This role is fully remote!

Description:

• Support updates to Veeva meta-data, including review of existing configuration and making necessary changes required for system integrations.
• Provide document processing support, including review of controlled GxP documentation for compliance with GDocP standards and internal processes.
• Provide customer support with Veeva Quality Systems issues.
• Support other process improvement initiatives as required.
• Manage Global Quality Systems SOP revisions

Skills:

Quality assurance, veeva, veeva vault, SOP, Quality system, documentation review, regulatory, GXP

Additional Skills & Qualifications:

• Bachelor’s Degree (BA/BS) and 3-4 years’ experience in an FDA regulated environment or similar experience preferred.
• Prior system administration experience required, with administration of Veeva Quality Suite preferred.
• Strong understanding of GxP Regulatory Requirements around Document Control and Training.
• Understanding of GxP Regulatory Requirements around Quality Management System

Job Type: Full-time

Pay: From $40.00 per hour

Expected hours: 40 per week

Benefits:

• 401(k)
• Dental insurance
• Employee discount
• Health insurance
• Life insurance
• Vision insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Work Location: In person