Pharma QA Specialist - GMP & Regulatory Compliance

Legalpmpartners

El Paso (TX)

On-site

USD 55,000 - 83,000

Full time

5 days ago
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Job summary

Legalpmpartners in El Paso, TX is seeking a Quality Assurance Specialist (Contractor, 1099) to support QA operations in a pharmaceutical manufacturing setting. The role collaborates with Manufacturing, Validation, Engineering, and Quality teams to drive investigations, documentation, and continuous improvement.

The candidate will review GMP documentation, batch records, and reports, support deviations, CAPAs, change controls, audits, and ensure regulatory compliance.

Qualifications

  • Bachelor’s degree in a related scientific/technical field is required.
  • 3+ years of quality assurance in regulated manufacturing environments preferred.
  • Experience with GMP, deviations, CAPA, Change Control, and audits.

Responsibilities

  • Support daily QA activities in pharmaceutical manufacturing.
  • Review and approve GMP documents, batch records, procedures, 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 regulatory requirements.
  • Provide QA support to cross-functional teams and maintain records.
  • Assist with training, SOP implementation, and quality system activities.

Skills

Attention to detail
Documentation
Cross-functional collaboration
Communication

Education

Bachelor’s degree in Pharmaceutical Sciences
Chemistry
Biology
Engineering

Tools

Microsoft Office
Electronic quality systems

Job description

Legalpmpartners in El Paso, TX is seeking a Quality Assurance Specialist (Contractor, 1099) to support QA operations in a pharmaceutical manufacturing setting. The role collaborates with Manufacturing, Validation, Engineering, and Quality teams to drive investigations, documentation, and continuous improvement.

The candidate will review GMP documentation, batch records, and reports, support deviations, CAPAs, change controls, audits, and ensure regulatory compliance.

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