A new Job, ID: 215747 <http://ejobsville.com/display-job/215747> was added at eJobsVille.com - For the Best Tech Jobs in Town <http://ejobsville.com>
Title: Validation Engineer with Medical Device posted on 2014-07-30 15:57:51 Job Description:Job title: *Process Validation Engineer* Location: Irwindale, CA 91706 Duration: 6-12 Months Contract *Required Skills:* Need to have Strong Process validation experience in medical devices industry. Strong medical devices industry experience. Need to have Mechanical engineering background. 3+ years of medical device process development experience in production environment. Degree in Mechanical Engineering - B.E / B.Tech / B.S / M.E / M.Tech / M.S Knowledge of medical device design controls. Performs and directs process validations, IQ, OQ, PQ, TMVs as required. Oversees the validation program: schedules, files, and records. Administers validation training for the facility Demonstrated knowledge of risk management techniques. Interfaces with Quality and Manufacturing Engineers to review processes, determine validation requirements, and coordinate the validation. Demonstrated knowledge of CAPA process and root cause investigation. Coordinates and performs testing relating to the validation. Familiar with working within formal design control processes, writing test protocols and reports. Works with suppliers, management, Engineers, and Manufacturing Associates in the resolution of quality problems associated with the validation program. Performs internal and external audits associated with validation activities. Utilizes advanced statistical tools to determine sampling plans and to analyze data associated with validation activities. Oversees and directs the activities of the Validation Engineers / Technicians Proven record of interpersonal skills to handle client, Result oriented and self-driven. Job Requirements: Need to have Strong Process validation experience in medical devices industry. Strong medical devices industry experience. Need to have Mechanical engineering background. 3+ years of medical device process development experience in production environment. Degree in Mechanical Engineering - B.E / B.Tech / B.S / M.E / M.Tech / M.S Knowledge of medical device design controls. Performs and directs process validations, IQ, OQ, PQ, TMVs as required. Oversees the validation program: schedules, files, and records. Administers validation training for the facility Demonstrated knowledge of risk management techniques. Interfaces with Quality and Manufacturing Engineers to review processes, determine validation requirements, and coordinate the validation. Demonstrated knowledge of CAPA process and root cause investigation. Coordinates and performs testing relating to the validation. Familiar with working within formal design control processes, writing test protocols and reports. Works with suppliers, management, Engineers, and Manufacturing Associates in the resolution of quality problems associated with the validation program. Performs internal and external audits associated with validation activities. Utilizes advanced statistical tools to determine sampling plans and to analyze data associated with validation activities. Oversees and directs the activities of the Validation Engineers / Technicians Proven record of interpersonal skills to handle client, Result oriented and self-driven. *Click here to view full job description and apply <http://ejobsville.com/display-job/215747> (Registration not mandatory to apply for this job)* ------------------------------ Best regards, eJobsVille.com - For The Best Tech Jobs In Town -- You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To unsubscribe from this group and stop receiving emails from it, send an email to open-source-erp-crm+unsubscr...@googlegroups.com. To post to this group, send email to open-source-erp-crm@googlegroups.com. Visit this group at http://groups.google.com/group/open-source-erp-crm. For more options, visit https://groups.google.com/d/optout.
