Grifols Jobs

789 </p><p></p><p><img src="http://www.grifols.com/documents/239901/1137346/SuccesFactors_1020x93_jobposting_line_test.png/ec7da48f-8161-41cb-b53a-7a36f6a376a6" width="100%"></p><p></p><p></p><p><a href="http://www.grifols.com/es/web/international/home" target="_blank">Learn more about Grifols</a></p><p></p><br><strong>Req ID:</strong> 229652 <br><strong>
able.MiTabla { max-width: 1020px;!important </p><img align="top/" alt="" src="https://www.grifols.com/documents/239901/1024085001/SSFF_01_BSC.jpg/94a9db8b-2c43-45fd-994e-0896e715aac7"><p style="text-align:justify">Do you want to join an international team wor
vices in more than 100 countries and regions. </p><img src="http://www.grifols.com/documents/239901/1137346/SuccesFactors_1020x93_jobposting_line_test.png/ec7da48f-8161-41cb-b53a-7a36f6a376a6"><p><strong>Manufacturing Quality Assurance Coordina

Job Information

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

SUMMARY:

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

requirements.

RESPONSIBILITIES:

  1. Assist management with planning, implementing, monitoring and maintaining the quality program

throughout the facility.

  1. Review all records as required by procedures, for completeness, correctness, and compliance to

product specifications.

  1. Host internal and external audits and inspections.

  2. Assist with the preparation of and/or reviews all manufacturing related validation protocols, as

assigned.

  1. Perform calibrations on equipment and instruments, as assigned.

  2. Assist with the maintenance of procedure manuals so that accurate and current SOPs are available for

employee use.

  1. Assist with the maintenance of files of customer specifications and procedures.

  2. Monitor employee compliance with procedures, GMPs, customer specifications, applicable government

regulations and industry practices; report any procedural or practice noncompliance.

  1. Promotes, complies, actively participates and enforces the Safety Procedures, to help maintain a safe

and healthy work environment.

  1. Assist in monitoring and timely resolution of all error and/or accident reporting.

  2. 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.

  1. Assist with the development and implementation of standard operating procedures for all

manufacturing operations.

  1. Assist in the initiation of continuous improvement activities utilizing the change

Page 2 of 2 JD-453 A (0712)

management process and incorporation of best practices.

  1. Inform Corporate Quality Assurance of any quality concerns.

  2. Perform other duties as required.

PERSONAL ATTRIBUTES:

  • 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

QUALIFICATIONS:

Requirements:

  • 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.

EEO Minorities/Females/Disability/Veterans

#biomatusa

CLK 789

Learn more about Grifols

Req ID: 229652

Type: Regular Full-Time

Job Category: Nursing/Healthcare

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