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Document Control Admin

Merrimack ManufacturingManchester, NH

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Overview

Schedule
Full-time
Career level
Senior-level
Remote
On-site

Job Description

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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FAQs About Document Control Admin Jobs at Merrimack Manufacturing

What is the work location for this position at Merrimack Manufacturing?
This job at Merrimack Manufacturing is located in Manchester, NH, according to the details provided by the employer. Some roles may also include multiple work locations depending on the requirement.
What pay range can candidates expect for this role at Merrimack Manufacturing?
Employer has not shared pay details for this role.
What employment applies to this position at Merrimack Manufacturing?
Merrimack Manufacturing lists this role as a Full-time position.
What experience level is required for this role at Merrimack Manufacturing?
Merrimack Manufacturing is looking for a candidate with "Senior-level" experience level.
What is the process to apply for this position at Merrimack Manufacturing?
You can apply for this role at Merrimack Manufacturing either through Sonara's automated application system, which helps you submit applications 10X faster with minimal effort, or by applying manually using the direct link on the job page.