Senior Validation Manager - cGMP & QA Systems (Hybrid)

Grifols, S.A; North Carolina; Hybrid; USD 120,000 - 170,000; Full time

Job summary

Grifols, S.A. is seeking a Manager, Validation for a hybrid role based in RTP with 2 days in the office and 3 days remote. The candidate will ensure cGMP compliance, Quality System alignment, and oversee validation/documentation across manufacturing processes and equipment.

Strong collaboration with Donor Center/Field Quality is required. The role emphasizes developing validation strategies, testing, data analysis, and timely regulatory-compliant reporting while driving continuous improvement

Qualifications

• Bachelor's degree in a scientific field is required.
• Typically requires 8 years of quality and validation experience in a cGMP/IT environment.
• Strong knowledge of cGMP operating procedures, validation standards, guidelines, and SOPs.

Responsibilities

• Manage department resources and prioritize work to meet timelines.
• Develop cGMP operating procedures related to validation/qualification.
• Ensure SOP compliance and support investigations and corrective actions.

Skills

cGMP knowledge

Quality systems

Analytical skills

Communication skills

Education

Bachelor's degree in a scientific field

Tools

Microsoft Office

Job description

Grifols, S.A. is seeking a Manager, Validation for a hybrid role based in RTP with 2 days in the office and 3 days remote. The candidate will ensure cGMP compliance, Quality System alignment, and oversee validation/documentation across manufacturing processes and equipment.

Strong collaboration with Donor Center/Field Quality is required. The role emphasizes developing validation strategies, testing, data analysis, and timely regulatory-compliant reporting while driving continuous improvement