Pharma QA Specialist: cGMP Compliance & CAPA Expert

Legal Project Management Partners; El Paso (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Legal Project Management Partners is seeking a Quality Assurance Specialist to support quality operations in a pharmaceutical manufacturing environment, ensuring compliance with FDA, cGMP and company quality standards. You will collaborate with Manufacturing, Validation, Engineering and Quality teams to support quality systems and documentation.

This on-site, full-time role requires a Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering or related field and 3+ years of

Qualifications

• 3+ years of QA experience in pharmaceutical manufacturing (regulated environment).
• Strong knowledge of FDA regulations and cGMP requirements.
• Experience with deviations, CAPA, Change Control, and audits.

Responsibilities

• Support daily Quality Assurance activities within pharmaceutical manufacturing operations.
• Review and approve GMP documentation, batch records, procedures, protocols, and reports.
• Support deviations, investigations, CAPAs, change controls, and non-conformances.
• Participate in GMP audits, inspections, and quality improvement initiatives.
• Ensure compliance with FDA, cGMP, and applicable regulatory requirements.
• Provide QA support to Manufacturing, Validation, Engineering, and other cross-functional teams.
• Review quality and validation documentation for compliance and completeness.
• Support training, SOP implementation, and quality system activities.
• Identify compliance gaps and assist with corrective and preventive actions.
• Maintain accurate and timely quality records and documentation.

Education

Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering or related field

Job description

Legal Project Management Partners is seeking a Quality Assurance Specialist to support quality operations in a pharmaceutical manufacturing environment, ensuring compliance with FDA, cGMP and company quality standards. You will collaborate with Manufacturing, Validation, Engineering and Quality teams to support quality systems and documentation.

This on-site, full-time role requires a Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering or related field and 3+ years of