Hello Partner, Hope you are doing great.
Please let me know you have suitable consultants for *Validation Engineer** with Medical Devices industry experience* Please send resumes to *[email protected] <[email protected]>* *Title: Validation Engineer* *Location: *West Chester / PA, Jenner vile / PA, Monument / CO, Palm Beach Gardens / FL and Elmira / NY *Duration: 9 months* *Required Skills:* · *Medical Devices , Manufacturing/ Test equipment validation* · *Must have Medical Devices industry experience ONLY. * *Overall Responsibilities: * § Project Quality Support in the CSV Equipment Legacy Review § Project Quality Support in CSV Equipment Remediation Projects *Tasks: * § Cover the part of the GxP-Compliance in the project. § Creation of the Validation documentation for GxP relevant system elements. § Know and follow the guidelines regarding the code of conduct, ethics and compliance programs and other relevant regulations *Extended Duties: * § Planning, coordination, execution and reporting of activities related to the project Requirements: § Higher education (Engineer or similar) and background in IT § Experience in similar position or extended experience as executer required. § Knowledge of national and international regulations and standards § GAMP5, ISO 13485, ISO 62304, FDA QSR, 21 CFR, Part 820, Part 11 § CSV Experience in the area of Medical Devices Manufacturing § Team Player § Excellent Communication skills *Title: Sr Validation Engineer* *Location: *West Chester / PA, Jenner vile / PA, Monument / CO, Palm Beach Gardens / FL and Elmira / NY *Duration: 9 months* *Required Skills:* · *Medical Devices , Manufacturing/ Test equipment validation* · *Must have Medical Devices industry experience ONLY. * *Overall Responsibilities: * § Project Quality Support in the CSV Equipment Legacy Review § Project Quality Support in CSV Equipment Remediation Projects § Team Lead of Site CSV Equipment Team *Tasks: * § Cover the part of the GxP-Compliance in the project. § Creation of the Validation documentation for GxP relevant system elements. § Know and follow the guidelines regarding the code of conduct, ethics and compliance programs and other relevant regulations *Extended Duties: * § Planning, coordination, execution and reporting of activities related to the project Requirements: § Higher education (Engineer or similar) and background in IT § Experience in similar position or extended experience as executer required. § Knowledge of national and international regulations and standards § GAMP5, ISO 13485, ISO 62304, FDA QSR, 21 CFR, Part 820, Part 11 § CSV Experience in the area of Medical Devices Manufacturing § Team Player § Excellent Communication skills § Leadership skills Thanks & Regards *Srikanth Kumar.V* IT Recruiter Email: [email protected] Phone:732-659-5594 *Gtalk: srikanthkumar.recruiter* *YIM: srikanthv.recruiter* *www.Yochanait.com* <http://www.yochanait.com/> *Best Way to reach me through EMAIL....................* [image: image006] [image: image003] -- You received this message because you are subscribed to the Google Groups "Open Source J2EE frameworks" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/open-source-j2ee-frameworks. For more options, visit https://groups.google.com/d/optout.
