Senior CAPA Associate, Quality Systems

Job overview

The Senior CAPA Associate, Quality Systems role is onsite in Puerto Rico; the listing identifies the location as postal code 00777. Compensation is not specified. Validation & Engineering Group provides laboratory, compliance, computer, engineering, project management, and validation services to regulated industries. The associate supports nonconformance investigations and corrective and preventive action processes in pharmaceutical or medical device manufacturing environments. The work helps document root causes, implement mitigation actions, and verify the effectiveness of corrective actions while supporting timely record closure.

What you'll do

• Execute and document nonconformance investigations
• develop investigation strategies with multidisciplinary teams
• prepare technical reports
• apply root cause analysis tools
• coordinate scientific and technical input from subject matter experts
• support mitigation actions, CAPA implementation, and effectiveness checks
• participate in review boards and continuous improvement
• coach others on nonconformance and CAPA processes
• promote EHS compliance.

What we're looking for

Skills & competencies

senior capa associate

quality systems

puerto rico 00777

validation & engineering group

nonconformance investigations

corrective and preventive actions

root cause analysis

gmp

pharmaceutical industry

medical device industry

technical documentation

english and spanish

Work arrangement

• Weekend coverage required

About the employer

Validation & Engineering Group, Inc is hiring for this role. Industry: Engineering Services. Sector: 54.