Quality Inspector I, II (Evenings 3:00pm to 11:30pm)

LSI Solutions Inc•Victor, NY

6h•$22 - $28•Onsite

About The Position

LSI SOLUTIONS® founded in 1986, located in Victor, New York, is a dynamic and growing medical device company with over 500 employees dedicated to advancing minimally invasive surgical instruments through research, development, manufacturing, and marketing. The company has doubled in size in the last 4 years and its campus includes 10 buildings on 95 meticulously cared for acres. LSI SOLUTIONS® is an ISO 13485 certified company, seeking passionate individuals to join an energetic team focused on relentlessly pursuing better patient outcomes with state-of-the-art devices. The Quality Inspector Level I and II are responsible for completing assigned inspections of vendor related and in house manufactured parts, working with the Quality Department to support manufacturing.

Requirements

High School Diploma or GED required.
For Level II: 3 years’ experience and Certified Quality Inspector (ASQ CQI) OR 5 years’ experience in Manufacturing or inspection.
Good verbal and written communication skills.
Ability to work independently as well as alongside team members with minimal supervision.
Attention to detail.
Hand-eye coordination and manual dexterity for the ability to manipulate and evaluate small parts and components under magnification.
Understanding of quality and improvement concepts and tools including, but not limited to, quality audits, sampling plans, and problem solving.
Understanding of basic statistical concepts, particularly as applied in statistical process control (SPC).
Familiarity with the selection and use of variable and attribute gages, hand tools, vision systems, and other appropriate gages for inspection.
Blueprint reading.
Mathematical skills including, but not limited to, rounding, significant figures, basic algebra, basic geometry, and conversion within and between English and metric measurement systems.

Nice To Haves

Some post-high school course work in a technical field.
Experience in Medical Device or other regulated industry (for Level II).
GD&T knowledge (for blueprint reading).

Responsibilities

Inspecting materials throughout assembly process, from raw materials to finished goods, for compliance.
Reading and interpreting blueprints in order to perform inspections.
Selection and use of variable and attribute gages, hand tools, vision systems, and other appropriate gages for inspection.
Auditing or sorting component lots for visual or measurement characteristics as assigned.
Reading, understanding, and application of sampling plans as specified in inspection plans.
Utilization of software, particularly but not limited to, office software such as spreadsheets and word processors.
Understanding and compliance with quality system requirements.
Completion and reviewing of quality paperwork ensuring compliance to quality system requirements.
Participation in periodic cleaning activities, including maintaining a clean, neat and organized work space.
Adherence to all company policies and procedures per the LSI Solutions Employee Manual.
All other duties as assigned.
Basic knowledge of SPC.
Ability to run existing programs on CMM to perform in-process inspections.
Advanced knowledge of QMS system and process documentation.
Assist Supervisor with Training & Coaching Inspectors.
Assist with IQ, OQ, PQ activities.
Participate in data collection for GR&R measurement studies.
Proficient in Microsoft Excel.
Assist with prioritizing workflow in inspection area.