About this Process Development Engineer II role at Abbott
JOB DESCRIPTION:
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
This position works out of our Santa Clara, CA location in the SH division.
Structural Heart Business Mission: Why We Exist.
Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease.
As the Process Development Engineer II, you will serve as the primary engineering personnel supporting manufacturing operations. The individual performing this role will have strong collaboration with the line supervisor, Quality Engineer and operators to address all the opportunities found in the assigned manufacturing line. This role will be accountable on quality, output and yield of the assigned manufacturing line. Will also serve as the engineering management representative in the manufacturing line, executing initiatives and working directly with the DL workforce. This person may also have a role beyond the line support engineering as a sustaining engineer for the department.
What You’ll Work On
- Responsible for assigned line output, safety, yield and quality. Responsible for identification of product defects and determination of operational and process related actions to reduce the defects. This may also include equipment trouble-shooting and sub-sequent work order request.
- Works with line support team (QC supervisor, Mfg. Supervisor, Quality Engineer and Operations) to perform on line issue triage to evaluate issues and determine if non-conformance is present, determine initial bracketing and containment, and generate corrective actions/preventative actions as needed.
- Responsible for product/process knowledge and understanding of basic cause and effect of line changes. Considered and expert in statistics, product and Engineering process.
- Responsible for modeling/drafting assemblies; fixtures & tools; Solidworks mid to advance level.
- Responsible for providing the line with related Engineering fixes, such as tooling (TLTs) and manufacturing aids (from idea definition to implementation). Knowledgeable of procedures related to equipment controls.
- Support technicians and supervisors in equipment availability issues.
- Supports Training and Certification Program. Provides additional insight on how to improve trainings and certifications in the best interest of the business.
- Responsible for determining quality impact of Out-of-Tolerance documents.
- Responsible for execution of line related change management (material, equipment and process changes). Responsible for CO and CR generation related to moderate to complex changes impacting the manufacturing line.
- Responsible for continuous improvement projects development and execution, including CAPAs implementations. Responsible for exception subtask execution.
- Evaluates ideas for continuous improvements.
- Leads root cause analysis efforts for high complexity manufacturing events, utilizing DMAIC model and A3s. Leads CAPA (Major) investigations with data gathering and analysis as needed. Owns CAPA activities without oversight.
- Runs studies and validations on the line as needed.
- Be the ME representative for manufacturing related projects including yield, CIP's, productivity, quality and safety.
- Responsible for coordination of product builds through the NPI process.
- Generates all types of changes to the eLHR system.
- Leads ME support during external and internal audits.
- Acts as coach and mentor to more inexperienced engineers or technical personnel.
- Leads statistical analysis for complex events at the site.
- Can generate qualification and validation protocols and reports with minimal oversight.
- Owns basic to medium to high complexity CR activities with no oversight.
- Demonstrates comprehensive understanding of regulations in area of work and where to look for information. Considered SME for most Engineering matters.
- In conjunction with RA:
- Understands regulatory implications of proposed changes.
- Understands what types of changes require filings. Completes documentation to support regulatory filings with oversight. - Minimal oversight required for problems or assignments of reasonable difficulty. Makes decision in an efficient manner, even when having limited information.
- Considers risk mitigation in planning based on lessons learned or from peers. Reviews previous similar projects and activities as part of the decision-making process. Anticipates potential situations that may impact projects timeline and resolves them before they become an issue.
- Prepares and provides well thought out contribution to meetings. Provides technical guidance to peers that facilitates the progression of the project, group or person.
- Can present information and collaborates with peers across functions (both internally and externally). Exposure to cross functional mgmt. communications.
- Leads manufacturing engineering projects of high complexity, including CIPs, CAPA, Validations.
- May have delegation authority for area manager.
Required Qualifications
- Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, or equivalent experience.
- 2-5 years of related work experience with a good understanding of specified functional area.
- Basic knowledge of applicable US non-US applicable regulations.
- Knowledge and proficiency in the application and principles of Manufacturing/Process Engineering.
- Ability to effectively communicate cross-functionally to assist with resolving Quality/Engineering issues.
- Excellent written, verbal and interpersonal communication skills
- Ability to interact effectively with all levels of employees.
- Knowledge of common office applications: Word, PowerPoint, Excel.
- Knowledge of statistical analysis.
- 3-D drawing (Solidworks required).
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
$85,600.00 – $156,000.00In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Manufacturing
DIVISION:
SH Structural Heart
LOCATION:
United States > Santa Clara : Building A - SC
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes, 10 % of the Time
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
