Equipment Validation Specialist, Level III

US - Portsmouthonsitemid

Posted today · via Workday

About this role

Equipment Validation Specialist, Level III Location : On-site, Portsmouth, NH. Relocation assistance is available for eligible candidates and their families. The Equipment Validation Specialist 3 ensures all critical GMP equipment and systems are validated and maintained in compliance with user requirements, process parameters, and global regulatory guidelines. This role provides Operations, Quality Assurance, clients, and regulatory bodies with scientifically sound, documented evidence that systems and processes perform reliably to maintain a compliant manufacturing environment. What you will get: A collaborative and inclusive work environment. Opportunities for career growth and development. Access to cutting-edge technologies and tools. Competitive compensation and benefits package.…

Read the full description on SG02 Lonza Biologics Tuas Pte.Ltd.'s site →

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reqspace match rubric

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1

Skills match

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2

Level fit

This role is mid-level. We check your trajectory against it.

3

Domain experience

Your work in the role's domain matters more than your years total. We weight recent and direct experience.

4

Recency

A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.

5

Location fit

This role is based in US - Portsmouth. We weight your proximity and willingness to relocate.

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