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Hi Partners, Please find below requirement and kindly send me suitable profiles ASAP * * *Validation Engineers* *Location: Menlo Park, CA * *Duration : 6 months+* *Job Description:* Skilled Validation Engineer to perform process and equipment validation functions including protocol generation and execution, risk assessments and validation impact assessments to maintain a high level of compliance with GMP *General Summary:* Participates in the development, implementation and adherence to validation test procedures (processes & equipment) ensuring product(s) meet appropriate regulatory agency validation requirements, internal company standards and current industry practices. This may include one or more of the following: · Prepares and reviews validation protocols and final reports (IQ, OQ and PQ). · Develops and revises standard operating procedures (SOPs). · Assists with equipment selection and specification. · Coordinate the proper approval of plans and protocols. · Monitors validation change control and/or corrective actions. · Writes validation protocols and final reports (IQ, OQ and PQ). · Documents and reviews standard operating procedures (SOPs). · Coordinates the proper approval of plans and protocols. · Supports regulatory inspections or audits. · Tracks and coordinates validation change control and/or corrective actions. *Job Requirements:* · Bachelor’s degree in a scientific or engineering discipline or equivalent. · Proficient in MS Office applications. · Experience with medical device based products and processing and technologies · Experience with Cordis/Conor Medsystem -- You received this message because you are subscribed to the Google Groups "OracleD2K" group. To post to this group, send email to oracle...@googlegroups.com. To unsubscribe from this group, send email to oracled2k+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/oracled2k?hl=en.