Lead QA Inspector - 1st Shift

PDI•Orangeburg, NY

10h•$65,000 - $75,000

About The Position

Driven by a commitment to research, quality and service, PDI provides innovative products, educational resources, training and support to prevent infection transmission and promote health and wellness. Encompassing three areas, our Healthcare, Sani Professional and Contract manufacturing divisions, we develop, manufacture and distribute leading edge products for North America and the world. We have several locations across the US and are looking for new Associates to join our team! POSITION PURPOSE This position is for 1st Shift (Mon-Fri, 7:00am - 3:30pm) The Lead Quality Assurance Inspector responsible for day to day in process quality checks across manufacturing lines to ensure all Finished Goods meet product specifications. The Lead QA Inspector will also assign and balance work across their assigned shift.

Requirements

High School Diploma; College Preferred
Proficiency in Microsoft Office Suite
3-5 Years of experience working in regulated industry
Excellent organizational skills, and ability to interact with cross functional teams throughout the organization
Ability to lift 25LBs

Responsibilities

Perform daily inspection of all production lines to assure compliance to GMPs and company.
Ensure that all manufacturing specifications for components, labeling and product are correct, clear and complete
Inspects work areas for removal or all previous products and components.
Verifies readiness of work areas prior to use (Line Clearance).
Monitor, sample and inspect in-process, finished product, for quality, by performing appropriate tests.
Determine final disposition on products inspected and verify information on transfer tickets.
Apply appropriate disposition label to material.
Execute Rework protocols as required.
Accurately and completely document all inspection information on Daily Inspection Report (DIR).
Collects data and samples to support disposition of product.
Documentation required includes but is not limited to: incoming lot #, liquid lot #, item #s, fill weights, defects, etc.
Initiation/Login of LIMS Samples.
Notifies and follows through with production and Quality when discrepancies from procedures and specifications are observed.
This function includes, but is not limited identifying non-conforming material, management of this material within BPCS (Hold procedure) recording of it and distributing required documentation.
Collect samples as required by customers or Nice Pak’s specifications.
This includes any retain sampling as per manufacturing specifications.
Retain evaluation as requested.
Execution of Validation Protocols
Review of documentation to assure accuracy prior to submittal to QA Release team
Identifies means for continuous improvement and to promote a quality culture.
Identifies and works with the Lead to resolve problems in a timely manner, and supply alternate solutions.
Handle assignments as requested by supervision to establish and maintain product quality.
Perform any required testing as per SOPs and WIs.