Sr. Technical Writer Job at Meet Life Sciences in Acton

MediabistroActon, MA, United States

27 days ago

Job type

Full-time

Job description

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.

Seniority level

Mid-Senior level

Employment type

Contract

Job function

Writing / Editing

Industries

Medical Equipment Manufacturing

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Sr Technical Writer • Acton, MA, United States