Medical Device Quality Engineer

3 weeks ago


Manchester, United Kingdom Merrimack Manufacturing Full time

Merrimack Manufacturing is seeking an experienced professional to support design transfer activities and quality operations in a fast-paced, medical device-manufacturing environment. This role includes generation and maintenance of control plans, risk management files, validation protocols, and other QMS documentation to support initial qualification and launch of commercial production activity.

Key Responsibilities:
  • Leverage your engineering and technical experience to evaluate new products, manufacturing processes, and ensure compliance with applicable regulatory standards throughout the New Product Introduction process.
  • Provide input to the development, review, and update of User Requirements, critical quality attributes, and other design documentation.
  • Lead project teams through protocol generation, execution, documentation organization, report writing, etc. while meeting schedule for final approval and release for use.

This role also requires leading investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem solving skills.

The estimated salary for this position is $80,000 - $110,000 per year, based on industry standards and location.



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