Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

Here are a few things you should know:
  • This site is mobile friendly. You do not need a log-in or password to access information.
  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
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  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.

Job Information

J&J Family of Companies Senior Engineer, Mfg. Engineering in Irving, Texas

Senior Engineer, Mfg. Engineering - 2406188972W

Description

Johnson & Johnson is recruiting for a Senior Engineer, Mfg. Engineering in Irving, TX.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

Job Summary:

  • 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.

Key Responsibilities:

  • 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.

Qualifications

Experience and Education:

  • 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.

Required Knowledge, Skills, Abilities, Certifications/ Licenses:

  • 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.

Other:

This position will be in Irving, TX.

This position could have up to 30% travel both domestic and/or international.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com (http://www.careers.jnj.com).

Primary Location NA-US-Texas-Irving

Organization Mentor Texas LP (6182)

Travel Yes, 25 % of the Time

Job Function Manufacturing Engineering

Req ID: 2406188972W

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