Grifols Plasma Jobs

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Interstate Blood Bank Quality Assurance Manager 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.

This position is responsible for creating high quality technical content that is clear, concise and technically accurate; editing or designing technical documentation, including Standard Operating Procedures, forms, job aids, technical instructions and bulletins; providing an information resource/contact; and performing Quality Assurance reviews for IBBI Business units.


  • Understand processes of all IBBI business units; obtain, evaluate and assess new information and incorporate into Standard Operating Procedures and associated documentation.

  • Distinguish global changes from individual incidents and proceed accordingly.

  • Evaluate document/system changes for effect within and across business units.

  • Apply skills to resolve problems not covered by existing procedures or practices; update documentation accordingly when necessary.

  • Adhere to established guidelines for style and format.

  • Continuously assess existing procedures, forms and associated documents for accuracy/completeness.

  • Act as contact person, information resource for Regional Managers, Center Management, and QACs.

  • Participate in project planning and work independently to meet established deadlines.

  • Perform Quality Assurance review of Error and Accidents, Customer Complaints, and completed Validations and Qualifications, etc.

  • Evaluate the effectivity of corrective action.

  • Collaborate with Corporate RA/QA and operation staff to produce documents which are accurate and executable.

  • Participate in training (conference calls, development of position assessments, cGMP, Safety, etc.

  • Perform equipment and material evaluation to support new processes and procedures.

  • Demonstrate excellent communication skills and interpersonal skills.

  • Perform necessary computer function in Word, Excel, Access, and Word.

  • Perform other duties as assigned.


  • Completion of secondary education or equivalent

  • Knowledge of FDA, GMP, OSHA, CLIA, AABB, iQPP practices and regulation

  • Minimum of ten years full-time, practical workplace experience

Individual must possess the ability to:

  • Perceive situations in a realistic way

  • Understand complex operations from a broad perspective

  • Understands the role of individual units and the interaction of units within the overall organization

  • Read and understand SOPs, and evaluate their proper use

  • Clearly and fluently express concepts and ideas verbally and in writing

  • Fluency in speaking and writing English

  • Work effectively in Microsoft Word to create documents and forms

EEO Minorities/Female/Disability/Veterans


Learn more about Grifols

Req ID: 273028

Type: Regular Full-Time

Job Category: Quality