Remote Regulatory Pro: Veeva Quality Docs

Jobgether; Oregon; Hybrid; USD 110,000 - 150,000; Full time

Benefits offered by this job

Health, vision, and dental insurance

401(k) retirement plan matching

Tuition reimbursement

Paid vacation, holidays, and sick time

Flexible remote working environment

Job summary

Jobgether in the United States (remote) seeks a Regulatory Affairs Consultant specializing in process and compliance with Veeva Quality. You will act as a SME for controlled document management, ensuring GxP documentation is accurate, inspection-ready, and aligned with regulatory standards.

You will collaborate across Regulatory, Quality, CMC, Clinical Operations, and Pharmacovigilance to strengthen document governance, training, and QMS processes, support inspections, and drive continuous

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Engineering, or a related field.
• At least 8 years of experience in regulatory compliance, quality assurance, or related GxP functions.
• Hands-on experience with Veeva Vault or similar eDMS for controlled documents.
• Strong knowledge of FDA, EMA, ICH, and global GxP regulations.
• Experience supporting regulatory inspections and audits.

Responsibilities

• Oversee controlled document management in Veeva Quality or similar eDMS, including creation, review, approval, and archiving.
• Support global GxP compliance activities and mitigation of compliance risks.
• Prepare for and support regulatory inspections and audits by health authorities.
• Manage GxP training governance and assign role-based curricula.
• Support and improve QMS processes including deviations, CAPAs, and change controls.

Skills

Regulatory compliance expertise

Quality management

Document governance

Stakeholder collaboration

Attention to detail

Analytical skills

Leadership and communication

Education

Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Engineering, or related field

Tools

Veeva Vault

LMS platforms

QMS tools

Job description

Jobgether in the United States (remote) seeks a Regulatory Affairs Consultant specializing in process and compliance with Veeva Quality. You will act as a SME for controlled document management, ensuring GxP documentation is accurate, inspection-ready, and aligned with regulatory standards.

You will collaborate across Regulatory, Quality, CMC, Clinical Operations, and Pharmacovigilance to strengthen document governance, training, and QMS processes, support inspections, and drive continuous