Master Batch Record & BOM Technician
Core
Ensure quality compliance across manufacturing operations through detailed documentation review, process monitoring, and GMP adherence.
Role type
Quality Specialist I (GMP Manufacturing)
Builds
Life-changing products for customers in healthcare, food safety, and environmental protection sectors.
Domain
Life Sciences / Pharmaceutical Manufacturing / GMP Compliance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP documentation review, FDA/EMA regulation knowledge, quality management systems (CAPA, change control), root cause analysis, environmental monitoring principles, gowning procedures, shift flexibility, physical capability for manufacturing environments
Preferred skills
Chemistry/Biology/Engineering degree, ISO auditor certification, Six Sigma certification, English fluency
Technologies
Quality systems software, Microsoft Office applications
Responsibilities
Review and approve GMP documentation and batch records, investigate quality events, conduct root cause analysis, monitor processes for compliance, collaborate with cross-functional teams, maintain quality-focused culture
Seniority
Entry-level, no prior experience required