Pharma engineering consulting for equipment qualification and GMP compliance
PHARMACOS is an engineering consulting firm focused on pharmaceutical and biotech manufacturing. The tech stack—heavy on industrial control systems (SCADA, DCS, MES, PLC) and CAD (CREO)—reflects their core work in equipment design and process validation. Active projects cluster around production-unit commissioning and regulatory compliance (FAT/SAT, CDISC programming, risk management plans), while pain points center on GMP adherence and integrating new equipment into existing installations—typical friction points when scaling manufacturing operations.
PHARMACOS provides engineering consulting services to pharmaceutical manufacturers and biotech firms across France, ranging from large-cap pharma to mid-market biotech. The firm operates at three layers: design assistance across all project phases, project execution with equipment and process qualification, and risk mitigation for pressurized equipment and piping systems. Their client base spans both multinational pharmaceutical groups and smaller biotech companies. The current hiring profile—balanced across engineering, healthcare, and quality roles at manager, mid, and senior levels—suggests active growth in production support and regulatory functions.
PHARMACOS serves pharmaceutical manufacturers and biotechnology companies, offering design assistance, project management, equipment qualification, and compliance support for GMP manufacturing environments.
Primary tools include SCADA, DCS, MES, and PLC systems (Siemens S7, Emerson DeltaV, TIA Portal, WinCC) for process control, plus CREO for CAD and design work—standard for pharma equipment engineering.
PHARMACOS is based in Lyon, Auvergne-Rhône-Alpes, France, with all current hiring concentrated in France.
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