Job Description
<p><p>This role is within OmniaBio’s PS&AD team which is a multidisciplinary group responsible for Process Development (PD), Analytical Development (AD), Manufacturing Sciences & Technology (MSAT), Analytical Sciences & Technology (ASAT) functions to support client and internal programs. As an <b>Associate Scientist</b> at OmniaBio, you will be part of a team focused on defining and executing process and/or analytical development/optimization projects as well as the technology transfer of programs into programs into OmniaBio’s cGMP manufacturing unit. Supported by other members of the team, you will be responsible to design/draft protocols, execute and author documents supporting program deliverables. With guidance and mentorship, you will also be involved in troubleshooting & investigations, supporting the PS&AD team to deliver project tasks. The Associate Scientist is part of a multidisciplinary team bringing new and innovative products to market to enable life-saving advances in cell and gene therapy and regenerative medicine.</p><h3>Responsibilities</h3>
<ul><li>Project task execution for process and/or analytical optimization and technology transfer programs in cell and gene therapy and regenerative medicine. This includes experiment planning and execution, data analysis, documentation and reporting.</li><li>Presentation & communication of scientific data, predominantly to internal audiences.</li><li>Execute on project milestones as part of a diverse and multi-disciplinary team.</li><li>Applies standard approaches to routine problems. Seeks guidance for novel issues. Understands daily lab operations. Follows SOPs and project plans.</li><li>Drive effective communication across the organization and leadership team.</li><li>Assist in the evaluation of new and existing technologies to improve workflows.</li><li>Demonstrate continuous integrity, credibility and positivity, and motivate others to do the same.</li><li>Continuously grow and adapt in a fast-moving field to keep yourself and the organization at the forefront of the cell and gene therapy and regenerative medicine fields.</li></ul>
<h3>Qualifications</h3>
<ul><li>B.Sc. or M.Eng/MSc with 0-2 yrs industrial exp</li><li>This is a lab based role</li></ul>
<h3>Desired Characteristics</h3>
<ul><li>Practical experience in cell and gene therapy or regenerative medicine.</li><li>Industry experience in cell and gene therapy or regenerative medicine.</li><li><b>PD-Specific Roles</b>: Hands-on experience working with human primary and/or stem cell cultures. Experience with bioreactors and/or other equipment relevant to cell and gene therapy.</li><li><b>AD-Specific Roles</b>: Experience with cell and molecular analytic techniques, such as flow cytometry and q-PCR.</li><li><b>MSAT-Specific Roles:</b> Experience with technology transfer of processes & platform technologies into a cGMP environment. Supporting investigations of routine cGMP manufacturing.</li><li><b>ASAT-Specific Roles: </b>Experience executing method transfer to QC and support qualification activities.</li><li>Experience in statistical design and analysis.</li><li>Independent, detail-oriented, self-starter with excellent analytical skills and the ability to multitask and succeed in a team environment.</li><li>Demonstrated initiative and the ability to deliver high quality outcomes</li></ul></p>
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