CMM Programmer/Quality Inspector
CMM Programmer/Quality Inspector
We are seeking an experienced, high caliber Quality Inspector/CMM programmer to work under general supervision and be accountable for providing support services to the Quality Assurance function by performing inspection of precision machined parts in accordance with policy and procedures.
We are team-oriented, fast-paced and progressive company. We value people with great ideas who partner with others both internally and externally to take action and accomplish goals.
Roles & Responsibilities:
- The Quality Inspector is responsible for incoming, in-process, and final inspection of medical devices and precision machined components. This includes the physical inspection of custom and off-the-shelf parts, sub- assemblies, and final product, to ensure compliance to specifications and engineering drawings.
- Performs visual, dimensional and functional inspection and testing according to documented policies and procedures.
- Records inspection and test data as prescribed by written instructions and procedures.
- Operates all associated test and measurement equipment, including CMM, as instructed and as documented in procedures.
- Recommends changes to policies and procedures.
- Documents non-conformances in Non-Conforming Material Review system.
- Collects data for First Article inspections.
- Assists in gathering, analyzing, and trending of data.
- 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.
- Minimum of five years of experience in a Quality inspection role.
- CMM programming experience highly preferred. PC-DMIS experience a major plus.
- Experience with optical measurement equipment, hand tools, gages, and visual inspection.
- Experience with reading and understanding engineering drawings and have a firm understanding of GD&T.
- Experience with inspection sampling techniques.
- Knowledge of ISO 9001, ISO 13485, AS9100 or 21 CFR 820 preferred.
- Good communication and computer skills, including Microsoft Word and Excel.
- Prior medical device or aerospace component inspection experience preferred.
- 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 projects.
- 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.
Research & Recruitment Specialist
Paula joined the Morisey-Dart Group in August of 2017. She is the firm’s research and recruitment specialist for the medical device and precision machining/manufacturing teams. She is responsible for sourcing and recruiting, lead generation, internet research and various other responsibilities within both the medical device and precision machining industries.
With 25 years at Xerox Corporation in New York, Paula had a prosperous and noteworthy career where she excelled during her tenure. She brings her vast knowledge and expertise in procurement, supply chain, contract administration and project management to the firm. She is a creative and natural problem-solver with proven success in developing and implementing new procedures and processes as well as integrating newly acquired subsidiaries.
Now, she’s using her expertise to build a network of solid relationships in the medical device and precision machining industries that help hiring managers find the top talent they need to improve their organizations.
Paula is Lean Six Sigma certified (Green Belt), has a Master of Science in business management and a Bachelor of Science in education.