TAPI is a pharmaceutical manufacturing company producing active pharmaceutical ingredients and contract development and manufacturing services (CDMO). The hiring mix is heavily weighted toward manufacturing (27 roles) and engineering (15), with concurrent projects in compliance, quality strategy, and facility upgrades—suggesting a company in operational scale-up mode rather than product innovation. Pain-point clustering around GLP/GMP compliance, audit readiness, and process optimization indicates internal focus on regulatory maturity and manufacturing efficiency over new capability development.
Notable leadership hires: Quality Head, Project Track Lead, Quality Compliance Head
TAPI manufactures active pharmaceutical ingredients (APIs) and provides CDMO services to pharmaceutical partners globally. The company operates manufacturing sites across multiple countries including Hungary, Israel, India, Mexico, Italy, Czechia, and Croatia. Operations are anchored in SAP for resource planning, LIMS for lab data management, and advanced analytical equipment (HPLC, LC-MS, MALDI-TOF) for quality control. The company maintains a public company structure with 1,001–5,000 employees, the majority concentrated in manufacturing and engineering roles. Current operational priorities center on GMP/GLP compliance, quality strategy execution, facility QC upgrades, and technology transfer across manufacturing sites.
TAPI operates manufacturing and R&D sites across Hungary, Israel, India, Mexico, Italy, Czechia, and Croatia, reflecting a globally distributed manufacturing footprint.
TAPI uses SAP for ERP, LIMS for lab data management, HPLC and LC-MS for analytical testing, Salesforce for CRM, and GCP for cloud infrastructure, alongside manufacturing automation systems (SCADA, PLC).
Yes. Manufacturing represents the largest hiring category with 27 active roles across the company's global sites, out of 87 total open positions.
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