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Supports validation activities and develops Master validation plans. Collaborates with the Process Development team and leads quality improvement efforts, focusing on compliance and system adequacy.

Manage all facets of pharmaceutical projects including planning, execution, budget tracking, and ensuring compliance with industry standards. Requires bilingual skills in English and Spanish and substantial project management experience.

As a Cost Control Specialist, you will manage cost control frameworks, establish project budgets, monitor costs, report financials, and ensure compliance in capital project management within biopharma environments.

The Project Engineer will manage all phases of Project Engineering in Capital Projects within the Pharmaceutical industry, providing technical direction, maintaining effective communication among project parties, and ensuring quality standards are met.

The role involves resolving equipment issues, providing technical solutions, collaborating on projects, and ensuring compliance in the medical devices or pharmaceutical industry.

The Jr. Automation Engineer will maintain process equipment, manage PLCs and automated systems, ensure compliance with regulations, and resolve technical issues.

The Product Engineer supports production engineering in testing methods, device issues, equipment design, and ensures compliance with quality standards in manufacturing operations.

Manage DeltaV automation upgrade projects in regulated environments, coordinating engineering, IT, and vendors while ensuring compliance and risk mitigation.

The C&Q Lead will develop and execute commissioning and qualification strategies, managing documentation, leading teams, and ensuring regulatory compliance in biotech manufacturing.

Lead projects to implement automation in a regulated environment, define project scope, manage vendors, and ensure compliance with procedures.