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Company | Abbott |
Address | Los Angeles, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-07-31 |
Posted at | 10 months ago |
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
- 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.
- Contributes to the evaluation and validation of a specific subsystem or project prior to submission.
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
- Facilitates the transition of algorithms and system requirements into new projects through collaborative review and evaluation. Assesses the clinical and software risks of new algorithm designs and features, and identifies potential interactions with existing ones.
- Gathers and analyzes input requirements for medical devices, supporting instrumentation/service infrastructure, and translates these into specific system requirements/interface specifications. Participates in broad cross functional review of work output. Updates and maintains feature specifications for one major project and may support one or more minor project.
- Provides input into the development of clinical system validation plans, and the conduct of those tests.
- Identifies and resolves issues, escalating as appropriate.
- Leads/owns pre-defined tasks within a larger effort such as definition or product development of a sub-system, and drives them to on-time, high quality completion.
- Interacts with functional groups as necessary to conduct technical feasibility, understanding of requirements and correct interpretation of software requirements.
- Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
- Multitasks, prioritizes and meets deadlines in timely manner. Strong organizational and follow-up skills, as well as attention to detail.
- Relevant, progressively more responsible work experience in medical product development.
- Experience working in a broader enterprise/cross-division business unit model preferred. Ability to work in a highly matrixed and geographically diverse business environment.
- Professional certification or designation preferred.
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
- Ability to leverage and/or engage others to accomplish projects.
- Ability to travel approximately 10%, including internationally.
- Demonstrated ability to effectively integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. Medical device industry experience preferred.
- The stability of a company with a record of strong financial performance and history of being actively involved in local communities
- Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
- Training and career development, with onboarding programs for new employees and tuition assistance
- Paid time off
- 401(k) retirement savings with a generous company match
- Financial security through competitive compensation, incentives and retirement plans
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