logo inner

Principal Mechanical Engineer - Consumables

CellaresSouth San Francisco, California, United StatesOnsite
We are seeking an innovative and highly motivated Mechanical Engineer who will contribute significantly to developing our advanced cell therapy manufacturing platform. The primary focus of this position will be the design, prototyping, production, and verification of highly complex plastic injection-molded consumable assemblies.
As a Principal Mechanical Engineer (consumables), you will be responsible for component selection, design tasks, manufacturing coordination, sterilization coordination, and initial quality assurance efforts of both individual components, and finished assemblies. Additionally, you will be required to provide in-depth analysis and CAD data to help guide important decisions during design reviews. This is a multidisciplinary role, and this individual will further interface across many parts of the company to develop novel products used in cell therapy and gene therapy.

The successful candidate will be experienced in plastic injection molding, material selection, and component selection for complex biomedical consumable device design. This is a hands-on position.Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows.

Responsibilities


  • Responsible for the design, development, prototyping, and volume manufacturing of complex injection molded assemblies and high-precision mechanical components & assemblies
  • Specifying injection molding tooling with state-of-the-art capabilities: Variotherm, vacuum assist, hot runners, etc
  • Design and development of manufacturing test fixtures as required
  • Identify & interface with key component vendors (suppliers of tubing, valves, etc, that may be integrated into our consumable design)
  • Interface with R&D systems & mechanical engineering teams to negotiate designs that meet product requirements & are feasible to manufacture economically
  • Conduct design reviews and present fresh ideas, new technologies, and creative solutions to design problems
  • Show proof of concept through rapid prototyping
  • Work closely with the scientific team through the creation of verification/validation protocols (IQ, OQ, PQ) as well as successful execution, data generation, reporting, and documentation
  • Work with external companies as needed to outsource injection molding activities and manage the vendors through all phases of the projects, including user requirements, RFQ, vendor selection, and concept & design, followed by verification/validation
  • Work with external companies as needed to outsource consumable assembly and sterilization activities through all phases of the project(s)
  • Create comprehensive work instructions and manufacturing SOPs as needed 

Requirements


  • 15+ years of hands-on experience with plastic injection molding, including but not limited to component design, design optimization, mold design
  • 5+ years of experience designing and building one-time-use tubing sets or consumables for the medical or biotech industry
  • In-depth knowledge of materials science/plastics properties and metrology techniques
  • Experience with drafting engineering drawings, BOMs, and product specifications
  • Good understanding of DFM and lean manufacturing
  • Excellent verbal, written, presentation, and interpersonal skills. Strong analytical and problem-solving skills
  • Prior experience with FDA regulations and ISO, cGMP, QMS standards & with USP class VI materials
  • Knowledge and hands-on experience with machine shop tools
  • Strong proficiency with SolidWorks CAD tools
  • Work history with several successful iterations of molded components transferred successfully to volume manufacturing
  • Working knowledge of manufacturing techniques, including machining, injection molding, and bonding of consumables (ultrasonic welding, laser welding) for biotech components
  • Desire to be part of a rapidly evolving organization with compelling technology, and ready to take products and processes to the next level
  • Self-awareness, integrity, authenticity, and a growth mindset

$150,000 - $240,000 a yearCellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.Apply for this job

Life at Cellares

Cellares is revolutionizing cell therapy manufacturing. We are developing a one-of-a-kind solution, The Cell Shuttle, to overcome the challenges associated with manufacturing so these life-saving therapies are affordable and widely available to patients who can benefit. The clinical impact of cell therapy in treating cancer has been proven, but this therapeutic approach has several limitations, especially in manufacturing, leaving extremely sick patients waiting for treatment and desperate for hope. Since cell therapy is currently produced for a single patient at a time, it is expensive to manufacture, requiring significant time and resources, and is difficult to scale. Preclinical and clinical scientists, as well as commercial cell therapy manufacturers also lack the options to fully automate their manufacturing process quickly, safely, cost-effectively and at the scale they need. The Cell Shuttle is an automated and closed end-to-end manufacturing solution that is flexible and scalable, enabling customers to run exact processes specified for their cell therapy. Compared with the current manual manufacturing processes for cell therapy, the Cell Shuttle’s next-generation automated manufacturing solution has 10 times the scalability (meaning 10 times more patient doses can be produced simultaneously), enables a three-fold reduction in process failure rates and will reduce the per-patient manufacturing cost by up to 70 percent for most processes.
Thrive Here & What We Value- Fastpaced, mission-driven environment- Collaborative and knowledge-sharing environment- Total patient demand for cell therapies at global scale- Industry 4.0 approach to mass manufacturing living drugs of the 21st century- Integrated Development and Manufacturing Organization (IDMO) with flexible, high-throughput platform- Accelerating access to life-saving cell therapies- WalkAway, end-to-end automation
Your tracker settings

We use cookies and similar methods to recognize visitors and remember their preferences. We also use them to measure ad campaign effectiveness, target ads and analyze site traffic. To learn more about these methods, including how to disable them, view our Cookie Policy or Privacy Policy.

By tapping `Accept`, you consent to the use of these methods by us and third parties. You can always change your tracker preferences by visiting our Cookie Policy.

logo innerThatStartupJob
Discover the best startup and their job positions, all in one place.
Copyright © 2024