Find & Apply For Quality Inspector / Technician Jobs in Greenville, North Carolina

Deviation Investigator Indotronix International Corporation

•4.1 Greenville, NC Job Details Contract $40

•$50 an hour 4 hours ago Qualifications Six Sigma Certification Microsoft Excel Investigations regulatory compliance Regulatory documents Quality records maintenance Defect resolution root cause analysis Incident report management Preventive action implementation Technical writing experience within manufacturing Production deviation management Good documentation practices (GDP) Quality control preventive actions Corrective and preventive actions (CAPA) GMP Mid-level Internal investigations Trend analysis Quality reports Bachelor's degree in engineering Quality assurance standard operating procedures Compliance documentation Regulatory/legal compliance standards in production Management reporting Associate's degree in engineering Investigative reports Continuous quality improvement (CQI) Productivity software Investigating compliance violations Root cause analysis Cross-functional collaboration

Full Job Description Location:

Greenville, NC 27834

Duration:

12 months

•

Contract Pay Rate:

$40.00 $50.00/ hr w2

Shift:

M-F 8-5

Key Responsibilities:

Identify and document deviations from standard operating procedures (SOPs), quality standards, or regulatory guidelines. Conduct thorough investigations to determine the root cause of deviations. Collaborate with cross-functional teams to develop and implement corrective and preventive actions (CAPAs).

Documentation and Reporting:

Maintain accurate and detailed records of all deviations, investigations, and CAPAs. Prepare and present deviation reports to management and regulatory authorities as required. Ensure documentation is completed in accordance with Good Documentation Practices (GDP).

Compliance and Quality Assurance:

Ensure all deviations are managed in compliance with company policies, industry standards, and regulatory requirements. Participate in internal and external audits and inspections, providing necessary documentation and information related to deviations.

Continuous Improvement:

Analyze deviation trends and provide insights for continuous improvement initiatives. Participate in training programs to enhance knowledge and skills related to deviation management and quality assurance.

Qualifications:

Regulated Industry, cGMP environment experience, deviation management, or a e.g., Pharmaceuticals, Manufacturing, Engineering, Medical, Law Enforcement, etc.]. Strong Attention to details, technical writing, Analytical and problem-solving skills. Knowledge of regulatory requirements and standards. Intermediate to Advanced skills in Microsoft Suite (Word, Excel, PowerPoint) Excellent communication and interpersonal skills.

Preferred Qualifications:

Associate or bachelor's degree in a relevant field such as Life Sciences, Engineering, Medial, or Quality Management with 2+ years of related experience.

Preferred Experience:

Biologics, Aseptic, Filling Isolators, Six Sigma Certification, Electronic documentation systems. Familiarity with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP)

Engineering Role:

IICIT01