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Your role at Baxter: This description outlines the employment prerequisites and job responsibilities for the position of Manufacturing Engineer within the Continuous Improvement Team. Provide support in the execution of the site’s operational optimization and quality improvement projects to achieve Medina Plant goals and objectives. Drive/support various quality improvement, business continuity/expansion, and cost reduction initiatives from identification through implementation while working with cross functional resources to ensure results are achieved in a timely manner
Job Responsibility:
Creation/modification of process flows within the Manufacturing/Service Departments
Development and maintenance Manufacturing/Service Work Instructions and related documents
Creation/modification of fixtures, tooling, equipment and systems to support operations
IQ, OQ, and PQ of fixtures, tooling, and equipment
Identify, investigate, and resolve operational issues to improve First Pass Yield and reduce waste
Improve throughput constraints and capacity management
Monitor and drive corrective action and continuous improvement activities that directly impact performance measures by performing primary investigations, conducting data analysis, and implementing corrective actions
Support corrective and preventive actions in manufacturing using formal problem-solving tools and documentation
Requirements:
Medical Device Experience with knowledge of 21CFR820 preferred
Must be able to work well as a member of a team with the ability to adapt quickly to changes and work efficiently in a fast-paced environment
Experience with statistical software packages (Minitab is a plus)
Experience with Quality Systems and process controls in the medical device industry is desirable
Knowledge and working application of FDA cGMP
ANSI/ISO/ASQC requirements
Knowledge and working application of technical part drawings and GD&T principles (experience with CAD or SolidWorks is desirable)
Demonstrated application of engineering principles on individual/small projects and ability to work with cross functional teams to successfully implement quality improvement and cost reduction initiatives
Demonstrated strong analytical problem solving (Root Cause Investigations)
Lean Six Sigma Certification is preferred
Computer competency in MS Office Suite is required
statistical software experience (ex: Minitab) is desirable
Ability to multi-task and methodically manage projects
A bachelor’s degree in engineering is required
Preferred candidates will have an engineering discipline focus in Biomedical, Mechanical, Industrial, Electrical or Chemical Engineering
1-3 years of Medical Device experience is preferred
Nice to have:
Experience with statistical software packages (Minitab is a plus)
Experience with Quality Systems and process controls in the medical device industry is desirable
Knowledge and working application of technical part drawings and GD&T principles (experience with CAD or SolidWorks is desirable)
What we offer:
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
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