Technical Writer- Assay Development

Job Description

Our client, a world leader in diagnostics and life sciences, is looking for a "Technical Writer- Assay Development" based out of Tucson, AZ.

Job Duration : Long Term Contract (Possibility Of Conversion & Extension)

Pay Rate : $27 / hr on W2

Company Benefits : Medical, Dental, Vision, Paid Sick leave, 401K

Responsibilities

• Create, edit, and maintain technical documentation and product labeling for assay development and diagnostic products.
• Collaborate closely with R&D, Product Development, Quality, and Regulatory Affairs teams to gather and verify technical information.
• Ensure all documentation complies with internal standards, FDA, ISO 13485, and 21 CFR Part 11 requirements.
• Support the preparation and control of SOPs, work instructions, product manuals, and labeling content.
• Attend project team meetings and provide updates to supervisors on documentation progress and timelines.
• Participate in document review, approval, and change control processes within an electronic documentation management system (eQMS).
• Maintain version control and ensure timely updates to technical and regulatory documentation.
• Coordinate with cross-functional teams to ensure consistency and accuracy across all technical content.
• Assist in audits and inspections by providing compliant documentation as required.
• Identify opportunities to improve document templates, style guides, and documentation processes.

Qualifications & Education

If interested, please send us your updated resume at

hr@dawarconsulting.com / sanya@dawarconsulting.com