
Advanced Process Optimization Specialist
2 days ago
Transform Your Career as a Senior Manufacturing Engineer
About the RoleAs a Senior Manufacturing Engineer, you will be responsible for developing and optimizing advanced manufacturing processes for Class II/III medical devices.
Collaborate with a growing team to support business growth and ensure compliance with international standards.
Key Responsibilities:- Provide technical leadership and mentorship to engineers and technicians to ensure stable, efficient, and compliant manufacturing operations.
- Lead complex troubleshooting efforts for equipment, tooling, process, or material issues using advanced problem-solving techniques.
- Drive continuous improvement initiatives using Lean, Six Sigma, and other structured methodologies.
- Own and oversee process and equipment change control activities, ensuring quality and regulatory compliance.
- Lead the strategy, planning, and execution of equipment and process validations (IQ, OQ, PQ).
- Guide root cause investigations for non-conformances and ensure effective corrective and preventive actions (CAPA).
- Bachelor's degree in Engineering (Mechanical, Manufacturing, Biomedical or related discipline).
- 6-9 years' experience in medical device or pharmaceutical manufacturing, with proven leadership and mentoring responsibilities.
- Strong knowledge of medical device quality standards (ISO 13485, FDA QSR, EU MDR).
- Demonstrated expertise in process validation (IQ/OQ/PQ) and change control.
- Skilled in continuous improvement methodologies (Lean, Six Sigma – Green Belt preferred).
- Opportunity to work on cutting-edge MedTech manufacturing processes.
- Career development with leadership exposure and cross-functional project ownership.
- Competitive salary and benefits package.
- Collaborative and innovative team environment.
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