[9747MSCRMCV] Urgent Opening::::Software Engineer::::Northridge, CA::::12+ Months

Hi ,

 

Please review the following job description and if interested please share updated resume and best time to reach you.

 

Position:  Software Engineer - 46998

Location: Northridge, CA

Duration: 12+ Months

 

Job Duties: Contributes to the Verification Testing Process, Participates in Design and Code Reviews, Specifies, Designs, and Debugs, and Verifies Medical Applications Software, Participates in Software Requirements Specifications inspections

 

Required:

Education Level:                                                          Undergraduate Degree

Industry Experience:                                                    3 - 5 Years

Software Application Knowledge/Engineering: Acrobat Reader

                                                                                    MS Word

                                                                                    MS Excel

                                                                                    Software Application Knowledge

 

Written Communication:                                              Excellent

 

Desired:

Industry Experience:                                                    Greater than 5 Years

Software Application Knowledge/Engineering: MS Visio

                                                                                    MS Project

 

HM Notes:

·         Actual title is Requirements /Systems Engineer.

·         Experience in Requirements Management (gathering, creating, tracing) required, and requirements management systems (e.g., ReqPro, DOORS).

 

Required;

·         Experience in creating engineering documents in Word required. IBM ReqPro highly desired.

·         Contribute to the system design analysis and requirement analysis discipline for the array of CareLink Informatics medical device systems and products.

·         This engineering role requires a combination of disciplines to provide high quality product and software lifecycle development for a medical device information data management platform.

·         This role may involve team lead responsibilities.

 

Position Responsibilities

·         Interface with key stakeholders on new feature requirements for medical device software systems and products.

·         Perform requirements gathering, formulation, and analysis to capture needs and understanding of the requests and provide feedback to the stakeholders on these issues.

·         Create and manage Design Input requirements.

·         This includes system and product level requirements, use of a requirements management system and creation and management of requirements documents.

·         Interface with the development team and the test team on understanding, implementing, and testing of requirements.

·         Ensure complete coverage of requirements throughout the software lifecycle.

·         Work with stakeholders to help define product features that meet user needs and business goals.

·         Maintain and produce Design Control and software lifecycle procedures and plans to conform to department and company policies and procedures.

 

Basic Qualifications:

·         BSEE, BSCS or comparable industry experience.

·         At least 5 years' experience with software development lifecycle and/or engineering development practices.

·         Experience with configuration management tools and requirements management tools.

·         Experience with system design, component interfacing, complex systems architectures.

·         Requirements writing with an understanding of the key aspects of capturing and documenting high quality requirements, the different forms of requirements types and analysis.

·         Highly competent with MS Word. Capable with Excel.

·         Ability to work in a team environment.

·         Excellent verbal and written communications skills.

 

Desired/ Preferred Qualifications:

·         Experience with medical product development, design control process and quality system or regulatory environments (FDA/QSR, ISO 13485, standards and the basic Medical Device Directives requirements).

·         Programming/interfacing of medical devices in application use.

·         Experience with software test plan creation and management.

·         Project planning and scheduling.

·         Rational Requisite Pro experience.

·         PTC Integrity experience

·         Software programming experience.

·         Competent with UML or other modeling language.

·         Good meeting management techniques and skills.

                                                  

If interested revert with the following details:

 

First Name
Middle Name
Last Name
Postal Address
Contact Phone
Email Address
Education
Expected Rate
Willing to relocate/ Commute?
Work Authorization Status
Availability for Discussion
Availability for Face-Face
Availability to Join

 

 

Thanks & Regards

 

Aman Singh

Technical Recruiter

Email: asingh@syglo.com

www.synico.com

 

 

 

--
You received this message because you are subscribed to the Google Groups "CVMSCRM" group.
To unsubscribe from this group and stop receiving emails from it, send an email to cvmscrm+unsubscribe@googlegroups.com.
To post to this group, send email to cvmscrm@googlegroups.com.
Visit this group at http://groups.google.com/group/cvmscrm.
For more options, visit https://groups.google.com/d/optout.