Document Control Specialist (Manufacturing) Position Available In Hillsborough, New Hampshire
Tallo's Job Summary: As a Document Control Specialist in the manufacturing sector, you will manage critical documentation throughout the product lifecycle. Reporting to the Quality Manager, you will ensure compliance with ISO 13485 and ISO 9001 standards, utilizing skills in document management systems, records management, technical writing, and data management to enhance operational efficiency in our manufacturing processes.
Job Description
Document Control Specialist (Manufacturing) Connexion Systems and Engineering, Inc. Manchester, NH Job Details Full-time $24•$28 an hour 22 hours ago Benefits Health insurance 401(k) matching Qualifications ERP systems
ISO 9001
Mid-level Administrative experience Records management Bachelor’s degree Data management SharePoint Technical writing Manufacturing Order entry Documentation review Product lifecycle management
Full Job Description Hours:
Monday•Friday 7am or 8am to 4pm or 5pm. (Flexible)
Payrate:
$24/hr•28/hr
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
Desired Qualifications:
Bachelor’s or comparable experience 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 #CNX200 Summary As a Document Control Specialist in the manufacturing sector, you will be essential in managing and organizing critical documentation throughout the product lifecycle. Reporting to the Quality Manager, you will utilize your core skills in document management systems and records management to ensure compliance with ISO 13485 and
ISO 9001
standards. Your premium expertise in quality management and SharePoint will enhance operational efficiency. Additionally, your relevant skills in technical writing and data management will support the creation and maintenance of accurate records, contributing to the overall success of our manufacturing processes.
Job Type:
Full-time Pay:
$24.00•$28.00 per hour Expected hours: 40 per week
Benefits:
401(k) matching Health insurance
Schedule:
8 hour shift Monday to Friday Ability to
Commute:
Manchester, NH 03108 (Required) Ability to
Relocate:
Manchester, NH 03108: Relocate before starting work (Required)
Work Location:
In person