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Background Investigator Jobs in North Carolina

Deviation Investigator

Integrated Resources, Inc

  • Greenville, NC
  • 30 days ago

    Highlights

    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. Qualifications: Regulated Industry, cGMP environment experience, deviation management, or a e.g., Pharmaceuticals, Manufacturing, Engineering, Medical, Law Enforcement, etc.].

    Numbers & Facts

    LocationGreenville, NC

    Description

    Title: Deviation Investigator
    Location: Greenville, NC 27834 (Full onsite)
    Duration: 12 months
    Shift time: Shift: Monday-Friday 8-5

    Description: 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).

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