Description
I am equipped with 25+ years of experience in Documentation Design/Development and Technical Writing. I am currently exploring gainful opportunity prospects in Pharma and Bio Research. * Analytical and detail-oriented Technical Writer, with vast experience in technical documentation development across various industries. Strong background in writing with superb written communication skills. Expert knowledge in document life cycle management in support of cGMP, cGDP, CFR, and ISO standards compliance. * Notable skills: * Expert in Microsoft Office, Visio, SharePoint, TrackWise
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| (Confidential) | Senior Technical Writer (Contractor) | 1/2018 - Present |
| Immunomedics | Senior Technical Writer (Contractor) | 10/2017 - 1/2018 |
| Adaptimmune, Llc | Senior Validation Consultant (Contractor) | 9/2016 - 3/2017 |
| Merck & Company | Learning Objective Document Author/Technical Writer (Contractor) | 6/2016 - 9/2016 |
| Ortho Clinical Diagnostics | Change Author/Technical Writer (Contractor) | 2/2016 - 5/2016 |
| Glaxo Smith Kline St Louis Operations | Facility Engineer/Technical Writing (Contractor) | 8/2014 - 9/2015 |
| Quality Packaging Systems International, Inc. | Technical Writer/Contractor | 4/2014 - 7/2014 |
| J&J De Puy Synthes | Technical Writer | 7/2013 - 10/2013 |
| J&J Mc Neil | Technical Writer | 7/2012 - 3/2013 |
| Merck & Company | Technical Writer/Data Analyst/Contractor | 11/2009 - 5/2012 |
| Ricoh | Technical Documentation/Data Analyst/Contractor | 10/2008 - 10/2009 |
Accomplishments
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