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This role is part of the site’s Quality Systems team and will primarily focus on maintaining the Quality risk management program at the manufacturing facility. The program is intended to promote self-identification of risk areas and implementation of risk mitigation measures for operations, cGMP compliance, and business continuity. Additionally, this role supports the use of various risk management tools to lead complex cross-functional issue resolution by employing a methodical approach to root cause analysis and implementing appropriate corrective and preventive actions.
Key Responsibilities:
Contribute to the writing, coordination, review, and maintenance of the Risk Management Standard Operating Procedures (SOPs) and associated documents.
Ensure product risk management documentation/files are maintained, with good documentation practices and in compliances with company Quality System
Facilitate planning, execution and completion of risk assessments by providing guidance to cross-functional team members
Conduct risk reviews and escalate findings, as appropriate, to QRM team
Track the status of risk mitigation actions through to completion
Track the implementation of corrective actions associated with risk assessments and verify the actions are align with source event
Responsible for maintaining the Bothell Quality Risk Catalog/Registry
Support the creation, revision and approval of Quality Risk Management Reports
Proactively deploy methods and techniques (e.g. Six Sigma/Lean, FMEA, Root Cause Analysis, etc.) to improve effectiveness of the Risk Management program.
Collaborate to improve Quality Risk Methodologies and practices
Generate data for Quality Risk Management Performance Metrics.
Desired Profiles:
A minimum of 5 years of relevant Quality experience in a GMP/FDA regulated environment.
Understanding of Quality Risk Management principles and application within the quality systems
Strong technical writing skill set and ability to critically review reports while effectively expressing Quality principles.
Quality and continuous improvement
Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationships.
Strong project planning skills.
Strong knowledge of cGMPs and Health Authority requirements
Knowledge of manufacturing quality (manufacturing, packaging, facilities, critical systems)
Strong experience and thorough understanding of risk management tools with in-depth knowledge of cGMPs and applicable FDA regulations guidelines and industry best practices
Proven experience working as a detailed oriented team player with effective planning, organization and execution skills
Experience with performing risk assessments using a variety of tools (e.g. FMEA, FTA, HACCP, etc).
Strong computer skills with MS Office (e.g. Word, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System).
Ability to work effectively at a fast pace with cross functional departments to finalize time-sensitive deliverables.
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