EPA Sterility QC Technician - 3rd Shift
Location:
South Brunswick Township , New Jersey
Posted:
February 03, 2017
Reference:
00001H5U
PharMEDium Services, a division of AmerisourceBergen, is a growing outsourcing compounding organization servicing hospitals nationwide. Our growth now has encouraged our business to seek QC staff to perform sterility testing in ourtesting lab. This position will report to the Quality Organization of PharMEDium

Sterility Technician at this facility will perform solution preparation and maintain a properly supplied laboratory. Technicians will abide by all documentation procedures and maintain a level of professionalism throughout each working day. The technician must be familiar with cGMP/GLP and 21 CFR Part 11 procedures. All applicants for this position must embody and demonstrate the PharMEDium Core Values: Patient Safety, Flawless Quality, Operational Excellence, Employee Well Being, Service Excellence, and Respectful and Collaborative Environment.

JOB RESPONSIBILITIES:

  1. Perform tests using aseptic technique in a Laminar Airflow Clean Bench
  2. Per Procedures Maintain all Document for laboratory analysis
  3. Perform rapid sterility testing per procedure and report results
  4. Receiving, storage, and logging in samples for testing analysis.
  5. Setting up and ensuring appropriate solutionsand standards are prepared daily.
  6. Keeping the laboratory clean
  7. Ordering supplies and other materials
  8. Maintains the supply inventory for the laboratory.
  9. Maintains the daily cleanliness of the laboratory.
  10. Follow Standard Operating Procedures
  11. Maintenance of Laboratory Notebooks
  12. Support in all regulatory inspections: FDA, DEA, Board of Pharmacy, and Internal Audits.

Qualifications:
  1. Associate degree in science with knowledge of Aseptic Technique
  2. Knowledge ofbasic laboratory equipment
  3. Ability to execute planned projects
  4. Excellent communication skills
  5. Computer knowledge of spreadsheet software, Microsoft Word and Excel
  6. Knowledge of GMP documentation and Qualitative testing

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