Quality Systems Document Control

Scorpion Therapeutics; Indiana (PA); Hybrid; USD 52,000 - 76,000; Full time

Job summary

Scorpion Therapeutics seeks a Temporary Document Control Support to manage and review quality and regulatory documents within a biopharma setting.

Your role includes interacting with global stakeholders, creating and releasing documents, and supporting QMS software implementations, with a focus on GxP and regulatory compliance.

Qualifications

• HS diploma or higher; BA in English or technical writing preferred
• Experience in administrative, quality, or document control roles
• Proficiency in MS Office, SharePoint, Adobe Acrobat; strong attention to detail

Responsibilities

• Interact with global stakeholders to ensure document alignment with regulatory standards
• Create, revise, and release controlled documents across QA/QMS
• Maintain document lifecycle and support special projects within the QMS

Skills

written communication

organizational ability

QMS document management

Education

HS diploma or higher; BA in English/technical writing preferred

Tools

MS Office

SharePoint

Adobe Acrobat

Job description

Role

Temporary Document Control Support specializing in the management and review of quality and regulatory documents within a biopharma setting.

Objectives

ensure document compliance, facilitate review/approval workflows, and support QMS software implementation.

Responsibilities

interact with global stakeholders, create/revise/release documents, maintain document lifecycle, and support special projects.

Qualifications

HS diploma or higher (preferably Bachelors in English or technical writing), experience in administrative, quality, or document control roles, proficiency in MS Office, SharePoint, Adobe Acrobat, and strong attention to detail.

Skills

effective written/verbal communication, organizational ability, and understanding of formal QMS document management.

High-Value

role involves GxP compliance, document control within quality systems, and support for biopharma regulatory standards.

Work setup

hybrid (minimum 3 days onsite), temporary (6-8 months), with physical requirements related to office work. No specific therapeutic areas or development stages specified, but focus on supporting document workflows for quality assurance and regulatory compliance.