Inspector II, In-Process & Finished Product, QC (2nd Shift)

MicroVention

80d•$19 - $25•Onsite

About The Position

Proficient in performing all duties and responsibilities of Inspector I, In-Process & Finished Product, QC and assist the QC Lead in reviewing device history record to assure compliance. Perform quality control inspections on products at various stages of production from sub-assemblies to final assemblies to assure quality and conformance to specifications and procedural requirements.

Requirements

High school diploma or equivalent.
Minimum three (3) years of relevant experience in medical device manufacturing or inspection.
Strong reading, verbal, and written communication skills.

Nice To Haves

Demonstrated knowledge of inspection techniques, understanding and reading technical documentation including product drawings.
Interpersonal savvy, able to clearly and effectively communicate (read, write, and speak in English).
Detail oriented.
Knowledge of cGMP, GDP, QMS, and/or ISO regulations.
Knowledge of basic measuring techniques including scales, rulers, calipers, micrometers, etc.
Knowledge of computer software, including MS Word, Excel, Outlook, Teams, etc.
Ability to work in a fast-paced environment and to balance and prioritize workload to support production’s schedule.
Ability to work with a culturally diverse work population.
Previous experience with video inspection equipment and other inspection tools.

Responsibilities

Conduct visual/dimensional QC inspection and/or testing of incoming materials, in-process materials, sub-assemblies, labeling, and final inspection of finished goods while utilizing visual inspection systems and other inspection tools per inspection requirements to ensure conformance to Quality Specification and procedural requirements.
Accurately measure and record data on data collection forms.
Read and understand Product Drawings and specification dimensions.
Input data into online tracking software.
Provide feedback to Quality and/or Manufacturing on quality issues.
Record, maintain, and communicate all nonconformance to relevant parties involved to ensure timely Corrective Action completion.
Coordinate with production associates to perform in-process, finished product, and final documentation reviews to release finished goods.
Maintain a safe and clean working environment following 5S principles.
Train other inspectors on QSs, TMs, and procedures as required.
Consistently review in-process batch documentation to ensure real-time compliance with product specifications, Good Documentation Practices, SOPs, and cGMPs.
Coordinate calibration of equipment/tools as required and maintain calibration records.
Assist QC Lead in reviewing, closing, scanning, and uploading Build Records into the network drive.
Must be able to work overtime when needed.
Comply with applicable Laws and Regulations, adhere to Quality Management System processes and requirements as well as demonstrate Ethics and Integrity in all matters and at all levels throughout the organization.
Perform additional duties as assigned.