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Supplier Quality Engineer | Quality Engineer in Quality Assurance Job in Memphis TN | 7278686014

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Supplier Quality Engineer

Location:
Memphis, TN
Description:

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well:being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary This position reports to the Associate Director Regulatory Affairs and Compliance and will be responsible for supporting the improvement, implementation and continuous maintenance of the Supplier Quality Management Program. This position will also collaborate with key internal and external (i.e. clients) business stakeholders and work cross functionally on continuous improvement activities to drive effective, compliant, and sustainable solutions/ outcomes. Incumbent will apply quality management and continuous improvement theory, technical principles and expert judgment to proactively assist the business in the identification of potential risk. Incumbent will lead activities to ensure mitigation, improve compliance and enhance performance of key Quality activities. Core to these activities will be the ability to effectively manage projects and foster effective interdepartmental and cross:functional partnerships. typedisc:: Develop, improve and maintain the Supplier Quality Management Program.: Lead, support, and/or perform activities in the following areas: Supplier Audits, Supplier Qualifications/ Re:qualifications, Supplier Corrective Action Reports (SCARs), Internal Corrective Action/Preventative (CAPAs), Non:Conformances (NCs), Change Controls, and Training.: Compile and report key performance indicators (KPIs), metrics and compliance status of Supplier Quality Management Program for Quarterly Management Review (QMR), Weekly Site Performance and other Quality Systems as needed.: Communicate weekly with manager on KPIs for Vendor Management.: Maintain the Approved Supplier List (ASL) in the Electronic Data Management System (EDMS).: Maintain the supplier scorecard.: Create and maintain supplier audit schedule.: Provide exceptional customer service to Cognate's internal and external customers in all assigned tasks and foster a GMP compliant culture.: Establish a continuous improvement program through the use of Total Quality Management (TQM) techniques.: Ensure compliance to quality policies, procedures, and governing regulations. Job Qualifications typedisc:: Bachelor's degree in Life Sciences, Engineering or related field with minimum three (3) years experience in a biologics, biotechnology, pharmaceutical, medical device, or related industry : OR : Associates degree in Life Sciences, Engineering or related field with minimum five (5) years experience in a biologics, biotechnology, pharmaceutical, medical device, or related industry.: Six Sigma experience or certification and/or Supplier Quality Engineer certification desired, not required.: Ability to work independently and in a group on a variety of projects.: Ability to maintain a high degree of accuracy and attention to detail.: Ability to handle a fast:paced, multi:tasking environment, and prioritize effectively.: Competency with electronic document managements systems, preferably MasterControl.: Proficiency in Microsoft Office (Word, Excel, Outlook, etc.).: Prior experience SOP, and or Procedure Development writing.: Excellent written and oral communication skills with a thorough knowledge of grammar, spelling and punctuation. The pay range for this position is 85,000 : 89,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. About Biologics Tes
Posted:
May 22 on Tip Top Job
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