We are seeking motivated and detail-oriented Entry-Level Engineers to join our Pharmaceutical and Medical Device manufacturing teams. This is an excellent opportunity for recent graduates or engineers with up to 2 years of experience to gain hands-on exposure to regulated manufacturing environments while working alongside experienced engineering and operations teams. The selected candidates will support manufacturing operations, process improvements, equipment qualification, validation, quality initiatives, and continuous improvement projects in compliance with FDA and GMP requirements.

Required Qualifications

Bachelor's degree in one of the following:
Mechanical Engineering
Chemical Engineering
Biomedical Engineering
Electrical Engineering
Industrial Engineering
Manufacturing Engineering
Mechatronics Engineering
Pharmaceutical Engineering
1–2 years of engineering experience
Basic understanding of manufacturing processes and engineering principles.
Strong analytical, problem-solving, and communication skills.
Ability to work effectively in a team-oriented environment.
Willingness to learn and work in a regulated manufacturing setting.

Preferred Qualifications

Experience in Pharmaceutical, Biotechnology, Medical Device, or Manufacturing industries.
Basic knowledge of:
FDA cGMP
ISO 13485
Good Documentation Practices (GDP)
Lean Manufacturing
Six Sigma
Validation concepts (IQ/OQ/PQ)
Familiarity with AutoCAD, SolidWorks, or other engineering software is a plus.
Exposure to SAP, TrackWise, or MES systems is advantageous.

Technical Skills

Manufacturing Operations
Process Improvement
Equipment Qualification (IQ/OQ/PQ)
Process Validation
Root Cause Analysis
CAPA
Change Control
Engineering Documentation
GMP Compliance
Microsoft Office Suite

Commissioning Partners

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