Company Type
Manufacturer
Location
Melville, New York
Job Description
• Review customer complaints, conduct product investigations, and assure proper complaint closure
• Conduct medical device reporting assessments and process potential MDR reports
• Ideal candidate should possess good problem solving & logical decision-making abilities
• Develop sampling plans for evaluating, and reporting quality and reliability data
• Demonstrate continuous effort to improve product quality and manufacturing processes
• Working knowledge of FDA regulations, cGMP, US-FDA’s 21 cfr part 820 and 21 cfr part 803
Job Skills
• Quality Engineering and customer complaint investigation experience
• Medical device industry experience preferred.
• Strong MS office skills
• Excellent communication and interpersonal skills
• 4 Year College Degree or equivalent work experience
Job ID: 9908
