Reliability Engineering Intern
Core
Execute equipment requalification (IQ/OQ/PQ), manage SOP updates, and ensure GMP compliance for facility operations.
Role type
Reliability Engineering Intern
Builds
Compliant pharmaceutical manufacturing equipment and documentation
Domain
Life Sciences / Pharmaceutical Manufacturing
Deliverable
client delivery
Required skills
Equipment requalification planning, SOP management, GMP compliance, audit support, deviation investigation, CAPA implementation, document control, vendor liaison
Responsibilities
Plan and execute periodic equipment requalification activities, review and update Standard Operating Procedures (SOPs), support internal and external audits, conduct annual facility reviews, review annual pest control reports
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