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Deviation Investigator - Bothell, United States - Integrated Resources
Description
Job Title: Deviation Investigator
Location: Bothell, WA
Job Duration: 12 Months
Pay Rate: $63.86/Hr. on W2
Job Description:
The MSAT (Manufacturing Sciences and Technology) team is responsible for overseeing and supporting the management of deviation records through the electronic quality record management system at client Manufacturing Plant (Jump) located in Bothell, WA.
The Deviation Investigator on the MSAT team is an individual contributor role responsible for investigating No Impact, Minor, Major, and Critical deviations to determine root cause, corrective actions, ensuring the written report contains the technical merit and completeness according to regulatory expectations.
This position will be responsible for operating cross-functionally, collecting necessary data and information associated with the manufacturing and laboratory investigations and determine the associated corrective action to prevent the deviation from reoccurring.
This person will be a key player in the Jump MSAT team and a champion for quality priority principles and compliance within the Jump organization.
A minimum bachelors degree in relevant Science or Engineering discipline and/or equivalent combination of work experience is required.
5+ years of relevant cGMP experience. Experience in FDA/EMA regulation in the biotechnology and/or cellular therapy field is preferred.
Minimum of 2 years working within quality systems managing deviation and CAPA records.
Experience authoring deviation and CAPA records
Demonstrated proficiency in selection of team and effectively managing personnel issues is highly desired. Proven ability to demonstrate attention to detail, personal and team accountability where it is critical to success.
Knowledge, Skills, and Abilities:
Expertise in GMP compliance and FDA/EMA regulations.
Demonstrate excellence in written and verbal communication.
Demonstrated ability to work cross-functionally and to develop and maintain strong business partner relationships.
Innovative, proactive, and resourceful; committed to quality and continuous improvement.
Ability to anticipate and mitigate challenges.
Key Responsibilities
Actively manages deviations to achieve RFT (right first time) and on-time phase completion, including deviation closure by the original due date.
Immediately upon assignment of an investigation, partners with their investigation team (QA Reviewer/ Approver, SMEs [subject matter experts], and necessary stakeholders) on definition and alignment of the investigation plan, required data, and timing for completion. Continues to partner with investigation team throughout the investigation process to ensure agreement / alignment on root cause and CAPA.
When CAPA is needed, facilitates the investigation / CAPA team to define objectives, deliverables, ownership, due dates, and effectiveness requirements.
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
Owns and investigates department-specific trend deviations. Leads investigation team to perform deep-dive analysis of department-specific trends, including to:
Assess trend details to ensure accuracy and alignment across the team.
Facilitate in-depth root cause analysis to determine additional process and system failure modes.
Evaluate previous root causes and CAPA (in-progress or implemented) identified to lessen the trend.
Determine if previous identified CAPA are sufficient to reduce the trend by defined targets.
Leads GEMBAs and interviews the people closest to the work to identify failure modes and seek further understanding of the deviations.
Applies HOP (Human and Organizational Performance) principles to investigations.
