
Senior Manufacturing Engineer
2 days ago
Senior Manufacturing Engineer / Manufacturing Manager
Reporting to the VP of Engineering & Manufacturing; this is a newly created position and will be setup, qualify and oversee the manufacturing processes for the company's products.
Responsibilities:
- Manufacturing Process Development & Compliance - Define, validate, and scale up manufacturing equipment and processes for Class I & II products in line with ISO 13485, FDA (21 CFR Part 820), and EHS requirements.
- Process Optimization & Continuous Improvement - Enhance existing processes to improve efficiency, yield, and cost-effectiveness, while driving Lean/Six Sigma initiatives to eliminate waste and ensure quality.
- Technology & Product Introduction - Lead implementation of new technologies, materials, and processes, and support new product introduction through DFM, process development, and production readiness.
- Cross-Functional & Vendor Collaboration - Partner with engineering, QA, supply chain, regulatory, and contract manufacturers to resolve issues (CAPA), develop documentation, and ensure smooth product lifecycle management.
Requirements:
- Bachelor's Degree in Engineering (Mechanical / Biomedical / Manufacturing) with minimum 8-10 years' experience in the medical devices industry. You should be familiar with setting up of manufacturing line, developing processes as well as optimization.
- Must be able to speak English and Mandarin (in order to deal with suppliers in China)
- Comfortable with being the 1st dedicated hire in manufacturing to take on all manufacturing related tasks and issues.
- Good knowledge and experience with various manufacturing processes eg. automation, semi-automation, assembly, injection molding, extrusion, blow molding, leak tester, packaging sealing, ultrasonic welding, UV adhesive curing etc.
- Develop manufacturing processes for medical devices using methodologies such as Design Thinking, DFM and DFSS techniques.
- Hands-on experience with equipment qualification and buy-off of manufacturing equipment with contract manufacturers.
- Hands-on experience with process validation, test method validation (MSA, GR&R), risk management with responsibility in developing process FMEA, root cause analysis and CAPA.
About the company:
- American startup with senior management team; based in Europe
- Hybrid work arrangement - 2 days in office, 3 days working from home
- Excellent medical insurance coverage
- Good variable bonus structure
- Great working culture
- Excellent office location (Central - just beside MRT)
Interested applicants, kindly send in a copy of your updated resume in WORD document to stating your current and expected remuneration together with notice period required to current employer.
You can also contact Vincent Low for a confidential discussion at .
EA Personnel Registration No: R
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