Technical Writer

Rbm-Services,-LLC-; Oak Ridge (TN); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Full benefits package

Job summary

RbM Services in Tennessee is seeking a Technical Writer/Protocol Development Specialist to document design verification activities, engineering reports, and manufacturing/service procedures for medical devices. You will work with engineering staff to create comprehensive documentation and maintain records to support compliance.

The role emphasizes developing verification and validation protocols, planning test approaches, and releasing technical reports within a full-time, on-site position.

Qualifications

• Experience documenting design verification activities and engineering reports.
• Familiarity with medical device compliance documentation.
• Ability to develop verification and validation protocols.

Responsibilities

• Work with engineering staff to document project plans, inputs, design reviews, outputs, and verification/validation protocols and results.
• Develop Verification and Validation Protocols.
• Plan how a set of requirements will be verified and validated.
• Outline the general approach to test each specific requirement.
• Develop individual test steps for each requirement.
• Release Engineering Technical Reports.
• Incorporate engineering information into a standardized technical report format.
• Develop and maintain Engineering Library.
• Create a library of example images for manufacturing and servicing procedures.

Skills

Technical writing

Documentation

Job description

Founded in 2000, locally owned and operated, RbM Services is a growing turn-key design, manufacture, and service solution provider for medical devices in Tennessee's Technology Corridor. With over 100 years of combined experience in the medical device industry, our management staff has extensive experience in intellectual property development, contract design, product development, field service support, and product support of medical devices and laboratory instrumentation. Our team is passionate and even obsessed with providing solutions that deliver cutting-edge technology that improves patient experiences and outcomes. Our passion lies in the pursuit of perfection. We value our employee family and foster opportunities for us to engage in meaningful connections, and we reward employees who exceed expectations.

Job Description

The Technical Writer/Protocol Development Specialist works with the engineering staff to document design verification activities, engineering technical reports, and manufacturing/service procedures. This position will focus on creating comprehensive technical documentation and support record-keeping activities necessary in the world of medical device compliance.

Job Duties:

• Working with engineering staff to document project plans, inputs (requirements/specifications), design reviews, outputs, and verification and validation protocols and results
• Development of Verification and Validation Protocols
• Working with engineering staff to plan how a set of requirements will be verified and validated.
• Outline the general approach to test each specific requirement.
• Develop the specific individual test steps for each specific requirement.
• Release Engineering Technical Reports
• Incorporate engineering information into a standardized technical report format
• Development and Maintenance of Engineering Library
• Develop and maintain a library of example images to use in manufacturing and servicing procedures.

As a full-time team employee, you are eligible for all RbM Services benefits including medical, dental, vision, long-term, short-term disability, 401k, PTO, 10 paid holidays, etc.

All your information will be kept confidential according to the EEO guidelines.