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Sr. Manufacturing​/Process Engineer

Job in San Diego, San Diego County, California, 92101, USA
Listing for: Ledgent Technology
Full Time, Contract position
Listed on 2026-07-20
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer, Lean Manufacturing / Six Sigma
  • Manufacturing / Production
    Manufacturing Engineer, Quality Engineering, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 45 - 48 USD Hourly USD 45.00 48.00 HOUR
Job Description & How to Apply Below
Position: Sr. Manufacturing/Process Engineer (Contract)

Sr. Manufacturing/Process Engineer (Contract)

Temporary $45.00 - $48.00/hr Onsite

6-month contract (40 hours/week) - possibility of extension and/or conversion

Location:

100% Onsite in Tustin

Pay: $46/hr

Primary Job Function

Responsible for providing engineering support to develop and transfer processes of new medical device.

The successful candidate will have a track record of driving and improving manufacturing processes. The engineer will be a key liaison between our product development team and production team with a focus on delivering quality, cost efficiency and productivity improvements. The ideal candidate will be a strategic thinker, have strong business acumen and have a 'hands on' approach to problem solving.

They will be comfortable working in a dynamic and fast-paced manufacturing environment and have experience with lean/six sigma practices.

Preferred Qualifications

The ideal candidate will be a strategic thinker, have strong business acumen and have a 'hands on' approach to problem solving and with strict attention to details. They will be comfortable working in a dynamic and fast-paced development and manufacturing environment and prefer to have experience with lean/six sigma practices.

You must have:

  • A Bachelor's degree in Engineering or related field with minimum of 8 years' experience in a manufacturing engineering or process transfer role.
  • Strong in communication, organizational, and problem-solving skills, and have the ability to work independently and as part of a team.
  • Experience in improving manufacturing processes as well as a passion for leading improve manufacturing processes to increase cost efficiency and productivity.
  • Knowledge of applicable FDA regulations for medical device industry.
Responsibilities
  • Contribute as part of a product development team to transfer pilot processes to high volume site.
  • Develop and improve manufacturing processes to improve cost and productivity.
  • Identify, troubleshoot, and resolve any production scale-up issues on design and process.
  • Perform investigations and plan/execute matrix experiments to identify solution for improvement. Perform qualification on improvements.
  • Develop equipment IOQ, process validation and operational qualification protocols.
  • Execute equipment IQ, OQ, PQ and validation protocols.
  • Utilize lean six sigma and related practices to streamline production processes.
  • Maintain and update engineering documents and records.
  • Work with suppliers to resolve material quality issues.
  • Design fixtures to improve process output and product quality.
  • Coordinate with other departments to ensure effective execution of the transfer and scale-up.
  • Ability to manage competing priorities in a fast-paced environment.

All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance.

Job Reference: JN -

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