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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.