Product Inspector

4 weeks ago

Clayton, Ohio, United States GRIFOLS, S.A. Full time

We are seeking a highly skilled Product Inspector to join our team at Grifols, S.A. in Clayton, NC. As a Product Inspector, you will be responsible for scanning and removing unsuitable plasma units utilizing the Plasma Management System (SGP). A visual inspection of plasma units is also performed, removing any units which are unacceptable (e.g. damaged, broken port/tube, RBC, or backup sample rejections).

The ideal candidate will have a high school diploma or equivalent and one year of experience in Manufacturing, Pharmaceutical or other FDA licensed Industry. Knowledge of cGMPs and Industry Standards is also required. The ability to follow Standard Operating Procedures and possess good verbal and written communication skills are essential. Basic math skills (addition, subtraction, division, multiplication) and basic computer skills are also necessary.

The work environment is a manufacturing setting with rotating shifts. Exposure to biological fluids with potential exposure to infectious organisms is possible. Personal protective equipment is required, including protective eyewear, safety shoes, gloves and garments. The ability to stand and walk for 6-8 hours per day, bend and twist neck and waist for 6-8 hours per day, and perform frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists is required.

We offer a competitive benefits package, including medical, PTO, up to 5% 401K match, and tuition reimbursement. Grifols, S.A. is committed to offering our employees opportunities for professional growth and career progression.

We are an equal employment opportunity employer and welcome applications from diverse candidates. We will consider for employment all qualified Applicants, including those with Criminal Histories, in a manner consistent with the requirements of applicable state and local laws.

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.

Requirements:

  • High school diploma or equivalent.
  • One year 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.

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