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QA Documentation Specialist
Job Location:
Job Location:
Juncos - Puerto Rico
Monthly Salary:
Not provided by the employer
Monthly Salary:
Experience Required:
5years
Experience Required:
Posted:
24 September 2026 (11 hours ago)
Posted:
Application Deadline:
22 December 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Quality Documentation Specialist with strong expertise in GMP documentation and quality systems. This role blends traditional QA responsibilities with a focus on managing reviewing and controlling documentation to support compliance and operational excellence.
Key Responsibilities:
Review approve and maintain GMP documentation including batch records protocols CAPAs NOEs and change controls.
Ensure documentation aligns with regulatory requirements and internal quality standards.
Support internal audits inspections and document readiness for regulatory agencies.
Collaborate with cross-functional teams to implement document revisions and updates.
Manage document control systems and ensure timely issuance and archiving of controlled documents.
Assist in training personnel on documentation procedures and compliance practices.
Requirements
Bachelors degree completed.
Minimum 5 years of experience.
Strong background in GMP documentation and quality systems.
Proficiency in document control platforms and Microsoft Office tools.
Excellent attention to detail organizational skills and written communication.
Ability to work independently and in cross-functional environments.
Required Skills:
Minimum 5 years of experience. Strong background in GMP documentation and quality systems. Proficiency in document control platforms and Microsoft Office tools. Excellent attention to detail organizational skills and written communication. Ability to work independently and in cross-functional environments.
Required Education:
Bachelors degree
