Full-Time

Manager – External Quality Control

Posted on 2/10/2023

AbCellera Biologics

AbCellera Biologics

501-1,000 employees

Accelerates antibody drug discovery with data science

Data & Analytics
AI & Machine Learning
Biotechnology

Senior

Vancouver, BC, Canada

Requirements
  • A Bachelors or Masters degree in a relevant discipline and 8+ years of GxP industry experience within biotechnology, pharmaceuticals, or life sciences
  • 5+ years of Quality Control experience in a GxP regulated environment such as biotechnology, pharmaceuticals, or life sciences
  • Strong comprehension of current pharmaceutical regulations and guidances (FDA/Health Canada/EU/ICH) and regulatory expectations for assigned function
  • Good ability to assess vendor quality core processes ensuring compliance with relevant guidelines and procedures
  • A thorough understanding of drug substance development process and monoclonal antibody manufacturing processes and testing
  • Strong experience with various software/databases such as, but not limited to, ERP, MES, eQMS and LIMS
  • Excellent communication and presentation skills with an ability to adjust to both technical and non-technical audiences
  • Results oriented, and able to effectively execute on projects with minimal supervision
Responsibilities
  • Overseeing all the QC subcontracted activities, such as Cell Banking preparation, Reference Standard, Reference Samples and Reference Material management, Manufacturing and testing operations
  • You will be accountable for the Contract Laboratories quality management activities including Deviations, Change Management or Complaints
  • Working with key groups such as, Procurement, Operations, QC, Supply Chain, and Process Development, for the Selection, Qualification and Management of Contract Laboratories
  • Negotiating and maintain Quality Agreements between AbCellera and Contract Laboratories
  • Supporting CMC Regulatory submissions
  • Representing Quality Assurance for Analytical and Technical transfers
  • Defining, monitoring and reporting quality performance metrics
  • Ensuring implementation at the Contract Laboratories of a compliant Data management process and other AbCellera quality initiatives
  • Performing quality risk assessments, develop mitigation plans and follow up on implementation
  • Maintaining site readiness for Health Authority regulatory inspections & for AbCellera /partners/ 3rd parties audits
  • Participating in on-site regulatory inspections and audits
  • You will be responsible for reporting the Health Authority inspections and audit outcomes and ensure implementation of associated action plans
  • Maintaining current knowledge of applicable Quality & Regulatory requirements and evolving trends and supporting the Contract Laboratories to meet these standards

AbCellera stands out as a leader in the biotech industry due to its unique approach to antibody drug discovery, combining expert teams, advanced technology, and data science to expedite the process from target to clinic across various therapeutic areas. The company's competitive edge lies in its ability to enable swift progress, cost reduction, and problem-solving in drug development for both innovative biotechs and leading pharmaceutical companies. Furthermore, AbCellera's commitment to technical innovation is evident in its recent presentation of new data on two T-Cell Engager Programs at SITC 2023, demonstrating its active role in advancing the field.

Company Stage

Series A

Total Funding

$393.1M

Headquarters

Vancouver, Canada

Founded

2012

Growth & Insights
Headcount

6 month growth

-3%

1 year growth

16%

2 year growth

77%
INACTIVE