Quality Engineer (DAYS)

Experis Technology Group; Greenville (NC); On-site; USD 4,496,000 - 7,737,000; Full time

Benefits offered by this job

Medical and Prescription Plans

Dental Plan

Vision Plan

Health Savings Account

Health Flex Spending Account

Dependent Care Flex Spending Account

Supplemental Life Insurance

Short/Long Term Disability Insurance

Business Travel Insurance

401(k) Plus Match

Weekly Pay

Job summary

Experis Technology Group seeks a Quality Engineer (DAYS) to join their team in Greenville, NC. The role supports sterile operations across manufacturing, filling, packaging, and inspection with a focus on cGMP compliance and quality culture.

The DAYS shift (6a-6p) runs on a 2-2-3 rotation. A Bachelor’s degree and 4+ years in QA/QC or manufacturing are required. Pharmaceutical aseptic experience is preferred; a 9-month contract is offered with competitive pay.

Qualifications

• Requires strong data capture, analysis and troubleshooting of process issues and equipment problems.
• Experience with aseptic/sterile processes is preferred in regulated environments.
• Technical writing experience is beneficial; certifications like CQA and Six Sigma training are a plus.

Responsibilities

• Perform daily quality assessments of facility, personnel and documentation to ensure cGMP compliance.
• Provide guidance for troubleshooting, documentation corrections and aseptic technique execution.
• Champion a quality culture and apply policies to protect product quality.
• Support deviation and change control activities, including RAPID event responses and quality guidance.
• Complete quality reviews and approvals for procedures, training docs, forms and deviation/change controls.

Skills

Data analysis

Troubleshooting

Technical writing

Six Sigma

CQA certification

Education

Bachelor’s degree in science/engineering-related field

Job description

Our client, a leading provider of sterile operations and regulated manufacturing services, is seeking a Quality Engineer (DAYS) to join their team. As a Quality Engineer (DAYS), you will be part of the Quality organization supporting sterile operations across manufacturing, filling, packaging, and inspection, including non-batch-specific activities for both commercial and product development services products. The ideal candidate will have strong ownership and responsibility, the ability to troubleshoot and analyze process issues, and the drive to champion a quality culture that supports cGMP compliance.

Job Title:Quality Engineer (DAYS)
Location:Greenville, NC
Schedule: DAYS 6a-6p, 2-2-3
Contract: 9 months
Pay Range:$52-54/hr

What's the Job?

• Perform daily quality assessments of facility, personnel, and documentation in classified and non-classified areas to uncover errors or deficiencies and ensure compliance with site procedures and cGMPs.
• Provide daily guidance to employees for troubleshooting, documentation corrections/notes, and support for aseptic technique execution.
• Champion a strong quality culture by helping personnel understand and apply policies and controls that protect product quality.
• Support deviation and change control activities by participating in RAPID event response, advancing deviation events to the appropriate area, and providing quality guidance.
• Complete quality reviews and approvals for procedures, training documents, forms, deviation/change control items, and perform quality batch record review for moderate to high complexity items.

What's Needed?

• Bachelor’s degree, preferably in a technology, engineering, or microbiology-related field; equivalent combinations of education, training, and relevant experience may be considered.
• Minimum of 4 years of experience in Quality Assurance or Quality Control, or in Operations/Manufacturing.
• Pharmaceutical industry experience preferred, with aseptic or sterile process experience strongly preferred; experience in other regulated environments (e.g., ISO 9001) may be considered.
• Ability to capture data, analyze and troubleshoot process issues and equipment problems alongside production leadership.
• Technical writing experience; professional certifications (e.g., CQA) and Six Sigma training are a plus.

What's in it for me?

• Opportunity to drive quality execution across sterile operations, including manufacturing, filling, packaging, inspection, and associated non-batch-specific activities.
• Role focused on practical process improvement and continuous improvement initiatives, including support for deviation investigations and Root Cause Analysis.
• Structured day shift schedule with typical hours of 6a–6p on a 2-2-3 rotation.
• Chance to provide quality guidance that strengthens aseptic technique and documentation accuracy across the production floor.
• Support for a quality culture through daily interaction with employees and hands‑on compliance oversight.

Upon completion of waiting period consultants are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• Health Savings Account
• Health Flexible Spending Account
• Dependent Care Flexible Spending Account
• Supplemental Life Insurance
• Short Term and Long Term Disability Insurance
• Business Travel Insurance
• 401(k), Plus Match
• Weekly Pay