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The Opportunity

We're looking for a Senior Quality Engineer, working in the Biotechnology/Medical Devices industry in Danvers, Massachusetts, United States.

  • Manages MDR Remediation Activities
  • Executes test method validations
  • Assists with protocol and implement process validation procedures in accordance with QSR, FDA, and international guidelines.
  • Performs risk assessment activities to identify the product quality or compliance risks and lead efforts to mitigate those risks. 

We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.

Our Client

Our client is an award-winning clinical development company.  Improving lives globally with 20+ years experience in clinical research and strategic resourcing.  Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities.  Industry expertise sets you up for success with helpful insights, career coaching, and professional training.  Grow and learn while you put your skills to work.  

Experience Required for Your Success
  • Bachelor's degree in an engineering discipline 
  • 5+ years Quality Assurance experience in a GMP environment or highly regulated industry with a BS degree.
  • 2+ years with a Master's degree 
  • Demonstrated working knowledge of process validation, statistical methods, risk management (preferred)
  •  5+ years of Quality Assurance experience in a QSR (GMP), disposable medical device environment (preferred)
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.