Material Handler II

Equiliem; Greenville (SC); On-site; USD 35,000 - 55,000; Full time

Job summary

An established industry player is seeking a detail-oriented individual to operate collator equipment for the production of medical devices. This role involves ensuring quality compliance, maintaining documentation, and adhering to safety regulations. Ideal candidates will have a background in regulated environments, showcasing strong attention to detail and effective communication skills. Join a team dedicated to excellence in medical device manufacturing and contribute to impactful projects that prioritize quality and safety.

Qualifications

• Experience in medical device or regulated work environments.
• Strong attention to detail, especially with documentation.

Responsibilities

• Operate collator equipment for processing multi-part forms.
• Ensure quality compliance and proper documentation.

Skills

Attention to Detail

Basic Math Skills

Communication Skills

Job description

What You'll Do:

• To run collator equipment that completes and processes the multi-part forms into the finished medical device.


• Ensure all previous steps have been finished and that QC Manager has signed off on each step.


• Align the multiple form parts in the collator in the correct positions according to the original copy and ensure correct cutting head is loaded in the collator.


• Ensure that the proper glue setup is in place for both the form and filter paper per the job specifications.


• Ensure that the forms are picked up in correct order and placed on a skid in order to optimize the finishing operation.


• Ensure that all quality issues including splices and machine stoppages, are properly identified and the product segregated and identified for further finishing.


• Maintain all required documentation and traceability of the work and ensure all forms and materials are labeled properly.


• Assure compliance with safety and health regulations and good housekeeping practices within assigned areas, as well as compliance with all quality specifications.


• Move completed orders to the designated Finishing staging areas.


• Comply with all regulatory and cGMP policies and procedures.


• The list of duties and responsibilities is not exhaustive and may be substituted as necessary.

Requirements:

• Medical device background or other regulated work experience.


• Attention to details, especially with numbers and documentation


• Must have basic math skills and be able to read a ruler


• Must have proficient communication skills with others


• Machining type backgorund is beneficial