Quality Supervisor (219650-052) Job in Danville 24541, Virginia Us

Quality Supervisor (219650-052)

Biomat USA, Inc., a part of the global Grifols family of companies, specializes in the collection of plasma for use in life-saving therapies. Biomat USA, Inc., along with PlasmaCare, Inc., have a network of over 80 plasmapheresis donor centers throughout the United States. These state-of-the-art facilities collect plasma from donors and operate according to the highest standards of quality.

Under the supervision of the Quality Manager perform Quality Assurance functions to ensure compliance with internal and external regulations and protocol.

  1. As a member of the facility management team, work to ensure compliance with all regulatory and quality standards.
  2. Provide accurate reports of the facility’s state of quality and compliance to the Division Head of Quality.
  3. Oversee the workload and assign tasks to the Quality Associate.
  4. This may include participation in the evaluation and counseling of the Quality Associate in conjunction with the Quality Manager.
  5. Participate in internal and external audits of the facility.
  6. Release product for shipment after review of pertinent DMS and facility records for conformance to requirements described in SOPs relating to production, testing, and storage of plasma.
  7. Perform weekly Quality Assurance observations of center employees.
  8. Verify that samples shipped to the testing laboratories are correctly labeled and prepared for shipment.
  9. Assure that all center incidents are properly documented using the error management system (e.g. Internal Investigation Report); perform root cause analysis and determine corrective actions.
  10. Review reports generated in various product management procedures for accuracy and completeness.
  11. Review information in selected donor record files for accuracy and completeness.
  12. Inspect supplies and materials for compliance with requirements prior to release for use.
  13. Review equipment maintenance, calibrations, and incidences for accuracy and completeness.
  14. Assure that CLIA proficiency test surveys, customer complaint investigations and employee training have been properly documented.
  15. Perform internal audits as required by SOP.
  16. Review quality control for test reagents to ensure they have been performed as required and are within acceptable ranges.
  17. Provide suggestions to corporate management proposing updates and revisions to standard operating procedures.
  18. Verify that the most recent approved procedures and forms are in the center’s procedure manuals.
  19. Perform all Quality Supervisor duties as defined in SOP.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

  1. High School Diploma or GED.
  2. Evaluation and/or translation of any foreign education (high school, university, or professional training) must be provided.

REQUIRED EXPERIENCE/SKILLS

  1. Must have legible handwriting.
  2. Must be able to use a PC.
  3. Ability to read and write the English language.

PHYSICAL REQUIREMENTS

  1. Ability to read and review documents for up to four (4) hours at a time.
  2. Ability to stand for extended periods of time – up to four (4) hours at a time.
  3. Ability to lift, tug, pull up to fifty (50) pounds.
  4. Ability to view video display terminal less than 18’’ away from face – up to four (4) hours a time.
  5. Ability to travel by via automobile and /or airplane.

Submitting a resume online at a job site could cause valuable screening information to be missed.

Please apply directly at:
http://hostedjobs.openhire.com/epostings/submit.cfm?fuseaction=app.dspjobjobid=219650company_id=16052jobboardid=24

We are an Equal Opportunity Employer