ARCH Cutting Tools
Essential Duties and Responsibilities
Program Coordinate Measuring Machines (CMMs) for high volume production inspection using applicable metrology software such as PC-DMIS and Calypso. Lead troubleshooting efforts for CMM operation. Lead measurement system analysis activities as required by internal and customer requirements on relevant equipment. Identify opportunities for measurement process improvement and implement automated solutions. Read and interpret blueprints, technical drawings, schematics, to ensure that requirements are met for measurement based activities. Confer with engineers or other personnel to implement operating procedures, resolve issues, or provide technical information. Investigate CMM equipment failures or difficulties to diagnose faulty operation and recommend remedial actions such as recalibration, sensor repair, software conflicts, fixture improvements, etc. Exercises independent judgment on selection of inspection equipment for use on new and established processes through the process of technical assessment and analysis. Provides technical support for project planning, development, installation, validation and modification of inspection assets. Assists in development of inspection fixtures to ensure minimum measurement error during inspection. Write/ edit/ assesses programs utilized in manufacturing using CMM programming platforms such as Calypso, PC-DMIS, etc. Education and Experience
Minimum 2 years experience in CMM programming platforms such as Calypso, PC-DMIS, etc. Bachelor’s Degree in an engineering field such as Mechanical and Manufacturing Engineering preferred. Job Knowledge, Skills and Abilities
Proficient in set-up and operation of inspection equipment. Proficiency in writing and/ or editing CMM programs (Calypso & PC-DMIS preferred) Proficient in reading/interpreting engineering drawings and the application of Geometric Dimensioning & Tolerancing (GD&T) per ASME Y14.5 Strong math skills, trigonometry. Knowledge of standard mechanical inspection methods, tools, and tolerances used to determine product acceptance. Knowledge of regulations associated with the medical device industry preferred. Experience with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) preferred. Working knowledge of Quality Systems (FDA/ISO) within a regulated environment preferred. Physical Demands
Light to moderate physical exertion required Lifting/carrying Maximum lbs: 25 Regularly required to stand, reach and move about the facility Some extended periods of sitting at desk/computer required EEO Disclaimer
ARCH Global Precision is an Equal Opportunity Employee and wholeheartedly supports diversity in the workplace as a basic premise for business success. All employees of ARCH Global Precision are employed on an at-will basis. This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employee(s) will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. A review of this position has excluded the marginal functions of the position that are incidental to the performance of fundamental job duties. All duties and responsibilities are essential job functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbent(s) will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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Program Coordinate Measuring Machines (CMMs) for high volume production inspection using applicable metrology software such as PC-DMIS and Calypso. Lead troubleshooting efforts for CMM operation. Lead measurement system analysis activities as required by internal and customer requirements on relevant equipment. Identify opportunities for measurement process improvement and implement automated solutions. Read and interpret blueprints, technical drawings, schematics, to ensure that requirements are met for measurement based activities. Confer with engineers or other personnel to implement operating procedures, resolve issues, or provide technical information. Investigate CMM equipment failures or difficulties to diagnose faulty operation and recommend remedial actions such as recalibration, sensor repair, software conflicts, fixture improvements, etc. Exercises independent judgment on selection of inspection equipment for use on new and established processes through the process of technical assessment and analysis. Provides technical support for project planning, development, installation, validation and modification of inspection assets. Assists in development of inspection fixtures to ensure minimum measurement error during inspection. Write/ edit/ assesses programs utilized in manufacturing using CMM programming platforms such as Calypso, PC-DMIS, etc. Education and Experience
Minimum 2 years experience in CMM programming platforms such as Calypso, PC-DMIS, etc. Bachelor’s Degree in an engineering field such as Mechanical and Manufacturing Engineering preferred. Job Knowledge, Skills and Abilities
Proficient in set-up and operation of inspection equipment. Proficiency in writing and/ or editing CMM programs (Calypso & PC-DMIS preferred) Proficient in reading/interpreting engineering drawings and the application of Geometric Dimensioning & Tolerancing (GD&T) per ASME Y14.5 Strong math skills, trigonometry. Knowledge of standard mechanical inspection methods, tools, and tolerances used to determine product acceptance. Knowledge of regulations associated with the medical device industry preferred. Experience with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) preferred. Working knowledge of Quality Systems (FDA/ISO) within a regulated environment preferred. Physical Demands
Light to moderate physical exertion required Lifting/carrying Maximum lbs: 25 Regularly required to stand, reach and move about the facility Some extended periods of sitting at desk/computer required EEO Disclaimer
ARCH Global Precision is an Equal Opportunity Employee and wholeheartedly supports diversity in the workplace as a basic premise for business success. All employees of ARCH Global Precision are employed on an at-will basis. This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employee(s) will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. A review of this position has excluded the marginal functions of the position that are incidental to the performance of fundamental job duties. All duties and responsibilities are essential job functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbent(s) will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. Equal Opportunity Employer. This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
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