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Tech Ops Process Engineering Supervisor – Self Care | Fixed Term: 12 months

Latin America, Brazil, Sao Paulo, Sao Jose dos Campos💼 Full-time🗓 2026-09-14 → 2026-09-26

Core

Lead Tech Ops Process Engineering agenda across multiple pharmaceutical product platforms, driving innovation, industrialization, process excellence, and technology deployment.

Role type

Senior Process Engineering Supervisor (Pharmaceutical Manufacturing)

Builds

Scalable, sustainable, and competitive manufacturing solutions for liquids, solids, and semi-solids pharmaceutical products.

Domain

Pharmaceutical manufacturing and process engineering

Deliverable

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

Required skills

Process engineering, technology transfer, industrialization, NPI, lifecycle management, troubleshooting, regulatory compliance (GxP, ANVISA, FDA), capital project governance, technical writing, cross-functional collaboration

Preferred skills

Statistical tools (Minitab, JMP, DOE), validation activities, automation, emerging manufacturing technologies, stakeholder influence, global organization experience

Technologies

Minitab, JMP, Design of Experiments (DOE)

Responsibilities

Lead and develop process engineering individuals across multiple technologies; Drive development, scale-up, and implementation of breakthrough process technologies; Provide technical leadership in machine-material interactions; Collaborate with suppliers and cross-functional teams to deploy emerging technologies; Partner with R&D, Supply Chain, Quality, and Operations for manufacturability and compliance; Lead technology transfer, industrialization, and commercialization activities; Plan and execute machine trials, pilot plant studies, and manufacturing runs for NPI and LCM; Provide governance for capital projects, technical documentation, and change management; Act as technical authority for product, process, and equipment changes; Drive process optimization and continuous improvement; Lead scientific investigations and root cause analyses; Develop and maintain protocols and validation documentation in compliance with GxP.

Seniority

Senior, hands-on IC with leadership responsibilities

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