Contract Opportunity: Quality Engineer Analytics _Carlsbad, CA@ lisa@sriventech.com

Hi Partners,

This is Lisa, Sr. Technical Recruiter with Sriven Technologies. I have an exciting or challenging contract job as below, Please have a look at the detailed job description below and reply back with your latest updated word resume for client submission. If you have best consultant please call me on 703 842 4866 Ext 316.

Position: Quality Engineer Analytics

Location : Carlsbad, CA

Duration: Long Term

Job Description:

The Quality Engineer will report into the Analytics Manager and will assist in the daily support/maintenance of data/reporting needs of the Patient Monitoring & Recovery (PMR) unit.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

· Design, create, verify/validate routine and adhoc reports regarding various aspects of complaint activities to a multitude of different departments located in different locations.

· Designing and maintaining SharePoint sites that are related to Post Market Vigilance (PMV) Activities. Information loaded to the site is used by the department as reference material, so up-to-date data is essential.

· Build and maintain Access databases used for monthly and adhoc reporting

· Develop and maintain tools for use by business operations where they can pull data on demand and tools to assist in their analysis of business operations

· Suggest and implement system improvements based on user requests

· Provide training and administer the Complaint Tracking System (CTS) or other tools developed within the team

· Generate T-SQL and Access queries, charts and perform analysis of complaint data in support of

· Monthly metrics

· Corporate metrics

· Product Quality Improvement Teams

· Provide technical support to projects related to CTS, as required.

· Support MITG-wide PMV Analytics improvement projects, as required.

· Generate/develop trend reports

· Participate in process improvement projects such as:

· Complaint tracking system improvements

· Provide backup support for other CTS administrators.

· Provide backup support for the corporate monthly metric report

· Assist with various Analytic projects (i.e. data mapping, validation, database table assessments, etc).

Required

· Education: Associate Degree or 3+ years of experience in a similar role

· Data management: 2+ years in a data management, statistical, and/or analytical role in medical devices, pharmaceuticals, biotechnology or healthcare. Candidates with data management, statistical and/or analytical experience from other industries will be considered

· Project Management: Small scale project management

· D/B Management: Familiar with T-SQL, Access, Business Objects

· BI Tools: Familiar with BI software/tools such as Tableau, TIBCO SpotFire, SAS

· Query Writing: Advanced level building queries in Access, SQL or in similar languages tools

· Excel Experience: Solid background with standard formula building, nested IF statements, standard calculations, Vlookup, Hlookup, charting/graphing, pivot tables and can build advanced formulas (macro knowledge is a plus)

· System Validation: 2+ years’ experience validating systems, writing test protocols preferably in a regulated industry such as biotechnology or healthcare

· SharePoint: Working knowledge of SharePoint sites and is able to build SharePoint sites for collaboration and documentation purposes. InfoPath experience a plus.

· Proficiency in Word, PowerPoint, Visio

· Have the ability to write work instructions in an easy to understand manner for the non-technical audience.

· Demonstrated ability to communicate clearly both verbally and in writing

· Must be a team player – willing to work with other departments and divisions

· Excellent documentation and communication skills.

· Attention to detail and a commitment to quality work

· Detail oriented and highly organized

· Excellent customer service skills

· Requires some direction but then is able to work with minimal supervision on repeated/similar tasks

Preferred

· Programming experience a plus

· Knowledge of quality control concepts a plus

· Knowledge of the FDA Quality System Regulations and ISO Quality System Standards a plus

· Post-Market Vigilance/Surveillance and/or Patient Safety/Risk Management experience a plus.

Please Fill the details:

Candidate Information

Full Name:

Rate:

Current Location with Zip code:

Telephone Numbers:

Email ID:

Work Authorization & Expiry:

Education Qualification along with University and Year of passing:

Date and Time available for interview:

Date available to start (After confirmation):

Interested in Face to Face Interview:

Reason For Change:

Currently ON or OFF the Project:

Last project ended (MM/YY):

Relocation:

Total IT Experience:

USA Experience:

Skype ID:

Two References:

Name:

Client:

Phone:

Email:

Name:

Client:

Phone:

Email:

Thanks & Regards . . . ?

LISA

Technical Recruiter

Lisa

Direct # 703 842 4866 EXT 316 | Fax # 866-725-286

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