Senior Manufacturing Engineer
Company: BAXTER
Location: Skaneateles
Posted on: August 7, 2022
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Job Description:
This is where you save and sustain lives At Baxter, we are
deeply connected by our mission. No matter your role at Baxter,
your work makes a positive impact on people around the world.
You---ll feel a sense of purpose throughout the organization, as we
know our work improves outcomes for millions of patients.
Baxter---s products and therapies are found in almost every
hospital worldwide, in clinics and in the home. For over 85 years,
we have pioneered significant medical innovations that transform
healthcare. Together, we create a place where we are happy,
successful and inspire each other. This is where you can do your
best work. Join us at the intersection of saving and sustaining
lives--- where your purpose accelerates our mission. Your role at
Baxter The Senior Manufacturing Engineer reports to the Senior
Manager Manufacturing Engineering. In this role you will support
several manufacturing assembly lines within the Final Assembly
Department. You will partner with cross - functional operations
teams members (i.e. Production Supervisor, Quality Assurance
Engineer, and Materials Planning) to optimally identify,
investigate and resolve manufacturing process related issues. In
addition, you will drive continuous improvement initiatives in
support of departmental, site and corporate objectives for Safety,
Quality, Delivery, Productivity, and Cost Performance. Your team We
are a team of inquisitive individuals who embrace a collaborative
environment to tackle sophisticated challenges that meet the needs
of our patients. We often need to change directions and respond to
issues to avoid disruptions in our fast-paced manufacturing
environment. Together, we build and maintain a positive work
environment. Our engineering team at Skaneateles Falls is dedicated
to quality. Delivering life-saving products is about getting them
right, and our technical expertise and experience working in a
manufacturing environment empower us to meet that challenge. When
you join us, you will work with a team of committed individuals who
trust each other to deliver on the tasks at hand. We support
innovation and out-of-the-box thinking balanced with teamwork
across functions and other teams. Our leadership understands the
need for continuous education and provides opportunities for
further development. What you'll be doing Member of
multi-functional Final Assembly ---Gemba--- Team with
responsibility for 10-12 medical device manufacturing assembly
lines. Develop and maintain manufacturing process documentation
including but not limited to: Manufacturing Process Specifications,
Device History Records, Tooling/Equipment Specifications,
Preventative Maintenance and Calibration procedures through
Engineering Change Management (ECM) process. Perform and document
root cause analysis for Non-Conforming Material Reports. Summarize
and report on departmental Safety, Quality, Delivery, Productivity,
and Cost performance measures. Use Lean/Six Sigma methodology to
identify and drive Continuous Improvement Projects to improve
Safety, Quality, Delivery, Productivity, and Cost performance
measures. Develop and manage process and Equipment
Validation/Verification Strategies for new or changing
manufacturing process elements. Develop and implement Engineering
Builds and assist with Material Qualification Planning to support
new or changing component requirements. Perform and document Impact
Assessments and Corrective Actions for Equipment Remediation---s
associated with out of tolerance calibration results. Proactively
identify and address safety related issues through Near Miss
Reporting Process. What you'll bring Required: A Bachelor---s
degree, or equivalent, in a relevant Engineering subject area. Two
to four years of solid work experience in a related field.
Preferred: Experience in the Medical Device or a similar regulated
industry. SAP, CAD modeling, Schematic drafting, PLC programming,
and/or Visual Basic programming experience is a plus. LI-AD
IN-USOPS The successful candidate for this job may be required to
verify that he or she has been vaccinated against COVID-19, subject
to reasonable accommodations for individuals with medical
conditions or religious beliefs that prevent vaccination, and in
accordance with applicable law. Equal Employment Opportunity Baxter
is an equal opportunity employer. Baxter evaluates qualified
applicants without regard to race, color, religion, gender,
national origin, age, sexual orientation, gender identity or
expression, protected veteran status, disability/handicap status or
any other legally protected characteristic. EEO is the Law EEO is
the law - Poster Supplement Pay Transparency Policy Reasonable
Accommodations Baxter is committed to working with and providing
reasonable accommodations to individuals with disabilities
globally. If, because of a medical condition or disability, you
need a reasonable accommodation for any part of the application or
interview process, please click on the link here and let us know
the nature of your request along with your contact information.
Recruitment Fraud Notice Baxter has discovered incidents of
employment scams, where fraudulent parties pose as Baxter
employees, recruiters, or other agents, and engage with online job
seekers in an attempt to steal personal and/or financial
information. To learn how you can protect yourself, review our
Recruitment Fraud Notice .
Keywords: BAXTER, Syracuse , Senior Manufacturing Engineer, Engineering , Skaneateles, New York
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