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Posted: 07/01/2026 Industry: Biotech/ Clinical/ R&D/ Science Job Number: 26-90840 Pay Rate: 30-33.41 USD/Hour

Job Description

Title: CAPA Process Analyst II:
Location: Gretna, LA 70053
Duration: likely be somewhere between 6-12 months.

Looking for experience with CAPA systems and assisting with helping to administer the process.
Must be able to use EQMS.

Description:
Years Experience: 4+ Years

Conducts investigations of nonconformances/quality events and progresses the associated quality records through Client QMS platform in accordance with established procedures.
Collaborates with cross-functional teams to support investigations and ensure corrective actions are appropriate.
Ensures that corrective and preventive actions are appropriate, accurately and completely documented, implemented on time, and meet the required procedural and regulatory standards.
Interacts cross-functionally, ensuring that all communications, interpersonal interactions, and business behaviors are consistent with the Client Code of Conduct.

Main Responsibilities:

Leads the investigation of complex and highly technical quality issues and ensures the timely completion of CAPA system activities initiated to address nonconformances, potential nonconformances, deviations, and/or complaints.
Executes investigations and CAPAs in accordance with established procedures, ensuring consistency with quality system requirements.
Serves as a subject matter expert in conducting investigations and performing root cause analysis to ensure that root and potential causes are appropriately identified and mitigated/eliminated.
Collaborates with laboratory operations and technical staff to conduct investigations and ensure corrective actions are appropriate and effectively implemented.
Maintains CAPA system records to ensure audit-readiness for internal and external quality system audits.
Ensure CAPA documentation is accurate, well-structured, and compliant with procedural requirements and regulatory guidelines.
Supports the initiation and implementation of improvement activities associated with identified trends.
Escalates potential compliance risks, quality concerns, or procedural gaps to the Quality Manager to ensure timely evaluation and resolution.
Demonstrates effective written and verbal communication skills.
Prioritizes workload in relation to business needs.
Supports the attainment of Client goals and objectives.
Performs other duties as assigned by the Quality Manager.

Required Qualifications:

Bachelor s degree in Life Sciences
Experience with Corrective and Preventative Action process in regulated environments, pharmaceuticals medical devices or laboratories
Excellent communication and technical writing skills
Experienced in working with QMS platforms

Preferred Qualifications:

ASQ CQA
Project management experience
Knowledge of College of American Pathologists (CAP) regulations, NLCP regulations, or similar regulations (i.E., FDA).
Experienced in navigating Agile

Meet Your Recruiter

Calling all job seekers! Explore exciting job opportunities in and around Gretna, Louisiana. Located just across the Mississippi River from New Orleans, Gretna offers a unique blend of historic charm and modern amenities. With its vibrant culture, renowned cuisine, and proximity to iconic attractions like Jackson Square, French Quarter, and Mercedes-Benz Superdome, this area provides an ideal setting for career growth and personal enrichment. Discover the art galleries, theaters, and professional sports teams that make this region so special. Start your job search today and embark on a career journey in a place where work meets play!