Quality Assurance Work Instruction Intern

Quality Assurance Work Instruction Intern Norwich Pharmaceuticals 18.00 To 18.00 (USD) Annually United States, York, Norwich Apr 10, 2026 SUMMARY

OF POSITION

The Quality Intern will primarily support document formatting and conversion from PDF to Microsoft Word for electronically stored work instructions to align with current process. Other duties may be assigned by the direct manager based on priorities and business need.

ORGANIZATION STRUCTURE

The QA Intern reports directly to the Quality Assurance Laboratory Lead.

RESPONSIBILITIES

Primary responsibilities of this role include the following: Work with the SOP coordinator to convert existing electronic PDF documents to updated Microsoft Word format. Input updated versions into eQMS system to ensure appropriately formatted documents are stored electronically and available for review by SMEs. Assist with other document maintenance activities as required.

QUALIFICATIONS

Currently enrolled in a college or university Experience with Microsoft Word and Adobe Strong organizational skills and ability to work independently. High level of attention to detail Strong written and oral communication skills, including the ability to work effectively with diverse groups of customers, management, and technicians. This includes the ability to work in a team environment.

GMP DECISION-MAKING AUTHORITY

Has the authority to manage, execute, and report on all aspects of the specified assignment. Additional approval authority may be designated by Quality Assurance Management. The anticipated base hourly rate for this position is $18.00. This role is temporary and not benefit eligible. We anticipate this position will be posted on April 10, 2026, and remain open for at least 30 days. To apply, select the apply button and submit your application. "An Equal Opportunity Employer, including disability/vets."