
Quality Control Engineer
3 days ago
WALK-IN for Quality Engineer -TRAINEE
A Quality Engineer for medical devices ensures products meet stringent safety and quality standards by overseeing production processes, performing risk assessments, and managing quality data.
Key responsibilities include validating equipment, implementing corrective actions (CAPA), analysing quality trends, ensuring regulatory compliance, and collaborating with cross-functional teams to resolve issues and drive continuous improvement throughout the product lifecycle.
Responsibilities
- Process & Equipment Validation: Oversee and document the validation of manufacturing processes and equipment to ensure they consistently produce compliant medical devices.
- Quality Data Analysis: Collect, analyse, and interpret quality data and trends to identify areas for improvement in product quality and manufacturing efficiency.
- CAPA Implementation: Initiate and manage corrective and preventive action (CAPA) protocols to resolve quality issues and prevent their recurrence.
- Regulatory Compliance: Ensure all production processes and documentation adhere to relevant regulatory requirements and industry standards, such as ISO 13485.
- Risk Management: Perform risk assessments, including Process FMEAs (Failure Mode and Effects Analysis), to evaluate potential defects and implement necessary risk mitigation techniques.
- Cross-Functional Collaboration: Work with R&D, manufacturing, and other departments to address quality-related issues and improve product quality.
- Quality Documentation: Prepare & maintain critical quality documents, including process instructions, control plans and QMS documentation.
- Process Monitoring: Implement methods to monitor and control manufacturing processes, effectively distinguishing between common and special cause variation.
- Continuous Improvement: Actively identify and drive opportunities to enhance product quality, reduce costs, and increase efficiency within the manufacturing line.
Key Skills and Qualifications
- Education: Bachelor's degree in BIO-MEDICAL/MECHANICAL engineering or scientific field.
- Experience: Freshers or lesser experience in the medical device industry are preferred.
- Technical Skills:
- Expertise in quality management systems (QMS).
- Proficiency in process monitoring, risk assessment, and validation techniques.
- Familiarity with regulatory standards for medical devices.
- Soft Skills:
- Strong problem-solving and analytical abilities.
- Excellent attention to detail and critical thinking.
- Effective communication and interpersonal skills.
If the above job profile suits your interest please walk-in to below factory location from Monday-Saturday 10am-4pm
GESCO Healthcare Pvt. Ltd.
43F, TASS INDUSTRIAL ESTATE, AMBATTUR, CHENNAI 600098
Job Type: Full-time
Pay: ₹15, ₹16,000.00 per month
Benefits:
- Food provided
- Provident Fund
Application Question(s):
- PLEASE MENTION YOUR WALK-IN DATE in DD/MM/YYYY format.
Shift availability:
- Day Shift (Preferred)
- Night Shift (Preferred)
Work Location: In person
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