Manufacturing Process Engineer at Delcath Systems Inc
Queensbury, NY 12804, USA -
Full Time


Start Date

Immediate

Expiry Date

28 Nov, 25

Salary

70000.0

Posted On

28 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Mechanical or Industrial Engineering

Description

The primary responsibilities of a Manufacturing Process Engineer include:
· Support day to day manufacturing operations through process control and improvement initiatives to minimize downtime and maximize production.
· Develop and implement new processes, process improvements, to improve process reliability and reduce customer complaints and costs.
· Work with cross-functional internal teams and external vendors to coordinate implementation of new equipment and processes to optimize production and increase capacity.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
· Develop and implement new processes and process improvements which foster lean manufacturing principles
· Plan and coordinate the selection, procurement, installation, start-up, and qualification of new equipment/technology, tooling, fixtures for manufacturing
· Innovate and define technical solutions for production, engineering or quality process-related concerns and lead efforts to realize the solutions
· Communicate/interface internally and externally to understand technical requirements, resolve issues, develop and maintain knowledge of equipment and processes
· Perform cost improvement projects, quality improvement projects, and equipment troubleshooting to support the Company’s manufacturing goals
· Perform and/or assist with root cause investigations associated with product/process non-conformances and implement robust corrective actions to prevent recurrence
· Collect and analyze process data to monitor process/equipment performance
· Lead and/or participate in cross-functional project teams, providing input to design control deliverables including project plans, design review requirements, and development of use, design & process FMEA’s
· Write protocols/reports, implement and lead process validation activities
· Write test methods and test method validation protocols/reports
· Perform and/or oversee equipment, test method validations and/or product testing
· Create, maintain and improve process documentation, work instructions and standard operating procedures
· Establish and implement effective preventive maintenance (PM) on equipment, as required
Job Type: Full-time
Pay: From $70,000.00 per year

Benefits:

  • 401(k)
  • Dental insurance
  • Employee assistance program
  • Flexible spending account
  • Health insurance
  • Paid time off
  • Professional development assistance
  • Vision insurance

Education:

  • Bachelor’s (Preferred)

Experience:

  • Medical Device Manufacturing: 3 years (Required)

Ability to Commute:

  • Queensbury, NY 12804 (Required)

Work Location: In perso

How To Apply:

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Responsibilities

Please refer the Job description for details

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