Pharma QA Specialist: CAPA & Deviation Expert

Grifols, S.A; Los Angeles (CA); On-site; USD 75,000 - 80,000; Full time

Job summary

Grifols, S.A in Los Angeles, CA is seeking a QA Specialist to oversee Quality Systems including Deviation Management, CAPA, and Customer Complaints to ensure compliant product release. The role interfaces with multiple departments, supports regulatory reporting, and leads improvement projects within a GMP environment.

The ideal candidate holds a biology/chemistry related degree with at least 2 years of pharmaceutical QA experience, strong technical writing skills, and proficiency in MS Office.

Qualifications

• Bachelor’s degree in Biology, Chemistry, Microbiology, Biochemistry or closely related scientific/technical discipline is required.
• Minimum of 2 years of experience in a pharmaceutical, GMP, or FDA regulated environment is required.
• Requires a basic understanding of pharmaceutical manufacturing and Quality Assurance/Operations.

Responsibilities

• Investigate and report issues under deviation management system and manage databases.
• Perform thorough investigations with root cause analysis and corrective actions.
• Coordinate and manage investigations related to trend analysis and problems.
• Assist in regulatory submissions and provide written responses as applicable.
• Generate written reports summarizing investigations for out-of-specification results.

Job description

Grifols, S.A in Los Angeles, CA is seeking a QA Specialist to oversee Quality Systems including Deviation Management, CAPA, and Customer Complaints to ensure compliant product release. The role interfaces with multiple departments, supports regulatory reporting, and leads improvement projects within a GMP environment.

The ideal candidate holds a biology/chemistry related degree with at least 2 years of pharmaceutical QA experience, strong technical writing skills, and proficiency in MS Office.