Synthetic Biology Manufacturing Lead

3 days ago


Menlo Park, California, United States Elegen Full time
Overview

Elegen is a pioneering biotechnology company that is revolutionizing the field of DNA synthesis with its cutting-edge approach. Our team of experts in biology, chemistry, hardware, and software engineering is dedicated to delivering innovative solutions to our customers in pharma, biotech, agbio, and biomanufacturing.

Salary and Benefits

The annual base salary compensation for this role, based on location, is $120,000 - $145,000. Compensation may vary depending on factors such as skill, experience, expertise, and location. The package also includes bonus, equity, and benefits. Specific offer packages are determined by multiple factors.

**Benefits:**

  • Healthcare
  • Dental
  • Vision
  • Learning Allowance
  • 401K
  • Flexible PTO
  • Short Term Disability
  • Fitness Allowance
  • Long Term Disability
  • Parental Leave Program
  • Commuter Benefits
Job Description

We are seeking a highly motivated Manufacturing Manager to champion the success and efficiency of our oligo synthesizing processes. This role will encompass supporting new technology transfer from R&D to production for oligo synthesis, adeptly managing manufacturing batches, personnel, and shipping schedules, fostering collaboration with cross-functional teams, and providing inspirational leadership to our production associates.

Key Responsibilities:
  • Lead and Manage production operations of Oligo Synthesis: In partnership with the R&D team, implement new processes in production, set throughput, cost, and quality goals for production operations and streamline and optimize production processes.
  • Timely Manufacturing of Oligo: Manage and execute batches in the lab to ensure the timely manufacturing of oligo. Coordinate with relevant teams to optimize efficiency and meet production targets. Manage day-to-day scheduling for technicians through the shifts. Assist in scheduling shipping and customer manifest generation.
  • Quality Control Inspection: Perform the QC of incoming raw material and ensure they meet specification before being released for production use, conduct QC of molecular kits, interpret and respond to validation data, and ensure that production outputs meet all specifications for high-quality reagents.
  • Data Analysis: Perform preliminary analysis of the production data and build dashboards and KPIs. Keep a detailed laboratory notebook for batch records.
  • Process Improvements: Collaborate closely with the Process Development (PD) and Research and Development (RD) teams to drive process improvements.
  • Software Development: Build a LIMS for daily production execution and enhance features over time to meet production needs, while actively participating in end-user validation for software support.
  • Team Management: Hire and manage a small team of production associates, providing guidance, training, and support as needed. Ensure effective communication, teamwork, and adherence to safety and quality standards.
  • Troubleshooting and Weekend Support: Provide troubleshooting assistance to address any production issues that may arise. Additionally, offer support over the weekend to maintain production continuity and resolve any urgent matters.


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