Fran Blauw

As a technical writer, editor, and project manager, I enjoy creating quality documentation in challenging and professional environments with motivated coworkers. For the last almost 20 years, I have worked as a contractor in the pharmaceutical industry, networking with process owners, business analysts, subject matter experts, and end-users to evaluate, create, and revise validation documentation. Projects involve software systems and related equipment. I preserve the integrity of my work by following FDA guidelines; best practices; GxP guidelines; and corporate and divisional procedures, standards, and practices. As my history demonstrates, I enjoy working independently, as part of a team, and in leadership positions. I am proactive and detail-oriented, possess strong organizational skills, and am an excellent communicator. I manage multiple projects and understand the importance of meeting all deadlines. I am a dedicated worker, take ownership of and responsibility for all assigned tasks, and am flexible by working extra hours when necessary. Two positive comments heard most from managers are that I work well with others and that I meet and exceed client expectations. If you have read my resume, this profile will serve as a more detailed overview of each of my positions in chronological order. Specialties: Validation and Technical Writing • Editing • Gap Analysis and Remediation • Life Sciences • Policy and Regulation Compliance • Project Management and Facilitation • Quality Assurance • Software Development Life Cycle • Documentation and Records Management • Team Leadership, Training, Mentoring