HCLTech is a global technology company, home to 222,000 people across 60 countries, delivering industry-leading capabilities centered around digital, engineering and cloud, powered by a broad portfolio of technology services and products. We work with clients across all major verticals, providing industry solutions for Financial Services, Manufacturing, Life Sciences and Healthcare, Technology and Services, Telecom and Media, Retail and CPG and Public Services. Consolidated revenues as of 12 months ending December 2022 totaled $12.3 billion. To learn how we can supercharge progress for you, visit ;/p>

HCLTech is looking to hire a Jr. Verification engineer with experience in Lab Equipment, software verification or development.

This opportunity requires to work onsite at St. Paul, MN. No privilege for remote or hybrid.

Detailed description/responsibilities:

• Bachelors in Engineering (Computers, Electrical, Bio-medical or any other related). Master s degree in relevant field is preferred.
• Minimum of 0-2 years of experience in medical device domain or related industry. Experience in verification/testing is preferred.
• Good Documentation and communications skills to perform test method development, technical report writing and client interactions.
• Strong analytical and troubleshooting skills for investigations.
• Knowledge of Basic Electrical Engineering principles
• Experience using Lab Equipment
• Experience in software verification or development is preferred.
• Knowledge in programming language
• Knowledge and experience of Computer Software Architectures, Networking protocols, and embedded software & devices.
• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
• Ability to leverage and/or engage others to accomplish projects.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.
• Strong organizational and follow-up skills, as well as attention to detail.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
• Performs other related duties and responsibilities, on occasion, as assigned.
• Ability to maintain regular and predictable attendance.