Quality Engineer

COMPANY OVERVIEW

Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life.

This position will support manufacturing quality operations in a dynamic, fast‑paced, medical device manufacturing environment. This environment includes the manufacture, inspection, and test of devices for design verification, design validation, and commercial production.

• Work cooperatively with other team members and in compliance with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 to transition products from development to manufacturing.
• Use experience within medical devices to provide guidance and assistance in the development of new production processes.
• Drive the development, implementation, and approval of PFMEAs and control plans.
• Develop inspection processes and sampling plans according to the risk level of the components, material and devices.
• Use experience with engineering and technology to ensure compliance with applicable standards and regulations.
• Ensure all product, processes, and components are within specifications and work with internal team and customers to resolve any nonconformance issues.
• Facilitate the development, implementation, and approval of Device Master Records and Device History Records.
• Review existing procedures for continuous improvement and improved workflow.
• Lead investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem solving skills.
• Use critical thinking and deductive reasoning to make risk‑based decisions.
• Develop and approve technical documents to plan work, such as Master Validation Plans, Quality Plans, and Qualification Protocols; support execution of work product.
• Collect and evaluate data, lead system and process improvements using six sigma tools.
• Provide reliability and statistical analysis of data for investigations, qualifications, test method validations and other quality‑related activities.
• Participate in ISO 13485 audits and assist in FDA and other regulatory inspections. Use Microsoft Office software (Word, Outlook, Excel).

• 3+ years of experience in occupation related to Quality Control of medical devices.
• Experience with compliance, with applicable standards and regulations such as 21 CFR 820 and ISO 13485:2016 is required.
• Experience participating in internal and external audits.

Bachelor’s degree or equivalent experience in Industrial, Mechanical or related engineering / life sciences related discipline.