Quality Engineer; Nights

Our client, a regulated pharmaceutical manufacturing environment is seeking a Quality Engineer (Nights) to join their team. As a Quality Engineer (Nights), you will be part of the Quality organization supporting sterile operations across manufacturing, filling, packaging, and inspection. The ideal candidate will bring strong ownership, a detail-focused mindset, and the ability to collaborate effectively with production teams to drive practical quality improvements and continuous improvement initiatives.

Job Title:Quality Engineer (Nights)
Location:Greenville, NC
Schedule:Nights 6p-6a 2-2-3
Contract: 9 Months
Pay Rate:$56.50/hr

What's the Job?

• Perform daily quality assessments of facility, personnel, and documentation in both classified and non-classified areas to uncover errors or deficiencies and assure quality and compliance per site procedures and cGMPs.
• Provide daily interaction and on-the-floor support to troubleshoot issues, guide documentation corrections/notes, and reinforce aseptic technique expectations.
• Champion a quality culture by helping personnel understand how policies and controls are applied in day-to-day work.
• Participate in RAPID event response, provide quality guidance for deviation events, and advance deviation events to the appropriate area and quality management.
• Complete quality reviews and approvals for procedures, training documents, forms, deviation/change control items, and moderate-to-high complexity Root Cause Analysis support, including quality batch record review.

What's Needed?

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

What's in it for me?

• Opportunity to drive quality execution across sterile operations, supporting both commercial and product development services products.
• Hands-on role with consistent production floor presence, where your guidance directly strengthens compliance and aseptic practices.
• Meaningful involvement in deviation, change control, and Root Cause Analysis activities to improve processes and outcomes.
• Clear pathway to contribute to practical process improvements and continuous improvement initiatives.
• Weekly pay and eligibility for comprehensive coverage after the waiting period.

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