Gandiv Insights LLC
Overview
Are you passionate about quality systems, root cause analysis, and regulatory compliance? We’re looking for an experienced
CAPA Investigator Owner
to join our team and support non-conformance investigations and corrective/preventive actions (CAPAs) within a highly regulated environment. ✔ Investigate non-conformances (NCRs) using TrackWise 8 ✔ Execute and implement CAPAs with precision ✔ Ensure compliance with FDA, international regulations, and corporate quality standards ✔ Coach and guide others on DMAIC and process improvement initiatives What You Bring: Responsibilities
Investigate non-conformances (NCRs) using TrackWise 8 Execute and implement CAPAs with precision Ensure compliance with FDA, international regulations, and corporate quality standards Coach and guide others on DMAIC and process improvement initiatives Qualifications
2–4 years of experience in a
cGMP-regulated or clinical
setting Bachelor’s degree in
Science, Engineering , or related field Strong problem-solving, analytical, and communication skills TrackWise experience strongly preferred Green Belt or experience with Six Sigma/Lean tools is a plus Must not be allergic to Penicillins or Cephalosporins Additional Information
Flexibility to support investigations or training during off-shift/weekend hours may be required. If you’re ready to make a meaningful impact in a critical quality role, let’s connect! Email: anupam@gandivainsights.com
#J-18808-Ljbffr
Are you passionate about quality systems, root cause analysis, and regulatory compliance? We’re looking for an experienced
CAPA Investigator Owner
to join our team and support non-conformance investigations and corrective/preventive actions (CAPAs) within a highly regulated environment. ✔ Investigate non-conformances (NCRs) using TrackWise 8 ✔ Execute and implement CAPAs with precision ✔ Ensure compliance with FDA, international regulations, and corporate quality standards ✔ Coach and guide others on DMAIC and process improvement initiatives What You Bring: Responsibilities
Investigate non-conformances (NCRs) using TrackWise 8 Execute and implement CAPAs with precision Ensure compliance with FDA, international regulations, and corporate quality standards Coach and guide others on DMAIC and process improvement initiatives Qualifications
2–4 years of experience in a
cGMP-regulated or clinical
setting Bachelor’s degree in
Science, Engineering , or related field Strong problem-solving, analytical, and communication skills TrackWise experience strongly preferred Green Belt or experience with Six Sigma/Lean tools is a plus Must not be allergic to Penicillins or Cephalosporins Additional Information
Flexibility to support investigations or training during off-shift/weekend hours may be required. If you’re ready to make a meaningful impact in a critical quality role, let’s connect! Email: anupam@gandivainsights.com
#J-18808-Ljbffr