Technical Writer III – Technical Operations
Core
Prepare and revise master batch records (MBRs) for manufacturing and packaging, providing support to Technical Operations and Process Technology groups.
Role type
Technical Writer (Pharmaceutical Manufacturing)
Builds
Master batch records (MBRs) and technical packages for GMP-compliant manufacturing and packaging.
Domain
Pharmaceutical manufacturing / Technical Operations
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP compliance, SOP adherence, MBR template maintenance, change control management, SAP report generation, internal log/metrics maintenance, hazard reporting, shift work adaptability
Preferred skills
Pharmaceutical development knowledge, improvement project leadership, problem solving
Technologies
SAP, Microsoft Office
Responsibilities
Generate and develop master batch records in a GMP environment; Maintain and upgrade MBR templates; Work with engineers and project managers to understand MBR requirements; Attend project meetings and on-site visits; Perform investigations into departmental deficiencies; Assign change controls and technical packages; Maintain internal logs and metrics; Create change controls; Assist with SAP report generation; Maintain a safe working environment and report hazards.
Seniority
Mid-level, hands-on IC
