trial design and execution, and impactful reimbursement strategies — accelerating market entry and commercial growth. We partner closely with manufacturers across device types and therapeutic areas to deliver life-changing technologies to patients: faster, safer, better.
We don’t make MedTech. We make MedTech happen.
We're looking for a Technical Writer ideally from the Medical Device industry who can help create and maintain documentation for an ISO 13485 Quality Management System. In this role you will work with stakeholders to ensure that documentation is accurate, complaint and meets the needs of the users.
Primary Responsibilities
- Create documentation Write manuals, guides, and standard operating procedures (SOPs) that explain technical processes
- Updates documentation: Keep documentation up to date to reflect changes in processes and procedures
- Prepares 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
Requirements
- Bachelor’s degree in a related field
- Technical or engineering degree preferred
- 3- 7 years of experience
- Medical Device experience preferred
- Knowledge of ISO 13485 preferred
- 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
Behaviours
- Action-Oriented, Analytical Mindset, Approachability, Business Acumen, Career Ambition, Composure, Courage, Customer Focus, Decision Quality, Detailed Oriented, Communication, Integrity Trust, Interpersonal Savvy, Planning, Prioritizing, Time Management
Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!
We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.
Job Opportunity Verification
At RQM+, we prioritize the security of our job applicants. To ensure a safe application process:
All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careers
Every candidate going through the interview process will participate in a voice and/or video interview.
Exercise caution with unsolicited job offers or requests for sensitive information.
AL, AD + 48 more
