Group Leader Quality Control
: Job Details :

Position Details: Our client, a world-leading Pharmaceutical Company in Parsippany, NJ is currently looking for a Veeva Vault Systems Analyst to join their expanding team. Job Title: Veeva Vault Systems Analyst / Pharma Industry / REMOTE WORK Duration: 6 months contract, extendable up to 24 months Location: Parsippany, NJ Note: The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract. You may participate in the company group medical insurance plan Job Description: Position Title: Veeva Quality Business Support Temp to perm: This is a contingent assignment only. Working 3 to 6 months. Shift Schedule: Monday - Friday , 40 hours a week Onsite or Remote: Onsite preferred (remote to be considered depending on candidates available) Candidates should have these core essential skill sets to be considered for the role: Bachelors of Science 5+ years using GxP systems with experience on projects including implementation/deployment and data migration in the pharmaceutical industry Experience working in large, multinational companies in the Quality department Experience in project/program management Client Veeva Quality Team Support Resource - Requirements Client is looking to supplement the current Global Quality team resources in support of the deployment of the Veeva Quality Vault program for Global Quality Management / Electronic Document Management Systems (QMS/EDMS). The candidate for this role should have extensive business experience in workstream project management for large global GxP systems (Veeva Quality systems highly preferred) in the pharmaceutical industry, as well as demonstrated capability working with large cross-functional global teams. Location: Onsite in Parsippany, NJ (preferred) or available remotely working according to Eastern US time zone (to be considered). 1. Required Deliverables The following services are required: Complete required internal training on Client's System Development Lifecycle (SDLC), Business SOPs, etc. related to the activities in scope. Support overall Client Quality team with daily operational activities such as attending meetings/training sessions, etc. Support all assigned business-related design and configuration activities for the Veeva Vault implementation program under the leadership of the Client Quality Veeva team. Support business workstream activities for the Veeva project including, but not limited to: Participate in all functional and process design review sessions, assist Business Leads with documenting open questions, addressing follow-ups, etc. Provide support to project Subject Matter Experts (SMEs) as needed (e.g. during process review sessions, testing activities, etc.) Execute system testing and raise feedback as needed Assist with creation/review of associated work instructions, procedures, training modules for business workstream Work closely with IT teams and support Business and IT Deployment Leads with deployment and migration related activities Additional activities per Client's request 2. Qualifications The following qualifications are required: Bachelors of Science is required and advanced degree preferred in science/regulatory/computer science/management field 5+ years using GxP systems with experience on projects including implementation/deployment and data migration in the pharmaceutical industry Experience working in large, multinational companies Prior experience with Veeva Quality Vault is preferred Experience in project/program management Excellent communication skills English fluency Proficiency in MS Office tools Provide qualification records: CV Related Veeva Quality Vault and pharmaceutical industry experience/history Candidates will be subject to interviews prior to selection.