Technical Writer - OQSIE
Andover, MA 01810
About the Job
The client is in the process of standardizing its Quality Systems across 27 sites.
Location: Wilmington, MA - Important Note: Initial week or two in Wilmington to meet key contacts, understand processes / systems. From there remote unless required to be
on-site at client's request.
Duration: Initial duration is three (3) months with likely extension.
Requirements & Responsibilities:
• Bachelor's degree
• Must have a foundation in ISO 13485 (Medical Device Quality Management System)
• Experience with technical writing, e.g., SOPs, policies and work instructions across Quality System components
o Work is focused on Level 1 – (Quality Policy and Quality Manual, Corporate Quality System)
• Understanding of standard terminology, e.g., 'as required', 'if required' to support discussion facilitation toward defining standardization across sites
• Support and facilitate meetings as needed
• Computer with video conferencing capability for remote activity
Location: Wilmington, MA - Important Note: Initial week or two in Wilmington to meet key contacts, understand processes / systems. From there remote unless required to be
on-site at client's request.
Duration: Initial duration is three (3) months with likely extension.
Requirements & Responsibilities:
• Bachelor's degree
• Must have a foundation in ISO 13485 (Medical Device Quality Management System)
• Experience with technical writing, e.g., SOPs, policies and work instructions across Quality System components
o Work is focused on Level 1 – (Quality Policy and Quality Manual, Corporate Quality System)
• Understanding of standard terminology, e.g., 'as required', 'if required' to support discussion facilitation toward defining standardization across sites
• Support and facilitate meetings as needed
• Computer with video conferencing capability for remote activity
Source : OQSIE