RC-REGULATORY COMPLIANCE-REGULATORY COMPLIANCE-Senior

We are seeking a highly experienced and detail-oriented Senior CSV Specialist with significant experience in Veeva Vault validation to lead and manage validation activities for GxP-regulated computerized systems.

Requirements

• Bachelor’s or Master’s degree in Life Sciences, Engineering, or related field
• 5-8 years of experience in CSV within the pharmaceutical industry or consulting environment
• Strong knowledge of GxP, GAMP 5, 21 CFR Part 11, and Annex 11
• Experience with regulated systems such as SAP, LIMS, MES, ELN, and Veeva Vault
• Excellent communication, documentation, and stakeholder management skills

Benefits

• Support, coaching and feedback from some of the most engaging colleagues around
• Opportunities to develop new skills and progress your career
• The freedom and flexibility to handle your role in a way that’s right for you