Manufacturing Engineer II
Apply NowCompany: Mindlance
Location: Atlanta, GA 30349
Description:
We are seeking an experienced, high caliber Engineer II, Manufacturing. This position will design and develop manufacturing processes, tooling, and fixtures in order to meet daily production schedules while enhancing productivity and product quality. This position will also support the development/transfer of new product design into manufacturing and provide technical solutions. And may require to work in ISO class 5 and class 7 cleanroom environments and required handling production materials and process chemicals.
Each employee can make a difference at and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals.
Responsibilities
Design and develop manufacturing processes, tooling, and fixtures in order to meet daily
production schedules while enhancing productivity and product quality
Evaluation and management of production equipment
Production support and process validation(s)
Interface with vendors for incoming components
Troubleshoot manufacturing processes and equipment(s)
Utilize tools like Gage R&R, Cp, Cpk, and SPC to improve processes
Understanding of and ability to utilize electronic data collection systems and computer software packages and possibly ability to analyze data using basic statistics.
Understand manufacturing concepts like Value Stream mapping, 5S and Visual Workplace to improve quality, labor efficiency, and throughput
Protocol and report writing
Generate and modify manufacturing process documentation
Work with cross functional teams as required
Develop and implement process improvements
Resolves and/or facilitates resolution of problems including identifying causes to prevent re-occurrence
Support all Company initiatives as identified by management and in support of Quality
Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory
requirements, Company policies, operating procedures, processes, and task assignments
Maintains positive and cooperative communications and collaboration with all levels of
employees, customers, contractors, and vendors
Performs other related duties and responsibilities, on occasion, as assigned
Qualifications
Electrical, Mechanical, Chemical, Biomedical, Manufacturing, related engineering degree or equivalent experience required
3-5 years of relevant engineering experience with a variety of Semiconductor, MEMS and Medical Device manufacturing processes, process validation processes and Clean Room equipment required.
Experience with various solvent and acid cleans, Wet and Dry etch, PVD and sputtering metal deposition, wire-bonding equipment and processes.
Wafer alignment and bonding, laser cutting, various test and measurement equipment.
Requires solid computer skills using Microsoft Office, Proficient using Microsoft Word and Excel.
Excellent wafers and individual device handling.
Demonstrated experience with Solidworks, Minitab, and CAD systems
Experience working in a broader enterprise/cross-division business unit model preferred.
Ability to work in a highly matrixed and geographically diverse business environment.
Ability to work within a team and as an individual contributor in a fast-paced, changing
environment.
Ability to leverage and/or engage others to accomplish assigned tasks.
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
Multitasks, prioritizes and meets deadlines in timely manner
Strong organizational and follow-up skills, as well as attention to detail
Ability to travel approximately 5%, including internationally
EEO:
"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."
Each employee can make a difference at and has the power, either individually or as a team, to influence the success of the company. We are team-oriented, fast-paced and progressive. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals.
Responsibilities
Design and develop manufacturing processes, tooling, and fixtures in order to meet daily
production schedules while enhancing productivity and product quality
Evaluation and management of production equipment
Production support and process validation(s)
Interface with vendors for incoming components
Troubleshoot manufacturing processes and equipment(s)
Utilize tools like Gage R&R, Cp, Cpk, and SPC to improve processes
Understanding of and ability to utilize electronic data collection systems and computer software packages and possibly ability to analyze data using basic statistics.
Understand manufacturing concepts like Value Stream mapping, 5S and Visual Workplace to improve quality, labor efficiency, and throughput
Protocol and report writing
Generate and modify manufacturing process documentation
Work with cross functional teams as required
Develop and implement process improvements
Resolves and/or facilitates resolution of problems including identifying causes to prevent re-occurrence
Support all Company initiatives as identified by management and in support of Quality
Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements
Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory
requirements, Company policies, operating procedures, processes, and task assignments
Maintains positive and cooperative communications and collaboration with all levels of
employees, customers, contractors, and vendors
Performs other related duties and responsibilities, on occasion, as assigned
Qualifications
Electrical, Mechanical, Chemical, Biomedical, Manufacturing, related engineering degree or equivalent experience required
3-5 years of relevant engineering experience with a variety of Semiconductor, MEMS and Medical Device manufacturing processes, process validation processes and Clean Room equipment required.
Experience with various solvent and acid cleans, Wet and Dry etch, PVD and sputtering metal deposition, wire-bonding equipment and processes.
Wafer alignment and bonding, laser cutting, various test and measurement equipment.
Requires solid computer skills using Microsoft Office, Proficient using Microsoft Word and Excel.
Excellent wafers and individual device handling.
Demonstrated experience with Solidworks, Minitab, and CAD systems
Experience working in a broader enterprise/cross-division business unit model preferred.
Ability to work in a highly matrixed and geographically diverse business environment.
Ability to work within a team and as an individual contributor in a fast-paced, changing
environment.
Ability to leverage and/or engage others to accomplish assigned tasks.
Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization
Multitasks, prioritizes and meets deadlines in timely manner
Strong organizational and follow-up skills, as well as attention to detail
Ability to travel approximately 5%, including internationally
EEO:
"Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of - Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans."