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Job Title, Keywords, Req ID
  • Canada ● Req #201
    Thursday, September 14, 2023
    Position Summary: As the head of Quality and Regulatory Compliance at the OmniaBio Facility located at the McMaster Innovation Park in Hamilton, ON, you are a seasoned individual in the field of GMP commercial and clinical phase manufacturing supply. You will have demonstrated effective leadership of successful Quality organizations. Your experience will include the manufacturing of biologic Drug Substances and Drug Product. Ideally you have experience in Advanced Therapy Medicinal Products (ATM ... More
  • Canada ● Req #198
    Monday, August 14, 2023
    Role Summary: OmniaBio, Inc. has a newly formed Director of Marketing role for candidates with strong experience in creating and implementing marketing programs in the biopharmaceutical CDMO industry. Responsibilities include: OmniaBio’s strategy to develop and execute all marketing programs related to process development and GMP services.  The focused audience will include companies within the highly technical, global Cell and Gene Therapy industry.  This role will be an integral member of a dy ... More
  • Canada ● Req #197
    Friday, August 11, 2023
    Role Summary: OmniaBio, Inc. is looking for a BD Associate with strong experience in prospecting, lead generation, and qualification in the biopharmaceutical CDMO / industry. The Associate will be responsible for developing the early-stage cell and gene therapy customer pipeline for OmniaBio’s process development and good manufacturing practices (GMP) manufacturing services and for supporting the BD team in pipeline development and expansion activities. You will work closely with technical exper ... More
  • Canada ● Req #196
    Thursday, August 10, 2023
    Position Summary: As a Project Manager at OmniaBio, a subsidiary of CCRM, you will be part of a diverse bioengineering team working with the Centre for Advanced Therapeutic Cell Technologies (CATCT), the Centre for Cell and Vector Production (CCVP) and OmniaBio, focused on designing and implementing Research & Development and/or Good Manufacturing Practices (GMP) production projects within the cell and gene therapy, and regenerative medicine fields. You will apply project, client, and contract m ... More