Product Inspector (2nd shift) 1

Grifols•Clayton, NC

46d•Onsite

About The Position

Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. This position is for a Plasma Classification Certified Inspector on the 2nd Shift, working Monday - Thursday from 1:30 PM to 12:00 AM. The role requires scanning and removal of unsuitable plasma units using the Plasma Management System (SGP), as well as performing visual inspections to remove unacceptable units (e.g., damaged, broken port/tube, RBC, or backup sample rejections). The employee will also perform secondary verifications and end-of-PU line clearances.

Requirements

High School diploma or equivalent.
Two years’ experience in Manufacturing, Pharmaceutical or other FDA licensed Industry is desirable.
Knowledge of cGMPs and Industry Standards.
Ability to follow “Standard Operating Procedures”.
Possess good verbal and written communication skills.
Possess basic math skills (addition, subtraction, division, multiplication).
Basic Computer skills.

Responsibilities

Scanning of plasma units assigned to a PU utilizing a barcode reader.
Scanning of archive samples assigned to a SA utilizing a barcode reader.
Transferring units to a Sub-shipment during the PU process.
Entering “Statistics” during the PU process.
Sub-shipment verification at the end of the PU process.
“Blocking” of units which do not meet customer requirements.
Responsible for various rejections found during visual inspection.
Removal of unsuitable plasma units marked for removal in SGP during the PU process.
Able to maintain record accountability.
Able to perform job duties with minimum supervision.
Ability to follow written procedures.
Monitoring plasma time out of freezer.
Department housekeeping and safety practices.
Processing of unsuitable plasma units during any step of the plasma process.
Transfer of unsuitable plasma units (status 100) to correct reject inventory.
Transferring units between PU/LOT to a PU.
Ability to consistently meet department average throughput.
Knowledge of SGP Status codes and Disposition Codes.
Knowledge of labeling Requirements.
Scanning of case/units to a 3rd party sale utilizing Disposition Module.
Scanning of case/units to a MDO process utilizing Disposition Module.
Completing the partial PU cases between PU’s.
Line Clearance at the end of a Plasma Process.