Jobs at Roche

Supports biochemical manufacturing by preparing equipment and solutions, cleaning and sterilizing vessels, operating processing equipment, sampling materials, monitoring environments, documenting production activities, and maintaining housekeeping. The role follows cGMP, safety, and quality standards; supports continuous improvement and process optimization; operates computer-based systems; and collaborates with shift teams. Weekend, off-shift, overtime, and physical lifting requirements apply.

Complete scheduled biochemical manufacturing tasks in compliance with cGMP, safety, and quality standards. Responsibilities include equipment preparation, vessel cleaning and sterilization, solution preparation, process equipment operation, raw-material sampling, environmental monitoring, documentation, troubleshooting, housekeeping, computer-based process control, and process improvement. The role requires collaboration across shifts, incident reporting, and the ability to work weekends, off-shifts, and overtime while handling loads up to 25 kg.

Leads pharmaceutical capital projects from design and procurement through installation, commissioning, qualification, and technology transfer. Ensures equipment, piping, facilities, documentation, and engineering assets meet cGMP, safety, regulatory, reliability, and operational requirements. Coordinates contractors and internal teams, supports capital planning and budgets, develops maintenance and manufacturing capabilities, contributes to root cause analyses and CAPA, and applies Lean Production System principles for continuous improvement.

Support Quality & Regulatory team by preparing and submitting product registration updates, monitoring regulatory sources, maintaining tracking databases, leveraging internal tools to automate processes, and collaborating with cross-functional stakeholders on regulatory and quality projects.