Our client is looking to fill the role of Pharmaceutical Technical Writer. The Technical Writer serves as the primary documentation specialist for commercial manufacturing operations and technical transfer processes. This role encompasses comprehensive document management, process improvement initiatives, and specialized support for R&D documentation requirements. The position involves evaluating current documentation systems (Batch Records, SOPs, OIMs), identifying enhancement opportunities, and executing improvements that advance Manufacturing's continuous improvement objectives.
Responsibilities:
Documentation Management & Development
Deliver comprehensive documentation support to Technical Services team, encompassing creation, revision, formatting, processing, archival, and maintenance of both physical and electronic documents
Develop and maintain critical documentation including batch production records, standard operating procedures, protocols, and technical reports
Prepare incident documentation, investigation summaries, and quality event reports with accuracy and timeliness
Quality Systems Administration
Administer Quality Systems processes for Technical Services, including CAPA management, Change Control procedures, and quality event tracking and analysis
Collaborate with subject matter experts to develop and document effective Corrective and Preventive Actions (CAPA), ensuring complete and compliant documentation
Serve as departmental Subject Matter Expert for Electronic Quality Documentation Management Systems, providing user support and training as required
Regulatory Compliance & Reviews
Lead the biennial SOP review cycle for Technical Services, managing revisions and ensuring adherence to established timelines
Coordinate Validation Section contributions to Periodic Quality Reviews (PQRs), including data compilation, document preparation, and CAPA identification
Maintain strict compliance with FDA regulations, cGMP guidelines, and all applicable regulatory standards
Scientific Communication & Marketing Support
Facilitate development of scientific publications and technical materials that enhance Adare Technologies' market presence and support business development initiatives
Create diverse content for Technical Services and R&D departments including research papers, conference posters, white papers, presentations, and webinar materials
Operational Excellence
Champion continuous improvement initiatives across departmental functions
Promote and support Safety and cGMP program implementation
Ensure adherence to all regulatory frameworks (GMP, ISO, FDA, internal policies) within scope of responsibility
Required Qualifications:
Education & Experience
High School diploma with 3-5 years of technical writing and procedure development experience in FDA-regulated environments, OR
Bachelor's degree with 2-3 years of technical writing and procedure development experience in FDA-regulated environments
Technical Proficiencies
Advanced proficiency in Microsoft Office Suite (Excel, Word, PowerPoint)
Demonstrated capability in data synthesis from multiple sources and creation of comprehensive reports and executive summaries
The Solomon Page Distinction
Solomon Page offers a comprehensive benefit program for hourly employees. We pride ourselves on offering medical, dental, 401(k), direct deposit and commuter benefits to our employees, including freelancers - which sets us apart in the industries we serve.
About Solomon Page
Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook, and LinkedIn .
Opportunity Awaits.
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