*Hi,* *Hope you are doing great!*
Please find the detailed job description mention below. It will be really appreciated if you can provide me the updated resume at your earliest. *Looking forward for your response.* *Role:* Validation Lead *Location: *Waukegan, IL *Duration: *12 months *JOB DESCRIPTION:* *Technical/Functional Skills * • 7 to 10 minimum years of experience in the Pharmaceutical industry. • 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) • Associate Degree minimum or equivalent combination of education in science and work experience. *Roles & Responsibilities * • Lead/support validation efforts and deliverables for systems used for Discovery/Development Sciences/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. • Review and Trace validation test scripts and documented test results, in accordance with company standards, to verify full test coverage, based on VRB Approved Validation Strategy, and acceptable results. • 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/Development Sciences/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 • File validation documentation within Quality Assurance Library guidelines. Ensures that project documentation is in compliance with AbbVie’s policies and procedures • Provide regular status reports on of validation activities in the organization to Validation SME, PM and/or Validation or IT Manager, as requested. Please provide me the updated resume at your earliest. Thanks and Regards, *Anurag Singh* Email: [email protected] Gtalk: *[email protected] <[email protected]>* Ph: 609-897-9670 x 2188 Fax: 609-228-552 Address: 38 Washington Road, Princeton Jn, NJ 08550 *[image: cid:[email protected]]* <http://www.sysmind.com/> [image: cid:[email protected]] [image: cid:[email protected]] [image: cid:[email protected]] NOTE: Under Bill s.1618 Title III passed by the 105th U.S. Congress this mail cannot be considered Spam as long as we include the contact information for removal from our mailing list. To be removed from our mailing list please reply with 'remove' in the subject heading and your email address in the body. Include complete address and/or domain/aliases to be removed. If you still get these emails, please call us at the number in the signature. -- You received this message because you are subscribed to the Google Groups "GTA DBA" 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/gtadba. For more options, visit https://groups.google.com/d/optout.
