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Project Management Associate

Louisville, KY, us💼 Full-time🗓 2026-08-28 → 2026-09-25

Core

Manage oligonucleotide manufacturing operations and key customer projects to meet production, quality, and cost objectives while ensuring regulatory compliance.

Role type

Senior manufacturing project management associate

Builds

Oligonucleotide production runs and validated manufacturing processes

Domain

Life sciences / Oligonucleotide manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

Organic synthesis and purification techniques, GMP/ISO/QSR regulatory knowledge, experimental data analysis, team leadership, project coordination, schedule administration, KPI reporting, Kaizen improvement, document management

Preferred skills

Experience in manufacturing or oligonucleotide field, proficiency in electronic document management systems

Technologies

Electronic document management systems, HPLC, MS

Responsibilities

Lead teams including supervisors, team leads, production chemists, and lab technicians; coordinate project timelines, costs, and process implementation; manage Red Folder/VIP customer projects; develop and monitor schedules against KPIs; lead validation activities for new projects and equipment; coach subordinates on performance; ensure GMP compliance and maintain traceable work environments; act as point of contact for QC questions regarding RF/VIP projects; track project delays and provide updates; coordinate safety training and recruitment processes.

Seniority

Mid-level, hands-on IC with team leadership

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