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Document Control Admin

Merrimack Manufacturing

Manchester, NH

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Administrative Skills, Bill of Materials (BOM), Board Meeting, Change Control, Change Requests/Orders, Cross-Functional, Detail Oriented, Document Control, Document Management, Documentation, ERP (Enterprise Resource Planning), ISO (International Organization for Standardization), ISO 9000, Manufacturing, Medical Equipment, Organizational Skills, Problem Solving Skills, Product Documentation, Product Lifecycle Management, Quality Management, Source Code/Configuration Management (SCM), Support Documentation, Team Player, Time Management
LOCATION
Manchester, NH
POSTED
6 days ago
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.

Position Overview:
This Document Control Administrator provides support our document control processes as well as other related quality systems. This role will report to the QMS Manager and contributes as a critical facilitator between manufacturing, engineering, and project teams.

Responsibilities:
  • Support change control administration, part number management, BOMs and BOM structure, and applying revision control within the Product Lifecycle Management (PLM) and Enterprise Resource Planning (ERP) systems
  • Review all changes and in a timely manner with high level of detail
  • Contribute to cross-functional improvement initiatives
  • Provide input during weekly change board meetings to facilitate change review and closure
  • Support the proper organization, filing, archiving, and secure destruction of all controlled documents whether electronic or paper
  • Ensure all change requests and documents within the Quality Management System are reviewed by the appropriate department
  • Review change orders for accuracy, completeness, and impact to other documents, products, processes, and the PLM or ERP systems
  • Review documents for the proper formatting and editing prior to submitting for approval
  • Provide Good Documentation Practices guidance to the team as needed
  • Support the maintenance of design history files, device master records, and device history records as needed
  • Proactively interface with internal and external customers to convey requirements, resolve issues, fulfill documentation requests, and otherwise facilitate the change process
Qualifications and Skills:
  • Experience working in a manufacturing company required
  • Familiarity with GDP and working in the medical device field preferred
  • Familiarity with ISO 9000 and/or ISO 13485 preferred
  • Systems oriented with solid and demonstrable PLM and/or ERP experience
  • Team player who prefers to take a collaborative approach in problem solving
  • Organized, detail oriented, and self-directed; able to meet goals and deadlines without constant supervision

Education: Bachelor’s or comparable experience.
 

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Merrimack Manufacturing

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