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Validation Specialist II
Framingham, MAMarch 28th, 2026
Roles & Responsibilities: 8 years of experience in validating GxP-regulated systems and your strong skills in risk assessment and protocol generation, bring a wealth of expertise that aligns perfectly with what our client is looking for. Hands-on experience with validation documentation and compliance, combined with your understanding of industry standards, makes you an excellent candidate for this role. Track record in the pharmaceutical industry and your technical skills in regulations like GAMP 5 and 21 CFR Part 11 will be invaluable in ensuring the shipping and transport validation processes are executed flawlessly.
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