Head of Validation Strategy – GMP/Pharma

Grifols, S.A; Los Angeles (CA); On-site; USD 160,000 - 190,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Life insurance

PTO

Paid holidays

401(K) match

Tuition reimbursement

Job summary

Grifols, a global healthcare leader, seeks an Associate Director of Validation to drive the GBIs Validation program in California, ensuring qualification of critical equipment, utilities, processes and systems. The role requires directing a team, developing strategy, and aligning with GMP and regulatory standards.

Responsibilities include reviewing validation protocols, prioritizing high-impact projects, coordinating regulatory submissions, and improving training to enhance validation knowledge

Qualifications

• Bachelor's degree in a technical or scientific field required; Master’s or PhD preferred.
• Minimum 6 years of validation experience in a pharmaceutical, GMP, or FDA-regulated environment.
• Strong knowledge of validation principles and qualification requirements for sterilization and aseptic processing.

Responsibilities

• Direct GB Grifols Validation program to ensure qualification of equipment, utilities, processes and systems.
• Develop validation strategy and policy to streamline validation approaches.
• Review and approve validation protocols and reports to meet regulatory and quality requirements.

Skills

Validation leadership

GMP knowledge

Project management

Analytical skills

Communication skills

Cross-functional teamwork

Education

Bachelor's degree in a technical field

Master's degree preferred

Job description

Grifols, a global healthcare leader, seeks an Associate Director of Validation to drive the GBIs Validation program in California, ensuring qualification of critical equipment, utilities, processes and systems. The role requires directing a team, developing strategy, and aligning with GMP and regulatory standards.

Responsibilities include reviewing validation protocols, prioritizing high-impact projects, coordinating regulatory submissions, and improving training to enhance validation knowledge