Job Title: Technical Writer Location: Fort Washington, PA 19034 Duration: 12 months Hybrid schedule: 3 days remotely and 2 days onsite
Job Description:
The Technical Writer is responsible for developing, editing, and maintaining Packaging Development documentation, including Package Development Reports (PDRs), Package Development Assessment Plans (PDAPs), validation documentation, technical assessments, specifications, and supporting reports.
This role partners with Packaging Development, Technical Operations, Quality Assurance, Manufacturing, Regulatory Affairs, R&D, and external suppliers to collect, organize, and communicate technical information in a clear, compliant, and traceable manner.
Key Responsibilities:
Author and maintain PDRs, PDAPs, technical assessments, validation reports, and related documentation.
Coordinate cross-functional reviews and approvals.
Consolidate technical data into compliant documentation.
Support change controls, CAPAs, and audit activities.
Develop templates, SOPs, and work instructions.
Ensure documentation complies with GMP, GDP, and quality standards.
Qualifications:
Bachelor's degree in Technical Writing, Packaging Science, Engineering, Life Sciences, Communications, or related field. 3-7 years of technical writing experience in a regulated industry preferred.
Preferred Qualifications:
Experience in pharmaceutical, medical device, consumer healthcare, or packaging development environments. Familiarity with TrackWise, Veeva, SAP, or other document management systems.
Key Competencies:
Technical writing, document control, attention to detail, project coordination, cross-functional collaboration, analytical thinking, and regulatory compliance.
Looking for a great job? Join eTeam. We’re looking for talented staffing professionals to join our staff. We also provide contract assignments and full-time jobs at Fortune 2000 Companies. We’ve been named one of the best companies to work for by Staffing Industry Analysts and New Jersey Business.
Skills
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Change Controlunmatched
Cross-Functionalunmatched
Detail Orientedunmatched
Document Controlunmatched
Document Managementunmatched
Documentationunmatched
Editingunmatched
Functional Analysisunmatched
GMP (Good Manufacturing Practices)unmatched
Healthcareunmatched
Manufacturing Requirementsunmatched
Medical Equipmentunmatched
Project/Program Coordinationunmatched
Quality Assuranceunmatched
Quality Metricsunmatched
Regulatory Complianceunmatched
Reporting Skillsunmatched
Research & Development (R&D)unmatched
SAPunmatched
Standard Operating Procedures (SOP)unmatched
Technical Analysisunmatched
Technical Operationsunmatched
Technical Writingunmatched
Validation Documentationunmatched
Writing Skillsunmatched
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