Document Control Specialist

Company DescriptionAviva Natural Supplements is a GMP & USDA Organic turnkey contract manufacturer located in New Brunswick, NJ. Specializing in custom formulation, blending, encapsulations, compression and high-speed packaging lines, Role DescriptionThis is a full-time on-site role for a SOP Document Control Specialist at Aviva Natural Supplements in New...

Company DescriptionAviva Natural Supplements is a GMP & USDA Organic turnkey contract manufacturer located in New Brunswick, NJ. Specializing in custom formulation, blending, encapsulations, compression and high-speed packaging lines, Role DescriptionThis is a full-time on-site role for a SOP Document Control Specialist at Aviva Natural Supplements in New...

Hello,One of my clients is looking Role: Documentation Control Lead, if you’re interested or your skills matches, please share with me your updated resume to sushma@intellectt.comRole - Documentation Control LeadLocation: New Brunswick, New Jersey, United StatesDuration: Long-TermNote: NO C2CThe Document Control/QA Specialist will be responsible for...

Hello,One of my clients is looking Role: Documentation Control Lead, if you’re interested or your skills matches, please share with me your updated resume to sushma@intellectt.comRole - Documentation Control LeadLocation: New Brunswick, New Jersey, United StatesDuration: Long-TermNote: NO C2CThe Document Control/QA Specialist will be responsible for...

Job Title: Sr Specialist, Document Control Job ID: 24-03440 Location: New Brunswick, NJ, 08903 Duration: 12 Months contract on W2 Client Hybrid role Work Schedule: Monday - Friday, Business Hours The purpose of this role is to develop and deliver a Document Framework for the overall Autodesk Construction Cloud (Client) application and for the...

Job DescriptionThe Document Control/QA Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory standards.Key Responsibilities:• Manage validation documentation in automated systems,...

Sr Specialist, Document Control12+ monthsNew Brunswick, NJ 08903 The purpose of this role is to develop and deliver a Document Framework for the overall Autodesk Construction Cloud (ACC) application and for the Capital Project Realization and Information Management (CPRIM) configuration project. Key Responsibilities • Lead the development of the Document...

Sr Specialist, Document Control12+ monthsNew Brunswick, NJ 08903 The purpose of this role is to develop and deliver a Document Framework for the overall Autodesk Construction Cloud (ACC) application and for the Capital Project Realization and Information Management (CPRIM) configuration project. Key Responsibilities • Lead the development of the Document...

Immediate need for a talented Senior Specialist, Document Control. This is a 12+months contract opportunity with long-term potential and is located in New Brunswick, NJ(Onsite). Please review the job description below and contact me ASAP if you are interested.Job ID:24-35830 Pay Range: $60 - $67/hour. Employee benefits include, but are not limited to, health...

About the RoleMace is seeking an ambitious and forward-thinking Document Controls Specialist to join our established and growing team in New York. As a key member of our Consult business, you will play a crucial role in harnessing our unique combination of leading-edge practical expertise and project delivery consultancy to unlock the potential in every...

Job DescriptionThe Document Control Lead will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols, ensuring compliance with internal and regulatory standards.Key Responsibilities:Manage validation documentation in automated systems, including...

{"title": "Document Control Specialist", "description": "Job SummaryWe are seeking a highly skilled Document Control Specialist to join our team at Triumph Construction. As a key member of our project team, you will be responsible for managing and overseeing all project-related documentation to ensure accuracy and compliance.Key ResponsibilitiesManage and...

About the Role:We are seeking a highly skilled Senior Document Control Specialist to support our portfolio of projects.Key Responsibilities:Apply electronic document archiving procedures to support capital and non-capital rail-transit projects.Develop and maintain project files, adhering to file naming conventions.Assist and consult staff in retrieving...

Job SummaryWe are seeking a highly organized and detail-oriented Document Control Specialist to join our Program Management Services Division at LaBella Associates. This role will be responsible for maintaining accurate and up-to-date documentation for our clients' projects, ensuring compliance with established procedures and protocols.Key...

About the RoleMace is seeking an ambitious and forward-thinking Document Controls Specialist to join our established and growing team in New York. As a key member of our Consult business, you will play a crucial role in harnessing our unique combination of leading-edge practical expertise and project delivery consultancy to unlock the potential in every...

Job SummaryWe are seeking a highly organized and detail-oriented Document Control Specialist to join our team at Aspen Technical Staffing, Inc. The successful candidate will be responsible for assisting the document control team and project managers in delivering quality materials and input information on engineering projects.Key Responsibilities:Set up and...

About Orchestra BioMedOrchestra BioMed is a pioneering biomedical innovation company that accelerates high-impact technologies to patients through strategic partnerships with leading medical device companies. Our vision is to revolutionize medical innovation by forging collaborative relationships with industry leaders to drive successful global...

GxP Document Control Specialist - Contract - New Haven, CT Proclinical is seeking a GxP Document Control Specialist for our client based in New Haven, CT. Primary Responsibilities:The successful candidate will serve as the primary point of contact for on-site GxP records archiving. This role involves managing GxP archives, including receiving and logging...

About the Role:Parsons Corporation is seeking a highly skilled Senior Document Control Specialist to support our portfolio of projects. As a key member of our Critical Infrastructure team, you will play a critical role in ensuring the accuracy and completeness of project documents.Key Responsibilities:Support capital and non-capital rail-transit projects by...

About the Role:We are seeking a highly skilled Senior Document Control Specialist to join our team at Parsons Corporation. As a key member of our Critical Infrastructure team, you will play a critical role in supporting our portfolio of projects.Key Responsibilities:Support capital and non-capital rail-transit projects by applying appropriate and proper...