What are the responsibilities and job description for the Manufacturing Engineer position at Aroha Technologies, Inc?
Visa: Any VISA
Rate : $50 on C2C
Location: Marietta, Georgia
Duration: 6 Months with possible extension to 12 Months
Title: Manufacturing Engineer
Here are the key skills highlighted in the below JD:
Job Description
Role Summary:
The Manufacturing Engineer will support equipment and process validation activities (IQ/OQ/PQ) for a medical device production facility. The role involves ensuring that manufacturing systems, equipment, and processes meet regulatory, quality, and performance standards while supporting production readiness and compliance.
Key Responsibilities
Execute and support Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities for manufacturing equipment and processes
Develop, review, and execute validation protocols and reports in compliance with FDA and regulatory standards
Coordinate with cross-functional teams (Quality, R&D, Production, and Validation teams) for successful validation execution
Support equipment installation, commissioning, and troubleshooting activities
Ensure adherence to Good Manufacturing Practices (GMP) and quality systems
Perform risk assessments (FMEA) and contribute to process improvements
Maintain accurate documentation, traceability, and validation records
Participate in process optimization and continuous improvement initiatives
Support audits, inspections, and regulatory submissions as needed
Required Skills & Competencies
Bachelor s degree in Engineering (Mechanical / Electrical / Biomedical / Manufacturing) or equivalent experience with 3 years experience
Strong understanding of IQ/OQ/PQ methodologies and validation lifecycle
Knowledge of medical device regulations (FDA, ISO 13485)
Experience in manufacturing processes, equipment qualification, and process validation
Familiarity with GMP, CAPA, and change control processes
Ability to read and interpret engineering drawings, P&IDs, and technical specifications
Strong problem-solving and analytical skills
Excellent communication and documentation skills
Preferred Qualifications
Experience in medical device or regulated manufacturing environment
Exposure to cleanroom manufacturing environments
Familiarity with statistical tools and validation software
Experience supporting automation systems or complex manufacturing equipment
Work Environment
Full-time onsite role in a regulated medical manufacturing facility
Requires collaboration with cross-functional teams and shop-floor presence
Key Deliverables
Approved IQ/OQ/PQ protocols and reports
Equipment qualification and validation documentation
Compliance with regulatory and quality standards
Timely execution of validation and production readiness activities
Rate : $50 on C2C
Location: Marietta, Georgia
Duration: 6 Months with possible extension to 12 Months
Title: Manufacturing Engineer
Here are the key skills highlighted in the below JD:
Job Description
Role Summary:
The Manufacturing Engineer will support equipment and process validation activities (IQ/OQ/PQ) for a medical device production facility. The role involves ensuring that manufacturing systems, equipment, and processes meet regulatory, quality, and performance standards while supporting production readiness and compliance.
Key Responsibilities
Execute and support Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities for manufacturing equipment and processes
Develop, review, and execute validation protocols and reports in compliance with FDA and regulatory standards
Coordinate with cross-functional teams (Quality, R&D, Production, and Validation teams) for successful validation execution
Support equipment installation, commissioning, and troubleshooting activities
Ensure adherence to Good Manufacturing Practices (GMP) and quality systems
Perform risk assessments (FMEA) and contribute to process improvements
Maintain accurate documentation, traceability, and validation records
Participate in process optimization and continuous improvement initiatives
Support audits, inspections, and regulatory submissions as needed
Required Skills & Competencies
Bachelor s degree in Engineering (Mechanical / Electrical / Biomedical / Manufacturing) or equivalent experience with 3 years experience
Strong understanding of IQ/OQ/PQ methodologies and validation lifecycle
Knowledge of medical device regulations (FDA, ISO 13485)
Experience in manufacturing processes, equipment qualification, and process validation
Familiarity with GMP, CAPA, and change control processes
Ability to read and interpret engineering drawings, P&IDs, and technical specifications
Strong problem-solving and analytical skills
Excellent communication and documentation skills
Preferred Qualifications
Experience in medical device or regulated manufacturing environment
Exposure to cleanroom manufacturing environments
Familiarity with statistical tools and validation software
Experience supporting automation systems or complex manufacturing equipment
Work Environment
Full-time onsite role in a regulated medical manufacturing facility
Requires collaboration with cross-functional teams and shop-floor presence
Key Deliverables
Approved IQ/OQ/PQ protocols and reports
Equipment qualification and validation documentation
Compliance with regulatory and quality standards
Timely execution of validation and production readiness activities
Salary : $45 - $50