Mentor Technical Group seeks a detail-oriented Documentation Specialist to support cGMP-compliant activities for pharmaceutical and life sciences projects.
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You will manage technical documentation, ensure regulatory compliance, and contribute to ISO 17025:2017 standards while collaborating with MTG teams to meet client expectations.
Responsibilities include maintaining quality records, reviewing xqbhyrx procedures, and supporting audits; you will also coordinate with supervisors to ensure timely delivery
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📌 Documentation Specialist - Regulatory Records Life Sciences (Barcelona)
🏢 Mentor Technical Group
📍 Barcelona
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