Senior Quality Engineer

  • Anywhere

Company :

Location :
West Carrollton City, Ohio

Expiry Date :
Mon, 14 Jun 2021 23:59:59 GMT

Apply Job :
Open Link

Description :
Job Summary and Primary Responsibilities Designs, implements and maintains quality assurance protocols and methods for processing materials into finished products. Plans and manages the compliance of manufacturing and production processes with internal and external safety, quality and regulatory standard requirements for worldwide distribution. Develops methods and procedures for inspecting, testing and evaluation of the precision and accuracy of production processes and equipment. Performs report and production data analysis to identify trends and recommend updates or changes to quality standards and procedures. Upholds the company’s quality standards and testing systems to reflect efficiency, reliability and performance. Creates documentation to report issues and errors relating to the production process. – Evaluates product and process changes for qualification and validation requirements, and participates in change implementations – Develops and implements inspection criteria and ensures inspections are performed by qualified personnel, and that inspection results and documentation support the recommended disposition action – Conducts investigations, initiates, and processes all necessary actions from quality system feedback such as records review, non conforming materials reports, corrective action reports, complaints, and audit reports – Leads Design Control activities such as risk assessment, supplier quality plans, design verification and validation, cleaning validations, and sterilization and packaging validation – Identifies opportunities of improvement, and coordinates the development of criteria and documentation to facilitate the analysis and enhancement of various quality systems program elements – Perform other duties as assigned Required Skills / Capabilities – High proficiency in computer technology including MS Office applications, with strong analytical and problem-solving skills – Able to work efficiently in a team environment and collaborate cross-functionally – Strong attention to detail and solid organizational skills – Perform duties to compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13467 Education and Experience – Typically requires a minimum of 5 years of related experience with a Bachelor’s degree or 3 years and a Master’s degree; or a PHd without experience or equivalent work experience – Bachelor’s degree in an engineering discipline – American Society for Quality Certified Engineer (CQE) highly desirable NuVasive is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran status and will not be discriminated against on the basis of disability. The EEO is the Law poster options are available here. NuVasive’s EEO policy is available here. About NuVasive NuVasive, Inc. (NASDAQ: NUVA) is the leader in spine technology innovation, with a mission to transform surgery, advance care, and change lives. The Company’s less-invasive, procedurally integrated surgical solutions are designed to deliver reproducible and clinically proven outcomes. The Company’s comprehensive procedural portfolio includes surgical access instruments, spinal implants, fixation systems, biologics, software for surgical planning, navigation and imaging solutions, magnetically adjustable implant systems for spine and orthopedics, and intraoperative neuromonitoring technology and service offerings. With more than $1 billion in net sales, NuVasive has approximately 2,700 employees and operates in more than 50 countries serving surgeons, hospitals, and patients. For more information, please visit .