We are seeking an experienced and skilled CSSD Product Engineer to join our team. The successful candidate will be responsible for developing, and implementing sterile packaging and processing solutions for medical devices and equipment. The CSSD Product Engineer will play a critical role in ensuring the safety, quality, and efficacy of our products. Key Responsibilities: 1. Product Testing and Validation : Conduct testing and validation of sterile packaging and processing solutions to ensure they meet design specifications, regulatory requirements, and industry standards. 2. Process Improvement : Continuously evaluate and improve sterile packaging and processing solutions, implementing changes as needed to ensure optimal safety, quality, and efficacy. 3. Regulatory Compliance : Ensure compliance with regulatory requirements, such as FDA, ISO, and CE marking, for sterile packaging and processing solutions. 4. Collaboration and Communication*: Collaborate with cross-functional teams, including R&D, manufacturing, and quality, to ensure effective communication and coordination of product development and launch activities. 5. Technical Support : Provide technical support and guidance to internal stakeholders, including manufacturing, quality, and customer service, on sterile packaging and processing solutions. 6. Industry Trends and Standards : Stay up-to-date on industry trends, standards, and regulatory requirements, applying this knowledge to inform design and development activities. 7. Documentation and Record-Keeping : Maintain accurate and complete documentation and records of design and development activities, testing and validation results, and regulatory compliance. Requirements: - Bachelor's degree or Diploma in Engineering (e.g., Mechanical, Biomedical, Packaging), or related field. - Minimum 1-5 years of experience in product or a related field, preferably in the medical device industry. - Strong knowledge of sterile packaging and processing solutions, development, testing, and validation. - Experience with regulatory requirements, such as FDA, ISO, and CE marking. - Excellent problem-solving, communication, and collaboration skills. - Ability to work in a fast-paced environment and prioritize multiple projects simultaneously.,