Information Technology_USA - USA_Lead

Leading the Tech Writer team for preparing the test cases. Co-ordinating the testing with the business and automation test teams. Experience working within a FDA/Other regulated pharma industry. Roles & Responsibilities Meeting with system users to understand the scope of projects Participating in business requirement discussions to draft SDLC /CSV /Qualification documents. Developing validation/qualification/migration/verification strategies for software Executing validation/qualification/verification/migration strategies per quality assurance SOPs.. Providing validation/verification/qualification recommendations to stake holders as necessary. Managing relationships with customers, technical team, quality assurance team, testing team and other stake holders to ensure the validation/ verification/qualification solution delivered to the customer meets expectations. Ensuring SDLC/CSV/Qualification activities are conducted as planned Generate, review, and Computerized Systems lifecycle documentation including risk and impact assessments, user requirement specifications, functional specifications, traceability matrices, qualification protocols, validation plans, and validation summary reports etc. Working towards project deadlines Communicating findings to technical and non-technical colleagues. Liaising with project teams in other parts of the world Leading the validation effort., Responsibilities: Lead Health & Safety Officer (HSO) - Raritan & Northern NJ Projects HazTek Safety Management is seeking an experienced Health & Safety Officer (HSO) to suppor…

• 1 month ago

Role Descriptions: Demonstratable Experience in Computer System Validation (CSV) Experience in software development processes (SDLC) and software testing life cycle (STLC) Experience in drafting, reviewing, revising, and maintaining validation documents (CSV), including Compliance Analysis, Compliance Plan, Change Control Document, User & Functional Requirement documents, Risk Assessments (Risk Register), Test (ST/UAT/Regression) Protocol, Test Defect Report, Test Summary Report, Compliance Summary Report, Traceability Matrix, Hypercare Plan, Operation Run Book and other validation & technical documentation. Experience in drafting Standard Operating Procedures (SOP) and Work Instructions (WI Strong knowledge of JIRA, HP-ALM, qTest tools Knowledge of validation & testing in projects implemented using agile methodology Knowledge about Agile techniques like: User Stories, Continuous Testing, tasks, etc. Ability to take and understand the commitment to deliver the product on time. GxP experience is required Experience of validation support for 21 CFR Part 11 implementation in Pharma industries., Strong verbal and written communication skills with the ability to liaise with a variety of stakeholders Must be self-motivated and pro-active Need to show constant dynamism and able to manage pressure. Attention to detail Competent CSV skills The ability to work in a team and individually Organizational skills with the capability of working towards tight deadlines Able to work with demanding customer Essential Skills: Life Sciences : Computer System Validation Desirable Skills: Keyword: Skills: Life Sciences : Computer System Validation~Project Management Experience Required: 6-8 Comments for Suppliers

Allied Universal + Raritan, NJ + $20.85 per hour Overview Company Overview: Allied Universal®, North America's leading security and facility services company, offers rewarding careers that provide you a sense of purpose. Whil…, Allied Universal + Raritan, NJ + $20.00 per hour Overview Allied Universal®, North America's leading security and facility services company, offers rewarding careers that provide you a sense of purpose. While working in a dynam…