JT544 - MANUFACTURING ENGINEER II
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JT544 - MANUFACTURING ENGINEER II
Location
Villalba, Puerto Rico
Experience
Mid
Posted
Jul 10, 2026
Apply by
August 9, 2026
Applicants
0
Early applicantEasy applyTemporaryWork from Office
Job Description
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 (Mechanical, Chemical, Electrical Engineering preferred)
- 2+ years of relevant experience.
- Experience with ethylene oxide, steam, liquid chemical, and radiation sterilization methods
- Experience with no sterile package design or pharma package design
- Change control of Medical Devices
- Equipment Commissioning / Qualification
- Manufacturing, Packaging and Laboratory Equipment
- Technical experience (Trouble shooting) or any similar experience or background
- Quality / Process Control / Assurance of Medical Devices
- Process Validation and Computer software validation knowledge.
- Equipment Validations Manage Supplier Change Request
- 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.
Key Responsibilities
- Designs manufacturing processes, procedures, and production layouts for assemblies and equipment.
- Arranges machines within plant facilities to ensure efficient and productive layouts.
- Designs sequences of operations and specifies procedures for tool and equipment fabrication.
- Adapts machine or equipment design to factory and production conditions.
- Incorporates inspection and test requirements into production plans.
- Inspects machinery and equipment performance to verify efficiency and initiates corrective actions.
- Develops manufacturing processes applicable to statistical process control.
Requirements
- Bachelor’s degree in Engineering
Skills Required
Ethylene oxide sterilizationSteam sterilizationLiquid chemical sterilizationRadiation sterilizationNo sterile package designPharma package designChange control of Medical DevicesEquipment CommissioningEquipment QualificationManufacturing EquipmentPackaging EquipmentLaboratory EquipmentTroubleshootingQuality ControlProcess ControlProcess AssuranceProcess ValidationComputer software validationEquipment ValidationsSupplier Change Request ManagementMotivatedEnthusiastic
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