Description

You will design, develop, and update technical documentation for manufacturing, validation, and quality teams. This role is on-site.

Responsibilities

• Write, edit, and research technical documents including SOPs, change controls, protocols, deviations, and validation master plans.
• Navigate the Pasteur EDoc (Documentum) system to manage templates, workflows, and approval processes.
• Track and review change control documentation and programming standards.
• Collaborate with cross-functional teams to ensure documentation accuracy and regulatory compliance.
• Provide status reports to management regarding documentation activities and workflow issues.

Required Skills

• 3+ years of experience in technical writing or documentation roles.
• Proficiency in writing Standard Operating Procedures (SOPs).
• Experience using EDoc or Documentum systems.
• Strong analytical skills for root cause analysis regarding quality standards.
• Advanced proficiency in Microsoft Word and Excel.
• Competency in Microsoft PowerPoint and Outlook.
• Ability to document software capabilities and functionality clearly.

Preferred Skills

• Experience with Veeva Vault or Qualipso.

Key Skills

Education

Any Graduate