Current jobs related to Sr. Document Control Specialist - New Brunswick - SPECTRAFORCE
-
Document Control Specialist
4 weeks ago
New Brunswick, United States Aviva Natural Supplements Full timeCompany 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...
-
Document Control Specialist
4 weeks ago
New Brunswick, United States Aviva Natural Supplements Full timeCompany 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...
-
Document Control Specialist
4 weeks ago
New Brunswick, New Jersey, United States Aviva Natural Supplements Full timeJob Title: Document Control SpecialistCompany: Aviva Natural SupplementsLocation: New Brunswick, NJJob Type: Full-timeAbout Us: Aviva Natural Supplements is a GMP & USDA Organic turnkey contract manufacturer specializing in custom formulation, blending, encapsulations, compression, and high-speed packaging lines.Job Description:We are seeking a highly...
-
Document Control Specialist
4 weeks ago
New Brunswick, New Jersey, United States Intellectt Inc Full timeJob DescriptionIntellectt Inc is seeking a highly skilled Document Control Specialist to join our team. As a key member of our quality assurance team, you will be responsible for maintaining the lifecycle of validation documents within our automated system.Key Responsibilities:Manage validation documentation in automated systems, including document control...
-
Document Control Specialist
4 weeks ago
New Brunswick, United States Intellectt Inc Full timeRole: Documentation Control LeadLocation: New Brunswick, NJDuration: 24+ MonthsJob Description:The 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...
-
Document Control Specialist
4 weeks ago
New Brunswick, United States Intellectt Inc Full timeRole: Documentation Control LeadLocation: New Brunswick, NJDuration: 24+ MonthsJob Description:The 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...
-
Document Control Specialist
6 days ago
New Brunswick, New Jersey, United States Futran Tech Solutions Pvt. Ltd. Full timeJob Summary:As a Document Control Specialist at Futran Tech Solutions Pvt. Ltd., you will be responsible for the initiation, processing, routing, and archiving of cGMP documentation related to global specifications and methods. This role requires strong teamwork, time management, organizational, and communication skills, as well as excellent computer skills...
-
Document Control Specialist
2 days ago
New Brunswick, New Jersey, United States Futran Tech Solutions Pvt. Ltd. Full timeJob SummaryAs a Document Control Specialist at Futran Tech Solutions Pvt. Ltd., you will be responsible for the initiation, processing, routing, and archiving of cGMP documentation related to global specifications and methods. This role requires strong teamwork, time management, organizational, and communication skills, as well as the ability to follow...
-
Document Control Specialist
3 days ago
New Brunswick, New Jersey, United States Futran Tech Solutions Pvt. Ltd. Full timeJob SummaryAs a Document Control Specialist at Futran Tech Solutions Pvt. Ltd., you will be responsible for the initiation, processing, routing, and archiving of cGMP documentation related to global specifications and methods. This role requires strong teamwork, time management, organizational, and communication skills, as well as the ability to follow...
-
Documentation Control Lead
4 weeks ago
New Brunswick, United States Intellectt Inc Full timeHello,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...
-
Documentation Control Lead
4 weeks ago
New Brunswick, United States Intellectt Inc Full timeHello,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...
-
Documentation Control Specialist
4 weeks ago
New Brunswick, New Jersey, United States Pharmatek Consulting Inc Full timeJob Title: Documentation Control LeadThe Documentation 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 to ensure compliance with internal and regulatory standards.Key Responsibilities:Manage validation documentation in...
-
Documentation Control Specialist
2 weeks ago
New Brunswick, New Jersey, United States Pharmatek Consulting Inc Full timeJob Title: Documentation Control LeadThe successful candidate 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...
-
Documentation Control Lead
4 weeks ago
New Brunswick, United States Pharmatek Consulting Inc Full timeJob 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,...
-
Document Control Specialist
1 week ago
New York, New York, United States Pride Now Full timeJob OverviewWe are seeking a highly organized and detail-oriented Document Control Specialist to join our team at PrideNow. The successful candidate will have a minimum of three years of experience in administrative assistance or document control, with a strong background in computer software systems.As a Document Control Specialist, you will be responsible...
-
Validation Documentation Specialist
2 weeks ago
New Brunswick, New Jersey, United States Pharmatek Consulting Inc Full timeJob Title: Validation Documentation SpecialistThe Validation Documentation Specialist will be responsible for maintaining the lifecycle of validation documents within an automated system. This role involves performing quality reviews of validation protocols to ensure compliance with internal and regulatory standards.Key Responsibilities:Manage validation...
-
Document Controls Specialist
3 days ago
New York, New York, United States EXP Full timeJob OverviewAs a Document Controls Specialist at EXP, you will play a vital role in ensuring the smooth operation of our engineering projects. Your primary responsibility will be to coordinate the electronic, printing, and distribution process for engineering drawings and documents. This includes performing basic system maintenance, managing access requests,...
-
Document Control Lead
4 weeks ago
New Brunswick, New Jersey, United States Pharmatek Consulting Inc Full timeJob 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...
-
Document Control Specialist
4 weeks ago
New York, United States Pride Now Full timeJob DescriptionJob DescriptionAdministrative/Document Control(1) Will have a minimum of three (3) years of experience as an administrative assistant ordocument control clerk with a CM or construction organization, or(2) a technical degree from an accredited college and one (1) year experience as anadministrative assistance or document control clerk with a CM...
-
Documentation Control Lead
7 days ago
New Brunswick, New Jersey, United States Verista Full timeJob SummaryVerista is seeking a skilled Documentation Control Lead to join our team. As a key member of our quality assurance team, you will be responsible for managing validation documentation in automated systems, performing quality reviews of IQ/OQ/PQ protocols, and collaborating with cross-functional teams to ensure documentation aligns with project...
Sr. Document Control Specialist
2 months ago
Sr Specialist, Document Control
12+ months
New 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 Framework for the overall Autodesk Construction Cloud (ACC) application
• Lead the development of a Document Framework for the Capital Project Realization and Implementation
Management (CPRIM) configuration project in ACC
• Identify all required documentation for ACC and for the CPRIM project using IT-SOP-100 System Lifecycle
Solution and other BMS policies, procedures and BMS Design Standards
• Partner with BMS IT to ensure all required IT documentation is known/discovered and understand and advise on
correct use of various procedural document types
• Partner with Global Engineering and CPRIM Workstream Leads to ensure all documentation requirements have
been discovered
• Author or update documents identified in both Document Framework
• Review/edit documents for compliance with the IT-SOP-100 documentation requirements
• Update Project Management Standards documents, forms, templates, and job aids that are impacted by the CPRIM project, partnering with or assisting the Global Engineering Design Standard owner
• Develop training material for updated Project Management Standards
• Ensure training material and curriculum is made available on the BMS SuccessFactors training portal
CPRIM project Specific tasks
• Review business and administrative documents, training material and workflows delivered by Autodesk for the
configuration of ACC for CPRIM
• Review the functional requirements document developed by Autodesk for traceability to User Acceptance Testing scripts
• Author functional requirements documents, as needed
• Review User Acceptance Testing materials developed by a 3rd party vendor and ensure traceability to functional
requirements
• Develop User Acceptance Testing materials, as needed
• Participate in user acceptance testing
• Prepare training material for pre-pilot testing
• Deliver training to pre-pilot testing project personnel
• Support pre-pilot testing project teams
• Develop training plan for CPRIM rollout
• Develop training curriculum for CPRIM rollout
Qualifications & Experience
• Required Bachelor's Degree in Business Administration, Engineering or related field
• Advanced Level Experience with IT documentation requirements for software implementation.
• Advanced Level Experience authoring IT technical documents.
• Advanced Level Experience authoring Business Standards.
• Advanced Level Experience with Autodesk Construction Cloud (ACC).
•Advanced Level Experience with Training software such as Clipchamp or Simpleshow.
• Advanced Level Experience with software configuration and implementation.
• Advanced Level Experience with authoring functional requirements and user acceptance testing.
• Demonstrate excellence in writing clear, concise business-related documents
• Candidates must be effective in both a team environment and an individual contributor role.
• Works with limited supervision on the accomplishment of agreed upon goals and objectives.
• Ability to work in a fast-paced environment; able to prioritize tasks to meet multiple deadlines.
• Excellent planning, organizing, analysis and problem-solving skills.
Strong background and understanding in the planning and execution of capital projects.
• Minimum of eight years business writing experience, preferably in an IT environment