Abbott

Healthcare

SeniorManufacturingProcessEngineer

$0–0k Temecula, California, United States FULL TIME
The Brief

“Senior Manufacturing Process Engineer at Abbott. Skills: Manufacturing Process Engineering, Sterilization Engineering, Process Validation. Provide technical support. Provide sterilization engineering support”

What You'll Achieve.

Improve production efficiencies; Improve manufacturing techniques; Improve production yields; Meet daily production schedules; Enhance productivity; Enhance product quality; Improve product quality; Improve labor efficiency; Improve throughput

Industry & Context.

Healthcare
Problems you'll solve

Problem solving; Root cause analysis; Troubleshooting

Eligibility Requirements

5 % travel, Continuous standing, Continuous sitting, Awkward/forceful/repetitive

What They're Looking For.

Must Have

Bachelor's degree in Engineering, Minimum 5 years experience, Analytical skills, Problem solving skills, Verbal communication skills, Written communication skills, Multitask, Prioritize tasks, Meet deadlines, Organizational skills, Follow-up skills, Attention to detail

Nice to Have

Medical Device products experience, 4 years people management, Statistical techniques experience, Lean manufacturing technique experience, Value stream mapping experience, Continuous improvement methodologies experience, GMP knowledge, ISO regulations knowledge, Broader enterprise experience, Cross division business experience, International manufacturing experience, Six Sigma certification, Cross-division business unit model experience

What You'll Do.

Provide technical support

Provide sterilization engineering support

Develop manufacturing processes

Meet production schedules

Enhance product quality

Support new product introductions

Conduct Process FMEAs

Conduct Process Validations

Improve product quality

Improve labor efficiency

Use Lean manufacturing concepts

Coordinate procurement

Work with Product Development

Draft verification protocols

Review verification protocols

Execute verification protocols

Draft validation protocols

Review validation protocols

Execute validation protocols

Identify validation risks

Identify validation impacts

Develop engineering systems

Implement engineering systems

Train engineering systems

Monitor engineering systems effectiveness

Ensure FDA compliance

Ensure GMP compliance

Ensure regulatory compliance

Coordinate technicians

Implement resource planning

Manage resource planning

Implement project management

Manage project management

Monitor project progress

Evaluate project progress

Monitor department progress

Evaluate department progress

Support sterilization qualification

Evaluate variable factors

Select evaluation criteria

Network with contacts

Lead Continuous Improvement

Support Divisional initiatives

Comply with FDA regulations

Comply with regulatory requirements

Maintain positive communications

Maintain cooperative communications

Collaborate with employees

Collaborate with customers

Collaborate with contractors

Collaborate with vendors

How You'll Work.

Team & Collaboration

Cross-functional teams; Cross-functional agile teams; Cross-division business unit

Communication Scope

Verbal communication; Written communication; Effective communication

Process & Methodology

Project management, Resource planning, Lean manufacturing, Six Sigma

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