Pharma - Deviation Investigator

Net2Source

  • Bothell, WA
  • $55.00-63.00 per hour
  • Permanent
  • Full-time
  • 15 days ago
Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.Title: Quality - Deviation Investigator
Duration: 12 months
Location: Bothell, WA 98021Pay Range: $55-63/hr on W2 (Paid Weekly)
100% on-siteJob 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 the Juno 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.Minimum of Bachelor’s 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 are 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:
o Assess trend details to ensure accuracy and alignment across the team
o Facilitate 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
  • 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
  • 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
o Captures the necessary data to support containment activities and impact assessment
o Attaches all necessary supporting evidence to the electronic deviation and ensures all attachments have been referenced in the record
o Performs investigations and root cause analyses that are commensurate to the event being investigated
o Understands multiple RCA tools and when, where, and how to apply them
o Utilizes good technical writing skills
o Contacts vendor as needed to complete investigations in a timely manner
o May participate on deviation governance teams, projects, and other initiativesWhy work with us - At Net2Source, we believe everyone has an opportunity to lead. We see the importance of your perspective and your ability to create value. We want you to fit inwith an inclusive culture, focus on work-life fit and well-being, and a supportive, connected environment; but we also want you to stand outwith opportunities to have a strategic impact, innovate, and take necessary steps to make your mark. We help clients with new skilling, talent strategy, leadership development, employee experience, transformational change management and beyond.Equal Employment Opportunity Statement:
Net2Source is an Equal Opportunity Employer. We believe that no one should be discriminated against because of their differences, such as age, disability, ethnicity, gender, gender identity and expression, religion or sexual orientation. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.Awards and Accolades:
America's Most Honored Businesses (Top 10%)
Awarded by USPAAC for Fastest Growing Business in the US
12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020)
Fastest 50 by NJ Biz (2020, 2019, 2020)
INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list)
Top 100 by Dallas Business Journal (2020 and 2019)
Proven Supplier of the Year by Workforce Logiq (2020 and 2019)
2019 Spirit of Alliance Award by Agile1
2018 Best of the Best Platinum Award by Agile1
2018 TechServe Alliance Excellence Awards Winner
2017 Best of the Best Gold Award by Agile1(Act1 Group)
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