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The Senior Quality Systems Engineer is responsible for implementing quality systems, conducting audits, leading product improvement projects, managing CAPA programs, and ensuring compliance with GMP and ISO requirements. This role involves supervising staff and executing safety protocols related to handling hazardous materials.
The Senior QS Engineer will manage product quality within the healthcare field, specifically handling QMS systems per PMD Act. Responsibilities include managing customer complaints, performing investigations, managing nonconforming products, and supporting regulatory responses. Extensive collaboration with teams and conducting audits are crucial parts of this role.
The Supplier Quality Engineer will perform quality-related activities for medical device suppliers, including supplier selection, qualification, audits, and resolution of quality issues. This role involves collaboration with cross-functional teams to ensure compliance with regulatory standards and improvement in supplier performance.
The Principal Software Architect at Haemonetics leads all technical aspects of a key software platform, ensuring high-quality delivery and innovation. Responsibilities include mentoring developers, conducting design and code reviews, and prototyping features. The role also involves researching new technologies and collaborating with various teams for product advancement and support, particularly in regulated medical environments.
The Market Development Manager at Cardiva Medical is responsible for implementing market strategies to develop physician champions and drive product adoption, working closely with sales directors and hospital leadership. This role emphasizes building relationships, compliance, and achieving sales quotas.
The Field Implementation Specialist is responsible for planning and executing product implementations, managing customer resources, providing operator training, and ensuring quality throughout the project. The role requires extensive communication with stakeholders, project tracking, and adherence to company policies while traveling to client locations to support equipment setup and validation.
The Quality Systems Engineer is responsible for ensuring compliance with regulations and standards in process validation and product release. Duties include developing new product variants, leading measurement systems analysis, managing corrective actions, and supporting audits. The role involves working with cross-functional teams to investigate quality issues and ensure all processes meet specified requirements.
The Global Senior Product Manager for Structural Heart is responsible for managing the product lifecycle of medical devices, developing global product strategies, collaborating with cross-functional teams, conducting market analysis, and overseeing product launches and financial performance.
The Territory Manager will drive sales objectives, manage territory growth, develop business plans, oversee training during account launches, and build customer relationships while maintaining company standards. Responsibilities include executing sales strategies, providing product knowledge, and ensuring compliance with policies.
The Account Manager will drive sales objectives and territory growth by cultivating new accounts, executing business plans, and maintaining customer relationships. Responsibilities include training during account launches, making presentations, and ensuring compliance with company policies and regulations.
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