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.