Technical Writer I

Req#: 15356195
Name: Technical Writer I
Status: Pending
Client: Cardinal Health
Start: 03/21/2022
End: 09/23/2022
Location: Arcadia, CA, 300 West Huntington Drive, CA-Arcadia

Department: 1000000740 Medical Segment Quality Systems Job Category: QRA and Engineering Job Title: Technical Writer I

The main responsibility of the technical write is to edit and revise documents, e.g., SOPs, written by Cardinal quality professionals. Assist with harmonization of process and writing of user guides in support of the implementation of new enterprise electronic quality management system (eQMS).

The technical writer will collaborate closely with SMEs to gather, organize, format, draft, revise and implement a variety of quality management system documents associated primarily with quality system elements such as CAPA, Audit, Complaint Management, Supplier Management, NC, OOS, etc. This individual will also work with document change analysts to track and communicate the status of document changes to ensure the appropriate level of assessment and approval.

Skills: Must be proficient in Microsoft Word, Microsoft Excel, and Microsoft PowerPoint Must work well with others and understand how to be successful in a Team environment Must be detail oriented, organized, able to multi-task, a self-starter, and self-motivated. Solid working knowlege of FDA 21 CFR 820, ISO 13485 and other global medical device regulations preferred

Keywords:

Education: Minimum, B.S. degree in Life Sciences (Chemistry, Microbiology, Biology, etc.), Engineering Technology, or related science field
1-2 years of technical writing experience C34 Skills and Experience:

Req#: 15356195
Name: Technical Writer I
Status: Pending
Client: Cardinal Health
Start: 03/21/2022
End: 09/23/2022
Location: Arcadia, CA, 300 West Huntington Drive, CA-Arcadia

Department: 1000000740 Medical Segment Quality Systems Job Category: QRA and Engineering Job Title: Technical Writer I

The main responsibility of the technical write is to edit and revise documents, e.g., SOPs, written by Cardinal quality professionals. Assist with harmonization of process and writing of user guides in support of the implementation of new enterprise electronic quality management system (eQMS).

The technical writer will collaborate closely with SMEs to gather, organize, format, draft, revise and implement a variety of quality management system documents associated primarily with quality system elements such as CAPA, Audit, Complaint Management, Supplier Management, NC, OOS, etc. This individual will also work with document change analysts to track and communicate the status of document changes to ensure the appropriate level of assessment and approval.

Skills: Must be proficient in Microsoft Word, Microsoft Excel, and Microsoft PowerPoint Must work well with others and understand how to be successful in a Team environment Must be detail oriented, organized, able to multi-task, a self-starter, and self-motivated. Solid working knowlege of FDA 21 CFR 820, ISO 13485 and other global medical device regulations preferred

Keywords:

Education: Minimum, B.S. degree in Life Sciences (Chemistry, Microbiology, Biology, etc.), Engineering Technology, or related science field
1-2 years of technical writing experience C34 Skills and Experience: