This role focuses on continuously improving manufacturing processes, equipment, and designs while ensuring top-quality products and meeting regulatory requirements. You’ll collaborate across the organization with manufacturing, R&D, clinical teams, quality assurance (QA) and regulatory affairs (RA), as well as external suppliers. This position is primarily responsible for manufacturing improvements, with less emphasis on verification and validation (V&V).
Responsibilities:
- Analyze and lead efforts to enhance all production processes and methods to reduce costs and ensure quality compliance.
- Design and implement new tools, jigs, equipment, and technologies in production, while improving existing ones.
- Manage inventory to ensure the availability of necessary equipment, tools, testing equipment, and prototype parts.
- Provide support to the manufacturing floor, suppliers, and quality control activities.
- Create detailed test plans, protocols, and reports for both process validation and design verification.
Requirements:
- Bachelor’s degree in Mechanical Engineering.
- Minimum of 4 years of experience in a similar role within the medical device industry.
- Strong technical skills and a hands-on approach.
- Excellent written and spoken English.
To apply for this job email your details to jobs@insighthr.co.il