Job Description
Stefanini Group is hiring!
Stefanini is looking for
Manufacturing Engineer
for ST. Paul, MN Location.
For quick Apply, please reach out to Shubham Singh - call:
248-728-2629 / email: shubham.singh@stefanini.com
Work shift (days/times) - Mon-Fri (40 hours) 1st shift
Work Location - ST. Paul, MN
Description:
- Displays standard engineering principles to resolve difficult problems, from conception to final design with team input.
- Works as part of a team performing standard engineering work requiring application of standard engineering techniques, procedures and criteria. Work is closely supervised.
- Responsible for ensuring that the quality of all product/process design meet all customer requirements and are manufacturable at the time of transfer to Manufacturing/Operations under the guidance of senior personnel.
- Helps to performs engineering design evaluations.
- Recommends alterations to development and design to improve quality of products and/or procedures.
Essential Duties and Responsibilities:
- Performs routine engineering assignments of related tasks which are typically a focused portion of larger projects.
- These tasks provide experience and familiarization with the engineering staff,
methods, techniques, theories, Corporate and division SOP's, policies and projects.
- Document development work including writing specifications for manufacturing or scientific test results. Ability to solve routine design and engineering tasks with some assistance. Able to solve problems with periodic monitoring. Assists in the preparation and participation in technical reviews and responsible for organizing data and preparing appropriate
documentation for assigned projects.
- Performs routine engineering assignments of related tasks which are typically a focused portion of larger projects. These tasks provide experience and familiarization with the engineering staff, methods, techniques, theories, Corporate and division SOP's, policies and projects.
- Document development work including writing specifications for manufacturing or scientific test results.
- Ability to solve routine design and engineering tasks with some assistance. Able to solve problems with periodic monitoring.
- Support organization on Medical Device Regulations (MDR) deliverables as assigned
- Create or update Batch Records, Procedures, Processes, to meet MDR requirements
- Review site products manufacturing documentation to ensure compliance to MDR.
- Ability to work within Quality Systems to route updated documents and complete MDR assignments,
- Assists in the preparation and participation in technical reviews and responsible for organizing data and preparing appropriate documentation for assigned projects.
Qualifications:
- Ability to discuss normally encountered technical or project management issues, both
verbally and in written form.
- Ability to work as a collaborative team member.
- Ability to solve routine design, engineering problems with assistance.
- Effectively operate in and may facilitate cross-functional teams with guidance.
- Must be able to provide solutions that reflect understanding business objectives and cost implications.
- Strong communication skills
- Display a solid technical understanding of engineering principles and procedures (e.g. CAD and its application or scheduling a series of technical tasks utilizing software-based tools.
- B.S.in Engineering or other related technical field and a minimum of 1 year related experience (in-house, co-op or acquired outside).