Director of Quality Assurance

Overview Performing critical work that impacts our industry and our world’s health while problem solving and innovating in the field – that is what the Director of Quality Assurance at KCAS Bio gets to do every day. The Director of Quality Assurance leads one or more QA departments, interacts with executive management, clients, and regulatory agencies regarding quality systems, audits, and inspections, and guides interpretation and implementation of health agency regulatory requirements. As a member of the Senior Leadership Team, you will oversee the quality management system at KCAS Bio, meet department goals and objectives, and maintain expert knowledge of bioanalytical scientific trends and regulatory requirements. Responsibilities Assure Quality systems are designed and performing to meet industry, regulatory, and executive management requirements Initiate employee hire, promotion, discharge, or transfer Participate in the selection process for subordinate personnel including determining recruiting criteria, interviewing, and performing reference checks Perform annual performance evaluations for direct reports Require and monitor training for subordinates to develop them to their potential Effectively use delegation to develop subordinates Perform career planning for subordinates Provide encouragement and positive reinforcement to subordinates; require subordinate leadership staff to do the same Participate in the development of short and long-range goals and objectives, implement and attain short and long-range goals and objectives, and assure that year-end goals are attained Assure that all departmental management staff are working in concert with each other Coordinate activities of the department with related activities of other departments to ensure efficiency and economy Understand, communicate and cascade communication from Executive management Be knowledgeable of site departmental budget and monitor and analyze cost against budget Overall responsibility for the Quality Assurance operation, compliance and site department goals including budget management Interact with clients relating to quality audits, respond to client audit reports, and understand client needs/expectations Complete client QA questionnaires and respective QA-assigned sections of RFIs Forecast, recommend and justify strategies to accommodate growth when needed (space, equipment, staffing) Establish policies and procedures to ensure that QA operations maintain a high level of QA expertise and comply with related regulatory policies, OSHA and company SOPs/policies Audit reports, data, internal processes, computer system validations, facility, and procedures to support management to improve data integrity, reduce error rates, efficiency, and maintain compliance Manage internal auditing program including planning, conduct and reporting of audits Conduct annual management review of the quality system Manage digital quality systems, including eQMS administration, archiving, and related scanning Ensure appropriate validation of methodology and instrumentation per regulatory requirement/industry expectation Oversee CAPA system to ensure effective continuous improvement Coordinator and back-up within the department Perform and track vendor quality assessments Review/update SOPs to reflect current practice and regulatory requirements Maintain expert knowledge of bioanalytical scientific trends as well as regulatory requirements Perform complex quality assignments with understanding of underlying scientific principles Recommend and institute systems and programs to improve safety, work quality, cost saving and productivity Effectively interface with various functional units, groups or departments in the company Qualifications Bachelor’s degree in a related field Director-level experience preferred 10 years industry-related experience, including 2 years supervisory experience Experience in a CRO or pharmaceutical company is preferred Broad knowledge of regulatory requirements applicable to areas managed Extensive knowledge of processes applicable to subordinate groups Awareness of industry trends related to areas managed Computer proficiency Perform all aspects of the job in a way that supports the company brand and the company mission, vision, and values What you’ll get Our benefits include, and extend beyond, the traditional package. At KCAS Bio, you will enjoy company sponsored events like food trucks, family days and spirit days. You will grow in your career with KCAS University. You will be able to connect with like-minded employees to further KCAS Bio's approach to key areas such as wellness, inclusion, and community outreach. You will engage as an owner in our stock ownership program. You will have access to the latest technology. And you will be able to invest in the community with paid time off to volunteer. Who we are We are a fast-growing contract research organization (CRO) headquartered in Kansas City, pioneering the latest drug development in both human and animal health fields. We advance both great science AND great people. EEO and how to apply KCAS Bio is proud to be an Equal Opportunity Employer. We provide equal employment opportunities without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, sex, sexual orientation, gender identity, or any other legally protected category. We recruit qualified candidates without regard to citizenship status based on internal processes that enable us to hire the right candidates consistent with the appropriate U.S. Immigration framework. We work with and provide reasonable accommodations to individuals with disabilities and for sincerely held religious beliefs, observances, and practices. Anyone who needs reasonable accommodation may email View email address on click.appcast.io or call View phone number on click.appcast.io (for TTY assistance call 711) and ask for Human Resources.

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