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QA / Regulatory Affairs Specialist

Ensure compliance with GMP, ISO standards, and 21 CFR Part 11. Manage quality documentation, support audits, and contribute to continuous improvement of the quality system.

Type:: Full-time
Location:: Hybrid
Department:: Quality & Regulatory
Experience:: Senior

QA / Regulatory Affairs Specialist

If this opportunity inspires you and you’re ready to make an impact, we’d love to hear from you, apply now.

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QA / Regulatory Affairs Specialist

QA / Regulatory Affairs Specialist

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