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Quality Control Specialist
Job in
Norcross, Gwinnett County, Georgia, 30003, USA
Listed on 2026-07-29
Listing for:
Actalent
Full Time
position Listed on 2026-07-29
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Production QC/QA, Quality Engineering
Job Description & How to Apply Below
Actively Screening for a Quality Control Specialist to join Medical Laboratory in Norcross, GA!
Job DescriptionThe Quality Control Specialist reviews documentation and quality records to ensure that products and processes meet defined specifications and regulatory requirements. This role focuses on documentation review, quality systems compliance, and product assessments in an industrial or warehouse setting, as well as in a laboratory environment. The specialist supports quality management initiatives, participates in quality and compliance projects, and contributes to continuous improvement efforts across testing and quality assurance processes.
Responsibilities- Review documentation, including records, procedures, and forms, to ensure quality endpoints and compliance requirements are consistently achieved.
- Actively lead and contribute data relevant to Quality Systems Compliance during periodic Management Review meetings.
- Assist Quality Management in coordinating and actively participating in quality or compliance-related projects.
- Conduct product tests and assessments in an industrial or warehouse setting to verify that specifications are met and that products, materials, or supplies function as intended.
- Perform in-process and final product or result inspections and clearances on the production floor to ensure consistency and adherence to standards.
- Identify product defects or potential issues and determine appropriate actions to resolve these issues.
- Analyze the results of laboratory or usability tests to identify defects and ensure they do not persist in future production or testing cycles.
- Maintain detailed records of product defects and manufacturing issues to help identify and eliminate recurring problems and to provide a clear paper trail for accountability and error reporting.
- Notify supervisors or plant leadership of issues or defect reports to support informed decisions about manufacturing processes and practices.
- Support process improvements throughout testing and quality assurance processes to enhance product quality and reliability.
- Suggest improvements to address potential systemic problems discovered during quality control activities, ensuring products are produced consistently and defects or errors do not persist.
- Participate in structured training by reviewing each testing bench in the laboratory environment to gain a general understanding of workflows.
- Use a training booklet to document learnings, add notes, and capture key information communicated during training.
- Shadow Technologists to understand the testing processes and context for the documentation being reviewed, ensuring accurate and informed quality control review.
- Learn and use relevant computer applications to perform documentation review and quality control tasks effectively.
- Complete competency assessments after the training period to demonstrate understanding of quality control review responsibilities.
- Experience reviewing documentation, including records, procedures, and forms, for quality and compliance.
- Familiarity with laboratory environments and processes related to quality control and quality assurance.
- At least 1 year of experience within quality control, quality assurance, laboratory operations, document control, chemistry, biology, or related fields.
- Ability to conduct product tests and assessments in industrial or warehouse settings to verify specifications and functionality.
- Strong skills in identifying product defects or potential issues and determining appropriate corrective actions.
- Experience analyzing results from lab or usability tests to identify defects and prevent recurrence.
- Proficiency in maintaining detailed records of product defects and manufacturing issues for traceability and accountability.
- Knowledge of standard operating procedures (SOPs) and Good Manufacturing Practices (GMP).
- Strong data entry skills and attention to detail in documentation and recordkeeping.
- Ability to support and participate in Quality Systems Compliance activities and Management Review meetings.
- Effective communication skills to report issues and collaborate with supervisors and cross-functional teams.
- Associate's…
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