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The Director of Quality Control is responsible for technical, quality, and managerial oversight specific to the Quality Control Department to support the Company’s existing products and production.
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ADMA Biologics currently has an opening for a Director of Quality Control in Boca Raton, FL. Support tech transfer of new methods from analytical development and contract laboratories to the Quality Control Laboratory.
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Supervise, orient, train, evaluate, and counsel department employees to improve their job performance and to maintain high standards of performance and patient quality care, in conjunction with the Regional Director of Operations and Human Resources.
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The Director of Rehabilitation (DOR) is responsible for managing and supervising the rehabilitation department to meet resident needs, the company’s fiscal requirements, and federal and state regulations.
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A member of the DES executive team, the Quality Director is responsible for the oversight and strategic development of a comprehensive quality program and is accountable for quality assurance and compliance activities, focusing efforts on outcomes that will resolve program deficiencies and enhance the disability supplement process for both external and internal parties, most notably the main customer of the program (MassHealth disability applicants.
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The Director will be tasked to drive CMS Star and Leapfrog ratings, and other key quality metrics. JOB DETAILSNew Director Needed to Lead All Inpatient and Outpatient Quality Services with Reid Hospital and Health Care Services as Director of Quality.
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Assist in performance of all Quality Assurance functions as outlined in the GLPs and PSL SOPs. Assist the Quality Assurance Director as needed during inspections by EPA, FDA or clients.
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Working cross functionally with Analytical Development, Process Development, Manufacturing, MSAT, Regulatory, and Quality Assurance departments. Facilitate the maintenance of the lab including routine housekeeping, lab inventory, and equipment Contribute to team building, training, and problem-solving initiatives Professionally develop analysts to improve on individual and overall performance Communicate effectively with other relevant groups, including but not limited to Quality Assurance, Manufacturing, and Process Development Contributing to CMC sections of regulatory filings including IND, NDA, and BLA submissions.
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To support these requirements, the Director of Quality must be forward-thinking and work closely with the Director of Operations, Director of Sales, Director of Engineering, Director of Human Resources and Director of Finance/Systems.
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Reporting to the Director will be the Manager of Quality Management and Patient Safety Officer, Infection Prevention, and multiple Quality Analysts. Reporting up to the Chief Nursing Officer, the Quality Director oversees the regulatory preparedness throughout the hospital.
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JOB REQUIREMENTS: Your Job Phillips-Medisize, a Molex Company, isseeking a Director of Quality to oversee the effective execution ofquality systems, representing the business to align with FDA and otherregulated bodies, and provide global leadership and direction to theQuality teams globally.
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Primary Function: The Director of Quality requires a high degree of autonomy and creativity in analyzing and investigating causes for and variation in process improvement and workflows that result in error or critical events facilitating improvements at the FQHC. The Director is responsible for overseeing continuous quality improvement efforts at the federally qualified health center (FQHC) with special focus on clinical care, clinical quality and performance measures, and patient satisfaction.
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Associate Quality manager is the acting SQF Practitioner and assumes all SQF. Maintain written/signed records of each periodic inspection and submit written status reports of each study to management / study director.
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The Director of Quality must be extremely organized, detail-oriented, and bring positive and high energy to the position, supporting a culture of excellence and leading by example. The Director of Quality ensures TriMark products are made per specification and supports production in delivering quality products on time to the customer, with a sense of urgency.
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The Associate Director, In-Vitro Diagnostics/ Precision Medicine Quality supports the use of In-Vitro Diagnostics (IVD), including Companion Diagnostics (CdX), and Precision Medicine applications to clinical research and development.
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