Quality Specialist – II (Pharmaceutical)

TL;DR

Quality Specialist – II (Pharmaceutical): Support QA processes in GMP pharmaceutical manufacturing facility with an accent on batch record reviews, investigations, corrective actions, and documentation. Focus on data migration for Global Enterprise Asset Management System project, CoA/CoC generation and review, and quality system management.

Location: 100% Onsite in Wilson, NC (27893)

Salary: $89,000–$95,400

Company

Staffing firm partnering with pharmaceutical manufacturers to ensure high standards of quality and regulatory compliance.

What you will do

• Support Global Enterprise Asset Management System (EAMS) project including data migration from legacy systems and project documentation.
• Assist with batch record documentation, audits, CoA/CoC generation and review, and data updates.
• Participate in team meetings and cross-functional alignments to manage priorities and escalate issues.
• Handle additional QA activities as assigned.

Requirements

• Bachelor's degree preferred; Associates with relevant experience considered.
• 3-5 years in GMP pharmaceutical manufacturing with batch records, documentation reviews, investigations, corrective actions, complaints, quality systems.
• Experience in Quality Assurance and pharmaceutical packaging facility.
• SAP, maintenance systems, or SOP experience.
• Strong written/oral communication and problem-solving skills; ability to manage multiple projects.

Culture & Benefits

• For temporary assignments 13+ weeks: major medical, dental, vision, 401k, statutory sick pay where required.
• Reasonable accommodations for disabilities.
• Equal opportunity employer committed to diversity and fair chance hiring.