Compliance QA Manager - Systems - Onsite

Compliance QA Manager - Systems - Onsite (JN -092026-431285) Canada Salary: USD58 - USD70 per hour Onsite Location: Alameda, CA Pay: $58 - $70 per hour

SUMMARY/JOB PURPOSE:

QA Manager Systems and Process is responsible for oversight, support, and administration of Computer System Validation (CSV) and Data Integrity, assuring effective and efficient process maintenance to support GxP functions. Primary role is supporting end users, Business Owners (BOs), Systems Owners (SO and QA , assuring applicable requirements are in place and met, system compliance , managing accounts, evaluating and managing CSV/DI and related changes, deviations and CAPAs, executing on continuous system improvements, and supporting Quality Management Systems (QMS) activities, as applicable.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

As QA Core, support QA Partner: Analyze user enhancement requests to deliver solutions that establish and improve business processes, assuring process and system efficiency, elimination of process gaps, enabling automation Assemble document user and functional requirements Author and execute implementation plans, develop solutions, effectively manage timelines for timely execution Perform User Acceptance testing (UAT), Performance Qualification (PQ), Validation testing Create and run reports; track follow-up actions to ensure data quality and compliance Generate metrics to support business goals, as applicable Pro-actively improve monitoring, eliminate user issues, deliver better value to cross-functional teams Drive CSV/DI and QMS results, timeliness and compliance in QA , across System and Business Owners, and in cross-functional project forums Escalate timely and effectively Day-to-day business system administration: Manage system access and permissions Design solutions; manage configuration Work proactively with users to resolve issues and drive timelines Create reports based on defined requirements Maintain system documentation and associated records Create and run reports; track follow-up actions, ensure data quality and compliance Identify, mitigate, escrow and resolve issues and risks Author/review CSV, DI records, and QMS records, as applicable (policies, procedures, lifecycle documents) Generate metrics to support business goals as requested Revise business guidance and user reference documentation Support internal and external audits/inspections Support CSV/DI program Experience/The Ideal for Successful Entry into Job: At least 5 years of experience with validated applications in a pharmaceutical or regulated environment. Experience and knowledge of the quality and regulatory business processes. Direct hands-on experience implementing GxP computerized systems and maintaining validated state, and DI. Strong process improvement and negotiation skills, driving process excellence. Proven business and technology skills, successful in providing customer- oriented technology solutions. Proven excellent communication skills, with users, technical communities, cross-functional project groups. Communicates ideas in technical and user-friendly language. Collaborative team player, driving for results and timeliness. Knowledge/Skills: Knowledge of System Administration (Veeva Platform (Quality QMS, Quality QDocs)); SaaS systems; Other Regulated Applications (Learning Management Systems, QMS) #J-18808-Ljbffr Ledgent Technology