Department: Technical Operations - Engineering and Automation Compliance
Contract Type: Hourly Rate Contract
We are seeking experienced Technical Writers of ALL LEVELS to join our Technical Operations - Engineering and Automation Compliance team. This role offers an exciting opportunity to work within a leading biopharmaceutical company, contributing to the creation and maintenance of high-quality GMP documentation that supports key business functions.
Role Overview:
As a Technical Writer, you will be responsible for developing and maintaining accurate GMP documentation in collaboration with subject matter experts. This includes managing documentation workflows through the Electronic Document Management System (EDMS), ensuring compliance with industry standards, and supporting document-related activities across cross-functional teams.
Key Responsibilities:
Qualifications & Experience:
Associate Technical Writer:
Technical Writer:
Senior Technical Writer:
Knowledge, Skills, and Abilities:
What We Offer:
If you're a detail-oriented technical writer ready to make an impact in the biopharmaceutical industry, apply today by submitting your CV
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
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