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JT587 - MANUFACTURING ENGINEER II

Quality Consulting Group · Villalba, PRtoday

BS-level Process Engineering roles on Crosslinked list a median of $112k (563 that show pay). This posting does not list pay.

Design manufacturing processes, layouts and equipment validation for medical device production

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Worth knowing

Might not be for you. Heavy validation/documentation focus (IQ/OQ/PQ, SOPs, CSV) — more compliance than open-ended materials R&D

Generalist BS acceptable

Heads-up: Mostly boilerplate text

Adjacent materials roleExperience in injection molding processes

Seniority
Mid-level
Work
On-site
Type
Full-time
Degree
BS
Experience
3+ yrs
Industry
Medical devices
Role
Process Engineering

Role details

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities

  • Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling.
  • Designs arrangement of machines within plant facilities to ensure most efficient and productive layout.
  • Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance.
  • Adapts machine or equipment design to factory and production conditions.
  • May incorporate inspection and test requirements into the production plan.
  • Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.
  • Develops manufacturing processes that are applicable to statistical process control and may develop those techniques.

Qualifications

  • Bachelor’s degree in Engineering
  • 3+ years of relevant experience.
  • Process Development and documentation
  • Equipment validation
  • SOP Development
  • Special Build Documentation and Line Support
  • Experience in equipment IQ |Experience in OQ (Operational Qualification) and PQ (Performance Qualification) and/or process validation
  • Process Validation Lifecycle ( from process characterization, operational qualification to performance qualification)
  • SOP Development | Special Build Documentation and Line Support
  • Computer and software validation CSV
  • Change control of Medical Devices
  • MES system
  • Experience in injection molding processes
  • Shift: 1st shift

*Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.*

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Common questions

Does Quality Consulting Group sponsor H-1B visas?

Quality Consulting Group has filed H-1B petitions with the US Department of Labor in past years, but this specific posting does not explicitly mention sponsorship for the JT587 - MANUFACTURING ENGINEER II role. Confirm with the employer before applying if visa support is required.

Where is the JT587 - MANUFACTURING ENGINEER II role at Quality Consulting Group based?

This role is based in Villalba, PR.

What degree is required for the JT587 - MANUFACTURING ENGINEER II role at Quality Consulting Group?

This role requires a BS.

How many years of experience does this JT587 - MANUFACTURING ENGINEER II role require?

The posting calls for at least 3 years of relevant experience.