Data quality engineer serp_jobs.h1.location_city

The Opportunity

We are seeking a Quality Engineer to work at our Temecula, CA location in our Vascular division. This is a full on-site role.

Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.

WHAT YOU'LL DO :

Perform Abbott Vascular quality engineering activities by developing and maintaining data integrity and cybersecurity policy, standards, applications, systems, etc. Work closely with R&D, Equipment Engineering, Quality Engineering and IT on risk identification and mitigation activities. Facilitate cross functional team collaboration to achieve data management goals.

• Support project planning and perform assessments and mitigations with cross functional teams. Develop and manage training programs including training material and training audience. Track and report metrics.
• Provide support to internal and external audits. Manage relevant audit findings and CAPAs.
• Continuously improve processes to align with current and emerging regulatory and customer requirements and best industry practices. Collaborate with AV key stakeholders, Abbott corporate functional groups and other Abbott business units.
• Responsible for compliance with applicable Corporate and Divisional Policies and procedures.
• Independently, or lead a project team to, identify, plan and conduct medium-size assigned projects requiring a combination of conventional and custom risk-managed execution plans and investigations. manages multiple often concurrent projects.
• Lead technical projects with inter-coordinating elements where problem resolution may involve the application of new methods and / or approaches and may require consideration of impact with other system components and / or users.
• Lead and / or participate on cross-functional teams to support organizational goals.
• Responsible for completing documentation in a timely manner and in accordance with business standards.
• Serve as a subject matter expert (SME) on a subset or select subsets of a project's technical matters. may interface with external firms or agencies.
• Responsible for implementing the effectiveness and maintaining compliance of the Quality System. (e.g. compliance with internal procedures and FDA, BSI regulations etc).
• Interacts with internal and external customers, by meeting regularly, responding to requests and explaining procedures.
• Interprets and executes policies that affect work processes and personnel within the assigned organizational unit.
• Contributes to the development of operational policies and procedures that affect personnel within the assigned organizational unit.
• Assists with evaluating project costs.
• Identifies, develops and implements processes to improve department performance.
• Implements improvements to Quality Systems and tools by directing personnel to gather data on existing quality tools, identify weaknesses, and research / select new tools based on findings.
• Ensures sustaining support of Quality System and regulatory compliance by individually working quality system issues and by delegating project work for maintaining quality system capability.

Required Experience

Please note that the salary range listed is our full grade range. We usually hire based on the mid-point. There is no relocation offered for this role.