7 Records Management jobs in the United Arab Emirates
Document control
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Objectives:
The Document Controller ensures effective management and control of technical documentation within projects, aligning with contractual and organizational standards. This role requires a strong understanding of Vanderlande products, asset and documentation management processes, and the relationship between physical assets and technical documentation. Working closely with Project Managers, Engineering Project Leaders, and cross-functional teams—including Engineering, Planning, Commercial, and Integration Management—the Document Controller oversees the review, approval, distribution, and timely submission of documents and correspondence to support successful project execution and handover.
Main Tasks:- Implement and maintain the Document Management Plan, ensuring adherence to defined standards, processes, and templates.
- Support project teams in generating, updating, and validating documents using agreed templates and ensuring formal compliance (e.g., completeness, formatting, readability).
- Manage and control the preparation, submission, receipt, and distribution of all technical documents and contractual correspondence in line with the Project Submittal Plan and distribution lists.
- Maintain the document control system, ensuring availability of up-to-date information such as approval status, revision history, metadata, and planned submission dates.
- Ensure appropriate document review and approval workflows are followed, maintaining a clear audit trail and proactively following up on pending actions or deviations.
- Liaise with the client’s documentation/information management team to ensure smooth handover of records and compliance with client and contractual requirements.
- Coordinate with the Contract Team and stakeholders to define external deliverables and internal documentation needs; maintain the Document List and Project Submittal Plan.
- Prepare and maintain templates for technical documents, contractual correspondence, and forms (e.g., RFIs).
- Support official communication with the client, including submission and tracking of RFIs, comment sheets, and contractual correspondence.
- Ensure compliance with Vanderlande and client information management requirements, as well as legal and statutory regulations.
- Contribute to continuous improvement of information management tools and processes.
- Prepare status and progress reports based on submission schedules, workflow statuses, and KPIs.
- Organize and maintain both electronic and physical document archives as required.
Full access to project contract & documentation, baselines (time, scope) status and progress information.
Suggest and follow-up on improvements, if required, in relation to any document management & control activities.
Responsibilities:Ensures document deliverables and correspondence are generated, reviewed, approved, stored and distributed in time and in line with the applicable standards and regulations.
Skills:- Previous experience in information management / document control related activities
- Experience with EDMS, information management and collaboration applications such as SharePoint, Business Collaborator, Conject, Aconex, or Autodesk Construction Cloud
- A Bachelor's degree (or working towards) in Business, Administration, Engineering or a related field is desirable
- Strong interpersonal and stakeholder management skills, excellent communication skills
- Logical and systematic, IT literate, working with formulas and specifications, with strong attention to detail
5 years of experience in document management & control and project management of large-scale industrial projects
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Document control
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Document Control Coordinator
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Parsons is looking for an amazingly talented Document Controller to join our team in Dubai, UAE. In this role, you will get to establish and/or maintain filing systems, schedules, and records; file correspondence, reports, bulletins; log reports, and correspondence.
What You'll Be Doing :
- Establish and/or maintain filing systems, schedules, and records; file correspondence, reports, bulletins; log reports, and correspondence.
- Process contractor submittals and Requests for Information (RFIs). You will also support and review contractor submittals for compliance with contract documents and logs responses.
- Assist in providing technical and administrative review of construction documents to confirm design intent, RFIs, and submittals comparison, and coordination between projects.
- Develop simple, clear, consistent file structures and implement controls to ensure that communication and work flow protocols are easily to follow.
What Required Skills You'll Bring :
- Bachelor's degree or diploma in a related field
- Minimum 3 years of related work experience on a construction project
- Well versed in EDMS - Aconex software.
- Membership and/or certification in EMC (Enterprise Content Management) and/or ARMA (American Records Management Association) is preferred.
- Knowledgeable of document control work processes and utilization of electronic systems for document management, as well as corporate procedures related to document management.
- Excellent written and oral communication skills, and a thorough knowledge of industry practices and company policies and procedures are required.
- Must also possess a thorough knowledge of database concepts, project-related software, and the ability to train others in its use.
- Keys to your success will be your previous experience in providing document control on similar projects, your organizational skills, and knowledge of Electronic Document Management Systems.
Parsons equally employs representation at all job levels, no matter the race, color, religion, sex (including pregnancy), national origin, age, disability, or genetic information. We truly invest and care about our employee’s wellbeing and provide endless growth opportunities.
Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to .
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Quality Control - Document Administrator
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Quality Control – Document Administrator
Acino is a Swiss pharmaceutical company, leader in advanced drug delivery technologies. We have a clear focus on selected emerging markets in the Middle East, Africa, the CIS Region, and Latin America, and we operate in some of the most dynamic countries of the world. We value courage, commitment, trust, and empathy and provide an environment that supports initiative and effort. We are proud to be action-oriented and open-minded, with a strong focus on quality and product availability, even in remote and hard-to-reach areas of the world.
We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our Quality Control team in Dubai, UAE Site- Acino Pharmaceuticals FZ LLC
Job Overview:
The QC Document Administrator is responsible for ensuring effective control of all QC documentation and sample management processes, in alignment with GLP, GMP, and data integrity principles, supporting laboratory compliance, resources coordination, and ensures smooth execution of QC operations from material receipt to reporting.
Job Responsible:
- Manage QC documents (SOPs, specifications, STPs, release reports, logbooks, training records) in compliance with ALCOA+ principles.
- Ensure timely drafting, revision, approval, and archival of SOPs, specifications, standard test procedures, and reports.
- Maintain document storage, retrieval, and archival systems (manual and electronic such as SAP, Dot Compliance, etc.).
- Monitor document version control and ensure accessibility to authorized personnel only.
- Oversee receipt, registration, and distribution of QC samples as per lot management and sample receiving procedures.
- Ensure proper handling, storage, and tracking of samples (raw materials, packaging, intermediates, finished products, and stability).
- Performing sampling activities for raw materials and water system samples in compliance with GLP and SOPs.
- Maintain sample retention and disposal records as per regulatory and company requirements.
- Monitor and reinforce adherence to GLP practices within the QC laboratory.
- Support internal audits, inspections, and compliance activities by ensuring availability and accuracy of records.
- Report and escalate any observed deviations, non-compliance, or data integrity concerns to QC Manager.
- Coordinate usage and availability of sampling and testing resources (sampling tools, logbooks, controlled forms, etc.).
- Support QC Manager in managing laboratory schedules, prioritizing sample workflows, and aligning resources for timely completion.
- Ensure laboratory personnel training records are maintained, up-to-date, and available for audits.
- Ensure all activities are performed in compliance with EHS policy and PPE requirements.
- Maintain strict confidentiality of QC data, documents, and product information.
- Participate in improvement initiatives for QC operations and documentation processes.
- Provide inputs for system enhancements (SAP, LIMS, documentation tools) to streamline QC efficiency.
- Perform any other responsibilities assigned by the QC Manager to support department needs.
Qualifications & Skills:
- Bachelor’s degree in science or pharmacy with relevant experience.
- 1-3 years of experience in pharmaceutical QC role (GLP/GMP environment preferred).
- Knowledge of data integrity (ALCOA+), GLP, and regulatory requirements.
- Strong organizational skills, attention to detail, and ability to manage multiple priorities.
- Familiarity with SAP, LIMS, or other digital quality/document management systems is an advantage.
This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!
Only direct applications will be considered. Please apply via our HR system here.
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Quality Control - Document Administrator
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Job Overview
The QC Document Controller is responsible for ensuring effective control of all QC documentation and sample management processes, in alignment with GLP, GMP, and data integrity principles, supporting laboratory compliance, resources coordination, and ensures smooth execution of QC operations from material receipt to reporting.
Responsibilities- Manage QC documents (SOPs, specifications, STPs, release reports, logbooks, training records) in compliance with ALCOA+ principles.
- Ensure timely drafting, revision, approval, and archival of SOPs, specifications, standard test procedures, and reports.
- Maintain document storage, retrieval, and archival systems (manual and electronic such as SAP, Dot Compliance, etc.).
- Monitor document version control and ensure accessibility to authorized personnel only.
- Oversee receipt, registration, and distribution of QC samples as per lot management and sample receiving procedures.
- Ensure proper handling, storage, and tracking of samples (raw materials, packaging, intermediates, finished products, and stability).
- Perform sampling activities for raw materials and water system samples in compliance with GLP and SOPs.
- Maintain sample retention and disposal records as per regulatory and company requirements.
- Monitor and reinforce adherence to GLP practices within the QC laboratory.
- Support internal audits, inspections, and compliance activities by ensuring availability and accuracy of records.
- Report and escalate any observed deviations, non-compliance, or data integrity concerns to QC Manager.
- Coordinate usage and availability of sampling and testing resources (sampling tools, logbooks, controlled forms, etc.).
- Support QC Manager in managing laboratory schedules, prioritizing sample workflows, and aligning resources for timely completion.
- Ensure laboratory personnel training records are maintained, up-to-date, and available for audits.
- Ensure all activities are performed in compliance with EHS policy and PPE requirements.
- Maintain strict confidentiality of QC data, documents, and product information.
- Participate in improvement initiatives for QC operations and documentation processes.
- Provide inputs for system enhancements (SAP, LIMS, documentation tools) to streamline QC efficiency.
- Perform any other responsibilities assigned by the QC Manager to support department needs.
- Bachelor’s degree in science or pharmacy with relevant experience.
- 1-3 years of experience in pharmaceutical QC role (GLP/GMP environment preferred).
- Knowledge of data integrity (ALCOA+), GLP, and regulatory requirements.
- Strong organizational skills, attention to detail, and ability to manage multiple priorities.
- Familiarity with SAP, LIMS, or other digital quality/document management systems is an advantage.
This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If this sounds exciting, we would love to hear more about you!
Please apply via our HR system here.
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Master Data Management Lead
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Join us at Enquo, where we're dedicated to harnessing the transformative power of data and technology. As leaders in technology and data solutions, we prioritize humanity in everything we do. Our mission is clear: to empower organizations to unlock the full potential of their data through cutting-edge technology and exceptional services.
We envision a brighter future, where technology ignites extraordinary achievements and drives profound transformation. Here at Enquo, challenges are opportunities, and our passionate team thrives on making meaningful impacts on society. With humility and a collaborative spirit, we leverage teamwork and creative thinking to deliver optimal and trustworthy solutions.
Asa purpose-driven company, were passionate about using data and technology as catalysts for positive change. Our vision extends to a world where everyone can harness the power of data to reach their fullest potential. At Enquo, honesty, trust, and empathy form the foundation of our simple business language. Were agile, adaptable, and committed to bridging any business need with innovative data solutions.
Join our journey, where curiosity and entrepreneurship drive us to explore uncharted territories and create solutions that truly matter. We foster a collaborative and inclusive environment, valuing every team member's contributions. If you're a talented, curious, and creative individual who thrives in a fast-paced, dynamic setting, we invite you to be part of our mission. Together, let's create new opportunities through data and technology, shaping a more humane future for all.
Enquo: fueling a better future through innovation, data, and technology.
Role DescriptionThe Master Data Management Lead will be responsible for defining, designing, and building dimensional databases to meet business needs. Assisting in the application and implementation procedures of data standards and guidelines coding structures and data replication to ensure access to and integrity of data sets.
Key Responsibilities- Excellent experience in Master Data Management including include Meta-Data Management, Data Migration, Data Security and Data Transformation/Conversion
- Experience in ETL processes and advanced SQL skills.
- Intermediate Requirements Gathering/Elicitation, Documentation, and Source to Target mapping skills.
- Working knowledge of Conceptual, Logical and Physical Data Modeling concepts as well as Database design concepts
- Practical experience working in an Agile Methodology
- Bachelor’s or master’s degree in computer science, Information Technology, or a related field.
- Proven experience in data quality management, with at least 8 years of experience in a leadership role.
- Strong understanding of data quality frameworks, tools, and methodologies.
- Proficiency in SQL and experience working with data profiling tools.
- Excellent analytical and problem-solving skills.
- Leadership and team management abilities.
- Effective communication and collaboration skills.
- Familiarity with data governance principles is a plus.
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Manager - TSG - Data Management for UAE Nationals
Posted 128 days ago
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