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Johnson & Johnson · 3 days ago
Senior Engineer, Mfg Engineering
Irving, TX
Full-time
Hybrid
Mid Level
2+ years exp
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Responsibilities
Responsible to identify process improvement initiatives and develops proposals for problem solving, improvement or optimization.
Support process improvement projects that have the objectives of developing more cost efficient and quality enhanced processes.
Establish machine and process standards and overall equipment efficiency.
Assist in the development of more effective operational control systems.
Evaluate data generated through studies using statistical analytical methods.
Responsible for the development and/or revision of production standards and standard work documents.
Develops, writes and executes engineering studies, design of experiments, and IQ/OQ/PQ protocols and reports.
Works on optimization of process output and throughput, equipment utilization, equipment downtime, waste reduction/yield improvements, budget management, standard cost and capital investment management.
Provides technical support to the production areas evaluating process deficiencies, process changes, modifications and equipment failure. Defines, analyzes, reviews and evaluates problems for prompt solutions.
Determines, adapts, and modifies methods and standards to control all aspects of assigned projects or portions of major projects.
Coordinates phases of work with other departments within the company and with other Medical Device divisions.
Perform Investigation and writes NC reports following established timelines.
Routes and follows up on NC reports through the evaluation, review and approval processes to comply with the established timeline.
Coordinates and participates in Cross Functional Investigations (CFI)
Revise and maintain engineering and equipment procedures.
Follows Standard Operating Procedures (SOP), Good Manufacturing Practices (GMPs), Company Policies and Federal, State and Local Government Regulations.
Map processes and analyze current status and potential future states with improvements. Define and quantify improvements to further analyze the gains. Use tools from Lean and Six Sigma to create and execute CIP projects.
Participates in GMP audits regarding equipment recording and machine performance.
Coordinates communications and interfaces with end users, machine manufacturers and/or suppliers.
Participates in projects involving other departments and activities (CIM, QIP, CFM, etc.).
Writes, develops and implements validation procedures.
Qualification
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Required
At least a bachelor’s degree in an engineering discipline is required.
At least 2-4 years’ experience in engineering in a medical device environment preferred.
Advanced computer skills and use of software applications. Strong computer background (MS Office, MS Project Management, PowerPoint, Word, Excel, Outlook etc.)
Experience in a manufacturing environment developing manufacturing standards.
Proven ability to anticipate and solve problems.
Ability to prioritize multiple commitments and technical problem-solving duties.
Experience or knowledge in short and long-term project management.
Company
Johnson & Johnson
Johnson & Johnson develops medical devices, pharmaceuticals, and consumer packaged goods.
10,001+ employees
H1B Sponsorship
Johnson & Johnson has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Trends of Total Sponsorships
2023 (43)
2022 (55)
2021 (40)
2020 (30)
Funding
Current Stage
Public CompanyTotal Funding
unknown1978-01-13IPO· nyse:JNJ
Leadership Team
Alex Gorsky
Chairman & CEO
Dominic J. Caruso
Vice President, Finance and Chief Financial Officer
Recent News
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2024-05-24
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