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, Continuous Improvement. Provide technical support. Provide sterilization engineering support”

Industry & Context.

Healthcare
Problems you'll solve

Problem solving; Analytical; Root cause analysis

Eligibility Requirements

5% travel

What They're Looking For.

Must Have

Bachelor's degree in Engineering, Minimum 5 years experience, Analytical problem solving skills, Verbal and written communication skills, Multitask and prioritize, Organizational and follow-up skills, Attention to detail

Nice to Have

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

What You'll Do.

Provide technical support

Provide sterilization engineering support

Develop manufacturing processes

Recommend equipment modifications

Implement process modifications

Improve production efficiencies

Improve manufacturing techniques

Improve production yields

Design manufacturing processes

Develop manufacturing tooling

Develop manufacturing fixtures

Meet daily production schedules

Enhance product quality

Support new product introductions

Provide guidance to engineers

Provide guidance to technicians

Provide guidance to operators

Provide technical mentorship

Conduct Process FMEAs

Conduct Process Validations

Improve product quality

Improve labor efficiency

Coordinate design of tooling

Coordinate procurement of tooling

Coordinate build of tooling

Coordinate debug of tooling

Coordinate design of machinery

Coordinate procurement of machinery

Coordinate build of machinery

Coordinate debug of machinery

Coordinate design of test equipment

Coordinate procurement of test equipment

Coordinate build of test equipment

Coordinate debug of test equipment

Work with Product Development

Ensure Design for Manufacturability

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 on engineering systems

Monitor engineering systems effectiveness

Ensure FDA compliance

Ensure GMP compliance

Ensure regulatory compliance

Coordinate technicians for operations

Coordinate operators for operations

Coordinate technicians for projects

Coordinate operators for projects

Implement resource planning

Manage resource planning

Implement project management tools

Manage project management tools

Monitor project progress

Evaluate project progress

Monitor department progress

Evaluate department progress

Conduct CAPAs for non-conformances

Investigate biological indicator sterility

Support sterilization qualification

Evaluate variable factors

Select methods for results

Select techniques for results

Select evaluation criteria for results

Network with key contacts

Lead Continuous Improvement activities

Support Divisional initiatives

Comply with FDA regulations

Comply with regulatory requirements

Comply with Company policies

Maintain positive communications

Maintain cooperative communications

Work with cross-functional teams

How You'll Work.

Team & Collaboration

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

Communication Scope

Verbal communication; Written communication; Communicate at multiple levels

Process & Methodology

Project management, Resource planning

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