Senior Engineering Technician (R&D)

BlueRock Therapeutics, a wholly owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company with a mission to develop regenerative medicines for intractable diseases. BlueRock Therapeutics’ CELL+GENE™ platform harnesses the power of cells for new medicines across neurology, cardiology and immunology indications. BlueRock Therapeutics’ cell differentiation technology recapitulates the cell’s developmental biology to produce authentic cell therapies, which are further engineered for additional function. Utilizing these cell therapies to replace damaged or degenerated tissue brings the potential to restore or regenerate lost function. BlueRock’s culture is defined by scientific innovation, highest ethical standards and an urgency to bring transformative treatments to all who would benefit. For more information, visit www.bluerocktx.com.

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.

Description of Position

As part of BlueRock Therapeutics’ vision to change the future of medicine by enabling ground-breaking cell therapies, the Senior Engineering Technician will be a key contributor of a dynamic and progressive team in the development of devices to facilitate delivery of cell therapy products. The individual will support various R&D engineering-related tasks and projects, will perform technical job functions and work with various cross-functional groups to support day-to-day operations and special projects. The ideal candidate will be a highly motivated individual with hands-on experience. Collaboration with a highly motivated, world-class team of scientists and engineers promises an exciting and engaging work environment for self-starting candidates.

Responsibilities

• Support prototype builds and testing as needed.
• Perform mechanical assembly, bonding, welding
• Work with basic electronics
• Perform basic chemical formulation
• Produce small number of devices and prototypes adequate to support feasibility and verification studies
• Update controlled technical documents such as prints, bill of materials, test methods, fixtures, manufacturing materials, routers, and procedures
• Make recommendations and implement design improvements
• Collaborate closely with Supply Chain, Quality, and Operations to ensure smooth flow of daily work.
• Execute pilot manufacturing operations when needed to ensure smooth flow of daily work
• Support and collaborate with suppliers, including third party manufacturers
• Support and execute design verification testing and pay close attention to detail to ensure compliance to protocols and accurately record data.
• Coordinate IQ/OQ/PQ activities with 3rd party suppliers/partners
• Order and maintain R&D tools, supplies and equipment
• Perform duties in compliance with applicable regulations and standards such as FDA Quality System Regulation (21 CFR 820) and ISO (International Organization for Standardization) 13485
• Provide timely updates on progress and day to day activities

Requirements:

• Minimum of an Associate’s degree or equivalent experience is required, preferably in a related field
• Minimum of 3 years of experience in a related technical field (such as medical devices or electronics); 5 or more years of relevant experience is preferred
• Familiarity with cardiovascular or neurovascular devices is a plus
• Working knowledge of Microsoft Excel and Word, and ability to utilize computer-based equipment control and data collection systems are required
• Working knowledge of Geometric Dimensioning and Tolerancing (GD&T) is required
• Working knowledge of measurement equipment such as vision systems, manual height gages, general inspection tools, etc. is required
• Working knowledge of using an advanced three-dimensional CAD system such as SolidWorks is preferred
• Understanding of catheter-related manufacturing processes such as adhesive bonding, machining, welding, soldering, braiding, reflow, etc. is preferred
• Comfortable in a fast-paced, small company environment with minimal direction and ability to adjust work focus based upon changing priorities
• Strong attention to detail and demonstrated analytical skills, especially in the areas of process improvement, problem solving, and logical thinking; highly developed organizational skills and ability to handle multiple high priority tasks and projects concurrently
• Shares relevant information openly and seeks appropriate input from others outside of the direct team; develops and maintains effective cross-functional working relationships and partnerships; responds positively and constructively to requests for support from across the organization
• Demonstrated enthusiasm and willingness to learn
• Excellent interpersonal and communication skills
• Self-motivated and willing to accept temporary responsibilities outside of initial job description

Work Environment

• Candidate will be working mostly in engineering laboratory environments
• Work may periodically require moving heavy equipment and the ability to lift ~25 pounds
• There is a risk of potential exposure to chemicals and biohazards consistent with cell therapy
• Working in the laboratory requires mandatory use of personal protective equipment

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.