Sr. Technical Writer

Job DescriptionLike the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description. Position: Senior Technical WriterOverview: We are seeking a Senior Technical Writer to collaborate with Quality Management System (QMS) process owners and subject matter experts to develop and refine top-level Standard Operating Procedures (SOPs). This role will ensure documentation aligns with regulatory requirements, business needs, and industry standards.Responsibilities:Partner with subject matter experts across Quality Systems, Document Control, Regulatory, Design & Development, Supplier Quality, and Production Controls.Author new SOPs that incorporate regulatory requirements, standards, and business processes.Define and document key process inputs and outputs.Review and update existing SOPs to ensure compliance and accuracy.Contribute to documentation structure, design, and best practices.Qualifications:Bachelor’s degree or equivalent experience.5+ years of technical writing experience, with a focus on top-level procedures.3+ years in medical device manufacturing.Strong organizational, communication, and English writing skills.Proficiency with Microsoft Office applications.Ability to work independently, manage multiple priorities, and meet tight deadlines.Preferred Skills:Experience authoring and publishing controlled documentation.Familiarity with PLM systems (Arena preferred).Strong planning and multitasking skills.Why Apply: This is a great opportunity to play a critical role in shaping QMS documentation within a highly regulated industry. If you’re detail-oriented, collaborative, and passionate about creating clear, compliant processes, we encourage you to apply today.

Created: 2025-09-06