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The Warehouse/Production Quality Inspection Leader performs incoming and outgoing product inspection of finished products and assemblies for good manufacturing practices (GMP) to verify product meets specifications and are free of damage or defects.
This role is responsible for Material Identification & Segregation, documentation configuration control practices; performing incoming and outgoing product inspection of finished products, finished medical devices and assemblies for good manufacturing practices (GMP) to verify product meets specifications and are free of damage or defects.
This role will require autonomy to make decisions within a defined framework: Resolves issues in situations that require good technical knowledge and judgment within established procedures. Consults more senior team members for issues outside of defined instructions/parameters. Lead a team of Quality Inspectors through professional guidance and technical expertise.
Documentation & disposition of non-conforming material, and Good Documentation Practices requirements, as associated with this job type/position Aware of and comply with the company HC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.
Job Description
Essential Responsibilities
Conduct visual and measurement tests, read Specifications to understand the requirements of products Inspect, test, or measure materials, products, installations - verify comply with specifications to mark material as acceptance or rejection status Discuss inspection results with those responsible for products, and recommend necessary actions Select output samples and check them using predefined appropriate methods Communicate and escalate with production team leader quality control concerns to improve product excellence Work with cross-functional teams and assists with implementation of process improvements to increase quality and productivity.

Operates and maintains stations to assemble, align, and adjust fabricated parts, components, or units according to specifications and follows established manufacturing procedures. Uses hand tools, power tools, and other manufacturing assembly line equipment to assemble units. Tests and calibrates parts and mechanisms to ensure all components meet tolerances, product specifications, and quality standards. May repair or refit parts or units that fail tests or tolerance levels. Keeps daily assembly production records. Maintains a clean and organized work environment. Typically requires a high school diploma. Typically reports to a supervisor. Works under the close direction of senior personnel in the functional area. Possesses a moderate understanding of general aspects of the job. May require 0-1 year of general work experience.

As a Software Engineer - PET Data Acquisition, you will join a highly specialized team developing the real-time software stack at the core of our companys PET/CT imaging systems.
Our software directly impacts image quality and system reliability, enabling clinicians worldwide to provide accurate diagnoses and life-saving care.
You will work on a distributed, high-performance C++ system running on Linux, responsible for configuring detector hardware, processing high-throughput data streams, and enabling seamless integration across the scanner ecosystem.
Job Description
About the Team
Our team develops the data acquisition platform powering our companys PET/CT scanners.
This system:
Configures and interfaces with detector hardware
Receives high-rate event streams via UDP
Performs real-time sorting and time-stamping of coincidence events
Manages acquisition state and persistence
Exposes control and monitoring APIs to clinical applications
The platform is a distributed, multi-process, multi-threaded C++ system running on Linux, designed for deterministic, high-performance operation under demanding workloads.
Key Responsibilities
Design and develop end-to-end data acquisition features, from low-level UDP capture and event processing through service layers and client APIs
Optimize and maintain performance-critical code paths, including:
Lock-free / low-contention data structures
Thread affinity and NUMA optimization
Zero-copy buffer management
Deterministic real-time execution
Enhance and maintain inter-process communication mechanisms, including shared memory, message queues, and service interfaces
Work with embedded persistence layers (SQL-based) for configuration, metadata, and runtime state
Collaborate closely with hardware, physics, and system teams to integrate new detector and system components
Develop unit and integration tests, and actively participate in code and design reviews
Troubleshoot complex cross-process issues using advanced debugging and profiling tools (e.g., gdb, perf, tcpdump, strace).

This position refers to leading the design of parts and assemblies for the company imaging systems (PET, SPECT). The position includes working inside an NPI project or supporting the systems in the field (Install Base). The mechanical design of parts and assemblies includes working with multi-disciplinary teams including electronics, system engineering, service engineering and involves transfer of designs to production, support of high-level-assembly lines, etc. This position involves the writing of safety files, planning and execution of V&V tests, engineering calculations and FEA simulations, writing specifications and failure analysis.
Job Description
Essential responsibilities:
Mechanical design derived from specifications (as well as writing specifications), as part of a multi-disciplinary team of parts and assemblies while using off-the-shelf components, using 3D CREO CAD design package. Presenting the design in technical design reviews at the levels of concept and detail design is a part of this position,
Developing creative design solutions in response to the product requirements of functionality, reliability, cost, manufacturability, etc.,
Support of company products at hospital and customer sites via the Service Teams as needed,
Building safety files for products, including strength calculations, failure modes analysis (FMEA), compliance with safety and medical industrial standards as well as internal company standards,
Supporting transfer to production, defining basic assembly and service instructions, working with parts suppliers,
Defining verification and validation test procedure, tests execution and report writing.
Essential qualifications /requirements:
Mandatory: 1st degree in mechanical engineering
Mandatory: Good personal, teamwork and communication skills, enthusiasm from study, self-motivated, results oriented,
Work experience of 2 years in mechanical design, with experience in at least 2 of the following: design of motion systems, large welded or cast structures and frames, mechanisms, electronic packaging, large sculptured FRP covers, electrical design support (DXF, cables routing),
Experience in machining and sheet metal technologies,
Experience in prototype building (hands on), testing execution per test plan and failures troubleshooting
Fluent English at presentation level in technical design reviews, Zoom/Teams calls and in writing.
Desired Characteristics by priority:
Leading tasks from requirements to engineering change finalization,
System level understanding in multi-disciplinary project environment,
Definition of testing and report writing,
Experience in design for cost, reliability, serviceability and for manufacturability.
Ability to perform finite-element analysis and Excel level technical calculations,
we are a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the moments that matter. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world.

Description: Responsibilities may include manufacturing, assembly, basic testing, packaging and shipping of products.
Job Description
Essential Responsibilities
Reads and follows work procedures and schematics or receives verbal instructions regarding duties to be performed
Performs manufacturing/assembly operations and various tasks following procedures, bills of materials, work instructions, and process aid sheets
Maintains daily production output
Follows all EHS and Quality policies and procedures
May participate in quality control inspections
Works with team lead, engineers, supervisors, and managers to improve quality and process efficiency
Other duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teams
Comply with EHS regulations and policies.

Description: Responsibilities may include manufacturing, assembly, basic testing, packaging and shipping of products.
Essential Responsibilities
Reads and follows work procedures and schematics or receives verbal instructions regarding duties to be performed
Performs manufacturing/assembly operations and various tasks following procedures, bills of materials, work instructions, and process aid sheets
Maintains daily production output
Follows all EHS and Quality policies and procedures
May participate in quality control inspections
Works with team lead, engineers, supervisors, and managers to improve quality and process efficiency
Other duties as assigned, and may be asked to be included in quality activities, training sessions, and employee activity teams
Comply with EHS regulations and policies.

We are looking for an NPI Engineer for the R&D team. The NPI Engineer will own the end-to-end transition of multidisciplinary medical devices from R&D prototypes to stable, scalable serial production, serving as the bridge between product development and Operations.
If you want to work in an innovative, international environment and help push the boundaries of healthcare, well-being, and energy-based technology, this is your opportunity
Key responsibilities:
Lead the full NPI and design-transfer process from R&D handoff through pilot builds, qualification, production ramp-up, and stabilization.
Build and drive transfer plans, schedules, risk and action tracking, production-readiness criteria, and release gates.
Create and maintain the manufacturing package, including BOM/DMR content, drawings, work instructions, test methods, acceptance criteria, tooling, and training materials.
Lead DFM, DFA, and DFT reviews and drive design and process improvements that support quality, manufacturability, serviceability, and cost.
Define, develop, and qualify manufacturing processes, fixtures, equipment, and test setups; prepare and execute validation protocols where applicable.
Lead ECOs and configuration changes, and provide hands-on support for production, yield, quality, field, and obsolescence issues using structured root-cause and corrective-action methods.
Serve as the technical focal point across R&D, Operations, QA/RA, Supply Chain, Service, suppliers, subcontractors, and contract manufacturers.