Process Engineer in Lodi, California at Cepheid

Date Posted: 5/12/2018

Job Snapshot

Job Description

Job ID: CEP000579

About Us

 

Description

JOB SUMMARY:
Execute mold qualification protocol. Responsible for documentation, inspection, scheduling and coordinating all qualification
activities to ensure optimum production capability and product quality.


ESSENTIAL JOB RESPONSIBILITIES:
Perform basic setup and operation of plastic injection molding machines
Create process parameters using scientific processing and molding techniques.
Assist and execute validation protocols (IQ/OQ/PQ) for new equipment and molds
Document processes and procedures as per validation protocol
Create/modify SOP and work instructions
Manage validation projects in order to meet timelines
Implement and make recommendations to optimize process
Assist with set up and optimization of injection molding and auxiliary equipment
Inspect parts for qualification
Work productively and cooperatively with all departments
Help train new operators on injection molding machines and process
Work in a clean room environment
Other duties as assigned

Job Requirements



Qualifications

MINIMUM REQUIREMENTS:


Education or Experience (in years):


High School Diploma or GED


Must have minimum of 5 years experience in injection molding.




Knowledge and skills:


Experience in MS Office (Word, Excel, MS Project)


Experience in writing technical documents, including validation documents, procedures, and reports.


Must have strong ability to organize and manage multiple tasks in a fast-paced environment.


The ability to work effectively with team members and work under minimal supervision.


Must have strong project management skills and the ability to lead and train others in a matrixes environment.



Physical requirements/abilities:


Ability to work in an office environment




PREFERRED REQUIREMENTS:


-AS degree preferred


-Scientific process and molding experience is a plus


-Experience in validation process (IQ/OQ/PQ)


-Experience working in a Medical Device or FDA Regulated environment a plus.



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