Pharma Quality Assurance Specialist

LEGAL PROJECT MANAGEMENT PARTNERS LLC; El Paso (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

LEGAL PROJECT MANAGEMENT PARTNERS LLC is seeking a Quality Assurance Specialist to support QA operations in a pharmaceutical manufacturing environment in El Paso, TX. The contractor will review GMP docs, batch records, and reports while supporting deviations, CAPAs, and change controls and collaborating with cross-functional teams.

The role requires a Bachelor’s degree in a related field and 3+ years of QA experience in regulated manufacturing, with strong knowledge of FDA and cGMP requirements,

Qualifications

• Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or related field.
• 3+ years QA in pharma or regulated manufacturing.
• Experience with Deviation, CAPA, Change Control, SOPs, and Audits.
• Strong knowledge of FDA regulations and cGMP.
• Excellent documentation and attention to detail.

Responsibilities

• Support daily QA activities in pharmaceutical manufacturing.
• Review and approve GMP documentation, batch records, procedures, protocols, and reports.
• Assist deviations, investigations, CAPAs, change controls, and non-conformances.
• Participate in GMP audits and inspections.
• Ensure compliance with FDA and cGMP requirements.
• Provide QA support to cross-functional teams.
• Maintain quality records and documentation.

Skills

FDA regulations

cGMP knowledge

Documentation

Cross-functional teamwork

Audit & investigations

Education

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

Tools

Microsoft Office

Electronic quality systems

Job description

LEGAL PROJECT MANAGEMENT PARTNERS LLC is seeking a Quality Assurance Specialist to support QA operations in a pharmaceutical manufacturing environment in El Paso, TX. The contractor will review GMP docs, batch records, and reports while supporting deviations, CAPAs, and change controls and collaborating with cross-functional teams.

The role requires a Bachelor’s degree in a related field and 3+ years of QA experience in regulated manufacturing, with strong knowledge of FDA and cGMP requirements,