What qra management contributes to cardinal health qra management is responsible for strategic oversight and leadership direction over multiple job families or areas of expertise within the qra function. Accountabilities manage day-to-day quality control functions including
quality control: scheduling of inspections, line support and testing
document control: management of all pertinent data bases
quality related audits and certifications
partners with site director and managers to recruit, hire, develop/supervise and train quality control and document control personnel including performance reviews in accordance with departmental and corporate practices
define, communicate and enforce quality policies focused on cah and external compliance and regulatory
coordinate qra functions and activities between departments.
determine responsibilities and procedures for ensuring that this function is performed effectively, and objectives are achieved
participate and assist in the formulation and establishment of organizational policies and quality procedures for the quality control department
participate and lead systems improvements project teams as required
meet with production management on a regular basis and support goals outlined in the company's operating plan
budgeting, planning and resource evaluation in line with zero base management initiatives
develop strategies to implement quality system regulations and continuously improve quality processes
promote communication, development and process improvement
solid leadership skills with the ability to influence others to ensure adherence to quality excellence
qualifications (minimum requirements) bachelor's in engineering, life sciences or similar 5+ years' quality experience in related field within medical industry environment 3+ years management experience - solid leadership and influential partnership skills advanced fluency in english / spanish strong product manufacturing technical background as well as knowledge of medical device quality system regulations experience in product manufacturing transfers, facility/line startup, etc. Experience in product design and transfer processes usa to mex or similar experience managing external regulatory agency compliance audits (fda, iso13485) highly preferred kaizen, six sigma certification highly preferred ability to travel up to 20% what is expected of you and others at this level manages department operations and supervises professional employees, frontline supervisors and/or business support staff
participates in the development of policies and procedures to achieve specific goals
ensures employees operate within guidelines
decisions have a short term impact on work processes, outcomes, and customers
interacts with subordinates, peer customers and suppliers at various management levels and may interact with senior management
interactions normally involve resolution of issues related to operations and/or projects
gains consensus from various parties involved
#j-18808-ljbffr