ZipRecruiter

Log In

1

Associate Medical Device Labeling Jobs in Ohio (NOW HIRING)

Vein360

Quality Technician

Cincinnati, OH · On-site

$17.25 - $23.25/hr

Packaging & labeling * Sterilization load preparation * Device history record review * Supports ... Minimum: Associates degree Preferred: Bachelor's in science Experience: * 1+ years of quality ...

Exsurco

Manufacturing Associate

Wakeman, OH · On-site

The duties & responsibilities of the Manufacturing Associate include, but are not necessarily ... Assemble blades, handpieces and sub-assemblies for both the medical device and non-medical device ...

Bettcher

Manufacturing Associate

Wakeman, OH · On-site

The duties & responsibilities of the Manufacturing Associate include, but are not necessarily ... Assemble blades, handpieces and sub-assemblies for both the medical device and non-medical device ...

Rep-Lite

SPD Field Account Specialist - 61

Dayton, OH · On-site

$65K - $75K/yr

Associate Medical Device Representative * Scrub Tech or candidates with orthopedic or technical device exposure Education & Certifications * Associate's degree preferred, not required * CRCST / CBSPD ...

next page

Showing results 1-20

All JobsAssociate Medical Device Labeling JobsAssociate Medical Device Labeling Jobs in Ohio

Associate Medical Device Labeling information

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 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.
Associate Medical Device Labeling jobs near you

Quality Technician

Vein360

Cincinnati, OH • On-site

$17.25 - $23.25/hr

Full-time

Posted 10 days ago

Job description

Salary:

Quality Technician works under the supervision of the Quality Management Representative or their designee and is responsible for ensuring compliance to the requirements of the corporate Quality System and 21 CFR Party 820 (Quality System Regulation). Quality Technician applies relevant experience, knowledge and skill sets to review and approve the output of daily operations (device history records), release raw materials to production, actively drive and support the management of process improvement activities such as Corrective & Preventive Action (CAPA). The Quality Technician is to become an expert in each phase of reprocessing operations and able to provide meaningful input to operations leadership and quality assurance for the continuous improvement of these operations.

Essential Functions:

  • Works within a production, lab and office environment to ensure the safe, compliant and reliable execution of reprocessing operations which include:
    • Receiving used healthcare products
    • Incoming inspection and release of raw materials
    • Cleaning
    • Drying
    • Inspection & testing
    • Packaging & labeling
    • Sterilization load preparation
    • Device history record review
  • Supports critical to quality programs such as:
    • Process validation
    • Internal audits
    • CAPA
  • Strictly adhere to all corporate environmental health and safety programs including bloodborne pathogens and hazard communication.
  • Faithfully execute duties against the corporate Quality System.
  • Use measurement systems and analysis tools to support process improvement/validation activities or establish root cause of non-conformances.
  • Identify opportunities for improvement and provide feedback to operations and quality leadership.
  • Support quality system initiatives as assigned.
  • Comply with applicable FDA requirements and all associated standards / guidance

Education:

Minimum: Associates degree

Preferred: Bachelor's in science

Experience:

  • 1+ years of quality technician or relevant experience within FDA regulated medical device operation
  • Preferred Skills/Qualifications:
  • Working knowledge of various pieces of test and measuring equipment including:
  • Micrometers, calipers, digital force gages, motorized test stands, rulers, digital multimeters, laser diode counters, etc.
  • Familiar with critical manufacturing processes such as packaging and terminal sterilization, including monitoring of controlled environments.

Skills/Competencies:

  • Time management
  • Root cause analysis
  • Functional knowledge of Microsoft Office (Word and Excel)
  • Technical writing
  • Basic data aggregation and analysis capabilities (e.g., summary statistics)

About Vein360

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

11 - 50 Employees

Headquarters location

Blue Ash, OH, US

Year founded

2015

View All Vein360 Jobs