Technical Writer

Kelly Science, Engineering, Technology & Telecom; Largo (FL); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Paid time off

Medical benefits

Job summary

Kelly Science, Engineering, Technology & Telecom is seeking a detail-oriented Technical Writer in Largo, Florida. This full-time role supports biocompatibility compliance for medical devices by updating documentation for 132 technical files and 500 catalog numbers. Ideal candidates are quick learners with strong technical writing skills, detail-oriented, and have a background in manufacturing, preferably medical devices. Benefits include paid time off and medical coverage.

Qualifications

• Experience in manufacturing environments preferred, especially in medical devices.
• Ability to create detailed manufacturing process flow maps.
• Strong communication skills for cross-functional collaboration.

Responsibilities

• Review existing manufacturing documentation and collaborate with the engineering team.
• Identify and document all processes and materials used in manufacturing.
• Create detailed end-to-end manufacturing process flow maps.
• Maintain accuracy and organization in technical documents for compliance.

Skills

Technical writing

Process documentation

Collaboration

Detail-oriented

Job description

Technical Writer – Kelly Engineering, Project Services

Largo, Florida.

Client in medical devices is seeking a detail‑oriented Technical Writer to support biocompatibility compliance efforts driven by evolving EU MDR (European Union Medical Device Regulation) requirements. This contract role will focus on updating and documenting manufacturing process flows for approximately 130 technical files and nearly 500 catalog numbers related to our sports medicine disposable orthopedic devices. Team will provide guidance and tools for our process mapping approach to ensure your success. Join us to play a critical role in meeting new EU MDR standards and ensuring the continued quality and compliance of innovative medical devices.

Key Responsibilities

• Review existing manufacturing documentation and collaborate with the engineering team.
• Identify and document all processes and materials used in the manufacturing of finished goods and subassemblies.
• Create detailed, end‑to‑end manufacturing process flow maps to support technical file updates and biocompatibility needs.
• Maintain a high level of accuracy and organization in updating technical documents as required for EU MDR compliance.

Project Scope & Commitment

The project will cover 132 technical files and about 500 catalog numbers. Each technical file is estimated to take approximately 10 hours (~1,300 hours total). The role is full‑time, 40‑hour work week.

Ideal Candidate

• Quick learner who can “hit the ground running.”
• Experience in manufacturing environments is a plus but not required. Medical devices strongly preferred.
• Detail‑oriented with strong technical writing and process documentation skills.
• Effective communicator, comfortable collaborating with cross‑functional teams.

Benefits

Paid time off, medical benefits, and other standard benefits are included for contract‑to‑hire participants.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E‑Verify and will provide the federal government with your Form I‑9 information to confirm that you are authorized to work in the U.S.