Quality Manager - Plasma Center

rEVO Biologics, Inc.

  • Greenacres, WA
  • 30+ days ago
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    Skills

    • Analysis Skillsunmatched
    • Biologyunmatched
    • Communication Skillsunmatched
    • Computer Skillsunmatched
    • Corrective and Preventative Action (CAPA) Systemsunmatched
    • Current Good Manufacturing Practice (cGMP)unmatched
    • Data Collectionunmatched
    • Detail Orientedunmatched
    • Disciplinary Actionunmatched
    • Document Controlunmatched
    • Document Managementunmatched
    • Educational Technologyunmatched
    • FDA Requirementsunmatched
    • Follow Throughunmatched
    • Manual Dexterityunmatched
    • Mathematicsunmatched
    • Multitaskingunmatched
    • Operational Supportunmatched
    • Operationsunmatched
    • Organizational Skillsunmatched
    • Performance Analysisunmatched
    • Physical Demandsunmatched
    • Plasmaunmatched
    • Presentation/Verbal Skillsunmatched
    • Problem Solving Skillsunmatched
    • Quality Assuranceunmatched
    • Quality Assurance Methodologyunmatched
    • Quality Managementunmatched
    • Quality Metricsunmatched
    • Regulationsunmatched
    • Specimen Collectionunmatched
    • Standard Operating Procedures (SOP)unmatched
    • Technical Writingunmatched
    • Testingunmatched
    • Training/Teachingunmatched
    • Willing to Travelunmatched
    • Writing Skillsunmatched

    Description

    Essential Job Responsibilities and Duties

    • Facilitating and evaluating center and equipment readiness
    • Responsible for all quality personnel functions including hiring, assignment and direction of work, development and training, disciplinary actions and termination, and the maintenance of all quality personnel records
    • Oversee daily actions that facilitate product collection (sample collection and submission; testing results, staging)
    • Assist the Quality Assurance Unit (QAU) ensuring donor center records are complete and accurate
    • Ensure shipments (sample, product, waste, etc.) are managed and labeled accurately
    • The interpretation and application of SOPs; and, ensuring SOP revisions are implemented correctly, efficiently and effectively
    • The receipt, approval and release of donor center supplies.
    • Assist Center Management and Training Coordinator to ensure training is conducted and documented as directed, review and prepare for inspections/audits, and to develop CAPA, and other quality duties as assigned
    • Oversee and manage the center's Deviation Management System to ensure adequate investigations are completed, accurate root cause(s) identified, and CAPA process is identified and managed
    • Track and trend the center's quality and operational metrics with respect to applicable SOPs.
    • Perform periodic self-assessments of the center's quality and compliance
    • Administratively oversee the performance and submission of the center's Proficiency Testing process (Note: this does not replace any CLIA regulated process)
    • Manage the document control process of the center and suggest necessary SOP changes as required
    • Supervise the center's Quality Assurance Unit employees
    • Work effectively and partner with the Field Quality, Operations support, Center Director and Corporate staff to ensure daily operations are in full compliance
    • Maintain an open line of communication with Management
    • Responsible for working through multiple projects and managing multiple competing priorities.
    • Other duties as assigned

    Qualifications

    • Bachelor's Degree in a scientific discipline, life sciences or related discipline preferred or

    (12) twelve months experience related to quality, regulatory or related industry provided that the experience was obtained in a regulated environment.

    • Necessary education/experience may be substituted for the position with approval from the Director of Quality Assurance or VP of Quality Assurance.

    Requirements

    • Must be fully signed off and capable of performing duties of the Manager of Quality Assurance
    • Demonstrate expertise in interpreting cGMPs, FDA regulations, SOP development, as well as an understanding of quality principles
    • Good oral and written communication skills
    • Ability to work independently with little supervision
    • Demonstrated ability to define problems, collect data, establish facts and draw valid conclusions
    • Strong verbal and written communication skills
    • Must have above average problem-solving and decision-making abilities
    • Proficiency with computers
    • Must have explicit attention to detail
    • Must have excellent analytical skills, organization skills, and follow-up
    • Ability to read and interpret documents such as safety rules, operating and maintenance instruction, and procedure and technical manuals
    • Ability to interpret a wide variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables

    Physical Requirements

    • Use hands to handle or feel objects, tools, or controls; reach with hands and arms; and talk or hear
    • Frequent leaning, bending, stooping, crouching, and reaching above the shoulders and below the knee
    • Manual dexterity to perform all phases of donor plasmapheresis
    • Ability to stand for extended periods of time for up to four (4) hours at a time
    • Ability to sit for extended periods of time for up to (4) hours at a time and view a computer screen
    • Ability to lift, tug, pull up to fifty (50) pounds
    • Ability to travel by plane, or car as required to train or assist other centers as needed.

    Numbers & Facts

    LocationGreenacres, WA

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