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Project Support Engineer

Job

Experis

Scarborough, ME (In Person)

Full-Time

Posted 5 days ago (Updated 1 day ago) • Actively hiring

Expires 6/12/2026

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Job Description

Summer Work Location:
Scarborough, ME(100% Onsite)
Duration:
3 Months (Summer Work) This will also be a great opportunity to learn about facilities and utility equipment for use in GMP and clean environments and gain experience within the medical device industry. In the end, you will build your own capabilities through the job experience, mentoring and training. This job description will be reviewed periodically and is subject to change by management.
Responsibilities may include the following:
Leverages Lean Methodology to drive work process improvements. Train on facilities processes, run automation and work hands-on with facilities Create and revise training material/technical documents Retrain technicians to new or revised SOPs and PMSOPs Drive adherence to approved policies and procedures and motivate production to meet daily demand Understand product specification and manufacturing logistics, provide guidance for non-conformance or out-of-specification conditions. Effectively communicate pass downs for Engineering, Maintenance and Production Support material and equipment troubleshooting as needed, communicate and escalate findings to decision makers Work with other engineers and technicians in developing solutions and improvements in equipment and process as necessary Participates in teams as necessary to ensure continual improvement, safety and compliance Execute work in accordance with all Operations and Quality procedures The duration of our internships is 10 to 12 weeks starting in May.
BASIC QUALIFICATIONS
|
EDUCATION
Candidates pursuing a BS/MS degree in Electrical Engineering, Mechanical Engineering or Chemical/BioChemical/Biomedical Engineering. Ability to follow verbal and written instructions and provide training to new hires
PREFERRED QUALIFICATIONS
Experience working in a GMP, FDA, ISO and USDA regulated environment. Familiarity with cGMP and
ISO 13485
regulations and practices. Experience in a manufacturing environment (Production, Facilities, Engineering, Maintenance) Knowledge of manufacturing principles/techniques

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