CAPA Specialist

Hiring:

CAPA Process Analyst II Location:

Gretna, LA Type:

Contract (W2)

Duration:

6

Months Key Requirements:

Experience in CAPA and Quality Systems Strong experience with CAPA systems and EQMS platforms Experience in regulated environments such as Pharmaceuticals, Medical Devices, or Laboratories Hands-on experience with root cause analysis and investigation management Strong technical writing and documentation skills Ability to manage non-conformances, deviations, and complaints Knowledge of FDA, CAP, NLCP, or similar regulatory standards preferred ASQ CQA certification preferred

Key Responsibilities:

Lead investigations for quality events and non-conformances Drive CAPA activities through the QMS system Perform root cause analysis and implement corrective actions Collaborate with cross-functional teams to ensure timely resolution Maintain audit-ready CAPA documentation and records Support quality improvement initiatives and trend analysis Escalate compliance risks and quality concerns when necessary Ensure all CAPA activities meet procedural and regulatory requirements

Pay:

$26.00 - $30.00 per hour

Work Location:

In person