Senior Document Control & Training Specialist

Arrowhead Pharmaceuticals; Verona (WI); On-site; USD 78,000 - 98,000; Full time

Job summary

Arrowhead Pharmaceuticals, Inc. in Wisconsin is seeking a detail-oriented Document Control and Training Compliance professional to support day-to-day QA activities. You will manage controlled documents, records, and training data within the eQMS and LMS, ensuring accuracy and regulatory alignment.

This role emphasizes document control workflows, audits, and collaboration with Legal and Compliance. A BS/BA in a scientific field and at least five years in pharma/biotech documentation are required;

Qualifications

• BS/BA in an applicable scientific field such as chemistry, biology, or biochemistry.
• Minimum of 5 years in a pharmaceutical/biotech company writing and maintaining documents.
• Ability to follow company procedures, work instructions, and policies.
• Strong organizational and interpersonal communication skills.
• Experience with an eQMS/eDMS platform (e.g., Veeva) preferred.

Responsibilities

• Document control and records management within the eQMS and LMS.
• Maintain controlled documents, records, and training records for compliance.
• Assist with audits, regulatory inspections, and document change control.
• Support training administration and data reporting for compliance.
• Coordinate with Legal, Compliance, and IS&I on policy routing and review.

Skills

Document control

Quality Assurance

GxP regulatory knowledge

Communication

Organization

Education

BS/BA in scientific field

Tools

Veeva/eQMS

LMS software

Adobe Acrobat

Microsoft Word

PowerPoint

Excel

Job description

Arrowhead Pharmaceuticals, Inc. in Wisconsin is seeking a detail-oriented Document Control and Training Compliance professional to support day-to-day QA activities. You will manage controlled documents, records, and training data within the eQMS and LMS, ensuring accuracy and regulatory alignment.

This role emphasizes document control workflows, audits, and collaboration with Legal and Compliance. A BS/BA in a scientific field and at least five years in pharma/biotech documentation are required;