Production Specialist
Core
Support process excellence and continuous improvement in GMP pharmaceutical manufacturing operations through technical writing and documentation management.
Role type
Production Specialist (Technical Writing & Process Improvement)
Builds
GMP-compliant manufacturing processes and documentation for pharmaceutical production
Domain
Pharmaceutical manufacturing / Quality Systems
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP compliance, SOP creation and maintenance, technical writing, root cause analysis, CAPA support, lean manufacturing, process evaluation, cross-functional collaboration, PPE adherence
Preferred skills
Continuous improvement mindset, training production personnel, Microsoft Office proficiency
Technologies
Microsoft Office applications
Responsibilities
Create, revise, review, and maintain SOPs and manufacturing documentation; Partner with Manufacturing, Quality, and Engineering teams on process improvements; Conduct root cause investigations and support CAPA activities; Evaluate workflows for efficiency and compliance; Assist with implementing new processes and training personnel; Participate in cross-functional project teams; Maintain accurate documentation practices.
Seniority
Mid-level, hands-on IC
