Job information

Location: JR Spain

Client / Employer: Oxford Global Resources

Job reference:

Listing type: Basic

EU work permit required: No

Posted:

Role

QA Specialist – (GMP, GxP Quality Systems)

Reporting to the QA Manager, the role is responsible for ensuring compliance with our client's internal policies and applicable regulatory standards, including Pharmaceutical Quality System requirements, Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), Good Clinical Practices (GCP), Good Pharmacovigilance Practices (GVP), ISO 13485, MDR, and 21 CFR Part 210 & 211 GxP, within the assigned scope of responsibility.

Responsibilities

• Execute the Corporate Quality Assurance Program across all applicable sites, ensuring alignment with the Corporate Pharmaceutical Quality System standards and supporting continuous improvement initiatives.
• Manage the documentati...