Job title: Senior Engineer Clinical Software
Company: Abbott
Job description: JOB DESCRIPTION:
Senior Engineer Clinical Software
Working under limited supervision, performs complex and specialized level software project activities in such areas as
Development, Tools, Test, Requirements and/or related areas. Assignments may include, but are not limited to, analyzing
requirements, planning and scheduling data, updating and maintaining different software specifications based on analysis of
specifications, needs and improvements, as well as troubleshooting, debugging, and maintaining of software, test, or tool
designs, cases, scripts, procedures, and/or code based on strategic analysis. Functions as lead on project teams and may
supervise other engineers. Work requires the application of theoretical engineering principles, evaluation, ingenuity and
creative/analytical techniques typically acquired in a recognized four-year or more academic course of specialized study.
Applies engineering and scientific principles to the evaluation and solution of technical problems in a creative manner unique
to each study. Exercises level appropriate technical judgment in planning, organizing, performing, and/or coordinating
engineering work.
- Working from requirement specifications, develops, maintains, and updates detailed design and interface specifications;
- Participates in and supports the implementation, development, enhancements, and modifications to software source code,
scripts, and procedures;
- Debugs, troubleshoots, and isolates software problems as well as offers strategic solutions, analysis, and advice regarding
identified issues for future development;
- Identifies parameters, structure, and critical test components. Writes, updates, or executes test design, cases, as well as
procedures and reports results.
- Writes, updates, and maintains requirement and interface specifications;
- Contributes to and supports gathering, analyzing, and validating requirements;
- Contributes to and supports writing, updating, developing and maintaining Hazard/Risk analysis specifications;
- Contributes to and supports root-cause analysis of failures.
- Working from requirement specifications, develops, maintains, and updates test requirements and design;
- Supports implementation, enhancements, and modifications to test cases, procedures, scripts, and code;
- Debugs, troubleshoots, and isolates software problems and offers strategic advice regarding identified issues for future
development;
- Identifies parameters, structure, and critical test components. Writes, updates, or executes test design, cases, as well as
procedures and reports results.
- Presents at design reviews; documents and resolves issues as directed.
- Contributes to and supports a variety of test phase efforts.
- May write and update requirement specifications for an assigned area.
- Reviews project deliverables such as specifications, code, and test/tool procedures for feasibility, thoroughness, clarity,
correctness, and accuracy.
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS),
Environmental Management Systems (EMS), and other regulatory requirements.
- 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.
JOB FAMILY: Clinical Affairs / Statistics
DIVISION: MD Medical Devices
LOCATION: India
New Delhi : No. 100, 1st Floor, Okhla Industrial Estate, Phase III
ADDITIONAL LOCATIONS:
WORK SHIFT: Standard
TRAVEL: Yes, 10 % of the Time
MEDICAL SURVEILLANCE: Not Applicable
SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Expected salary:
Location: New Delhi
Job date: Fri, 03 Jun 2022 00:25:55 GMT
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