Senior Manager, Downstream Manufacturing Science and Technology

4 weeks ago


Vancouver, British Columbia, Canada AbCellera Full time

About AbCellera

AbCellera is at the forefront of transforming traditional drug development, dedicated to advancing antibody-based therapies from concept to clinical application. Our diverse team comprises scientists, engineers, creatives, and business professionals united by the belief that scientific progress enhances lives. We have pioneered technologies that unlock high-value drug targets, including antibody-drug conjugates and T-cell engagers for oncology, as well as complex transmembrane proteins for various health conditions.

Position Overview

We are seeking a (Senior) Manager, Downstream Site MSAT to serve as the primary expert in GMP-scale purification of monoclonal and bispecific antibodies. This pivotal role involves collaborating with various departments including manufacturing operations, process development, engineering, quality assurance, and other technical operations. You will be instrumental in driving technology transfer, establishing process controls, developing recipes and batch records, troubleshooting technical issues, and ensuring successful batch production within our state-of-the-art GMP manufacturing facility.

Key Responsibilities

  • Provide expert technical leadership in the purification of monoclonal and/or bispecific antibodies.
  • Act as the primary liaison during the technology transfer of new processes from development to scale-up, focusing on risk management, recipe formulation, batch record creation, and overall operational success.
  • Collaborate with the pilot plant operations team to conduct process risk assessments, raw material evaluations, control strategies, and documentation for technology transfer.
  • Contribute to the design of processes and facilities to implement best practices effectively.
  • Offer technical support to guide bioprocessing decisions in manufacturing, advocating for optimal process principles alongside quality and production teams.
  • Design manufacturing systems that are robust, promote efficient operations, and comply with cGMP standards.
  • Identify opportunities for implementing GMP-compliant technologies aimed at enhancing processing efficiency, yield, cost-effectiveness, and operational simplicity.

Qualifications

  • A minimum of 8 years of experience in the development and manufacturing of monoclonal and/or bispecific antibodies, along with a bachelor's degree in biotechnology, biochemistry, chemical engineering, molecular biology, or a related field.
  • Demonstrated expertise in purification processes, including chromatography, tangential flow filtration, depth filtration, mixing, column packing and maintenance, as well as viral inactivation and filtration techniques.
  • In-depth knowledge of downstream processing methods supporting pre-clinical and clinical programs, with a solid understanding of GMP compliance.
  • Experience in technology transfer and scaling monoclonal antibody processes from pilot to GMP production.
  • A passion for developing dynamic teams and capabilities to achieve significant objectives.
  • Creative and innovative mindset with the ability to foresee potential challenges.
  • Strong operational insight and risk management skills, with a focus on prioritizing scientific and engineering solutions to minimize process interruptions.

Compensation and Benefits

AbCellera offers a competitive salary range, along with equity options, an annual performance-based bonus, and a 6% RRSP contribution. Additional benefits include a yearly Active Lifestyle Allowance, vacation time, flexible work arrangements, opportunities for professional growth, and comprehensive health benefits. We prioritize scientific and technical mentorship and foster a community-oriented environment that encourages collaboration and connection among our teams.



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