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 leading consumer 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.

Pyramid Consulting Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race color religion age sex national origin disability status genetics protected veteran status sexual orientation gender identity or expression or any other characteristic protected by federal state or local laws.

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