Site-wide Validation Leader

AstraZeneca plc; California (MD); On-site; USD 139,000 - 208,000; Full time

Benefits offered by this job

401(k) plan

Paid vacation

Health benefits: medical, dental, and视

Job summary

AstraZeneca plc in Tarzana, California seeks an Associate Director – Validation to lead the site-wide validation program within the Facilities and Engineering department. You will oversee CQV for facilities and equipment, validation life cycle assessments, and comprehensive documentation to ensure cGMP compliance across the site.

You will lead cross-functional teams, develop strategy, manage complex projects, and coordinate audit responses while driving continuous process improvements to enhance

Qualifications

• GMP knowledge and regulatory familiarity (FDA/EMA)
• Strong project management and budgeting skills
• Excellent analytical, problem-solving, and communication abilities

Responsibilities

• Lead site-wide validation program within Facilities and Engineering
• Oversee commissioning/qualification/validation (CQV) of systems, facilities, and equipment
• Ensure regulatory compliance and alignment with internal standards
• Manage validation documentation and reporting within EQV
• Support internal and external audits as a SME
• Drive continuous improvement of validation processes and cost efficiency

Education

Bachelor’s degree in Engineering, or a related life sciences field

Master’s degree preferred

Job description

AstraZeneca plc in Tarzana, California seeks an Associate Director – Validation to lead the site-wide validation program within the Facilities and Engineering department. You will oversee CQV for facilities and equipment, validation life cycle assessments, and comprehensive documentation to ensure cGMP compliance across the site.

You will lead cross-functional teams, develop strategy, manage complex projects, and coordinate audit responses while driving continuous process improvements to enhance