Quick Summary
Overview
Technical Writer – Validation Location: Melrose Park, IL | 100% Onsite Type: 6-Month Contract-to-Hire Start: ASAP Ideal Candidate: 1–2 years of experience, ideally around 1.5 years, in Life Sciences,
Technical Tools
OtherTechnical Writer
- 1–2 years of experience, ideally around 1.5 years, in Life Sciences, Pharmaceutical Manufacturing, or a related regulated environment.
- Experience creating, reviewing, or maintaining technical/validation documentation.
- Exposure to equipment validation, process validation, IQ/OQ/PQ, protocols, reports, SOPs, and GMP documentation.
- Pharmaceutical manufacturing experience is highly preferred, especially equipment used in injectable/filling-line operations.
- Familiarity with MES systems, particularly PAS-X, is a strong plus.
- Candidates with strong college accomplishments, internships, projects, or early-career achievements should be considered.
- Excellent writing, documentation, organization, communication, and attention to detail.
- Determination, attitude, adaptability, and willingness to learn will be critical.
- Must be comfortable working 100% onsite in Melrose Park, Illinois.
Location & Eligibility
Where is the job
Chicago, United States
On-site at the office
Who can apply
US
Listing Details
- First seen
- August 13, 2026
- Last seen
- October 2, 2026
Posting Health
- Days active
- 49
- Repost count
- 0
- Trust Level
- 17%
- Scored at
- October 2, 2026
Signal breakdown
freshnesssource trustcontent trustemployer trust
External application
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