Cell and Gene Technical Writer

ABM•East Hanover, NJ

2d•$70,000 - $90,000

About The Position

The Cell & Gene Technical Writer is responsible for development, control, and maintenance of technical documentation supporting laboratory and facility operations within cell and gene environments. This role ensures all SOPs, work instructions, maintenance procedures, and operational documentation are accurate, controlled, and audit-ready. The Technical Writer works closely with engineering, QHSE, and laboratory teams to ensure documentation aligns with site procedures, quality standards, and regulatory expectations. The role supports documentation control, version management, and consistency across all technical processes. This position is critical for ensuring operational consistency, compliance, and readiness for regulated (GxP-adjacent) environments. Compensation: $70,000 - $90,000/YR Salary The pay listed is the hourly/salary rate for this position. A specific offer will vary based on applicant’s experience, skills, abilities, geographic location, and alignment with market data. Benefit Information: ABM offers a comprehensive benefits package. For information about ABM’s benefits, visit Annual Benefits-Staff and Management Responsibilities

Requirements

3–7 years of experience in technical writing, documentation control, or quality systems
Experience supporting SOP development and controlled documentation environments
Familiarity with QMS, document control systems, and audit processes
Strong attention to detail and documentation accuracy

Nice To Haves

Experience in life sciences, laboratory, or regulated environments strongly preferred

Responsibilities

Develops, maintains, and updates SOPs, work instructions, and technical documentation for engineering, laboratory, and facility operations
Ensures all documentation aligns with site procedures, QMS requirements, and QHSE standards
Manages document control processes, including versioning, approvals, and audit readiness
Works with engineering and operations teams to document maintenance procedures, job plans, and operational workflows
Maintains accurate and controlled records of all documentation changes, revisions, and approvals
Supports audit preparation by ensuring all technical documentation is complete, current, and compliant
Assists in development of deviation documentation, change control inputs, and continuous improvement documentation
Ensures consistency of documentation across laboratory, facility, and operational processes