GMP Analytical Documentation Specialist

Experic; Cranbury Township (NJ); On-site; USD 100,000 - 130,000; Full time

Job summary

Experic is looking for a Technical Writer, Analytical to support Quality Management System documentation in Cranbury Township, NJ. This role involves drafting, revising, and maintaining laboratory documentation while collaborating closely with lab personnel and Quality Assurance.

The candidate should have strong technical writing skills and experience in GMP documentation practices. The position offers a hybrid work schedule: 4 days in office and 1 day work from home.

Qualifications

• Minimum 2–5 years of experience in GMP laboratory environments.
• Experience authoring GMP laboratory documentation required.
• Working knowledge of cGMP, GDP, FDA regulations necessary.

Responsibilities

• Drafts and maintains controlled laboratory documentation.
• Coordinates document review and approval workflows.
• Supports onboarding and training documentation activities.

Skills

Technical writing

Project management

Collaboration

Attention to detail

Education

Bachelor’s degree in Chemistry, Biology, Pharmaceutical Sciences, or related discipline

Tools

Microsoft Office

QMS/document management systems

Job description

Experic is looking for a Technical Writer, Analytical to support Quality Management System documentation in Cranbury Township, NJ. This role involves drafting, revising, and maintaining laboratory documentation while collaborating closely with lab personnel and Quality Assurance.

The candidate should have strong technical writing skills and experience in GMP documentation practices. The position offers a hybrid work schedule: 4 days in office and 1 day work from home.