drjobs Quality Assurance Engineer

Quality Assurance Engineer

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1 Vacancy
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Job Location drjobs

Cambridge - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Nanobiosym is an innovative hightech company that is developing novel technologies at the nexus of physics nanotechnology and biomedicine. Founded by MIT/Harvard alum and located in Cambridge Massachusetts Nanobiosym was awarded the first XPrize to be given for healthcare.
The Compliance Engineer is responsible for the organization and the coordination of processes pertaining to regulatory compliance and quality systems to ensure regulatory requirements for compliance
DUTIES
  • Collaborate with team members and management to develop and improve injection molded and assembled products and processing thru numerous manufacturing steps.
  • Aid in Coordinating a production and Engineering Team in a variety of manufacturing processes.
  • Develop and Implement new processes including DOE IQ OQ PQ
  • Able to implement TAQ time analysis life flow studies and improvement plans in a ISO 13485 environment
  • Perform root cause analysis and help develop corrective actions.
  • Develop and assist in the process and product monitoring including the creation and documentation of validation protocols that comply with FDA regulations.
  • Provide troubleshooting focus and direction for the team with details of root cause analysis.
  • Utilizes DRM/COS/Lean principles to develop creative thorough and practical technical solutions.
  • This is a handson leadership position in a growing organization and an opportunity which will grow rapidly.
QUALIFICATIONS
  • Bachelors degree is required in an Engineering mechanical polymer or material science discipline
  • Plastic products understanding & Injection Molding Experience Strongly preferred
  • Minitab and PFEMA Experience defab
  • 815 years of experience in diverse technical materials manufacturing and process design
  • Experience in statistical analysis and statistical process control
  • Recent experience with an FDA regulated 21 CFR 820 and/or ISO 13485 environment
PERSONAL QUALITIES
  • You have leadership skills to enhance team dynamics
  • You are passionate about new product development healthcare and mobile technology
  • You are methodical detail oriented well organized and effective at time management
  • You are a selfstarter
  • You have good interpersonal verbal communication and documentation skills
  • You can function well in a challenging and fastpaced environment
  • You are enthusiastic and positive with strong skills in the areas of dependability flexibility and maturity

Employment Type

Full-Time

Company Industry

About Company

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