Description

The European Account Executive will lead the sales and marketing efforts in Western Europe. The areas of direct responsibility will include France and Switzerland. The ESR will play a lead role in development of sales and marketing strategy for Western Europe as well as assist in clinical studies/ strategy as needed.

Requirements

* College degree required, advance degree beneficial
* Minimum of 5 years experience in Cardiovascular Surgery. Adiditional experience in Cardiac Electrophysiology is a major benefit
* Fluent in French and English and at least one other launguage
* Well Developed computer, sales, presentation and communication skills.
* Demonstration of these skill sets in previous experience and success is needed.
* Demonstrated record of success. 
* Must be able to work in Operating Room and Electrophysiology Lab. 
* Must be able to  wear protective lead.
* Technically proficient, comfortable working with medical equipment
* Excellent problems solving skills
* Ability to function in a self- directed maner with a high degree of independence.
* Strong interpersonal and communication skills
* Ability to motivate in a dynamic environment

Description

The North American Clinical Specialist will play a key role in supporting the CryoCath electrophysiology divisions in the USA. The candidate will educate physicians and lab personnel as to the proper function and use of CryoCath Technologies systems in their hospital. The Clinical Specialist will be a key link between the physicians and clinical support staff and CryoCath Technologies.

Responsibilities
* Oversee all aspects of EP procedures in the USA and assist CryoCath as it moves into new areas
* Train physicians and EP lab personnel, CCT representatives and or distributors about CryoCath Technology
* Provide feedback on each EP case, and assist with data acquisition for the IPR.
* Direct, observe and interact (field questions) during EP cases
* Work with Electrophysiologists and Ancillary personnel, CryoCath personnel and distributor representatives and/or Distribution partner to understand the proper use of CCT products in order to enhance the clinical utility
* Assist with development of an ongoing clinical training tool for the Field Sales Organization, In-house organization and Distributor Network
* Assist with other related requests as needed
* Keep education current with medical literature

Requirements

* Strong knowledge of Cardiac Electrophysiology with a minimum of 2 years clinical experience in Cardiac Electrophysiology is required
* Prior Industry experience in a clinical and/or training position would be a significant benefit.
* Excellent English communication skills required.
* Well-developed teaching skills
* Experence in the development of clinical training programs
* Well-developed computer, sales, presentation, and interpersonal skills
* Demonstration of these skill sets in previous experience and success is needed.
* Must be comfortable with expected travel 30%
* Must be able to work in EP labs.
* Technically proficient, comfortable working with medical equipment
* Excellent problem solving skills
* Ability to function in a self-directed manner with a high degree of independence. * Ability to motivate in a dynamic environment.
* College degree required.
* NASPE certification a benefit.

Profile
The ideal Candidate will have a college degree and a minimum of 2 years of clinical experience in Cardiology specifically in Electrophysiology. This candidate will have been involved in EP procedures during their clinical experience The candidate will have a firm understanding of the challenges involved in catheter manipulation, 3-D space orientation and arrhythmias. The candidate will learn and then demonstrate the ability to design and teach both general and highly specific cardiology topics to both general and highly specialized audiences.

Description

The Clinical Specialist will play a key role in supporting the CryoCath electrophysiology divisions in Europe. The candidate will educate physicians and lab personnel as to the proper function and use of CryoCath Technologies systems in their hospital. The Clinical Specialist will be a key link between the physicians and clinical support staff and CryoCath Technologies.

Responsibilities:

• Oversee all aspects of EP procedures in Europe and assist CryoCath as it moves into new areas;
• Train physicians and EP lab personnel, CCT representatives and or distributors about CryoCath Technology;
• Provide feedback on each EP case, and assist with data acquisition for the IPR;
• Direct, observe and interact (field questions) during EP cases;
• Work with Electrophysiologists and Ancillary personnel, CryoCath personnel and distributor representatives and/or Distribution partner to understand the proper use of CCT products in order to enhance the clinical utility;
• Assist with development of an ongoing clinical training tool for the Field Sales Organization, In-house organization and Distributor Network;
• Assist with other related requests as needed;
• Keep education current with medical literature.

Requirements

• Strong knowledge of Cardiac Electrophysiology with a minimum of 2 years clinical experience in Cardiac Electrophysiology is required;
• Prior Industry experience in a clinical and/or training position would be a significant benefit;
• Excellent English communication skills required;
• Well-developed teaching skills;
• Experence in the development of clinical training programs;
• Well-developed computer, sales, presentation, and interpersonal skills. Demonstration of these skill sets in previous experience and success is needed;
• Must be comfortable with expected travel 30%;
• Must be able to work in EP labs;
• Technically proficient, comfortable working with medical equipment;
• Excellent problem solving skills;
• Ability to function in a self-directed manner with a high degree of independence;
• Ability to motivate in a dynamic environment;
• College degree required. NASPE certification a benefit.

Description

• Assembles products according to approved standard operating procedures;

• Works at different workstations as production requires;

• Conducts quality inspection of own or other’s work;

• Follows all safety and production standard operating procedures;

• Ability to follow procedures and execute them effectively;

• May perform assembly of custom products using little or no documentation;

• Maintains clean and orderly workstation;

• Accurately records and completes all manufacturing documentation;

• Identifies production problems and their causes. Suggest methods for improvement.

Requirements

• Assembles products according to approved standard operating procedures;

• Works at different workstations as production requires;

• Conducts quality inspection of own or other’s work;

• Follows all safety and production standard operating procedures;

• Ability to follow procedures and execute them effectively;

• May perform assembly of custom products using little or no documentation;

• Maintains clean and orderly workstation;

• Accurately records and completes all manufacturing documentation;

• Identifies production problems and their causes;

• Suggest methods for improvement.

• High school diploma or general education degree (GED);

• Three to five years experience in a GMP Environment;

• Ability to read technical documentation associated with production;

• Ability to use microscope to perform assembly and/or inspection process;

• Ability to use and read measuring devices;

• Ability to follow complex instructions;

• Understands the importance of regulatory (GMP, ISO) requirements.

Profile

Good 3D vision, calm, patient, enjoys working with small delicate parts, motivated and enjoys teamwork.

Description

Assembles Catheters in a GMP (Good Manufacturing Practices) environment

Requirements

• Assembles products according to approved standard operating procedures;

• Works at different workstations as production requires;

• Conducts quality inspection of own or other’s work;

• Follows all safety and production standard operating procedures;

• Ability to follow procedures and execute them effectively;

• May perform assembly of custom products using little or no documentation;

• Maintains clean and orderly workstation;

• Accurately records and completes all manufacturing documentation;

• Identifies production problems and their causes;

• Suggest methods for improvement.

• High school diploma or general education degree (GED);

• Three to five years experience in a GMP Environment;

• Ability to read technical documentation associated with production;

• Ability to use microscope to perform assembly and/or inspection process;

• Ability to use and read measuring devices;

• Ability to follow complex instructions;

• Understands the importance of regulatory (GMP, ISO) requirements.

Profile

Good 3D vision, calm, patient, enjoys working with small delicate parts, motivated and enjoys teamwork.

Description

The Electrical Engineering Specialist applies principles and techniques of electrical / electronic engineering to accomplish tasks and goals and utilizes computer-assisted engineering and design software and equipment to perform assignments. A wide degree of creativity and latitude is expected, as is the ability to work under minimal supervision.

Requirements

• The incumbent shall supervise subtasks and assignments related to product development and sustaining engineering.
• Subtask supervision of engineering resources in the performance of analysis related to the design, development and implementation of electrical / electronic hardware for products.
• Supervise and performs performance tests and trouble-shooting on a variety of electrical / electronic system hardware including circuit boards, processors and wiring.
• Supervise and performs testing, investigation and analysis on components, boards, sub-assemblies and systems related to customer complaints.
• Maintains accurate documentation in compliance with the company’s quality system.
• Is responsible for setting up, checking, and correcting operational and experimental electrical / electronic machinery, circuitry, and equipment adhering to pre-established guidelines of the organization's engineering specifications.
• Writes, implements and analyzes and executes test procedures for system verification / validation.
• Provides engineering support for clinical investigation and resolution of product complaints and safety issues.
• May be required to review and assess engineering design changes.
• Assists and supports Field Service in taking care of all customer needs.
• May work with other engineering teams to increase efficiency, production quality and volume.

Qualifications

• Bachelor degree in electronic engineering or biomedical degree with an electrical concentration, or equivalent. Master degree preferred.
• At least three years experience in comparable position. Experience in: design, assembly, inspection, testing and trouble-shooting of electronic circuits.
• Experience working with multiple energy modalities; experience with RF, ultrasound, or Cryo technology is preferred. RF circuit design experience (400 kHz to 10.0 MHz) with good working knowledge of EMC / EMI.
• Embedded design experience, including working FPGA, CPLD, PAL, GAL, micro-controller (Microchip / Motorola) with CAE / IDE tools; communication interface protocols (RS232, USB); memory storage devices, etc.
• Good written and verbal communication skills in English and French. Proficiency in MS Office products.
• C / C++, Visual Basic Programming Language experience / knowledge;
• Strong ability to analyze technical drawings and specifications.
• Familiarity with CAD (Orcad, Protel, etc.)
• Experience with statistics and data analysis.
• Customer service experience would be an asset.
• Knowledge of medical device industry, quality system, and FDA regulation a plus.

Profile

• Dynamic, leading by example, able to motivate others to proactively deal with complex challenges under pressure.
• Strong analytical judgment backed by a rigorous scientific and technical reasoning.
• Detail oriented, organized and effective.
• Excellent team player.