Kasmo Global
Job Title:
Logistics Engineer Job Description:
We are seeking a skilled
Logistics Engineer
to join our team in Goodfield, IL. The ideal candidate will have strong experience in
Corrective and Preventive Actions (CAPA) , root cause analysis, and compliance with
FDA regulations . This role requires expertise in data analysis, cross-functional collaboration, and investigative reporting to ensure operational efficiency and regulatory alignment.
Key Responsibilities: Conduct root cause analysis for each assigned
CAPA
to determine effective solutions. Gather and analyze data to support findings and drive continuous improvement. Collaborate with cross-functional teams to develop appropriate
corrective and preventive actions . Draft and finalize investigation reports with
clear justifications
under each CAPA. Ensure
CAPA documentation
aligns with
FDA 483 resolution
needs. Participate in internal meetings, provide regular status updates, and address any gaps in the investigation process. Support responses to
FDA inquiries
related to CAPA status as needed. Requirements:
5-7+ years
of experience in performing CAPAs and
root cause analysis . Strong knowledge of
FDA regulations ,
compliance requirements , and
CAPA documentation . Proficiency in
data analysis and reporting . Excellent
problem-solving
and
critical thinking
skills. Strong communication and collaboration skills to work effectively with cross-functional teams. Experience in
logistics, supply chain, or quality engineering
is a plus.
Logistics Engineer Job Description:
We are seeking a skilled
Logistics Engineer
to join our team in Goodfield, IL. The ideal candidate will have strong experience in
Corrective and Preventive Actions (CAPA) , root cause analysis, and compliance with
FDA regulations . This role requires expertise in data analysis, cross-functional collaboration, and investigative reporting to ensure operational efficiency and regulatory alignment.
Key Responsibilities: Conduct root cause analysis for each assigned
CAPA
to determine effective solutions. Gather and analyze data to support findings and drive continuous improvement. Collaborate with cross-functional teams to develop appropriate
corrective and preventive actions . Draft and finalize investigation reports with
clear justifications
under each CAPA. Ensure
CAPA documentation
aligns with
FDA 483 resolution
needs. Participate in internal meetings, provide regular status updates, and address any gaps in the investigation process. Support responses to
FDA inquiries
related to CAPA status as needed. Requirements:
5-7+ years
of experience in performing CAPAs and
root cause analysis . Strong knowledge of
FDA regulations ,
compliance requirements , and
CAPA documentation . Proficiency in
data analysis and reporting . Excellent
problem-solving
and
critical thinking
skills. Strong communication and collaboration skills to work effectively with cross-functional teams. Experience in
logistics, supply chain, or quality engineering
is a plus.