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Quality Assurance Specialist - Bothell, United States - Katalyst Healthcares and Life Sciences
Description
Responsibilities:
Actively manages deviations to achieve RFT (right first time) and on-time phase completion, including deviation closure by the original due data Leads/facilitate triage, deviation process, investigations (as applicable), and No Impact deviation closure of records, CAPA (Corrective and Preventative Action), change controls, process transfers, and other business drivers are supported in a compliant manner.
Immediately upon assignment of a deviation, partners with their investigation team/cross-functional team approve No Impact Deviations in a timely manner to support RFT.
May partner with (QA Reviewer/ Approver, SMEs (Subject Matter Experts) [subject matter experts], and necessary stakeholders) for deviations with higher classification to help on definition and alignment of the investigation plan, required data, and timing for completion as applicable.
Continues to partner with investigation team throughout the investigation process to ensure agreement / alignment on root cause and CAPA.
Partnering with functional areas to help drive on-time phase completion, including No Impact deviation closures, RCA Assessment approvals, and participates in cross functional project teams.
When CAPA are needed, partners/facilitates the investigation / CAPA team to define objectives, deliverables, ownership, due dates, and effectiveness requirements Partners with stakeholders to ensures smooth transition of the defined CAPA to the owning department SME and ensures the CAPA progresses to implementation timely to ensure on-time deviation closure Uses both soft-skills and technical skills to drive the deviation and CAPA processes: o Demonstrates good teamwork, collaboration, and communication skills with all internal and external customers o Seeks to understand, demonstrates humility, and shows curiosity for learning o Completes deviations that are thorough, accurate, and complete o Understands the overall deviation and CAPA processes including all phases of the records and proper content for each phase o Understands appropriate assignment of classifications and requirements for each o Understands the importance and impact of lot association within deviations and the relation to product disposition Partners to assist cross-functional teams on department-specific trend deviations to: o Assist with assessing trend details to ensure accuracy and alignment across the team o Participate in in-depth root cause analysis to determine additional process and system failure modes o Evaluate previous root causes and CAPA (in-progress or implemented) identified to lessen the trend o Determine if previous identified CAPA are sufficient to reduce the trend by defined targets Maintains and routinely communicates an up-to-date dashboard of department specific CAPA to show status, escalate issues, provide mitigation plans, and request additional supportUnderstands appropriate assignment of classifications and requirements for each: o Understands multiple RCA tools and when, where, and how to apply them o Utilizes good technical writing skills Participates on GEMBAs or process improvement projects to identify failure modes and seek further understanding of the deviations when needed.
Participate in deviation governance teams, projects, and other initiatives. Provide Quality support to Manufacturing personnel on the floor; provide guidance during GMP events and initiation of deviation investigations. Review deviations, product non-conformities, and GMP investigations to ensure adequate resolution and compliance with current Good Manufacturing Practices (GMPs). Ensures the necessary data to support containment activities and impact assessments have been provided.Ensures all necessary supporting evidence is attached to the electronic deviation and that all attachments are referenced in the record.
Ensures investigations and root cause analyses are commensurate to the event being investigated. Understands multiple RCA tools and when, where, and how they should be applied.Reviews deviation reports for good technical writing skills actively coaches and mentors' investigators through the review and approval processes Act as QA Subject Matter Expert (SME) and support cross functional groups on no impact deviation events and development of corresponding corrective and preventive actions as applicable.
Support internal and external audits, including documenting observations and may oversee implementation of corresponding CAPAs (Corrective and Preventative Action) as applicable.
Perform quality review and approval of standard operating procedures as applicable. Train and mentor junior associates.Requirements:
Bachelor's degree in relevant science or engineering discipline is preferred. Minimum of Associates degree and/or equivalent combination of education and experience is required. 3-5 years of experience in oversight and execution of deviation initiation, investigations, and approvals within a quality management system. Experience in cGMPs and FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing is preferred.
Licenses/Certifications:
N/A
