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Job Description
Genetic Science Division (GSD) is looking for a strong quality leader to lead the Austin Site Quality organization to achieve Quality objectives and assure compliance with industry standards.
The Sr Manager, Quality is a leadership position responsible for implementing and improving Site Quality Management System and Quality Assurance structure to cover various internal functions, build scale, and most importantly, better serve our customers.
This position reports directly to the Sr Director of Quality, GSD.
Key Duties and Responsibilities
Support and provide expertise to the Quality Management System (QMS) and Quality department to successfully meet or exceed goals and targets
Collaborate with the various functions to ensure the quality management system is comprehensive, incorporates standard processes, and is consistent with the strategic plan
Product Development responsibilities including design controls, risk management, document control and record management, and supplier management
Manufacturing responsibilities including master record, training, process controls, labeling, change control, and CAPA
Responsible for monitoring and measurement including validations, calibrations, customer feedback and complaints, internal audits
Responsible for all site quality metrics and reporting for monthly and quarterly business reviews - e.g., Product Complaint rates, Cost of Poor Quality, CAPA, etc.
Support and provide quality expertise to the business process transfer activities - e.g., process implementation/validation
Hire and retain a diverse, highly qualified staff and provides ongoing performance feedback. Set goals which align to department plans and lead the execution of goals through coaching and mentoring
Ensure continuous improvement through the Practical Process Improvement (PPI)
Install and maintain a quality culture - Right First Time
Minimum Requirements/Qualifications:
Bachelor of Science Degree in - Life Sciences, Engineering or related science/engineering degree preferred
10+ years of professional quality experience - quality leadership experience preferred
Understanding of the Life Sciences and IVD/Medical Devices industries and required compliance regulations for Genetic Sciences products and processes
Solid understanding and experience with ISO 9001 and ISO 13485 standards
Experience in MDSAP, IVD/IVDR, 510K and GxP requirements preferred
Ability to travel domestically and internationally - up to 15%
Expert knowledge and experience implementing the following:
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