Job description

Join Our Team as a Technical Writer in Fort Washington, PA Are you a detail-oriented Technical Writer with a passion for transforming complex engineering and technical documents into clear and compliant Standard Operating Procedures (SOPs)? Join us in Fort Washington, PA, where you'll play a crucial role in supporting the development, revision, and management of manufacturing and engineering documentation within a GMP-regulated environment. This is an exciting opportunity to work closely with cross-functional teams and ensure documentation aligns with industry standards. Key Responsibilities • Review and interpret engineering, technical, validation, and operational documents. • Transform technical content into clear, concise, and compliant SOPs, work instructions, and controlled documents. • Collaborate with engineers, quality, validation, manufacturing, and cross-functional teams to gather and verify technical information. • Ensure documentation aligns with GMP requirements, company standards, and document control procedures. • Manage document review cycles, incorporating stakeholder feedback and maintaining version control. • Coordinate approval workflows and actively facilitate the collection of required signatures and approvals. • Maintain documentation accuracy, consistency, formatting, and traceability. • Utilize Microsoft Word to develop and format professional documentation templates and final deliverables. • Use Adobe Acrobat to review, edit, compile, and manage controlled PDF documentation. • Support document archival, revision management, and document management system activities as required. • Identify opportunities to improve documentation processes and standardization. Requirements • Bachelor's degree in Technical Writing, English, Communications, Engineering, Life Sciences, or a related field, or equivalent experience. • 2-4 years of technical writing experience in a GMP-regulated environment. • Experience creating and editing SOPs, work instructions, controlled documents, or quality system documentation. • Proficiency in Microsoft Word, including advanced formatting, styles, templates, tables, and document controls. • Proficiency in Adobe Acrobat for document editing, review, and PDF management. • Strong attention to detail with excellent proofreading and editing capabilities. • Ability to interpret technical and engineering information and translate it into end-user documentation. • Strong organizational, communication, and stakeholder management skills. Preferences • Experience supporting pharmaceutical, consumer health, biotechnology, medical device, or manufacturing operations. • Familiarity with document management systems and controlled document workflows. • Experience working with Quality, Validation, Engineering, or Manufacturing teams. • Knowledge of GMP documentation practices, data integrity principles, and compliance requirements. Work Arrangement • On-site in Fort Washington, PA during onboarding and initial engagement period to support stakeholder collaboration, document reviews, approvals, and signature collection. • Opportunity for a hybrid schedule (1-2 remote days per week) once the individual has established working relationships, gained familiarity with documentation processes, and can operate independently. Apply today to become a vital part of our team and help ensure our GMP documentation is accurate, compliant, and ready for execution. We look forward to welcoming you to our team in Fort Washington, PA! Subject Line: Technical Writer Opportunity in Fort Washington, PA By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy - Abacus .

Requirements

Must-haves

Join Our Team as a Technical Writer in Fort Washington, PA
Review and interpret engineering, technical, validation, and operational documents.
Transform technical content into clear, concise, and compliant SOPs, work instructions, and controlled documents.
Collaborate with engineers, quality, validation, manufacturing, and cross-functional teams to gather and verify technical information.
Ensure documentation aligns with GMP requirements, company standards, and document control procedures.
Manage document review cycles, incorporating stakeholder feedback and maintaining version control.
Coordinate approval workflows and actively facilitate the collection of required signatures and approvals.
Maintain documentation accuracy, consistency, formatting, and traceability.
Utilize Microsoft Word to develop and format professional documentation templates and final deliverables.
Use Adobe Acrobat to review, edit, compile, and manage controlled PDF documentation.
Support document archival, revision management, and document management system activities as required.
Identify opportunities to improve documentation processes and standardization.
Bachelor's degree in Technical Writing, English, Communications, Engineering, Life Sciences, or a related field, or equivalent experience.
2-4 years of technical writing experience in a GMP-regulated environment.
Experience creating and editing SOPs, work instructions, controlled documents, or quality system documentation.
Proficiency in Microsoft Word, including advanced formatting, styles, templates, tables, and document controls.
Proficiency in Adobe Acrobat for document editing, review, and PDF management.
Strong attention to detail with excellent proofreading and editing capabilities.
Ability to interpret technical and engineering information and translate it into end-user documentation.
Strong organizational, communication, and stakeholder management skills.
Experience supporting pharmaceutical, consumer health, biotechnology, medical device, or manufacturing operations.
Familiarity with document management systems and controlled document workflows.
Experience working with Quality, Validation, Engineering, or Manufacturing teams.
Knowledge of GMP documentation practices, data integrity principles, and compliance requirements.

Nice-to-haves

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