Senior Pharmaceutical Auditor – Global Compliance & CAPA
Globalchannelmanagement
Paramus (NJ)
On-site
USD 80,000 - 120,000
Full time
14 days+
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Job summary
A leading company in pharmaceuticals is looking for a Sr. Auditor based in Paramus, NJ. The ideal candidate should have extensive experience in Radio Pharmaceuticals and auditing, along with knowledge of cGMP, FDA, EMA, and ICH regulations. Strong analytical skills and the ability to conduct various audits are essential. This role involves preparing audit plans, tracking corrective actions, and supporting regulatory inspections. A Bachelor’s degree in a relevant field and ASQ Certification are required.
Qualifications
35 years in Radio Pharmaceuticals.
At least 2 years in auditing.
Ability to travel (up to 10%) for audits.
Strong knowledge of RPT cGMP, GDP, and global regulatory requirements.
Excellent attention to detail and analytical skills.
Strong communication and report-writing abilities.
ASQ Certified Quality Auditor (CQA).
Responsibilities
Conduct routine, for-cause, and risk-based audits.
Prepare detailed audit plans, checklists, and schedules.
Ensure adherence to FDA, EMA, ICH, and other regulatory guidelines.
Review and approve deviations, CAPAs, and change controls.
Document audit observations and issue formal audit reports.
Track and verify implementation of corrective and preventive actions (CAPAs).
Provide guidance on compliance requirements and audit readiness.
Support regulatory inspections and customer audits.
Skills
cGMP
GDP
FDA
EMA
ICH
RPT cGMP
regulatory inspections
customer audits
CAPA
deviations
change controls
audit planning
audit checklists
audit schedules
audit reporting
process improvements
compliance requirements
audit readiness
report writing
analytical skills
communication skills
pharmaceutical quality system (PQS)
ISO 9001
GCP
GMP
ASQ Certified Quality Auditor (CQA)
Education
Bachelor's degree in Life Sciences, Pharmacy, or related field
Job description
A leading company in pharmaceuticals is looking for a Sr. Auditor based in Paramus, NJ. The ideal candidate should have extensive experience in Radio Pharmaceuticals and auditing, along with knowledge of cGMP, FDA, EMA, and ICH regulations. Strong analytical skills and the ability to conduct various audits are essential. This role involves preparing audit plans, tracking corrective actions, and supporting regulatory inspections. A Bachelor’s degree in a relevant field and ASQ Certification are required.