Top Skills & Experience Required:
Hands-on lab experience in product development & manufacturing of medical devices, drug-device delivery systems, or combination products.
Strong background in DOE, product functionality testing, reliability, and characterization.
Experience in product investigations, compliance, data analysis, technical reports & presentations.
Product/process design, verification, validation, and commercial scale-up knowledge.
Excellent communication, technical writing, and ability to work independently.
Education/Experience:
BS (5 yrs exp.); MS (3 yrs exp.); PhD acceptable (2 yrs exp.).
Fields: Biomedical, Mechanical, Chemical, Materials Science, Biotechnology, or related Engineering.
Nice to Have:
Knowledge of FDA/ISO standards, cGMP, design history file, tech transfer, and CMOs.
Experience with pre-filled syringes, auto-injectors, eye care devices, or pump systems.
Strong skills in documentation (SOPs, validation protocols), electronic notebooks, and cross-functional teamwork.
Responsibilities:
Support development, scale-up, and manufacturing of drug-device systems & combination products.
Conduct lab studies, DOE experiments, and product testing for accuracy, sensitivity & reliability.
Prepare technical documentation, reports, and presentations.
Collaborate with cross-functional teams (R&D, Quality, Regulatory, Manufacturing, CMOs).
Ensure compliance with FDA/ISO standards and troubleshoot manufacturing challenges.