Quality Control Specialist

The Quality Control Specialist is responsible for reviewing documentation, including records, procedures, and forms, to ensure quality endpoints and compliance requirements are achieved. This role involves actively leading or contributing to data relevant to Quality Systems Compliance during periodic Management Review meetings, as well as assisting Quality Management in coordinating and actively participating in Quality or Compliance related projects.

Responsibilities

• Conduct product tests and assessments in an industrial or warehouse setting to ensure that specifications are met and that the product, material, or supply will function as intended.
• Perform in-process and final product/result inspections and clearances on the production floor to ensure consistency.
• Identify product defects or potential issues and determine resolutions.
• Analyze lab or usability test results to identify defects and ensure they do not persist.
• Maintain detailed records of product defects or manufacturing issues to help identify and eliminate recurring problems and provide accountability and error reporting.
• Report issues or defect findings to supervisors or plant managers to aid in manufacturing decisions.
• Support process improvements throughout testing and quality assurance processes.
• Suggest improvements to address systemic problems found during quality control, ensuring consistent product production and error elimination.

• Quality Control Expertise
• Laboratory Experience
• Data Entry Proficiency
• Knowledge of Standard Operating Procedures (SOP)
• Bachelor's or Associate's Degree
• Minimum of 1 year experience in quality or lab setting
• Document Control Skills
• Quality Assurance Knowledge
• Accessioning Experience
• Quality Inspection Capabilities
• Batch Record Review
• Understanding of FDA Regulations

• Requires an Associate's Degree at minimum
• Preferred one or more years of Quality Assurance or Quality Control experience in a regulated environment or other job-related experience

The work environment is a clean and regulated laboratory setting with a friendly company culture. Training will last approximately 3-4 weeks, during which employees will review testing benches and shadow Technologists.

The pay range for this position is $18.00 - $20.00/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Norcross,GA.

Application Deadline

This position is anticipated to close on Jun 13, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email ... for other accommodation options.