Hello Employer, Hope you are doing well!
We have an opportunity for *SAP – Pharma Compliance and Validation Analyst* with one of our clients in *Raritan, NJ OR Rochester, NY**.* Please see the job details below and let me know if you would be interested in this role. If interested, please send me a copy of your resume, your contact details, your availability and a good time to connect with you. *T**itle: **SAP – Pharma Compliance and Validation Analyst* *Location: **Raritan, NJ OR Rochester, NY* *Terms: Contract* *Job Details:* - To manage and ensure that the project schedules are adhered to as per the client specifications and deliveries are as per the time and quality standards. - Minimum of 7 to 8 years of experience in a regulated environment: pharmaceutical, biotechnology r related industry. - Hands on experience in *Validation of SAP modules.* - *Good understanding of Supply chain and manufacturing of Pharma and medical devices* - 2 to 3 years of experience (preferred) in leading teams; - Good Understanding of FDA (21 CFR Part 210 & 211, 21 CFR Part 11)and European compliance regulations (Eudralex Vol 4) and GAMP guidelines applicable to computer system validation; - Authoring/executing Validation Master Plan, Installation Qualification (IQ), Risk Assessment/GxP assessment, Operational Qualification (OQ), and Performance Qualification (PQ) Protocols, Test Scripts, and Completion/Summary Reports as per the compliance requirements. - Possess excellent verbal and written communication skills; - Position demands an individual who is willing to travel. - Mentoring more junior members of the validation team, and for managing medium-sized projects independently as required. - Responsible for participating in and contributing to team meeting. *Basic Qualifications:* - Bachelor’s degree in computer science, computer engineering, life science, or any other pertinent degree; - Minimum of 2 years professional experience in pharmaceutical computer systems validation OR in computer systems quality assurance (pharmaceutical and/or consulting background). - Technical proficiency with the Microsoft Office suite of tools required, especially Microsoft Word and Excel - Experience with a Validation of GxP applications *Thanks,* *AMIT**CYNET SYSTEMS Inc* <[email protected]> <[email protected]> *[email protected]* <[email protected]> *Ph:703.880.5236 | Fx:866.838.0907 | WWW.CYNETSYSTEMS.COM <http://www.cynetsystems.com/>* *IT & ENGINEERING CONSULTING* -- 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.
