| Operations Quality Manager ||| No H1 CPT ||| Elkton MD ||| Onsite at Elkton, Virginia, USA |
| Email: [email protected] |
| From: mayank, winorbittech [email protected] Reply to: [email protected] Dear partners, Hope you are doing great. Please find below job requirements and share the details and resumes if you have any matching resource. Job Title: Operations Quality Manager Reporting to: Sr. Manager of Quality Operations Work location: required onsite located in 950 Elkton Blvd, Suite 200 Elkton MD 21921-5322 Visa : No H1/CPT Operations Quality Manager 10+ years of relevant experience including 5+ years of management experience Job #: Operations Quality Manager: A leading Global Medical Device company is looking to hire a Operations Quality Manager to start ASAP. Looking for Operations Quality manager with experience in Medical Device Operations Quality, CAPA, Management Experience, NCR, Root Cause, Statistical Background with 5+ years management experience. Required Quality Manufacturing Operations experience. We will review resume strong Quality Operation manager candidates with Medical Device experience. Terumo Medical Corporation (TMC) develops, manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range of applications for numerous areas of the healthcare industry. TMC places a premium on providing customers with world-class products, training and education programs that drive clear economic value, better clinical outcomes and improved quality of life for patients. TMC is part of Tokyo-based Terumo Corporation; one of the worlds leading medical device manufacturers with $5+ billion in sales, 20,000+ employees worldwide and operations in more than 160 nations. Terumo Medical Corporation is comprised of two strategic business divisions: Terumo Interventional Systems and Terumo Medical Products. Job Summary The Manager, Quality Operations is responsible for managing quality operations functions within the respective manufacturing facility. S/he is responsible for ensuring compliance with the applicable regulations of all countries in which Terumo Medical either manufactures or distributes products including, but not limited to the U.S. Quality System Regulation, Japanese Pharmaceutical Affairs Laws, the Canadian Quality System Regulation, and the Medical Device Directive. Job Details/Responsibilities Establish and promote a work environment that supports compliance with the TMC Quality System and company policies Support the development of efficient and effective methods for meeting Quality System requirements. Prepare, communicate, and evaluate team goals and objectives for continual improvement of the quality system. Ensure linkage to Strategic Quality Plan. Manage a team of Quality Engineers in driving robust problem solving, NC reduction and continual improvement efforts. Drive values stream optimization through the application of proven methodologies such as Six Sigma, LEAN, Kaizen events etc. Promote production line value stream characterization and optimization efforts. Ensure process control plans (SPC, sampling, inspection methods) are appropriate and effective. Ensure operations related CAPA activities are managed in a complete and timely manner. Effectively partner with Operations Managers and Supervisors to develop and implement strategies which promote the Terumo Quality Culture throughout operations. Ensure transfers to manufacturing are data driven and robustly executed. Job Responsibilities (continued) Partner with internal support functions (i.e. laboratory operations, calibration & metrology, supplier control, distribution etc.) to achieve functional excellence. Manage Quality Assurance inspection staff and processes related to incoming inspection and release of finished goods. Manage Quality Control staff activities. Support activities associated with environmental controls and monitoring. Prepare for, and support compliance audit activities in Operations Maintain Quality Performance Indicators in support of management oversight activities Support the preparation and conduct of compliance forums such as Quality System Management Reviews, Change Board Meetings, NC/CAPA Board meetings etc. Promote the professional growth and development of staff personnel Knowledge, Skills and Abilities (KSA) o Knowledge of national and international regulations applicable to medical devices including; Quality System Regulations, 21 CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO 14971, ISO 13485, and MDR etc., LEAN o Prior experience in medical device manufacturing environment coupled with certifications from ASQ preferred o Ability to identify the strategic direction of the quality assurance system required o Ability to analyze and interpret all regulatory and quality guidelines as needed o Demonstrate a strong understanding and working knowledge of the Quality Sciences (Acceptance Sampling, SPC, continual improvement, Six Sigma, LEAN, Design of Experiments, COQ, Cause & Effect analysis etc.) o Demonstrate a strong business partner approach and attitude providing creative and innovative solutions that meet quality standards Qualifications/ Background Experiences o Bachelor degree in science/math required o Minimum of 10 years Quality Assurance experience o Minimum 5 years management experience o Six Sigma/LEAN experience, expertise preferred o Must be proficient in Microsoft Excel, Word, PowerPoint, and Outlook Thanks and Regards, Mayank Bijlwan Technical Recruiter + 1 813 412 5257 Winorbit Tehnology LLC 10834 Breaking Rocks Dr Tampa, FL 33647 Keywords: Florida Maryland North Carolina |
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| Fri Aug 04 02:04:00 UTC 2023 |