דרושים Documentation Technical Writer ב-Ge Healthcare ב-United States, State College

• Create and edit operational, instructional, and maintenance/test procedures for paper, digital, or web-based publication.

• Convert existing documentation into data collection plans, for use in the digital record system.

• Communicate with various users and technical staff to gather data for documentation.

• Document Engineering processes and specifications. Recommend format, regarding technical and customer requirements.

• Produce documentation that conforms to the company documentation and quality assurance standards.

• Interface with process owner(s) to ensure documentation matches current best practices.

• Release and maintain documents in PLM system.

• Associate degree or equivalent work experience as a technical writer or generating documentation for medical devices.

• Experience working in a highly regulated industry and following mandatory processes (preferably in the medical device industry).

• Excellent written and verbal communication skills.

• Good organizational skills (task tracking and reporting).

• Strong experience with Microsoft Office (including redlining function), and Adobe Acrobat.

• Experience with document control software (ideally MyWorkshop PLM) is desirable

• Legal authorization towork in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.

• Sitting

• Standing

• Lifting <25 pounds

• Computer typing

• Computer monitor

• Create and edit operational, instructional, and maintenance/test procedures for paper, digital, or web-based publication.
• Convert existing documentation into data collection plans, for use in the digital record system.
• Communicate with various users and technical staff to gather data for documentation.
• Document Engineering processes and specifications. Recommend format, regarding technical and customer requirements.
• Produce documentation that conforms to the company documentation and quality assurance standards.
• Interface with process owner(s) to ensure documentation matches current best practices.
• Release and maintain documents in PLM system.

Qualifications Required

• Associate degree or equivalent work experience as a technical writer or generating documentation for medical devices.
• Experience working in a highly regulated industry and following mandatory processes (preferably in the medical device industry).

• Excellent written and verbal communication skills.
• Good organizational skills (task tracking and reporting).
• Strong experience with Microsoft Office (including redlining function), and Adobe Acrobat.
• Ideal candidate will have experience working in a regulated environment (Medical Device Industry).
• Experience with document control software (ideally Oracle Agile PLM and MyWorkshop PLM) is desirable

Physical Requirements:

• Sitting
• Standing
• Lifting <25 pounds
• Computer typing
• Computer monitor

Location

• State College, PA