Cleanroom Technician

2 months ago


Kennesaw, United States CryoLife Full time
Company Overview:

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in treating patients with aortic diseases. Artivion's four major groups of products include: aortic stent grafts, surgical sealants, On-X mechanical heart valves, and implantable cardiac and vascular human tissues. Artivion has over 1,400 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website,www.artivion.com.

Position Overview:

The Cleanroom Technician will assist the Tissue Processing Laboratory with general duties such as cleaning, preparing disinfectant and stocking supplies.

Responsibilities:

  1. Cleaning general lab area and processing areas, including laundering of laboratory scrubs and trash removal.
  2. Transferring of supplies from central storage to lab storage.
  3. Preparing disinfectants.
  4. Responsible for performing all functions within cGMP/cGTP compliance.
Qualifications:
  1. High School Diploma or equivalent (high school students age 18 or above may be considered).
  2. Experience in medical device or pharmaceutical industry preferred.
  3. Prefer knowledge of Good Documentation Practice (GDP), Good Tissue Practice (GTP), Good Manufacturing Practice (GMP) and AATB regulations.
  4. Organized, detail-oriented, and adaptable.
  5. Capable of following instructions and working without direct supervision.
  6. Good oral and written communication skills and problem-solving skills.
  7. Sense of urgency and ability to meet deadlines.
  8. Strict adherence to following aseptic technique and standard operating procedures.
  9. Generate manufacturing batch records to comply with regulatory requirements, good manufacturing/tissue practices and standard operating procedures


The schedule is Sunday - Wednesday, 11:30PM - 6:30AM. This is a Part-Time position.