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Technical Writer - Scientific-I
Ref No.: 18-08032
Location: Jacksonville, Florida
Position Type:Contract
Start Date: 09/07/2018
Please note the following from the manager:
- Manager is looking for candidate to update templates and documents.
- Would prefer candidates with Quality systems / document control experience. 
- A degree is not required
- Med Device / pharma experience preferred, but not required

Technical writer with excellent PC, oral and written communication skills. Experience working in an FDA regulated environment. Experience in creating/editing work instructions/procedures. Ability to interpret statistical data. Works closely with Medical Safety, Clinical Science, Regulatory Affairs, QA and Post Market Surveillance Staff to develop, review and implement Safety Surveillance Plans for Surgical Vision product families. Work closely with Post Market Surveillance, Product Safety and QA to coordinate procedure updates following through to procedure implementation. Assist Post Market Surveillance team with monthly trending and annual post market surveillance meetings and documentation. Facilitate of Monthly Trend Review Meetings via Skype as required per team schedule. Assist and facilitate various integration related projects for Post Market Surveillance Team. Tracks and reports progress across various post market surveillance projects and departmental commitments by reviewing schedules and due dates, identifying risks, and assisting teams with contingency plans.