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The Product Specialist - Clinical Lab at QuidelOrtho in Saudi Arabia is responsible for troubleshooting customer issues, supporting sales teams, and maintaining high customer satisfaction. The role requires a Bachelor's Degree in Biomedical Engineering, 3+ years of clinical lab experience, fluency in English and Arabic, strong communication skills, and the ability to influence others.
Seeking a Staff Quality Engineer to support complex quality engineering activities, monitor compliance with regulations, support quality systems, and lead improvement projects. This position is onsite in Pompano Beach, FL.
Seeking a Wave Planner to optimize inventory flow and order fulfillment in a distribution center. Responsibilities include creating and managing wave plans, monitoring order capacity, and collaborating with various departments. Requires high school diploma, 2 years of distribution center experience, and strong computer and math skills.
Responsible for installation, configuration, maintenance, and technical disaster recovery of SAP Basis environments. Involvement in SAP system upgrades within ECC and into S/4. Develop and implement SAP performance and maintenance monitoring processes. Assist in troubleshooting performance issues and ensure changes adhere to corporate practices. Experience in SAP administration, upgrades, cloud migrations, RDBMS management, SSO setup, and global SAP system deployments. Additional experience with various SAP tools and applications.
Key Account Executive at QuidelOrtho responsible for maintaining business relationships, forecasting product and equipment, evaluating sales reports, and managing distributor activities. Requires a Bachelor's degree in Medical Technology, 3 years of commercial experience in the diagnostic health area, and strong communication skills.
Provide legal and compliance support to the team, including evaluating interaction activities, assisting with legal reviews, drafting contracts, and maintaining internal trackers and databases. Requires LLB/LLM degree, experience in Ethics, Compliance, Legal matters, and strong communication skills.
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.
The Senior Quality Engineer at QuidelOrtho in Rochester, NY will provide quality engineering support, conduct root cause investigations, and drive quality improvement initiatives. This role requires a Bachelor's degree in a relevant discipline and 5-7 years of Quality experience in a regulated environment.
The Quality Control Scientist I at QuidelOrtho is responsible for testing product stability and release, ensuring compliance with standards and regulations, participating in investigations, and suggesting process improvements. This position requires a bachelor's degree in a related field and 1-3 years of experience with QC and GMP procedures.
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