Onsite Process Documentation Intern (SOP/GMP)

BioSpace; Lexington (MA); On-site; USD 28,929 - 63,369; Full time

Benefits offered by this job

Paid sick time

Civic Duty paid time off

On-site fitness center

Commuter Benefit

Job summary

A leading pharmaceutical company seeks a Process Documentation Intern to revise controlled manufacturing documentation. Responsibilities include updating SOPs and ensuring compliance with GMP Standards, while working collaboratively with cross-functional teams. Candidates should pursue a degree in life sciences or related fields, possess strong technical writing skills, and be available for a full-time commitment in Lexington, MA. The internship offers competitive pay and numerous professional development opportunities.

Qualifications

• Must be enrolled in a degree program graduating December 2026 or later.
• Previous technical writing experience is necessary.
• This position will be fully onsite and requires 4+ days in the Lexington, MA office.

Responsibilities

• Revise SOPs, Batch Records, and Form Preps.
• Ensure document consistency in compliance with SOP requirements.
• Coordinate document revisions for major projects.

Skills

Technical writing

Document management applications

Microsoft Office Suite

Communication skills

Attention to detail

Team player

Basic computer skills

Education

Undergraduate degree in life sciences, writing, project management, or similar

Tools

EDMS

TrackWise

Job description

A leading pharmaceutical company seeks a Process Documentation Intern to revise controlled manufacturing documentation. Responsibilities include updating SOPs and ensuring compliance with GMP Standards, while working collaboratively with cross-functional teams. Candidates should pursue a degree in life sciences or related fields, possess strong technical writing skills, and be available for a full-time commitment in Lexington, MA. The internship offers competitive pay and numerous professional development opportunities.