Biomat USA, Inc. Quality Assurance Coordinator- Interstate Blood Bank in Memphis, Tennessee
Do you want to join an international team working to improve the future of healthcare? Do you want to improve the lives of millions of people? Grifols is a global healthcare company which, since its foundation in Barcelona in 1909, has been working to improve the health and well-being of people all over the world. Our four divisions - Bioscience, Diagnostic, Hospital and Bio Supplies - develop, produce and market innovative medicines, solutions and services in more than 100 countries and regions.
Manufacturing Quality Assurance Coordinator
This position is responsible for monitoring and evaluating daily production activities, as well as
recommending and implementing process improvements for the Covington Way – BCI Manufacturing
facility. The responsibilities include, but are not limited to, the review of records and verifying all activities
for compliance to Standard Operating Procedures, customer specific requirements and regulatory
- Assist management with planning, implementing, monitoring and maintaining the quality program
throughout the facility.
- Review all records as required by procedures, for completeness, correctness, and compliance to
Host internal and external audits and inspections.
Assist with the preparation of and/or reviews all manufacturing related validation protocols, as
Perform calibrations on equipment and instruments, as assigned.
Assist with the maintenance of procedure manuals so that accurate and current SOPs are available for
Assist with the maintenance of files of customer specifications and procedures.
Monitor employee compliance with procedures, GMPs, customer specifications, applicable government
regulations and industry practices; report any procedural or practice noncompliance.
- Promotes, complies, actively participates and enforces the Safety Procedures, to help maintain a safe
and healthy work environment.
Assist in monitoring and timely resolution of all error and/or accident reporting.
Assist with the review of work orders at the end of manufacturing to confirm all elements are accounted
for and all steps have been properly signed off.
- Assist with the development and implementation of standard operating procedures for all
- Assist in the initiation of continuous improvement activities utilizing the change
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management process and incorporation of best practices.
Inform Corporate Quality Assurance of any quality concerns.
Perform other duties as required.
Self-directed and highly motivated
Excellent analytical, organizational and multi-tasking skills
Proven ability to effectively communicate through the written and spoken word
Proficiency with word processing, spreadsheets, and electronic editing programs
Strong interpersonal skills; a team player and independent worker
Demonstrated effect verbal and written communication skills
- BS in Biological Sciences or MLT
Preferred Education and/or experience
Previous Quality Assurance or Quality Control experience
MS in Biological Sciences or Public Health Management
Previous work experience with the Source Plasma Industry
Previous manufacturing experience
PBS, LLC may elect to train individuals in one or all of these qualifying areas.
Learn more about Grifols
Req ID: 229652
Type: Regular Full-Time
Job Category: Nursing/Healthcare