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This project manager will oversee capital projects in the medical devices or pharmaceutical sector, supporting engineering and manufacturing teams while ensuring compliance and efficiency in project execution.

Develop and maintain quality standards, collaborate with teams to ensure product quality, and implement testing methods for evaluation in manufacturing processes.

The Associate Engineer will support process validation, execute validation protocols, and participate in process improvement and technology transfer projects in a regulated manufacturing environment.

Lead cross-functional teams in product development projects, manage project timelines, budgets, and quality, and ensure stakeholder engagement for successful outcomes.

Responsible for quality services in engineering, supervising and coordinating a small staff, developing policies, and solving complex issues in the manufacturing process.

The Quality Engineer will develop and implement product quality plans, write protocols, and monitor project progress, ensuring compliance and addressing quality issues cross-functionally.

As a Specialist in Quality Assurance, you will lead investigations, review and approve product releases, and support environmental programs while ensuring compliance with quality standards in the pharmaceutical industry.

The Associate Tech Engineering role involves troubleshooting mechanical systems, ensuring compliance with industry standards, and improving engineering processes.

Manage an MES project focused on software integration, ensuring compliance, leading technical meetings, and coordinating cross-functional teams.

Manage capital projects in the pharmaceutical sector, overseeing budgets, schedules, design management, and construction implementation while coordinating with stakeholders and resources.