Sr. Technical Instrument Support Engineer
Job Title
Sr. Technical Instrument Support Engineer
We’re empowering smarter medical and economic decision making to help transform the way people manage their health at all stages of life. Every day, more than 10 million tests are run on Abbott’s diagnostics instruments, providing lab results for millions of people.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:
- Career development with an international company where you can grow the career you dream of.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- An excellent retirement savings plan with a high employer contribution
- Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
- A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
- A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
The Sr. Technical Instrument Support Engineer position works out of our South Portland, Maine location within the IDDM Infectious Disease Developed Markets Division. In this role, you’ll have the opportunity to work on integrated business initiatives for on-market instruments, with R&D, marketing, commercial, finance, operations, quality and regulatory.This role will work on the design, development, V&V and transfer to production of design changes to on-market instruments within our business. You’ll have a strong focus on ensuring compliance to our quality system, as well as other business and regulatory standards that apply instruments.
This function will execute project plans and create deliverables for each design change initiated, ensuring successful transfer to production and manufacturing flexibility.
What You’ll Work On- Drive technical design for hardware, PCBs, Mechanical assemblies, Software and requirements documents.
- Responsible for implementation and execution of the product lifecycle roadmap. Drive daily progress, as well as plan/maintain for strategic and supply considerations.
- Communicate effectively and participate on a cross functional design team.
- Develop manufacturing test specifications including ICT, functional, and final test. Conduct and participate in design specification reviews. Manually verify test processes prior to implementation using common electrical test equipment.
- Specify and validate manufacturing test processes for medical monitoring instruments in accordance with applicable regulatory standards. Utilize statistical methods for determining variation and performance of test equipment.
- Coordinating pilot builds, acceptance, and transition to production activities with US and OUS Contract Developers and Manufacturers.
- Plan and execute verification and validation testing for design changes of on-market instruments.
- Identify and implement alternate sources for obsolete parts.
- Familiarity with documentation control tools and writing Engineering Change Orders, as required.
- Strong knowledge of defined development process that is consistent with ISO, FDA or any recognized quality standards and requirements.
- Own and drive the closure of quality events, deviations and CAPA’s.
- Responsible for project delivery on time and within budget.
- Drive gross margin improvement from technical solutions.
- Identify and own implementation of method-based culture for problem solving.
- B.S. in electrical, biomedical, or mechanical engineering discipline
- Minimum five years total experience in supply chain, finance, engineering, quality and analytics
- Experience to include leading people (direct and indirect), preparation and delivery of presentations to senior stakeholders, audit and inspection readiness, business process mapping/optimization and cost improvement.
- Experience with Third-Party (Contract) Manufacturers and other external resources
- Direct manufacturing, or manufacturing support, experience
- Experience with FDA, ISO design control standards
- Experience with the product lifecycle – from transferring new products to market through sunset
- Proficient in understanding hardware and software interfaces and their impact to the customer experience
- Experience in process change management projects/initiatives
- Experience in working with supply chain and manufacturing to achieve business goals and drive results in a dynamic business environment
- Experience with SAP or equivalent
- B.S. in biomedical, electrical, or mechanical engineering discipline
Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.
The base pay for this position is $75,300.00 – $150,700.00. In specific locations, the pay range may vary from the range posted.