Jr. Manufacturing Engineer

SANTA ROSA VA, CA, US • Posted 1 day ago • Updated 1 day ago
Contract Independent
Contract Corp To Corp
Contract W2
6 Months
No Travel Required
On-site
Depends on Experience
Fitment

Dice Job Match Score™

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Job Details

Skills

  • GMP
  • validation
  • Manufacturing ENgineer
  • equipment qualification
  • IQ
  • OQ
  • PQ
  • FDA
  • ISO
  • Life Sciences
  • Medical Devices
  • regulated
  • TMV

Summary

NMK Global Inc is a global IT Services & Solutions company providing IT Staffing Services and Application Development Services necessary for technology leaders to deliver business value. We help our people and clients succeed by leveraging our expertise, deep industry and market knowledge, proprietary assessment tools and techniques, and project delivery methodologies. Through relationships with thousands of specialized professionals, we bring an unparalleled ability to match talent with opportunities by assessing, recruiting, developing and engaging the best and brightest people for our clients. We combine broad geographic presence, world-class solutions and a tailored, consultative approach to help our people and clients achieve higher performance and outstanding results.

Job Title: Jr. Manufacturing Engineer

Location: Camarillo, CA

Duration: 6+ Months

Job Description:

  • We are seeking a Jr. Manufacturing Engineer with 3+ years of experience in the Life Sciences or Medical Device industry.

  • The ideal candidate will have hands-on experience supporting manufacturing operations, process development and new product introduction activities within regulated environments.

Key Responsibilities:

  • Support manufacturing operations and process improvement initiatives.

  • Participate in New Product Introduction (NPI) activities and transfer products into manufacturing.

  • Develop, optimize and document manufacturing processes.

  • Execute equipment qualification and validation activities including IQ, OQ and PQ.

  • Perform Test Method Validations (TMVs) and maintain validation documentation.

  • Collaborate with cross-functional teams including Quality, Operations and R&D.

  • Identify and implement continuous improvement opportunities to enhance efficiency, quality and productivity.

  • Ensure compliance with GMP, FDA and ISO 13485 requirements.

  • Support root cause investigations, CAPA activities and process troubleshooting.

Required Skills:

  • 3+ years of Manufacturing Engineering experience.

  • Experience in Life Sciences, Medical Devices or regulated manufacturing environments.

  • Strong knowledge of NPI, process development and manufacturing operations.

  • Hands-on experience with Equipment Validation (IQ/OQ/PQ).

  • Experience with Test Method Validation (TMV).

  • Knowledge of GMP, FDA regulations and ISO 13485 standards.

  • Experience supporting manufacturing operations in plastic fabrication or plastic processing environments is highly preferred.

  • Excellent problem-solving, documentation and communication skills.

Education:

  • Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering or a related technical discipline.

NMK Global Inc is an equal access/equal opportunity employer and does not discriminate on the basis of age, color, disability, marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other classification prescribed by applicable law.

 

 
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 90773860
  • Position Id: 3213-4981-
  • Posted 1 day ago
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