Validation Engineer- Training And Placement

ABOUT E-CQR GROUP:-

E-CQR is a San Diego based company which serves the technology needs of fortune 500 businesses as well as some mid-sized organizations. We pride ourselves on our team of experienced professionals who understand that serving your needs directly translates to our mutual success.

Some of our Fortune 500 clients include Medtronic, Abbott, Boston Scientific, Pfizer, AT&T, Paypal, Ebay, PG&E, US Airways, Salesforce.com etc.

Why should you consider E-CQR?

• We train our professionals with real time industry based scenarios from the get go.

• Our mentoring team is a team of highly skilled technical experts dedicated to training you.

• Our marketing team consists of more than 100 members with seasoned IT staffing experience.

• Over 200 consultants on our payroll with leading clients.

• 50 plus direct customers.

• E-Verified Company.

• We sponsor H1B and Green card.

We are seeking fresh graduates for our Direct Clients. This will be a great opportunity for Mechanical, Chemical, Electrical, BioTech and Pharma graduates, as there are a number of Validation and Verification engineers positions that are available.

Our Clients are open to hire solid talent with any Visas. OPTs, Green card holders and US citizens from the relevant background are welcome to apply.

Training will be provided for the right candidates in order to ensure that they are well equipped to perform the required tasks.

RESPONSIBILITIES:

• Responsible for designing, developing and maintaining test cases.

• Responsible for executing Verification and Validation test cases and compiling results in

accordance with processes.

• Installing and maintaining test equipment in the lab for V&V activities.

• Uses Defect Tracking System to report and/or resolve product issues.

• Participate in cross-functional project team meetings.

• Performs duties in compliance with environmental, health and safety related site rules, policies or governmental regulations.

• Performs other related duties as assigned.

REQUIREMENTS:

• Familiarity with windows based applications.

• Detail oriented, strong analytical and problem solving skills.

• Flexible to work second shifts when needed.

• Self-motivated person that can work individually and be part of a cross functional team.

• Medical device and regulatory experience is a plus.

• Work well in a team-oriented environment as well as on your own.

Freshers who are looking to start their career are also welcome to apply.

Job Type: Full-time/ Contract

Salary: $28.00 to $32.00 /hour

with Benefits