QA Technical Writer – Life Sciences & Regulatory Docs

HonorVet Technologies; Memphis (TN); On-site; USD 65,000 - 90,000; Full time

Job summary

HonorVet Technologies in Memphis, TN is seeking a QA Technical Writer to create, edit, and maintain technical documentation for cell and gene therapy manufacturing. Reporting to the Manager Compliance, you will tackle deviations, CAPAs, change controls, SOPs, batch records, and technical reports within a regulated life sciences environment.

The ideal candidate has 2–6 years of biotech/pharma writing experience, strong editing skills, and proficiency with Microsoft Office and document management

Qualifications

• Associate's degree or higher in Life Sciences, Biotechnology, Biochemistry, or related field preferred.
• 2–6 years of technical writing experience in biotechnology or pharmaceutical industries, preferably cell and gene therapy.
• Exceptional writing, editing, and proofreading skills with attention to detail.
• Ability to interpret and present complex scientific data clearly and concisely.
• Proficient in Microsoft Office Suite and document management systems.
• Strong organizational and project management skills.
• Excellent communication and interpersonal skills.

Responsibilities

• Generate and lead the facilitation in the completion of quality system documents for the manufacturing site (Deviations, CAPAs, Change Controls, etc)
• Ensure all documentation is clear, concise, and adheres to company standards and regulatory guidelines
• Complete routine and some non-routine documentation assignments within prescribed timeline under general supervision
• Work closely with stakeholders to gather information and ensure accuracy and completeness of documentation
• Facilitate document reviews and approvals, incorporating feedback from cross-functional teams and clients
• Collaborate in writing and editing technical documents including standard operating procedures (SOPs), batch records, technical reports, etc
• Communicate results and/or concerns verbally and in writing
• Develop and maintain relationships with internal stakeholders as well as begin building relationships with clients
• Provides solutions of moderate to complex scope to continuously improve documentation processes and templates to enhance clarity, efficiency, and compliance
• Leads in performing trainings for internal team and functional departments as applicable
• Perform other duties as assigned

Skills

Technical writing

Editing

Documentation management

Biopharma knowledge

SOP writing

Communication

Education

Life Sciences degree

Tools

Microsoft Office

Document management systems

Job description

HonorVet Technologies in Memphis, TN is seeking a QA Technical Writer to create, edit, and maintain technical documentation for cell and gene therapy manufacturing. Reporting to the Manager Compliance, you will tackle deviations, CAPAs, change controls, SOPs, batch records, and technical reports within a regulated life sciences environment.

The ideal candidate has 2–6 years of biotech/pharma writing experience, strong editing skills, and proficiency with Microsoft Office and document management