Quality Assurance Specialist

Randstad USA; Greenville (NC); On-site; USD 25,000 - 36,000; Part time

Benefits offered by this job

Medical

Prescription

Dental

Vision

AD&D

Life insurance offerings

Short-term disability

401K plan (eligibility)

Job summary

Randstad USA in Greenville, NC, seeks a Quality Assurance Specialist to drive quality execution across sterile manufacturing, filling, packaging, and inspection operations on a predictable 2-2-3 day shift schedule (6:00 AM - 6:00 PM).

This contract role offers exposure to a top-tier pharma environment with a focus on cGMP compliance and real-time quality guidance on the production floor.

Qualifications

• Bachelor's degree in Technology, Engineering, Microbiology, or a related scientific field or equivalent
• 4+ years of QA, QC, or manufacturing operations experience in pharma
• Strong background in sterile or aseptic processing operations
• Proven technical writing experience for investigations, SOPs, and reports

Responsibilities

• Perform daily quality assessments of facility operations, personnel, and documentation for cGMP
• Provide real-time guidance on production floor operations, aseptic techniques, and batch record corrections
• Participate in RAPID events, deviation investigations, and root cause analyses
• Review and approve batch records, change controls, deviations, SOPs, and training documentation
• Collaborate with cross-functional teams to drive process improvements and CI initiatives

Skills

Microbiology

Aseptic Technique

GMP

QA

QC

Aseptic Processing

Education

Bachelor's degree

Job description

Job Summary

Advance your career in pharmaceutical manufacturing in vibrant Greenville, NC. A Top-Tier Global Pharma Leader is seeking a Quality Assurance Specialist to drive quality execution across sterile manufacturing, filling, packaging, and inspection operations on a predictable 2-2-3 day shift schedule (6:00 AM - 6:00 PM).

location: Greenville, North Carolina

job type: Contract

salary: $18 - 26 per hour

work hours: 9 to 5

education: Bachelors

Responsibilities

• Perform daily quality assessments of facility operations, personnel, and documentation in classified and non-classified areas for cGMP compliance.
• Provide real-time guidance on production floor operations, aseptic techniques, and batch record corrections.
• Participate in RAPID event responses, deviation investigations, and root cause analysis.
• Review and approve batch records, change controls, deviations, SOPs, and training documentation.
• Collaborate with cross-functional teams to drive practical process improvements and continuous improvement initiatives.

Qualifications

Required:

• Bachelor's degree in Technology, Engineering, Microbiology, or a related scientific field (or equivalent combination of education and experience).
• 4+ years of QA, QC, or manufacturing operations experience in the pharmaceutical industry.
• Strong background in sterile or aseptic processing operations.
• Proven technical writing experience for investigations, SOPs, and reports.
• Physical ability to work on the production floor, including prolonged standing, walking, and wearing required aseptic gowning.

Preferred:

• Professional certifications such as CQA or Six Sigma training.

Skills

skills: Microbiology, Aseptic Technique, Good Manufacturing Practices (GMP), Quality Assurance (QA), Quality Control (QC), Aseptic Processing

Equal Opportunity Employer

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Benefits

• medical
• prescription
• dental
• vision
• AD&D
• life insurance offerings
• short-term disability
• 401K plan (all benefits are based on eligibility)

This posting is open for thirty (30) days.