Senior Life Cycle Management Process Engineer
at Johnson Johnson
Blackpool, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 31 Aug, 2024 | Not Specified | 31 May, 2024 | 4 year(s) or above | Regulated Industry,Computer Skills,Minitab,Databases,Medical Devices,Manufacturing Engineering,Manufacturing,Design Control,Presentation Skills,Industrial Engineering,Project Management Skills,Interpersonal Skills,Microsoft Office | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
DEI:
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and a broad culture that values different perspectives and life experiences.
That is why we in Johnson & Johnson are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are.
Diversity, Equity & Inclusion at Johnson & Johnson means “ You Belong”!
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/.
PROFESSIONAL EXPERIENCE REQUIREMENTS:
- 4-6 years of experience in manufacturing and/or engineering is required.
- Previous experience working in a regulated industry, such as Medical Device is preferred.
- Six Sigma or Lean Sigma certification or 4 years of experience preferred.
- Medical device industry experience is required.
- Familiarity with ISO 13485 Design Control, and manufacturing process IQ, OQ, PQ qualifications as related to medical devices is required.
- Demonstrates leadership qualities including confidence, transparency, integrity, innovation, passion, patience and tenacity.
- Demonstrates strong written, verbal and presentation skills.
- Demonstrates strong computer skills, such as the use of Microsoft Office, Minitab, and databases.
- Demonstrates strong organizational and project management skills and are results oriented.
- Demonstrates positive interpersonal skills and professional interactions with coworkers.
- Demonstrates troubleshooting skills.
EDUCATIONAL REQUIREMENTS:
- Bachelor of Science Degree from accredited institution in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree.
- Master of Science Degree from an accredited institution in Manufacturing Engineering, Mechanical Engineering, Industrial Engineering, or a related degree, preferred.
Responsibilities:
OVERALL RESPONSIBILITIES:
The Senior LCM Engineer, a member of the Lifecycle Management will participate in projects that require the resoultion of challenging problems impacting the Supply Chain and multiple cross-functional areas. The Senior LCM Engineer will manage teams and support projects that will lead to solutions for new and improvements to existing products and processes.
- Lead multidisciplinary project teams in the design, development, and manufacturing of Power Tools or Velys products, and other novel medical devices, and be able to function also as a team member as required.
- Works within cross-functional project teams including R&D, Quality Assurance, Supplier Quality, Planning, Purchasing, Regulatory, and Manufacturing amongst others to develop innovative new products for the medical device industry. This position works as a recognized manufacturing and process technical expert who can provide process engineering knowledge.
- Provides direction and technical support in identifying continuous improvements to manufacturing operations and implementing new technologies including development of processes, researching current and emerging technologies and evaluating process quality, cost, capacity and capability alternatives.
- Provides direction in supporting the needs of manufacturing areas in terms of meeting the requirements for quality standards and compliant documentation, capacity, product availability and cost.
- Interact with outside vendors and academia to bring state-of-the-art technologies, techniques, processes, and equipment in-house.
- Performs assignments designed to continue the development of professional work knowledge and abilities requiring application of standard engineering techniques, procedures and criteria in carrying out a sequence of related engineering tasks, project management, statistical analysis and presentation of data and technical writing. Mentors engineering staff.
- Supports all supplier change projects, request and/or evaluations assessments for the Technical Lifecycle Management team.
POSITION DUTIES & RESPONSIBILITIES:
- Participates in local and multi-site projects.
- Leads and participates in complex engineering projects, either technically or with an extensive cross-functional team. This includes developing and executing to the plan and schedule and meeting the goals and objectives of the project. Tracks costs, prepares status reports, conducts meetings, and documents and communicates progress to management.
- Manages the implementation and validation of new manufacturing processes and equipment to support the assembly of new products.
- Provides financial cost assessments and labor assembly estimates for new products.
- Demonstrates solid hands-on engineering skills in the development of new processes. Identifies and provides innovative new manufacturing technologies from current industry best practices that can be applied to neurovascular products.
- Identifies, leads and implements process improvements for existing manufacturing processes utilizing appropriate engineering principles and standard strategies as e.g. Lean and Six Sigma principles.
- Leads new equipment acquisition efforts including user requirement specifications, machine selection, installation, validation, employee training, and other related equipment responsibilities as required.
- Participates in and leads cross-functional teams which may include, but are not limited to Manufacturing Engineering, Production, Quality Assurance, Finance, Product Development and personnel from other sites.
- Acts as a liaison to vendors with regard to contracted products, tools & fixtures, and their manufacture.
- Identifies and implements improvements to engineering business processes such as configuration management, ERP management, maintenance tracking, etc.
- Performs other related duties, as required.
LI-CM4
REQUIREMENT SUMMARY
Min:4.0Max:6.0 year(s)
Mechanical or Industrial Engineering
Engineering Design / R&D
Mechanical Engineering
BSc
Manufacturing engineering mechanical engineering industrial engineering or a related degree
Proficient
1
Blackpool, United Kingdom