
Randolph D.
Technical Writer SOPs, Compliance and Business Documentation
Skills

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Work experience
Technical Editor (Contract Position)
Hilton Hotels & Resorts • Full-time
Apr 2024 - Nov 2025 • 1 yr 7 mos
- Developed and standardized sales documentation, proposals, and training guides to ensure accuracy and consistency. - Authored operational SOPs, workflow documentation, and CRM process guides to support sales operations. - Collaborated with cross-functional teams to produce client-facing collateral and technical presentations. - Streamlined reporting templates and documentation practices, improving efficiency across sales and operations teams. Key Achievement: Increased group and corporate bookings by 40% within the first 3 months.
Technical Writer
Schneider Electric • Full-time
Sep 2012 - Jan 2022 • 9 yrs 4 mos
- Received the highest performance/competency review of all technical writers at Schneider Electric, awarded a 4.90 of 5.0 increasing overall company and department performance. - Wrote and edited 500-1000 standard operating procedures (SOP’s), instruction bulletins, catalogs, user guides, market required documents (MRD’s), white papers and application programming interfaces (API’s) regarding proper equipment usage and appropriate product installation methods. - Revitalized new product documentation development, streamlined document lead times, drove 107% quota achievement and pioneered considerable cost savings by creating 205 new and revised 375 legacy documents adhering to PMP, PEP, OCP, UL, NEMA, OSHA, and ANSI regulations and standards. - Awarded the “Digitize” award by Schneider Electric for technical communications excellence concerning the enhancement of an all-new HTML composition of Digest 177.
Technical Writer (Contract Position)
Pfizer • Full-time
Jan 2011 - Sep 2012 • 1 yr 8 mos
- Composed standard operating procedures (SOP’s) regarding proper equipment usage and facility production training methods. Incorporated diagrams, graphics, screenshots thereby increasing staff documentation comprehension. - Improved vaccine production, reduced deviations, diagnosed a increase in sales solution, and provided significant cost savings by creating new and revising batch records (Manufacturing Directions), adhering to 21 CFR, USDA, FDA, and EU regulations. - Revitalized batch records by creating an instructional step by step format to ensure cGXP standards were met. The initiative also reduced user errors by 30% and increased productivity by 43.4%. - Orchestrated several M1 investigations using DMAIC and developed a Corrective Action Preventive Action (CAPA) incorporating changes to documentation and process design in order to resolve minor to severe inventory deviation issues. - Researched and implemented over 60 CAPA’s and created over 100 quality assurance reports to resolve quality control issues and prevent future deviations.