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Document Control Specialist Jobs in New Jersey

1 - 14 of 14
1 - 14 of 14
Search Results - Document Control Specialist Jobs in New Jersey
US Tech Solutions, Inc.-South Plainfield
Duration: 24-month contract Job Description: Develop and maintain document control and record management systems for the P&C ET&D organization. Proficiency with file transfer protocols and procedures. Provide general support for ET&D utilizing our...
resume-library.com -
JUNE JACOBS LABS, LLC-Moonachie
with document control and QA support of manufacturing. Department: Quality & Compliance Primary Job Duties & Responsibilities:  •  Author, maintain, and update test method, protocol, policy, instruction, and SOP accordingly.  •  Review manufacturing batch...
mindmatch.ai -
HEPCO, Inc.-South Plainfield
Our client is seeking a motivated Document Control Specialists to join the Record Management Center within their Electric Transmission & Distribution (ET&D) Organization. This is an excellent opportunity for candidates with 1-3 years of experience...
resume-library.com -
Moorestown (NJ)
Essential Duties and Responsibilities This position supports the AEGIS TECHREP Activity Security Manager with tasks to include:  •  Responsible for all AEGIS TECHREP document control including receiving and processing incoming mission essential materials...
icims.com -
Intellectt Inc-New Brunswick
Role: Documentation Control Lead Location: New Brunswick, NJ Duration: 24+ Months Job Description: The Document Control/QA Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role...
mindmatch.ai -
Stefanini, Inc-South Plainfield
problem-solving and decision-making skills, strong organizing skills, and be results-oriented. Responsibilities:-Develop and maintain document control and record management systems for the P&C ET&D organization. -Printing and preparing drawing packages...
smartsearchonline.com -
Source One Technical Solutions-South Plainfield
Control Specialist (Contractor) Pay Rate: $22.50/hr (W-2) The contract duration is initially 2 years 40 hours/week, standard business hours, Mon-Fri This is a position within the Record Management Center of the Electric Transmission & Distribution...
mindmatch.ai -
Newark
processing.  •  Monitor vendor project commitment status and generate reports.  •  Maintain stringent document control processes for all project related information. Issue notes of meetings. Waste data entry and management for Utility wide data tracking...
tiptopjob.com -
Compunnel Inc.-Morristown (NJ)
quality, and regulatory standards.  •  Maintains and updates Quality System procedures and work instructions.  •  Manages document control electronic system (Control): schedules document and diagram reviews, maintains account users, maintains controlled copy...
mindmatch.ai -
Hamilton (NJ)
to indemnities, warranties, liabilities, pricing, schedule, etc.  •  Monitor and evaluate contract performance  •  Record keeping / document control with audit involvement  •  Processing vendor invoices for payment This position allows for a hybrid work schedule...
icims.com -
Crossfire Consulting Corporation-South Plainfield
Job Description: DOCUMENT CONTROLS SPECIALIST: This will be fully on site and in person, five days per week (Monday through Friday), 8 working hours per day. This is a position within the Record Management Center of the Electric Transmission...
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Axelon Services Corporation-Clifton (NJ)
Document Controls Specialist Clifton NJ 2+ Years Pay: $20-23 per hour drawing packages construction organization printing and engineering package Preferred document controls papers for drawing records and scanning process drawing packages...
resume-library.com -
1 similar job: South Plainfield
CS Energy-Edison (NJ)
will be responsible for performing scheduled audits and random spot inspections of the work in progress, the final/finished product and project quality document control to verify these items have been completed in compliance with all applicable codes, standards, plans...
resume-library.com -
Kaztronix-Parsippany
with document control group to ensure regulatory document archiving. Evaluates risks of product and clinical safety issues during clinical phases and recommends regulatory solutions. Evaluates proposed preclinical, clinical and manufacturing changes...
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