At Pajunk Medical Systems we believe that success derives from both, high-quality and innovative products, and excellent customer service. As a Manufacturing Supervisor, a majority of your day will be supervising and being responsible for medical device assembly in a cleanroom environment. This position reports to the Manufacturing Manager.

This position is an important role in a team-oriented work environment within a family owned, German medical device company.


Essential Duties and Responsibilities:

  • Supervise and guide daily cleanroom manufacturing operations, including manual assembly and wrapping of medical procedure trays and operation of packaging equipment, according to established procedures
  • Be able to perform all cleanroom manufacturing operations in order to accurately assess cleanroom personnel performance and fill in when necessary
  • Be fully responsible for execution of a bi-weekly build plan, from start to finish
    • generation of Work Order Travelers and printing of labels
    • track and log daily production metrics (including outputs and lot status)
    • perform inventory material issues in Sage ERP system
    • resolve quantity/lot discrepancies with cleanroom and material personnel
    • verify recording of accurate data on batch records and forms, following GDPs
    • verify final load readiness to go out for sterilization
    • identify and dissolve bottlenecks in production flow to stay on schedule
    • escalate issues to management/other departments as needed
  • Follow gowning and hygiene requirements for working in a cleanroom
  • Be responsible for inventory of cleanroom and gowning supplies, from counts to order requests to receipt of goods
  • Train new manufacturing employees according to approved documents
  • Participate in routine material inventory counts
  • Communicate issues, problems and concerns to management and other departments in an open and timely manner
  • Participate with Manufacturing Manager in setting/executing goals to continuously improve the operations
  • Periodically assist with qualification and validation activities
  • Performs other duties and responsibilities as assigned

Qualifications:

  • Bachelor’s degree or equivalent level of work experience
  • Ability to understand and communicate (speak, read, comprehend, & write) in English
  • Ability to manufacture safe, effective, and properly documented product by following written procedures and paying attention to details.
  • Previous experience working in an FDA regulated environment is a plus.
  • Ability to stand for extended periods of time while performing repetitive work that requires manual dexterity and visual acuity.
  • Ability to occasionally lift and/or move up to 50 pounds
  • A current US work authorization is required.

Please submit a Resume and Cover Letter in your application.

*Due to high level of applicants, we will reach out to qualified candidates only.

Pajunk USA

4575 Marconi Dr.

Alpharetta, GA 30005