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| Company: | Johnson Johnson |
| Job Role: | Manufacturing Engineer II |
| Experience: | Freshers (0 To 2 years): |
| Vacancy: | 30+ |
| Qualification: | Bachelor’s degree in ME, EE, IE, Engineering Management or related field |
| Salary: | $79,720 per year |
| Location: | Los Gatos, California United states |
| Join us on Telegram | Click Here |
| Apply Mode: | (Online) |
| Start Date: | Not Mentioned |
Job Description:
Biosense Webster, Inc.member of Johnson & Johnson's Family of Companies, is recruiting for a Manufacturing Engineer II!
At Biosense Webster, Inc. we have one goal — to ensure those with cardiac arrhythmias can live the lives they want. This means transforming the latest advancements in electrophysiology into a suite of tools that empowers physicians with a range of treatments for the best outcomes.
Quality products and approaches are achievable only through collaboration with the smartest minds in electrophysiology. For more than 30 years, we’ve been the global market leader in the science and technology of cardiac arrhythmia treatment, working with thousands of electrophysiologists to identify and develop diagnostic and treatment tools. And through onsite training, online courses and our global education centers, we work together to set new standards every day. Learn more about Biosense Webster at www.biosensewebster.com and follow us on LinkedIn.
Are you interested in making a difference in a growing company thriving on a diverse culture, celebrating the uniqueness of our employees, and committed to inclusion? Apply today for this phenomenal opportunity!
The Manufacturing Engineer II will be a key member of, and sometimes lead, multi-functional project teams in Manufacturing Operations. Major objectives may include improve manufacturing operational efficiency, optimize processes & MFG documentation, aid in the product transfer to another facility, improve product and/or process quality, or reduce manufacturing and material costs.
Key Responsibilities:
Product changes are typically multi-disciplinary: mechanical, electrical.
May also perform and document field failure investigations, identify root cause, and participate in corrective and preventative action efforts.
Must be able to implement effective solutions in a timely manner
Adept and experienced problem solver who is able to determine root cause of difficult technical issues
Recognizes problems and addresses them without waiting to be instructed to do so
Work with quality and reliability teams to conduct risk analyses, FMEA reviews and able to define critical-to-quality criteria and present test plans for proposed changes or solutions
Ability to be effective with minimal direction.
Qualifications
Education:
A Bachelor’s degree in ME, EE, IE, Engineering Management or related field is required
Experience and Skills:
Required:
A minimum of 2 years of experience in a medical device manufacturing environment
Must be proficient in the use of personal computers: Microsoft Windows tools, including MS Project, VisioMust have some Solidworks familiarity
Must be able to understand engineering drawings, Bills of Materials, and operational procedures Must have experience writing and reviewing Engineering Change Orders
Excellent written and verbal communication skills, must have good interpersonal skills: conflict resolution, negotiation, and time leadership skills
Experience developing manufacturing processes, writing procedures, and training assembly personnel
Familiarity with ISO 13485 standards
Preferred:
- Product Transfer Experience to another MFG site and/or CM
- Knowledge with flex circuit processing
- Catheter Production assembly experience
- Equipment Management & Validation Experience
Others:
Must be able to travel up to 20% of the time domestically.
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