Manufacturing Engineer

Company:  Lucid Scientific
Location: Atlanta
Closing Date: 05/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description

Company Information

Lucid Scientific, Inc. is an early-stage company creating proprietary cellular analysis equipment for life science researchers in academia and drug discovery. Backed by venture capital, Lucid is rapidly scaling its global customer base as it transitions from a start-up to a profitable enterprise.


Role Summary


Lucid Scientific is seeking a Process Engineer to assist with the scale-up of its manufacturing. This is a new position reporting to the Director of Operations.  As a key member of Lucid’s growing team, the Process Engineer will work to design and qualify new processes, troubleshoot problems and help build a scalable manufacturing process to support Lucid’s rapid growth. The role will require succeeding in a dynamic, high growth environment where a small team is expected to attain a high degree of success through impactful individual contribution and leadership across multiple disciplines. 


Key Responsibilities Include:

  • Assist with the design and development of processes and process parameters for new manufacturing processes and improvements to existing manufacturing processes for improved yield, throughput, and cost.
  • Plan and execute process qualification and validation activities 
  • Perform process risk assessments and implement changes to mitigate risks.
  • Create, maintain, and improve documentation for standard operating procedures for manufacturing processes.
  • Provide technical support for manufacturing processes in production.
  • Assist with transition of processes to new manufacturing locations and/or outsourcing to contract manufacturers.
  • Drive continuous improvement of the manufacturing process


Education, Qualifications and Professional Experience:

  • At least 2 years experience in a related role
  • Bachelor’s degree in mechanical engineering, electrical engineering, or a related discipline
  • Experience operating under a Quality Management System (ISO 9001, ISO 13485, FDA, etc.)
  • A self-starter who is accountable, results-oriented and motivated by a challenge
  • Excellent technical writing skills


*This is an on-site role at Lucid Scientific

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