Technical Writer

Immediate need for a talented Technical Writer. This is a 06 Months Contract opportunity with long-term potential and is located in Fort Washington PA(Onsite). Please review the job description below and contact me ASAP if you are interested.

Job ID:26-31629

Pay Range: $40/hour. Employee benefits include but are not limited to health insurance (medical dental vision) 401(k) plan and paid sick leave (depending on work location).

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.

Key Requirements and Technology Experience:

• 24 years of GMP-regulated experience creating and revising manufacturing SOPs and controlled documents.
• 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.
• Bachelors degree in Technical Writing English Communications Engineering Life Sciences or a related field or equivalent experience.
• 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.

Our client is a leadingconsumer packaged goods Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position please apply online for immediate consideration.

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