Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Technical Application Specialist (Northern NJ)

Expired Job

Siemens Corporation Bridgewater , NJ 08807

Posted 2 weeks ago

Division: Siemens Healthineers

Business Unit: Laboratory Diagnostics

Requisition Number: 231898

Primary Location: United States-New Jersey-Bridgewater

Other Locations: United States-New Jersey-Morristown

Assignment Category: Full-time regular

Experience Level: Mid level

Education Required Level: Bachelor's Degree

Travel Required: 80%

Division Description:

Siemens is a global technology powerhouse that has stood for engineering excellence, innovation, quality, reliability and internationality for more than 165 years. As a global technology company, Siemens is rigorously leveraging the advantages that this setup provides.

To tap business opportunities in both new and established markets, the Company is organized in nine Divisions: Power and Gas, Wind Power and Renewables, Energy Management, Building Technologies, Mobility, Digital Factory, Process Industries and Drives, Healthineers and Financial Services.

With 45,000 employees Siemens Healthineers is one of the world's largest suppliers of technology to the healthcare industry and a leader in medical imaging, laboratory diagnostics and healthcare IT. All supported by a comprehensive portfolio of clinical consulting, training, and services available across the globe and tailored to customers' needs. So that more people can have a life that is longer, richer, and more filled with happiness.

For more information, please visit:

Job Description:

Position Overview

Open to qualified candidates in the northern New Jersey area,the Technical Application Specialist (Chemistry and Immunoassay) will solveproblems independently and within established policies and procedures. Theprimary objective is "to do what it takes" to ensure customer satisfaction aswell as timely system implementation and training.


Management of customer base and growing the business in the Region. Thisposition is responsible for the orchestration of implementation plans withcustomers for new instruments; Facilitation of training rotations and scheduleswithin the lab to insure cross training for all operators on all shifts;Development of timeline for acquiring samples, implementing tests and start upstrategies within defined guidelines; Assistance in facilitating the propercustomer support for technical issues.

Required Knowledge/Skills, Education, and Experience

Demonstrates single system products, participates in customer training and pre-and post sales support of clinical product offerings. Participates in-houseclinical trials.

Participates in training courses for customers and companypersonnel on the working aspects of single system clinical equipment and communicatesthe technical and clinical information, ensuring customer utilizes equipmentwith efficiency and skill in appropriate applications. May participate inproduct promotion for tradeshows and seminars. Supports development of customerrelationship.

Provides most complex feedback and recommendations from customersto product development groups. Education: BS/BA in related discipline, oradvanced degree, where required, or equivalent combination of education andexperience. Certification may be required in some areas. Must have cleandriving record over past 3 years.

Preferred Knowledge/Skills, Education, and Experience

BA/BS preferably in MedicalTechnology; thorough technical knowledge of medical technology; 2+ years oflaboratory

experience; prior fieldexperience is preferred; prior field experience with Siemens Dimension , VISTAand ADVIA Centaur. IMMULITE family will be a plus, strong communication and interpersonal skills to effectively handle customerproblems and support the sales team's efforts; ability to prioritize

critical customers and handle thecrisis customers first; computer literacy is mandatory (Word, Excel,PowerPoint, Outlook, etc.); strong presentation and selling

skills; must be completely alignedwith the corporate Vision, Values and Beliefs; job requires a large amount ofdriving

within the region.


See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Application Development Lead Statistical Programming Bridgewater NJ


Posted 1 week ago

VIEW JOBS 11/11/2018 12:00:00 AM 2019-02-09T00:00 Provides technical leadership and application development support to project teams on all statistical programming matters involving standard tools and technologies utilized by the biostatistics & programming (B&P) user community. Provides technical expertise in SAS graphics, R and other statistical computing software, and serve as a go-to person on programming technical issues. Provides project management and support to the development and evaluation of department applications, tools, and standards. Serves as a B&P internal expert to provide sustained support on the future generation of B&P tools, leads the creation and maintenance of the B&P report template library in the implementation of B&P tools and applications. Provides support and mentoring to the junior level staff with an emphasis on technical capabilities. Responsibilities: * Collaborate with the ITS/systems group on the development and maintenance of tools and systems associated with department standards and technologies.     * Define and/or improve the strategy for the implementation of the global reporting standards in the department based on industry standards and regulatory requirements. * Lead the creation and maintenance of the department report template library in the implementation of department tools and applications. * Lead and/or contribute to programming development and quality control of the programming deliverables utilizing standard tools and methodologies. Mentor others on the use of department standard tools when programming clinical data or system application deliverables. * Create formatted output for use in clinical study reports, publications, presentations, submission and response to regulatory authority queries. * Provide user support of department tools and standards. Provide technical guidance to the project teams on all statistical programming matters involving standard tools and technologies related projects as needed. * Support department initiatives and task forces. Lead/participate in departmental or cross-functional working groups and process improvement activities. * Identify areas for improvement and recommend solutions related to systems, reporting tools, technologies, and best programming practices. * Actively participate in department working groups, provide input in development of tools applicable to process improvement.     Required Education/Experience: * A candidate with a Master degree and 5+ years of programming experience preferably in processing clinical trial data in the pharmaceutical industry. * A candidate with a Bachelor degree and 7+ years of programming experience preferably in processing clinical trial data in the pharmaceutical industry.  * Excellent technical skills in statistical programming, with advanced knowledge in SAS, R and other statistical computing software. Preferably with background in both statistics and computer science. * Demonstrated experience and strength in developing and maintaining statistical analysis and reporting tools / systems. Extensive understanding of reporting systems utilizing multiple data delivery applications. * Solid understanding of clinical trial data and the technical requirements of analysis and reporting in clinical trials. * Extensive experience in the development and execution of project user requirements, system design, validation plans, development and implementation. * Experience with other programming languages such as C++, Java, etc. typically used for software development in a global environment. * Strong understanding of pharmaceutical clinical development (i.e. understanding of statistical concepts, techniques and clinical trial principles) and ability to provide programming support needs for NDA and other regulatory submissions. * Understanding of regulatory requirements concerning electronic submission standards with particular emphasis on item 11 deliverables. * Knowledge of CDISC data structure requirements. * Understanding of relational database structures and their correlation to submission ready database structures. * Excellent project management skills. Ability to effectively organize and manage multiple assignments with challenging timelines for the development of tools to facilitate creation and execution of statistical deliverables by the end-user. * Collaborative teamwork and interpersonal skills that demonstrate initiative and motivation. Strong problem solving skills. Excellent verbal and written communication skills in a global environment. * Experience in collaboration with external partners and/or vendors. * Ability to estimate resource requirement.    Preferred Education: * A candidate with an advanced degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related field, preferred Sanofi US Services, Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. #LI-SA #GD-SA At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all. Apply For Role Sanofi Bridgewater NJ

Technical Application Specialist (Northern NJ)

Expired Job

Siemens Corporation