What are the responsibilities and job description for the New Product Development Manager position at International Medical Industries, Inc.?
Company Description International Medical Industries, Inc. (IMI) is a long-established leader in tamper-evident technologies for IV syringes, oral dispensers, and other delivery systems. For over 40 years, IMI has provided innovative products to admixture, compounding, and nuclear pharmacies, manufacturing a full line of sterile adapters, caps, plugs, aspiration needles, and venting needles. All products are produced in the USA to exacting quality standards, reflecting the company’s commitment to safety and reliability in medical device components. IMI holds certifications that meet the requirements of ISO 13485:2003, CMDCAS, and Medical Devices Directive 93/42/EEC, underscoring its adherence to global regulatory and quality frameworks. Candidates joining IMI will contribute to a mission-driven organization focused on secure, high-quality solutions for healthcare delivery.
Role Description The New Product Development Manager is a full-time, on-site role based in Pompano Beach, FL. This role oversees the end-to-end development of new products, from concept generation and feasibility studies through design, testing, and commercialization. Day-to-day responsibilities include coordinating cross-functional project teams, managing timelines and budgets, and ensuring compliance with applicable regulatory and quality standards. The manager collaborates closely with R&D, manufacturing, quality assurance, and marketing to identify market needs, define product requirements, and drive continuous improvement of existing product lines. The role also involves monitoring industry trends, engaging with key stakeholders to collect feedback, and preparing documentation and reports to support product launches and portfolio decisions.
Qualifications
- Strong Research and Development (R&D) skills, with experience leading innovation and new product initiatives.
- Demonstrated Project Management capabilities, including planning, execution, risk management, and stakeholder communication.
- Knowledge of regulated manufacturing or medical device environments, including quality systems such as ISO 13485.
- Ability to work on-site in Pompano Beach, FL and collaborate effectively with cross-functional teams.
- Excellent analytical, problem-solving, and decision-making skills, with attention to detail and a focus on product safety and reliability.
- Clear written and verbal communication skills for technical documentation, presentations, and cross-department coordination.
- Bachelor’s degree in Mechanical Engineering, Plastics Engineering, or a related field; advanced degree or relevant certifications are a plus.