Type d’emploi: Full-time

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le contenu du travail

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.

The Toronto, ON site is seeking a GMP Specialist I (Lab Operations) to oversee the day-to-day technical and administrative operations of the manufacturing laboratories. Reporting to the Senior Manager of GMP Manufacturing Operations, the successful candidate will be responsible for the laboratory’s routine operations including but not limited to inventory management, receiving and distribution of supplies, receiving raw materials, cycle counting, and assisting with administration and documentation.
This is an outstanding opportunity to contribute to bringing a new class of cell-based medicines to patients. Collaboration with a highly motivated, world-class team of scientists and engineers promises an exciting and engaging work environment for a motivated, self-starting candidate.

Responsibilities:

    • Responsible for physically receiving, storage and distribution of all reagents, supplies, consumables, equipment, parts, and any other inventory item(s) related to the operation of the laboratory following GMP procedures including generating labels RM # via QMS system.
    • Receive raw materials (all reagents, supplies, consumables, equipment, parts, and any other inventory item(s) related to the operation of the laboratory) into the BlueRock electronic system (D365, Quartzy, inventory smartsheet).
    • Ensures that laboratory staff are aware of goods received and their proper storage, coordinates distribution of supplies within the laboratory on daily basis.
    • Conducts periodic cycle counts based on ABC categorization as defined by Supply Chain
    • Assist GMP specialists with the transfer of Raw materials to external manufacturing partners, as required.
    • Update and maintain raw material and drug product inventory as consumed by Tech Ops functions (includes picklists and inventory trackers)
    • Pull raw materials retains as per GMP procedures.
    • As requested by supervisor, supports with sample shipments. May require engaging with cold chain logistics providers to safely transport temperature critical material.
    • Order processing equipment as required.
    • Perform other tasks as required.
    • Ensures safety measures in the laboratory are being followed and takes initiative to update safety SOPs, training material and documentation.
    • Will receive all necessary training to be able to work in BlueRock offices and controlled laboratory environments. Due to the nature of the work in the laboratory it is mandatory to wear personal protective equipment. There is a risk of potential exposure to chemicals and biohazards.

Minimum Requirements:

    • Degree in biological sciences preferred with 1+ years related experience, or a Diploma with 3+ years related experience.
    • Experience with shipping and cold chain logistics is an asset.
    • Demonstrated experience with logistics support.
    • Experience with writing and reviewing SOPs is an asset.
    • Competency in computer skills and familiarity with Microsoft Office programs (Word, Excel, PowerPoint, etc.) required.
    • Strong problem-solving skills and ability to work with a variety of software platforms.
    • Excellent communication skills, both oral and written; must be able to manage time and priorities efficiently.
    • Must have the ability to maintain a constructive working relationship with all staff, vendors, and co-workers.
    • A proven ability to be highly productive in a fast-paced work environment with excellent attention to detail.
    • Must be a self-starter demonstrating initiative, a positive attitude, and the ability to work in an independent and organized manner.
    • Ability to, on occasion, lift 20kg and/or work with a partner to lift anything heavier.
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.

Check us out on Comparably: https://www.comparably.com/companies/bluerock-therapeutics
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.
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Date limite: 16-07-2024

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