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Medical Device Quality Inspector

Mindlance

Madison, WI

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JOB DETAILS
SKILLS
Communication Skills, Corporate Compliance, Corrective Action, Cross-Functional, Detail Oriented, Documentation, FDA Requirements, GMP (Good Manufacturing Practices), Healthcare Quality, High School Diploma, ISO (International Organization for Standardization), Investigative Reports, Manufacturing, Manufacturing/Industrial Processes, Medical Equipment, Order Picking/Packing, Process Manufacturing, Product Support, Quality Assurance, Quality Control, Quality Management, Regulations
LOCATION
Madison, WI
POSTED
30+ days ago
Medical Device Quality Inspector

Responsible for assuring that materials, activities, processes, and specified conditions related to the daily device manufacturing, processing and packaging meet current GMP standards and comply with applicable procedures and standards such as ensuring the quality integrity of the product. Ensure work is completed in compliance with the company quality system and medical device regulations. Ensure work is completed in compliance with the company quality system and medical device regulations.

Essential Functions
" Performs one of three functions in the Quality department:
o Inspecting raw materials to meet production requirements
o Conducts in-process inspection of manufacturing product and processes
o Reviews final documentation and shipment packaging for medical devices, subassemblies, and kits
" Assists in the Madison Manufacturing documentation control room.
" Completes documentation of activities performed, prepares and attaches material quality status labeling. Ensures storage and handling of product and labeling in a controlled and secure manner.
" Supports Quality through occasional conduct of investigations of nonconformance, assists with preventive actions associated with the QA unit.
" Performs quality reviews for quarantine releases on non-reportable, non-complaint, RMF-3 internal to an RSC.

Minimum Requirements
Education / Experience / Skills:
" High School diploma or equivalent
" One year s experience in a regulated work environment preferred
" Knowledge of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing

Competencies:
" High Level of motivation; ability to work independently
" Detailed oriented
" Ability to work with computer-based systems daily
" Collaborator with strong levels of engagement with individuals and as a team member
" Good interpersonal skills; ability to communicate well, both verbally and written

Organizational Relationship/Scope:
Reports to the Quality Control Manager. This position is accountable for delivery of prompt investigative work and detailed reporting. Working across multiple functions, this position collaborates primarily with manufacturing, engineering and quality to assess nonconforming product and support supplier quality issues.

Working Conditions:
Manufacturing facility of medical devices and accessories. Controlled environmental working conditions.

EEO:
Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.

About the Company

M

Mindlance

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