Onsite Process Documentation Intern; SOP/GMP
Job in
Lexington, Middlesex County, Massachusetts, 02173, USA
Listed on 2026-10-06
Listing for:
BioSpace
Full Time, Apprenticeship/Internship
position Listed on 2026-10-06
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer -
Pharmaceutical
Pharmaceutical Manufacturing, Pharma Engineer, Validation Engineer
Job Description & How to Apply Below
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.
We invite applications for the Onsite Process Documentation Intern (SOP/GMP) position located in Lexington, MA, United States. This posting is for the Onsite Process Documentation Intern (SOP/GMP) role at Bio Space, based in Lexington, MA, United States. We are looking to fill the Onsite Process Documentation Intern (SOP/GMP) position at Bio Space in Lexington, MA, United States. The Onsite Process Documentation Intern (SOP/GMP) role at Bio Space is now open for applications in Lexington, MA, United States.
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