Pharma GMP Technical Writer – Hybrid Contract

Staffmark Group; Branchburg Township (NJ); Hybrid; USD 55,000 - 83,000; Full time

Job summary

Staffmark Group seeks a detail-oriented Technical Writer in Branchburg, NJ for a 6-month contract with potential extension. The role centers on GMP documentation, CAPA closures, and controlled documents to support supply chain and manufacturing operations.

You will collaborate with SMEs, Quality, and Supply Chain teams to develop clear, compliant SOPs, forms, and change controls, ensuring consistency and timely delivery while meeting regulatory requirements.

Qualifications

• Bachelor's degree in a scientific discipline or 5+ years in a related field.
• 3–6 years of relevant experience in pharma manufacturing or a regulated industry.
• Strong technical writing skills for controlled documentation.
• Excellent written and verbal communication across all organizational levels.
• Working knowledge of GMP documentation and change management processes.

Responsibilities

• Author, review, revise, and maintain GMP documentation and CAPA closures.
• Develop documentation standards, templates, and formatting guidelines.
• Collaborate with Supply Chain to ensure consistency and reduce gaps in documentation.
• Ensure documents meet GMP requirements and internal Quality standards.
• Support CAPA closures by updating required documentation and coordinating actions.
• Coordinate document change management activities and reviews/approvals.

Skills

Technical writing

Communication

Change management

Multitasking

Process improvement

Education

Bachelor's degree in a scientific discipline

Tools

Microsoft Office (Word, Excel, Access, PowerPoint)

Job description

Staffmark Group seeks a detail-oriented Technical Writer in Branchburg, NJ for a 6-month contract with potential extension. The role centers on GMP documentation, CAPA closures, and controlled documents to support supply chain and manufacturing operations.

You will collaborate with SMEs, Quality, and Supply Chain teams to develop clear, compliant SOPs, forms, and change controls, ensuring consistency and timely delivery while meeting regulatory requirements.