Overview

Senior Consultant- Key Account Management (Contract)

Job Title: Quality Management Documentation Senior Specialist

Location: Remote

Contract Type: Contract

About the Role

We are seeking a Quality Management Documentation Senior Specialist to support the development and maintenance of GxP Quality Management Documents (QMDs) in compliance with a global Quality Management System (QMS). This role requires exceptional attention to detail, strong communication skills, and the ability to work to tight timelines while ensuring accuracy and compliance.

Responsibilities

• Perform document control activities, ensuring consistency and compliance with applicable standards and procedures for QMD lifecycle management.
• Manage external distribution of QMDs to support project teams, audits, and inspections.
• Collaborate with internal stakeholders to ensure compliance with QMS and QMD lifecycle requirements.
• Format, QC, and publish QMDs and related deliverables with exceptional accuracy.
• Proofread and edit QMDs to ensure clarity, accuracy, and adherence to internal standards.
• Identify and correct errors and formatting issues.

Qualifications

• Bachelor’s degree in life sciences or a related discipline.
• Minimum of 3 years of experience with document management systems.
• Experience managing GxP procedural documents.
• Strong proficiency with Microsoft Word, Excel, SharePoint, PowerPoint, and Visio.
• Excellent written and verbal communication skills.
• Strong critical thinking, teamwork, and interpersonal skills.
• Experience in technical writing or editing is preferred.
• Familiarity with Visio or similar diagramming tools is a plus.
• Understanding of the drug development process is desirable.