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Manufacturing Engineer
Job Location:
Job Location:
Marietta, GA - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
8 September 2026 (17 hours ago)
Posted:
Application Deadline:
6 December 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Tekfortune is a fast-growing consulting firm specialized in permanent contract & project-based staffing services for worlds leading organizations in a broad range of this quickly changing economic landscape virtual recruiting and remote work are critical for the future of work. To support the active project demands and skills gaps our staffing experts can help you find the best job for you.
Role: Manufacturing Engineer
Location: Marietta Georgia
Duration: 6 months
Required Skills: Manufacturing Engineer
Job Description:
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:
Bachelors 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
For more information and other jobs available please contact our recruitment team at . To view all the jobs available in the USA and Asia please visit our website at .
Role: Manufacturing Engineer
Location: Marietta Georgia
Duration: 6 months
Required Skills: Manufacturing Engineer
Job Description:
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:
Bachelors 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
For more information and other jobs available please contact our recruitment team at . To view all the jobs available in the USA and Asia please visit our website at .
Required Experience:
IC
