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Associate Medical Device Labeling Jobs in Wisconsin

Medical Device Technician

Madison, WI · On-site

$38.80K - $48.90K/yr

Medical Device Technician Location: Madison, WI (Onsite) Scope of Work: Assemble and test medical ... Associate's degree with 2+ years' experience or High School Diploma with 6+ years of experience in ...

Medical Device QMS Auditor

Milwaukee, WI · Remote

$98.10K - $123.86K/yr

Associate's degree or higher in Engineering, Science or related degree required * Minimum of 4 years experience in the medical device field including at least 2 years must be hands-on medical device ...

Medical Device QMS Auditor

Madison, WI · Remote

$98.10K - $123.86K/yr

Associate's degree or higher in Engineering, Science or related degree required * Minimum of 4 years experience in the medical device field including at least 2 years must be hands-on medical device ...

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Associate Medical Device Labeling information

What are the key skills and qualifications needed to thrive as an Associate Medical Device Labeling Specialist, and why are they important?

To thrive as an Associate Medical Device Labeling Specialist, you need a strong understanding of regulatory requirements, attention to detail, and experience in technical writing, often supported by a degree in life sciences or a related field. Familiarity with labeling software, document management systems, and knowledge of FDA or EU MDR regulations are typically required. Excellent communication, collaboration, and organizational skills set top performers apart in this position. These skills are crucial to ensure label accuracy, regulatory compliance, and patient safety in a highly regulated industry.

What are some common challenges faced by Associate Medical Device Labeling professionals, and how can they be addressed?

Associate Medical Device Labeling professionals often encounter challenges such as keeping up with evolving regulatory requirements across different countries, ensuring accuracy and clarity in complex technical information, and coordinating input from multiple departments like regulatory affairs, engineering, and marketing. Addressing these challenges involves staying updated on global labeling standards, developing strong attention to detail, and building effective communication and collaboration skills. Leveraging project management tools and regularly participating in training can also help manage these complexities and ensure timely, compliant labeling deliverables.

What are Associate Medical Device Labeling professionals?

Associate Medical Device Labeling professionals are responsible for creating, reviewing, and maintaining the labeling and packaging materials for medical devices. Their work ensures that all product information, instructions, and regulatory warnings are accurate, clear, and compliant with industry regulations. They collaborate closely with regulatory affairs, quality assurance, and product development teams to make sure that labels meet local and international standards. This role is critical in helping ensure patient safety and regulatory approval of medical devices.
What are the most commonly searched types of Medical Device Labeling jobs in Wisconsin? The most popular types of Medical Device Labeling jobs in Wisconsin are:
What cities in Wisconsin are hiring for Associate Medical Device Labeling jobs? Cities in Wisconsin with the most Associate Medical Device Labeling job openings:

Medical Device Quality Inspector

Stellar IT Group

Madison, WI • On-site

Full-time

Posted 23 days ago


Job description

Overview:
Job Title: Medical Device Quality Inspector
Job Type: Contract (6+ Months)
Work Location: Madison, WI (53718)
Responsibilities:
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
Working Conditions:
Manufacturing facility of medical devices and accessories. Controlled environmental working conditions.
REQUIRED - experience in GMP environments or with the correct measuring equipment.
Working Hours: Mon-Thurs (7 AM to 4 PM), Fri (7 AM to 11 AM)
Inspection of final finished goods and packaging prior to shipment. Preference for Medical Device / Metrology experience
Min,High School Diploma
In-person Interview - Mon-Thurs (7 AM to 3 PM)
Skills:
quality,inspector