Hi, Hope you are doing great! Please find the requirement below , If you find yourself comfortable with the requirement please reply back with your updated resume and I will get back to you or I would really appreciate if you can give me a call back at my contact number *408-457-9399 ext 2050*
*Role::** Validation Lead* *Location::** Rosewood, CA* *Duration::** 12+ months* *Job Description::* *Job Title* Validation Lead *Relevant Experience* *(in Yrs)* 9+ *Technical/Functional Skills* · Excellent verbal and written communication skills, Customer Service Focused; Information Technology background, experience within a Quality/Regulated environment including SDLC. · Strong interpersonal and technical writing skills and the ability to interact across divisional boundaries. · Ability to manage multiple tasks and projects simultaneously, and to prioritize work, goals and tasks per the divisional and corporate objectives. - Ability to report results clearly and concisely. Sound reasoning and ability to quickly analyze and solve complex problems. - Significant Work Activities & Conditions Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) - Experience with Quality Center (HP Quality Center) preferred. *Experience Required* *Roles & Responsibilities* - Lead/support validation efforts and deliverables for systems used for Discovery/Instruments/Clinical/Pre-clinical with minimal oversight. - Develop the validation testing strategy for large and medium sized projects and develop the overall Validation plans and timetables. - Create and execute validation test scripts and document test results in accordance with company standards. - Review and evaluate validation assessments for application systems/projects. - Ensures that validation project documentation is in compliance with company policies and procedures - Prior Experience with validation of Discovery/instruments/Clinical systems preferred. - Require prior experience in creating Change Requests, Developing Validation Plan, test scripts, Summary Reports, Traceability Matrix and other validation project documents in the Pharmaceutical industry preferred. - Create and execute validation test scripts and document test results in accordance with standards (Manually or in Quality Center) - File validation documentation within following Quality Assurance Library guidelines. - Ensures that project documentation is in compliance with AbbVie’s policies and procedures - Provide monthly reports on of validation activities in the organization to Validation SME and/or Manager *Generic Managerial Skills* *Education* - Associate Degree minimum or equivalent combination of education in science and work experience. *Start date* (dd-mmm-yy) 1-Jun-2015 *Duration of assignment *(in Months) 12 months *Work Location* Rosewood, CA *Thanks & Regards,* Vaishali Tyagi Sr. Technical Recruiter *IDC TECHNOLOGIES INC* | *1851 McCarthy Boulevard, Suite 116, Milpitas, CA , USA, 95035* *Phone No.: 408-457-9398 ext-2050 I Email: **[email protected]* <[email protected]>* I* *Gtalk: **[email protected]* <[email protected]> *Web: **www.idctechnologies.com* <http://www.idctechnologies.com/> "Under Bill s. 1618 Title III passed by the 105th U.S. Congress this mail cannot be considered spam as long as we include a way to be removed from our mailing list. Simply send us an e-mail with REMOVE in the subject and we will gladly REMOVE you from our mailing list." -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" 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/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
