USA – Quality Analyst III Position Available In Marshall, Mississippi

USA – Quality Analyst III#25-59404
Byhalia, MS
All On-site Job Description

Overview:

Seeking a skilled IT Engineer with strong experience in software issue resolution and supply chain operations, ideally within the pharmaceutical industry. The ideal candidate will bring technical knowledge, root cause analysis capabilities, and cross-functionally experience with business and IT teams.

Key Responsibilities:

Perform daily IT operations support with a focus on identifying and resolving system issues.
Conduct root cause investigations and document resolutions, including escalation when necessary.
Analyze system data flow and support failure analysis as part of project-based work.
Monitor data interactions, investigate anomalies, and implement solutions to enhance operations.
Collaborate with integration teams and local stakeholders to maintain system compliance (e.g., SharePoint site support).
Drive data analysis to support diagnostics and ensure existing solutions remain effective.
Support corrective and preventive actions (CAPA) processes, and apply project management principles.
Collaborate with both internal teams and external customers/suppliers.

Preferred Experience & Skills:

Minimum of 3 years’ experience resolving IT/software-related issues.
Exposure to software engineering and basic coding (major plus).
Familiarity with BS-CSA
Background in pharmaceutical supply chain operations strongly preferred.
Experience with enterprise systems like JDE (JD Edwards) and TrackWise.
Responsible for reviewing pertinent documents, records and reports, primarily but not limited to manufacturing batch records, against Standard Operating Procedures (SOPs) for accuracy and compliance to procedures based on regulatory requirements and internal guidelines, etc., and approving conforming documents, records, and reports Identify areas of nonconformance and inform management via the drafting of Nonconforming Material (NCM) reports as needed Perform initial investigative actions on some NCMs, applying established techniques and procedures Revise or review standard procedures Collect data for metrics related to documentation review Prepare and issue reports as defined by the area May perform other quality duties, e.g., quality control/quality inspection, as assigned To perform essential duties and responsibilities of the position, the following knowledge, skills, and abilities are required. Knowledge and understanding of the purpose and use of manufacturing records including but not limited to batch records Knowledge and understanding of Device History Record (DHR) Knowledge and application of Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) Strong process orientation, including ability to understand and follow established processes consistently and participate in development of new processes Ability to adapt to changes in work processes and requirements Ability to communicate clearly and accurately in both verbal and written form in all job-related activities Ability to identify and communicate opportunities for improvement within work area Ability to work with minimal supervision Ability to manage workload effectively High attention to detail Strong organizational skills Strong interpersonal skills Good problem-solving skills Computer proficiency including use of standard business productivity software (e.g., Microsoft Office applications)