Software Quality Engineer M2S, Inc.
M2S, Inc. provides technology and services for the healthcare industry to manage clinical information and utilize it to improve the quality of patient care and reduce costs. Powered by our advanced technological infrastructure and years of experience working in a regulatory environment, M2S is the leader in enterprise healthcare management solutions.
We are seeking a Software Quality Engineer. This position will validate software and coordinate the implementation of the software into the production environment. It is a great opportunity to work in a fast paced, team oriented environment.
Software Quality Engineer
This position will work with the software development team throughout the software development life cycle to:
Assist in the creation of product requirements documentation.
Develop software verification and validation test plans for new products.
Perform the validation and verification of product upgrades.
Create, perform and maintain manual and automated software test scripts for web-based and client-server applications running on both Linux and Windows operating systems.
Create and maintain test data sets and test environments.
Generate detailed reports summarizing the testing effort.
Review and update software documentation and maintain bug records.
Schedule and drive design review meetings.
Manage the software release process.
Ensure compliance with M2S? quality system, ISO 13485, ISO 14971, and FDA QSR
Assist in the development of new software quality initiatives, participate in quality system development, write and review procedures to improve quality and reliability of software.
Candidates should be highly motivated, detail-oriented, self-directed, and flexible with the ability to handle multiple tasks simultaneously. Working in a team environment with constant communication and collaboration is a must to be successful in this position. Ideal candidates will meet the following requirements:
5 years? experience in Software Quality Assurance.
Demonstrated success in project team environment.
BS in computer science, or equivalent experience
Proactive, with strong analytical, team, time management, and project management skills.
Track record of successfully prioritizing, multi-tasking, and working to agreed schedules.
Experience handling multiple projects simultaneously with minimal oversight.
Excellent written and verbal communication skills.
Experience with GMPs, GCPs, ISO 13485, ISO 14971, 21 CFR Part 820 FDA standard, and HIPAA.
Experience in an agile environment.
Familiarity with FDA Guidance on Clinical Trials.
We recognize that talented people are attracted to companies that provide competitive pay, comprehensive benefits packages and outstanding advancement opportunities. For this reason we offer a Comprehensive Benefits Plan that includes the following:
401K and Company match
Discount fitness memberships
Flexible spending accounts
Employee life insurance
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