Job Details

Adecco Healthcare & Life Sciences is hiring for a leading life sciences and healthcare organization known for developing and supporting innovative products in a highly regulated quality environment in Greenville, NC.

Position Details

Location: Greenville, NC
Work Arrangement: 100% Onsite
Pay Rate: Up to $27/hour
Contract: 1-year contract with potential for direct hire
Schedule: 12-hour shift, 2-2-3 rotation
Hours: 6:00 AM–6:00 PM
Travel: Less than 15% may be required
Interview: (Interview format)

Position Overview

The Quality Assurance Specialist will support day-to-day quality operations while working directly with customers, suppliers, and internal teams to identify, investigate, and resolve quality-related issues.

This position will be responsible for executing core Quality Assurance processes, including customer complaints, product quarantine and recovery, quality investigations, corrective and preventive actions (CAPA), change notifications, quality reporting, customer surveys, internal audits, and continuous improvement initiatives .

The ideal candidate will have experience working in a regulated ISO and/or FDA environment , strong problem-solving and analytical skills, and the ability to communicate effectively with both internal and external stakeholders.

Key Responsibilities

• Support day-to-day execution of core Quality Assurance processes.

• Process and distribute customer complaints and identify issues requiring escalation.

• Work with Customer Service to fully document customer allegations and coordinate product returns for evaluation.

• Coordinate quality investigations with customers, suppliers, and internal stakeholders .

• Review and communicate root cause and corrective actions resulting from quality investigations.

• Facilitate product quarantine, recovery, and disposition activities.

• Support quality issues involving products that may have regulatory or legal considerations.

• Process change notifications, customer surveys, quality certificates, and related quality documentation.

• Collect, analyze, and report quality data.

• Run database queries and prepare quality reports and metrics.

• Support customer surveys and Requests for Proposal (RFPs) .

• Create, revise, and maintain QA procedures and work instructions .

• Participate in internal audits of the Quality Management System (QMS) .

• Support continuous improvement initiatives using Practical Process Improvement (PPI), Lean, Six Sigma , or similar methodologies.

• Develop and distribute supplier and team performance metrics.

• Provide training and presentations on QA processes to departments outside of Quality Assurance.

• Support projects and other quality-related initiatives as assigned.

• Maintain accurate and timely quality records in accordance with applicable procedures and regulatory requirements.

Required Qualifications

• Bachelor's degree in a technical or scientific field such as:

  • Engineering

  • Chemistry

  • Biology

  • Mathematics

  • Or a related discipline

• Equivalent relevant technical/scientific experience may be considered.

• 2+ years of experience working in an ISO-regulated and/or FDA cGMP environment.

• Experience working directly with customers and suppliers on quality-related matters.

• Demonstrated experience with root cause analysis and problem solving .

• Strong understanding of quality systems and regulated manufacturing environments.

• Excellent written and verbal communication skills.

• Strong organizational skills and attention to detail.

• Ability to manage multiple priorities and work with a sense of urgency.

• Strong computer, analytical, and data-management skills.

• Ability to work effectively both independently and as part of a cross-functional team.

Preferred Experience

Experience with:

• ISO 13485

• FDA cGMP

• Quality Management Systems (QMS)

• CAPA

• Customer complaints

• Supplier quality

• Internal or external auditing

• MasterControl or similar quality management systems

• Six Sigma

• Lean

• Practical Process Improvement (PPI)

• Minitab

• Pareto charts

• Run charts

• Flowcharting

• Pivot tables

• Data analysis and reporting

• Oracle or similar database systems

• Microsoft Excel, Access, Word, and PowerPoint

Lead Auditor experience is a plus.

What Makes This Role a Strong Opportunity?

This position offers the opportunity to work across several areas of Quality Assurance and Quality Systems , rather than focusing on a single laboratory or production function. You will interact with customers, suppliers, Quality, Manufacturing, and other internal teams while gaining exposure to investigations, CAPA, audits, quality metrics, and continuous improvement.

Schedule & Work Environment

• Fully onsite in Greenville, NC

• 12-hour 2-2-3 rotation

• 6:00 AM–6:00 PM

• Ability to work in laboratory, warehouse, and manufacturing environments as needed.

• Less than 15% travel may be required.

• Reliable attendance and punctuality are essential.

Why Work with Adecco?

• Up to $27/hour

• 1-year contract with potential for direct hire

• Weekly pay

• 401(k) options

• Medical, dental, and vision benefits for eligible employees

• Skills training and professional development resources

• Dedicated Adecco recruiter support

• Opportunity to build experience in a highly regulated Quality Assurance/Quality Systems environment

If you have experience working in an ISO or FDA-regulated environment and enjoy solving quality problems, working with customers and suppliers, and improving quality processes, this could be an excellent opportunity to take your QA experience to the next level.

Pay Details: $25.00 to $27.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:

• The California Fair Chance Act
• Los Angeles City Fair Chance Ordinance
• Los Angeles County Fair Chance Ordinance for Employers
• San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.