Who is BlueRock?
BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique cell+gene platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological, cardiovascular, and immunology diseases.
The convergence of cell biology and genetic engineering is creating fundamental new ways to impact disease. Founded in 2016 to capitalize on these technological breakthroughs, we are advancing our novel cell+gene platform to develop, manufacture, and deliver an entirely new generation of authentic and engineered cell therapies across three therapeutic areas: neurology, cardiology, and immunology.
What Are We Doing?
Our foundational science harnesses the ability to create and then direct the differentiation of universal pluripotent stem cells into authentic, functional cells that can be used as allogeneic cellular therapies to treat a broad array of diseases. We can also further engineer these cells, enabling them to produce enzymes, antibodies, and other proteins for additional therapeutic benefit.
We are passionate about delivering on the promise of cellular and gene therapy, shaping the future of cellular medicine, and delivering new therapies to millions of patients with treatment options.
We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to advance cutting-edge cellular therapies to impact patients’ lives.
We are in search of an enthusiastic, organized, and driven individual to join the Product Quality Team within BlueRock’s Quality Control and Analytical Sciences Technology Department. Reporting to the Product Quality Scientist II, this role will closely collaborate with the entire Product Quality team to bolster the analytical strategy for products in BlueRock’s pipeline.
The successful candidate will be primarily responsible for supporting the preparation of analytical strategy documents, GMP documents, data collection, and lifecycle management for our documents. Additionally, they will engage in collaborative efforts with other internal groups to contribute to the development of tools and templates aimed at ensuring product quality.
Responsibilities
- Prepare analytical strategy documents based on pre-aligned information
- Document life-cycle management via document control system
- Support implementation of guidelines into GMP documents
- Lead development of tools and templates for product quality team
- Drive re-organization of team share point site and folder system
Qualifications & Requirements
- Currently enrolled in a university program focused on Biology, Biochemistry, Biomedical studies, or a related field. A master’s degree in the relevant discipline is preferred.
- Be able to work a 6-month assignment, full-time.
- Must be 18 years of age by the start of the internship/co-op.
- Must have transportation to the site in Toronto, ON, CA.
- This position is intended to be hybrid and candidates will be informed should anything change.
- Excellent organizational skills, sufficient to multi-task in an extremely fast-paced environment with changing priorities.
- Excellent communication skills and ability to engage stakeholders.
- Excellent writing and editing skills with good attention to detail.
BlueRock Therapeutics Company Culture Highlights
Winner of Boston Business Journal’s Best Places to Work (Mid-size Company) 2023
Winner of Comparably’s Award for Best Company for Diversity 2022
Winner of Comparably’s Award for Best Company for Women 2022
Winner of Comparably’s Award for Best CEO 2022
BlueRock Therapeutics is ranked in the top 5% of companies for Overall Culture on Comparably.
Engineering Department is ranked in the top 5% of companies for Overall Culture on Comparably.
Follow us on Linkedin: https://www.linkedin.com/company/bluerocktx/
Equal Opportunity Workplace: At BlueRock, we welcome and support differences and diversity and we are proud to be an equal opportunity workplace. Please let us know if you require disability-related accommodation or other grounds protected by human rights legislation during the recruitment process so that we can work with you to meet your needs.
