QA Specialist | Pharmaceutical | El Paso, TX | On Site

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

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Contractor - 1099 Professional El Paso, TX, US

10 days ago Requisition ID: 1055

Position Summary

The Quality Assurance Specialist will support quality operations within a pharmaceutical manufacturing environment, ensuring compliance with FDA, cGMP, and company quality standards. This role will collaborate with Manufacturing, Validation, Engineering, and Quality teams to support quality systems, investigations, documentation, and continuous improvement initiatives.

Main Responsibilities

Support daily Quality Assurance activities within pharmaceutical manufacturing operations.

Review and approve GMP documentation, batch records, procedures, protocols, and reports.

Supportdeviations, investigations, CAPAs, change controls, and non-conformances.

Participate in GMP audits, inspections, and quality improvement initiatives.

Ensure compliance withFDA, cGMP, and applicable regulatory requirements.

Provide QA support toManufacturing, Validation, Engineering, and other cross-functional teams.

Review quality and validation documentation for compliance and completeness.

Supporttraining, SOP implementation, and quality system activities.

Identify compliance gaps and assist with corrective and preventive actions.

Maintain accurate and timely quality records and documentation.

General Requirements

Experience working in a pharmaceutical manufacturing environment.

Strong knowledge of FDA regulations and cGMP requirements.

Experience withdeviations, CAPA, Change Control, and investigations.

Experience reviewing GMP and quality documentation.

Strong attention to detail and documentation skills.

Ability to work effectively with cross-functional teams.

Strong written and verbal communication skills.

Proficiency withMicrosoft Office and electronic quality systems.

Ability to workon-site, full-time in El Paso, Texas.

Education and Experience Requirements

Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related scientific/technical field.

3+ years of experience in Quality Assurance within the pharmaceutical, biotechnology, or regulated manufacturing industry.

Experience in GMP-regulated manufacturing operations.

Experience with quality systems such as Deviation, CAPA, Change Control, SOPs, and Audits.

Experience supportingFDA-regulated environmentsis preferred.