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 "oraapps" 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/oraapps. For more options, visit https://groups.google.com/d/optout.
