Job description
Do you want to work for a company that still has that small, family-like feel, even though it’s growing at a sustainable rate? Do you want to work where the plant leaders are 100% approachable? Do you want to work where your thoughts, observations, and opinions are welcomed and appreciated? Does an average length of employment well over 10 years because the environment is pleasant, productive, and positive appeal to you? Then come, join Viant and be part of this amazing company.We offer a full comprehensive Benefit package that are effective on your first day of work! This includes Medical, Dental, Vision, 401k company with match, 17 days paid time off, 10 paid holidays, life insurance and so much more!!
The primary purpose of our Manufacturing Engineer position is to apply engineering principles to drive process improvements in the manufacturing of medical devices while positively affecting quality, delivery, cost, safety and moral. We are looking for someone with a positive attitude with excellent attention-to-detail who wants to grow professionally with high internal expectations.
PURPOSE: Every associate at Viant contributes to the lifesaving or life enhancing medical devices we produce. We are totally invested in the work we do.
GROWTH: Our Laconia site is growing! We are looking for individuals that are looking for development and up for a good challenge. There are many opportunities for personal growth and contributions to the success of Viant!
MISSION: We partner and innovate with our customers to provide the highest quality, life enhancing medical devices in the world.
Skills/Competencies
- Ability to effectively communicate with customers and internal business partners
- Must be able to handle multiple tasks/projects and manage priorities accordingly
- Hands on, collaborative, decisive self-starter
- Computer literacy in Microsoft WORD, EXCEL and POWER POINT
- Engineering or Bachelor’s degree in a technical field with applicable experience
- Proficient in Microsoft office suite (word, excel, outlook)
- Demonstrated proficiency in Solid Works and Minitab.
- 3-5 years’ experience in regulated industry
- Experience in executing Process and Test Method Validations (IQ.OQ,PQ,PPQ) in accordance with Viant Medical’s procedures and guidelines.
- Understands mechanical assembly processes
- Understanding of Root Cause Analysis
- Lean manufacturing and new product development or launch support experience is highly desirable.
- Knowledge of bonding processes, preferred
- Knowledge of statistical analysis, preferred
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