IT Documentation Specialist - Bedford, NH
5 days ago

Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
Haigh-Farr is a premier antenna design and manufacturing company seeking an IT Documentation Specialist to create manage and update technical documentation. · ...
5 days ago
Haigh-Farr is seeking an Information Technology Documentation Specialist to create, manage and update technical documentation. · ...
5 days ago
+Job summary · Support ZOLL's Quality System Documentation · Generate and process Engineering Change Orders , Engineering Change Requests , Manufacturing Change Orders , Process Deviation Authorizations by incorporating input effectively clarifying information · +Qualifications ...
1 week ago
Responsible for supporting ZOLL's Quality System Documentation and the Change Control process (ECOs, ECRs, MCOs, and PDAs) activities related to the ZOLL's Product Lifecycle Management (PLM) System. · ...
6 days ago
Support ZOLL's Quality System Documentation and the Change Control process activities related to the ZOLL's Product Lifecycle Management (PLM) System. · ...
1 week ago
Support ZOLL's Quality System Documentation and the Change Control process activities related to the ZOLL's Product Lifecycle Management (PLM) System. · ...
1 week ago
This Quality position is considered a global role reporting into the supplier management team within PharmSci QA who is responsible for supporting the Pharmaceutical Sciences R&D organization. · ...
1 week ago
We are seeking a detail-oriented Document Control Specialist to support the implementation of an electronic Quality Management System (eQMS) in a fast-paced medical device environment. · Develop, implement, and maintain comprehensive record retention systems, policies, and proced ...
1 month ago
This position is responsible for developing implementing and maintaining comprehensive record retention systems policies and procedures. Develop implement and maintain comprehensive record retention systems policies and proceduresImplement electronic file system · Ensure accurac ...
3 weeks ago
Provides medical device design and quality documentation creation and development as well as management and control of our Quality Management System. · Works with technical teams to establish criteria and best practices for document development, management, · and change control. ...
1 month ago
+This position is responsible for developing implementing and maintaining comprehensive record retention systems policies and procedures. · + · +Bachelor's Degree or equivalent combination of education and experience · ...
3 weeks ago
Provides for the creation and development of medical device design and quality documentation. · A minimum of 3 years of experience in a medical device design/manufacturer environment responsible for documentation control. · ...
1 month ago
The Quality Document Control Specialist implements and maintains the Engineering Change Notice (ECN) System. They will coordinate the interaction between engineering, manufacturing, field operations and marketing teams in order to ensure appropriate changes are properly documente ...
3 weeks ago
The RN Clinical Documentation Specialist facilitates concurrent documentation of health records to ensure accurate representation of Severity of Illness (SOI) and Risk of Mortality (ROM) for hospitalized patients, · Collaborate with Coding staff and Clinical Documentation Improve ...
1 month ago
We are looking for a Document Control Specialist to oversee and manage the structured control of Bill of Materials (BOMs), system settings and lifecycle processes within AX and related business systems. · ...
3 weeks ago
We offer all that and more at Microchip Technology Inc. We help design the technology that runs the world. · ...
1 month ago
The Quality Document Control Specialist implements and maintains the Engineering Change Notice (ECN) System. · Key Responsibilities:Responsible for issuing part numbers, ECNs, · ...
3 weeks ago
Join the Microchip team as a Document Control Specialist and work on technology that powers the world. You'll be part of a diverse and dynamic team with unlimited career potential. · ...
3 weeks ago
This is a dual role combining Document Control skills and the ability to create and enhance the training within Quality.The ideal candidate will conduct change impact assessments, develop and implement change management and training strategies, and provide coaching and support to ...
1 month ago
The RN Clinical Documentation Specialist facilitates concurrent documentation of health records to ensure accurate representation of Severity of Illness (SOI) and Risk of Mortality (ROM) for hospitalized patients, · Utilize clinical expertise to ensure documentation reflects the ...
1 month ago