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Manufacturing Engineer

Job in California, Moniteau County, Missouri, 65018, USA
Listing for: Kindeva
Full Time position
Listed on 2026-08-30
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Lean Manufacturing / Six Sigma, Manufacturing Engineer
  • Engineering
    Quality Engineering, Process Engineer, Lean Manufacturing / Six Sigma, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 90000 - 130000 USD Yearly USD 90000.00 130000.00 YEAR
Job Description & How to Apply Below
Location: California

19901 Nordhoff St, Northridge, CA 91324, USA

Job Description

Posted Tuesday, August 25, 2026 at 5:00 AM

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world

ROLE SUMMARY

This is a great opportunity to support commercial manufacturing operations within a 24/7 pharmaceutical manufacturing environment by providing technical support, troubleshooting processes, continuous improvement, and project execution. This individual will be supporting assigned production lines, driving corrective actions, and executing engineering deliverables that improve safety, quality, reliability, and productivity.

ROLE RESPONSIBILITIES Manufacturing Support (24/7 Facility)
  • Provide daily technical support for assigned production lines.
  • Support troubleshooting of equipment, process, and quality issues.
  • Participate in root cause investigations and corrective actions.
  • Maintain visibility online performance, downtime losses, and recurring issues
Process Ownership & Optimization
  • Serve as engineering owner for assigned manufacturing processes.
  • Manage assigned action items and corrective actions to closure.
  • Support OEE, uptime, yield, scrap reduction, and throughput improvements.
  • Develop and implement process improvements.
  • Support validation, qualifications, and change-control activities.
  • Maintain technical documentation and engineering records
CAPA, Quality, and Compliance
  • Support investigations, deviations, and CAPAs.
  • Complete assigned quality actions by committed due dates.
  • Maintain compliance with cGMP requirements.
  • Support audits and inspection readiness activities.
  • Participate in Engineering Change Control processes)
Project Execution
  • Execute assigned engineering projects and deliverables.
  • Manage multiple assignments simultaneously.
  • Communicate project risks and delays proactively.
  • Meet agreed-upon completion dates.
  • Provide regular status updates to management.
  • Support implementation of capital and continuous improvement projects
QUALIFICATIONS Required
  • Bachelor's degree in mechanical, electrical, systems engineering, manufacturing or other engineering discipline from an accredited institution or a bachelor's degree with manufacturing experience.
  • 3+ years in pharma/biotech/medical device manufacturing is preferred.
  • Working knowledge of root cause investigation methodologies and corrective action development.
  • Working knowledge of cGMP requirements, quality systems, change control, deviations, and CAPA processes.
  • Experience troubleshooting manufacturing processes, equipment, and production issues.
  • Ability to manage multiple assignments and priorities simultaneously.
  • Demonstrated ability to execute engineering projects from concept through implementation.
  • Strong written and verbal communication skills.
  • Experience supporting manufacturing operations in a production environment.
  • Proficiency with Microsoft Office applications and engineering documentation systems.
  • Ability to work effectively with Production, Maintenance, Quality, Validation, and Engineering teams.
  • Willingness to provide support within a 24/7 manufacturing operation when business conditions require additional engagement.
Preferred
  • Familiarity with automated systems and MES.
  • Experience with Lean Manufacturing, Six Sigma, DMAIC, Kaizen, SPC, or DOE methodologies.
  • Experience participating in equipment qualifications, validations, and commissioning activities.
  • Familiarity with RCAs, CAPAs, deviations, and investigation systems.
  • Experience supporting OEE, downtime reduction, scrap reduction, and productivity improvement initiatives.
  • Expertise in inhalation or transdermal manufacturing is preferred.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, & Vision, Health Savings Accounts, Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and 401k Benefits, etc.).

Equal Opportunity

Employer:

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

19901 Nordhoff St, Northridge, CA 91324, USA

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