We are currently seeking a detail-oriented and experienced CAPA Specialist to support a regulated quality environment within the pharmaceutical, medical device, biotech, or laboratory space. This role is ideal for professionals with hands-on experience driving Corrective and Preventive Action (CAPA) processes and managing quality system documentation within an electronic Quality Management System (eQMS).
Job Title: CAPA Specialist (Contract)
Location: Gretna, LA 70053 (Onsite)
Duration: 6+ Month Contract
Pay Rate: $28- $31/hr
- Lead and support CAPA investigations from initiation through closure
- Conduct root cause analysis for deviations, nonconformances, and quality events
- Ensure timely and compliant documentation of all quality records
- Collaborate with cross-functional teams including Quality, Manufacturing, and Regulatory
- Maintain and update records within eQMS platforms
- Support continuous improvement initiatives and audit readiness activities
- Experience working with CAPA, deviations, nonconformances, or quality investigations
- Hands-on experience with eQMS systems such as TrackWise, MasterControl, Veeva, ETQ, or similar
- Strong technical writing and documentation skills
- Bachelor’s degree in Life Sciences, Engineering, or a related field
- Experience in regulated industries (pharma, biotech, medical device, or laboratory environments)
- Knowledge of FDA, GMP, ISO, or similar regulatory standards
- Strong analytical and problem-solving abilities
- Ability to manage multiple quality records and priorities in a fast-paced environment
