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The Senior Quality Engineer oversees quality processes for in vitro diagnostic device manufacturing, mentors staff, resolves quality issues, ensures compliance with regulations, and collaborates with business partners on quality events. This position involves independent decision-making, root cause investigations, and driving improvements aligned with business goals.
The Operations Manager-RMM will lead the operations of the new MicroWell Factory, focusing on supporting R+D product development. Responsibilities include coordinating project goals, overseeing production processes, and maintaining communication with various teams. The role requires technical support for engineering solutions and the development of master production schedules.
The DRP Planner will develop inventory plans based on demand and actual orders, monitor inventory levels, manage customer backorders, and interact with various departments to optimize supply chain metrics. This role includes forecasting, reporting, and executing inventory plans responsibly for finished goods.
The Job Scheduling Engineer ensures the proper installation, configuration, and monitoring of job scheduling environments. Responsibilities include creating and updating jobs, maintaining system logs, responding to job failures, and collaborating with infrastructure and vendor teams for support and updates. The role also includes daily system administration tasks and enhancing service offerings through metrics and improvements.
The Post Market Risk Management Specialist II will assist with post-market product safety and quality issues, execute field actions, and support during audits. The role involves data collection, regulatory reporting, and collaboration with internal and external partners to ensure a high-performance culture and continuous process improvement.
The Operator II in Slides Manufacturing is responsible for meeting production metrics, assisting in equipment troubleshooting, performing data entry and quality checks, contributing to SOP updates, and participating in root cause analysis. This role emphasizes safety, teamwork, and effective communication while working on automated production machines.
As a Senior Manager, IAM, you will lead the implementation of security services related to access management while enforcing compliance and quality standards. Your role involves designing access authentication solutions, managing the IAM team, providing expertise on IAM issues, and aligning ERP controls with wider IAM requirements.
The Serologist I will perform manufacturing test methods for serological evaluation and processing of blood bank reagents. Responsibilities include executing tests, documenting results, maintaining inventory, and ensuring compliance with company policies and regulations in a CGMP environment.
The Strategic Account Manager is responsible for managing and directing sales and marketing operations in compliance with unit strategies, providing sales forecasts, monitoring sales performance across accounts and territories, ensuring contract compliance, and maintaining effective client communication to enhance customer experience.
The RA Specialist at QuidelOrtho will be responsible for regulatory submissions to ensure successful delivery of the regulatory plan. This role involves leadership in preparation and review of regulatory submissions, compliance with guidelines and timelines, liaising with regulatory agencies, and maintaining approved products. The specialist will also manage new product registration, develop documentation, anticipate regulatory changes, and collaborate with cross-functional teams for continuous improvement in regulatory compliance.
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