Senior Systems Integration Engineer (I,II,III) at Cellares

South San Francisco, California, United States

Cellares Logo
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Biotechnology, Cell TherapyIndustries

Requirements

  • BS in Engineering, Bioengineering, Physics, or related field with 5+ years of extensive, hands-on experience in developing analytical instrumentation and biotech automation OR MS or PhD in Engineering, Bioengineering, Physics, or related field with 3+ years of extensive, hands-on experience in developing analytical instrumentation and biotech automation
  • Extensive hands-on experience in integration testing and troubleshooting in highly complex instrumentation systems that combine fluidic handling, electronic sensors, gas mixing, and robotics
  • Experience in biomedical-related instruments and consumables development, integration, and verification activities
  • Experience with autologous and allogeneic cell therapy manufacturing processes (preferred)
  • Experience with scripting languages (MATLAB, Python, JMP, etc.) for modeling, simulation, and data processing (preferred)
  • Prior experience with ISO regulations, cGMP, QMS, and IEC 61010 standards (preferred)
  • Excellent verbal, written, presentation, and interpersonal skills
  • Strong analytical and problem-solving mindset
  • Self-awareness, integrity, authenticity, and a growth mindset

Responsibilities

  • Serve as technical lead to perform hands-on system characterization, integration, verification testing, troubleshooting, root-cause investigation, and continuous improvement of Cellares technology platforms
  • Work closely with the Hardware, Software, Firmware, Process, and Manufacturing teams to perform system characterization, testing, and continuous system improvement
  • Design and execute complex experiments, following scientific principles and statistical approaches, to support the development and characterization of customer processes
  • Author and present quality technical documents, procedures, and reports; produce technical reference documentation and reports; provide training and assistance for the operations team
  • Interface closely and actively with cross-functional teams; self-motivated to drive given tasks to completion
  • Learn and adapt to Cell Shuttle technologies; take ownership of various tasks and successfully drive them to completion

Skills

Systems Integration
Instrumentation Development
Fluidic Handling
Electronic Sensors
Gas Mixing
Robotics
Integration Testing
Troubleshooting
Python
MATLAB
JMP
Biotech Automation
cGMP
ISO
QMS
IEC 61010

Cellares

Develops and manufactures cell therapies efficiently

About Cellares

Cellares develops and manufactures cell therapies in the biotechnology sector, operating as an Integrated Development and Manufacturing Organization (IDMO). Its proprietary "Smart Factory" technology features an automated single-use cartridge system, which increases productivity and reduces costs and process failures compared to traditional methods. The company serves a range of clients, including pharmaceutical companies, and aims to provide efficient and cost-effective manufacturing services for cell therapies. Cellares stands out by combining development and manufacturing processes under one roof, making it a competitive option in the industry.

South San Francisco, CaliforniaHeadquarters
2019Year Founded
$345.3MTotal Funding
SERIES_CCompany Stage
Industrial & Manufacturing, BiotechnologyIndustries
201-500Employees

Benefits

Health Insurance
Dental Insurance
Vision Insurance
401(k) Company Match
Stock Options

Risks

Emerging biotech startups threaten Cellares' market share with similar solutions.
Potential regulatory delays could impact scaling of new automated systems like Cell Q.
Supply chain vulnerabilities may disrupt production timelines for Cell Shuttle and Cell Q.

Differentiation

Cellares' Cell Shuttle offers 10x scalability over manual cell therapy manufacturing.
The Smart Factory technology integrates development and manufacturing, unlike traditional CDMOs.
Cell Q automates QC processes, addressing bottlenecks in cell therapy quality control.

Upsides

Partnership with Sony enhances precision in cell therapy manufacturing processes.
Strategic partnership with Bristol Myers Squibb provides financial boost and validation.
Ossama Eissa's appointment as COO accelerates global expansion and operational capabilities.

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