Technical Writer

Industry

Manufacturing and Production

Advert ID

USA_426870

Location

Grand Rapids

Job Type

Contract

Hours

Full-Time

Salary Range

USD22.00-28.00/hr

No. of Openings

1

Branch Information

Grand Rapids MI Area - (USA) 2935 28th Street MI Grand Rapids , MI - 49512 Phone : 616-957-0461

ContactNumber

616-957-0461

Job Description

Manpower is actively recruiting for a Technical Writer with experience within a FDA-regulated facility.



Key responsibilities include:

* Writing and editing controlled documents such as protocols, reports, data sheets, work instructions, forms, drawings and process maps

* Works with departmental manager, leaders, and subject matter experts to review and assist in creating documentation that will support product testing, data collections, risk management, and process flow

* Performs gap analyses of current practices and procedures

* Create, update, and maintain trending charts as requested

* Other projects or tasks as assigned



EDUCATION and/or EXPERIENCE:

* Bachelor's Degree in Communications, English, Education, or accredited technical writing training is preferred

* 3-5 years experience writing procedures within a FDA-regulated facility is preferred

* 3-5 years experience within medical manufacturing or research & development is preferred



SKILLS, KNOWLEDGE AND EXPERIENCE REQUIRED:

* Strong computer skills and knowledge of MS Word, MS Excel, Access, Outlook, and MS Visio

* Must have strong verbal and interpersonal communication skills

* Strong English writing, editing, and grammar skills

* Excellent organizational, planning, and project management skills

* Must display a positive attitude while maintaining flexibility

* Team player with ability to facilitate meetings with cross functional teams



QUALITY AND REGULATORY REQUIREMENTS:

* Quality system knowledge including the quality manual, quality policy, and applicable procedures and work instructions

* Establishes, implements, and maintains the quality system in accordance to FDA Quality System Regulation, ISO 13485, European Union Medical Device Directives, and Canadian Medical Device Regulations

* Completes and documents all required quality, business, and departmental training