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Medical Device Manufacturing Packaging Operator I - 3rd Shift at Amneal Pharmceuticals LLC

Posted in Manufacturing 30+ days ago.

Type: Full-Time
Location: Piscataway, New Jersey





Job Description:

Description:


  • The Medical Device Manufacturing Packaging Operator is responsible for efficiently operating the medical device packaging equipment in order to complete packaging of commercial products, in accordance with standard operating procedures and cGMP compliance.


Essential Functions:


  • Run high tech packaging equipment and machines during the packaging process of the medical device product.


  • Wear protective equipment, gear, including respirator masks at times, to handle product. Follow all environmental, health and safety procedures during packaging process. Maintain a clean and organized work area.


  • Properly load and package medical device products into the machines as assigned.Identify product defects and make appropriate adjustment as needed to correct equipment.Inspect components for visible defects during the loading and packaging process.


  • Follow standard operating procedures and work instructions to operate, adjust, navigate, troubleshoot medical device packaging machines inorder to complete packaging process. Follow set up instructions to change over machines. Assure adherence to SOPs's GMP & ISO policies.

Education:


  • High School or GED - Required

Experience:


  • less than one year in Pharmaceutical Packaging

Skills:


  • Excellent attention to detail. • Observes safety and security procedures; reports potentially unsafe conditions. • Good written and verbal communication skills • Good record keeping skills • Ability to perform basic mathematical calculations • Experience in measurement methods and practices • Must be a team player • Must be able to wear required protective safety gear/equipment, including respirator mask - Advanced

Specialized Knowledge:


  • Good working knowledge of Optel Vision System, Label Vision System, Track & Trace System. • Knowledge of GMP documentation and regulations • Basic computer skills including the ability to input data, prior experience with computerized control panels preferred • Ability to communicate verbally, read, comprehend, and write in data onto documents.





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