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Non-Conformance Investigator

Indianapolis $80,000 - $90,000 Permanent

Job Responsibilities:


  • Draft and document deviations, ensuring clarity, accuracy, and compliance with internal and regulatory standards.
  • Work closely with operations, quality assurance, and other relevant teams to gather information related to deviations.
  • Classify and prioritize deviations based on risk assessment and impact.
  • Participate in deviation investigations, conducting interviews, reviewing batch records, and analyzing processes to identify root causes.
  • Utilize root cause analysis tools (e.g., 5 Whys, Fishbone Diagrams) to support investigations.
  • Develop and document effective CAPAs based on investigation findings.
  • Ensure timely implementation and verification of CAPAs to prevent recurrence.
  • Ensure all deviation reports are complete, concise, and submitted within defined timelines.
  • Maintain accurate and organized records for audits and inspections.
  • Generate and analyze deviation trend reports to identify recurring issues or trends.
  • Stay updated on relevant regulatory requirements (e.g., FDA, EMA, ISO) and industry best practices.
  • Propose process improvements to reduce deviations and enhance product quality.
  • Provide training and guidance to staff on deviation reporting procedures.


Qualifications:


  • Bachelor’s degree in a relevant field (e.g., Life Sciences, Chemistry, Engineering, or related discipline).
  • 2+ years of experience in quality assurance, manufacturing, or compliance within a GMP-regulated industry.
  • Hands-on experience with deviation investigations and root cause analysis.
  • Strong technical writing and documentation skills with attention to detail.
  • Excellent communication and interpersonal skills for cross-departmental collaboration.
  • Proficiency in using electronic quality management systems (eQMS) and deviation tracking tools.
  • Analytical thinking with problem-solving abilities.
  • Thorough understanding of GMP regulations and quality management systems.
  • Familiarity with manufacturing processes, batch record reviews, and laboratory investigations.
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