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Quality Project Manager | Project Manager in Executive Job at Monster in Van Nuys CA | 7186750138

This listing was posted on Professional Diversity Network.

Quality Project Manager

Location:
Van Nuys, CA
Description:

Title | Quality Project ManagerLocation | Van Nuys, CADepartment | Quality & ComplianceReports To | Director, QM Overview SOFIE is committed to all aspects of Quality and Compliance in the manufacture of Radiopharmaceutical products. SOFIE aseptically manufactures therapeutic and diagnostic radiopharmaceuticals across the USThe Quality Project Manager will manage high-criticality projects to support the long-term goals of the business. The Quality Project Manager will design and execute validations, qualifications, project plans, and will be tasked with supporting and managing Quality initiatives across the United States. The candidate must be strong at project management, technical and quality writing, root cause analysis, executing tasks to completion, electronic systems, and MS Office Applications Essential Duties and Responsibilities Plan and manage the execution of complex quality, verification/validation, and regulatory projects. Responsible for directly and indirectly leading cross-functional teams in the execution of project plans Build team ownership and commitment to project and business plans and define project milestones and resource requirements. Conduct routine meetings to ensure accountability and milestone achievements with team(s) Sets prioritization of team member activities and follow up on actions. Actively seeks collaboration and builds relationships with internal and external parties to improve overall outcomes and timely project completion. Manages and serves as the subject matter expert on the project team regarding validation/verification requirements, regulatory requirements and technical capabilities of the equipment/infrastructure to be deployed. Design, review, and execute validations and qualifications of equipment, facilities, processes, and infrastructure Proactively identify and assess areas of risk, escalate issues in a timely manner and proactively propose solutions. Implement and manage project changes and interventions to achieve timely project outputs. Provide regular project updates (written and verbal) to appropriate management. Serves on project steering committees. Develop a team culture of continuous improvement and teamwork that strives to improve in quality, safety, delivery and cost Responsible for opening change controls and initiating, maintaining, and reviewing SOFIE network and site-specific procedures. Apply quality assurance processes and procedures at the corporate level to ensure product quality and regulatory Write, review, and implement procedures, specifications, processes, and methods as Review executed CGMP records and product batch records to ensure compliance and product quality, when needed. Other essential duties as directed Qualifications Bachelor's degree in chemistry or a related scientific area preferred Minimum of 8 years of experience in a CGMP/FDA-regulated environment is required. Minimum of 3 years of experience in Project Management. Quality & Regulatory Assurance experience preferred. Experience and/or full knowledge of manufacturing operations and the preparation of sterile injectables is required. Knowledge of relevant USP and FDA regulations, as well as CGMP requirements, is required. Knowledge of how and ability to write, review and revise SOPs is required. Familiarity with radiopharmaceutical manufacturing processes and related QC release testing preferred. Working knowledge of US and ICH cGMP regulations and guidelines, risk management standards, quality attributes, and Quality Assurance best practices in the pharmaceutical industry required. Excellent analytical, prioritization, multi-tasking, communication, strong leadership skills, and the ability to work independently with limited supervision required. Ability to effectively communicate (written and verbal) with leadership, site personnel, corporate QA, customers, and regulatory agencies required. Ability to prepare and present written and verbal reports to upper management required. Domestic travel up to 60%. PDN-9b7263be-959d-43d0-a97c-a48a348ec3fc
Company:
Monster
Industry:
Other
Posted:
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