Responsibilities: Drive process validation activities to ensure compliance with medical device regulations. Design and develop equipment and tooling to support production needs. Provide hands-on production support to address and resolve manufacturing issues. Develop and maintain detailed documentation to support production processes. Requirements: 3+ years of experience in medical device manufacturing. Proficiency in process validation and documentation (IQ/OQ/PQ). Equipment/tooling design experience is required. Experience with either injection molding or laser welding is preferred.