Internship Length: 18 months internship

Role Summary:

We are seeking a motivated and detail-oriented co-op student to join our Manufacturing Science and Technology (MSAT) team to help develop the next generation of cell and gene therapy (CGT) manufacturing technologies and processes. You will gain first-hand experience with industrial cell culture technologies and a strong appreciation of Good Manufacturing Practices (GMP) manufacturing from technology transfer challenges for CGTs from academic and clinical research to a commercial setting. You will acquire the skills to understand the process of introducing innovative discoveries, leading to the delivery of cutting-edge solutions in cell and gene manufacturing.

Responsibilities

Assists in the preparation of new process technology transfer to GMP process improvements, including protocol generation, data analysis and report writing.
Works effectively with other team members in a multi-disciplinary environment.
Supports writing technical documents, including standard operating procedures, project plans and reports.
Develops and improves the skills and knowledge necessary to successfully support assigned projects.
Assists and helps with colleagues' training, as necessary.
Participates in cross-functional project teams to provide MSAT input and support.
Understands that the role and responsibilities may change with the evolving needs of the organization, requiring flexibility and adaptability.

Qualifications

Currently enrolled in undergraduate education in industrial engineering, bioprocess engineering, chemical engineering, biotechnology or similar.
Strong attention to detail.
Practical experience with computer programming, process modelling, databases and statistics.
Excellent analytical, problem solving and process development skills.
Excellent organizational skills.
Able to work independently and as part of a team.
Detail-oriented team player.
Strong English written and verbal communications skills.
Solid working knowledge of MS Office programs.
Demonstrated knowledge of laboratory safety plans and procedures to ensure compliance with applicable federal, provincial and local regulations.

This position may be fully or partially funded by Biotalent Canada. In order to be eligible for funding under Biotalent Canada the applicant must be a Canadian citizen, permanent resident, or a person to whom refugee protection has been conferred and such are legally entitled to work in Canada in accordance with relevant provincial or territorial legislation and regulations. As such, only applicants that meet the above criteria will be eligible for this opportunity.

Revision Number: CCRMDEVMSAT-20240507

CCRM is a developing organization and represents a fluid working environment. Flexibility and adaptability are essential, and duties will be influenced by the needs of the organization.

Applicants must be legally eligible to work in Canada.

An applicant’s compensation package is finalized once the interview process is concluded and accounts for the nature of the role as well as the experience, competencies (job knowledge, skills and abilities) of the applicant and internal equity.

CCRM is committed to accessibility, diversity, and equal opportunity. Requests for accommodation can be made at any stage of the recruitment process, providing the applicant has met the bona fide requirements for the open position. Applicants should make their requirements known once contacted to schedule an interview, or when the job offer has been made.

CCRM

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