Quality Associate
Job Location:
Juncos - Puerto Rico
Monthly Salary:
Not provided by the employer
Experience Required:
3years
Posted:
28 July 2026 (10 days ago)
Application Deadline:
25 October 2026
Vacancies:
1 Vacancy
Job Summary
We are seeking a Quality Associate to support and maintain quality systems ensuring compliance with GMP regulations industry standards and company policies within a regulated manufacturing environment. The successful candidate will be responsible for reviewing and managing quality documentation participating in investigations and corrective and preventive actions (CAPAs) providing quality support to manufacturing operations and helping ensure that products processes and systems consistently meet established quality and regulatory requirements. This role requires strong attention to detail a commitment to continuous improvement and the ability to collaborate effectively with cross-functional teams to drive quality excellence and operational compliance.
Requirements
Requirements:
- 3 to 5 years of experience in process quality areas.
- Experience in regulated manufacturing environments.
- Knowledge of GMP documentation.
- Experience with quality systems investigations documentation and support of manufacturing processes.
- Bilingual (English & Spanish).
Required Skills:
risk assessments SOPs and cross-functional collaboration
Required Education:
Bachelors degree in a technical field and experience in pharmaceutical safety or regulated environments.