2487 Document Management Jobs - Page 22

Are you passionate about Salesforce, automation, and leveraging AI to supercharge business workflowsDo you thrive at the intersection of technology, operations, and sales strategy At Sparkrock, we help social benefit organizations like nonprofits, school boards, and government agencies reach their greatest potential through technology. Every day, over 150,000 people use our ERP and product platforms to work more efficiently, freeing up time and resources to focus on the good they want to achieve. We are seeking a Sales Operations and Salesforce/Certinia Admin to manage Salesforce and Certinia to support business requirements. This role also includes owning financial management system configu...

As a Record to Report Specialist at White Horse Manpower Consultancy P Ltd., you will play a crucial role in managing records, performing account reconciliations, and ensuring compliance with company procedures. Your analytical skills will be utilized to maintain accuracy, while effective communication with team members and other departments will be essential for seamless operations. Key Responsibilities: - Manage records efficiently - Perform account reconciliations accurately - Handle document management tasks effectively - Utilize analytical skills to ensure compliance with company procedures - Communicate effectively with team members and other departments Qualifications: - Proficiency i...

You will be joining Slogans FIBC Pvt. Ltd., a leading manufacturer of FIBC bags, in the role of an Account Person at our facility in Morbi, Gujarat. Your responsibilities will include maintaining accurate financial records, organizing documentation, and utilizing Miracle Accounting Software and Tally ERP/Prime. Your expertise in accounting principles, attention to detail, and effective time management will be crucial for this full-time, on-site position. Key Responsibilities: - Bookkeeping & Record Keeping: Ensure all financial transactions are accurately recorded. - Document Management: Organize and maintain financial documentation systematically. Qualifications Required: - Proven experienc...

As an Executive Assistant at our company, you will play a crucial role in managing office operations and providing high-level administrative and executive support. Your attention to detail, multitasking abilities, and excellent communication skills will contribute to a well-functioning work environment. **Key Responsibilities:** - Provide high-level administrative support to C-Suite and senior leadership, including calendar management, travel arrangements, and correspondence. - Manage complex schedules, coordinate meetings, conferences, and events for executives, and prepare reports and presentations for executive review. - Handle confidential information with discretion and act as a point o...

As an Accountant & Admin Officer at our client's international finance team in Chennai, you will play a vital role in handling a hybrid position that combines accounting and finance tasks (80% of your time) along with administrative, facilities, and operational support duties (20%). Key Responsibilities Accounting & Finance (80%) - Support investor reporting and audit preparation for both the management company and managed funds. - Ensure compliance with Indian accounting standards, TDS, GST, and ROC filings. Administration & Operations (20%) - Coordinate with vendors and manage document management. - Provide reception and general office support. - Handle travel arrangements and assist with ...

Requirement of Office Administrative assistant An architecture and project management firm catering to Real Estate projects in Mumbai city for the last 41 years is looking for an office administrative assistant. Preferably Female candidate required between age group of 30-50 years. Job Profile Your primary responsibilities (but not limited to) for this post are as follows: 1. Provide administrative support to ensure efficient operation of office. Escort clients to scheduled meetings in conference rooms, cabins for meetings with respective clients. 2. Answer phone calls, schedule meetings and support clients/visitors. Spoken English is a must 3. Carry out administrative duties such as filing,...

Job Details Performing triage and review for initial validity assessment of cases including spontaneous, health authority, Clinical Trial and literature cases. Responsible for quality management, workload management, compliance management and document management for the assigned PV projects Evaluation of the need for expedited reporting to Health Authorities / partners of a client concerned, including reporting timelines Preparation of standard reporting forms (e.g., CIOMS I / MedWatch Forms and XML Preparation and sending of follow up requests Submission of ICSRs to Health Authorities and partners of a client Acts as line manager of assigned staff Manages project coordination and resource a...

Job Descriptions CMC review of technical documentation for regulatory filings to various markets market: US- Gap Analysis and Remediation for module 3 -CMC Development and implementation of regulatory strategies, processes and timelines for grant of MA- Africas, GCC, LATAM, ASEAN. Review of CTD dossiers , variations, change controls, renewals Affairs

Key Responsibilities The Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation. The Global Trial Acceleration Associate will interact with clinical study sites, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo.), the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies). As the main point of contact for essential document management, ethical and regulatory submission-related activities, develops and maintains collaborative wo...

Key Responsibilities The Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation. The Global Trial Acceleration Associate will interact with clinical study sites, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo.), the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies). As the main point of contact for essential document management, ethical and regulatory submission-related activities, develops and maintains collaborative wo...

Key Responsibilities: The Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation. The Global Trial Acceleration Associate will interact with clinical study sites, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo.), the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies). As the main point of contact for essential document management, ethical and regulatory submission-related activities, develops and maintains collaborative w...

[{"Salary":"3 LPA TO 6 LPA" , "Remote_Job":false , "Posting_Title":"Record Management Executive" , "Is_Locked":false , "City":"Faridabad" , "Industry":"Solar Energy","Job_Description":" Job Overview: We are looking for a detail-oriented and organized Records Management Executive to join our operations team. The ideal candidate will be responsible for maintaining and managing both digital and physical records across departments in compliance with internal policies and statutory requirements. Key Responsibilities: Maintain accurate and up-to-date records, including invoices, purchase orders, delivery notes, employee files, contracts, and customer documentation. Implement and follow best practi...

Title: Senior Executive/ Manager - Corporate Quality Compliance Business Unit: Global Quality and Compliance Job Grade: G10 Location: Vadodara Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” ...

The Senior Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation. The Senior Global Trial Acceleration Associate will interact with clinical study sites, Central/Local IRB/IECs, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo. ), the study team and other functional areas within BMS and will provide support to the Study Team throughout the study duration (start-up, maintenance, and close-out of clinical studies). As the main point of contact for essential document management, ethical and regulatory submission-related activities, develops and maintain...

We are seeking a skilled and detail-oriented Loan Underwriter to join our lending team specializing in manufactured housing chattel loans. As an Underwriter, they will play a pivotal role in evaluating loan applications and assessing the creditworthiness of borrowers seeking financing for manufactured homes. Their expertise in analyzing financial documents, assessing risk, and ensuring regulatory compliance. Desired Mentality: 1.) Passionate about improving consumer outcomes and addressing the affordable housing crisis. 2.) A critical thinker with a collaborative mindset, committed to excellence and innovation in lending. Responsibilities: Review loan applications and supporting documentatio...

Bid Preparation Coordination Assist in the preparation and assembly of tender documents, proposals, and presentations Coordinate input from multiple disciplines, including architecture, masterplanning, and interior design teams Maintain and update project databases, case study libraries, and staff CVs Ensure compliance with tender requirements and submission deadlines Document Management Quality Assurance Format and proofread bid documents to ensure professional presentation standards Manage version control and document distribution processes Coordinate with design teams to ensure accurate representation of project information Administrative Support Track bid opportunities and maintain submi...

1. SCM E2E Operations: Support end-to-end supply chain management operations from the back office. Assist in implementing and monitoring supply chain strategies. Collaborate with cross-functional teams to ensure alignment with business objectives. 2. Export Document Management: Prepare, verify, and submit export documentation. Ensure compliance with international trade regulations. Coordinate with logistics and customs teams. 3. KPI Metrics: Track and analyse key performance indicators (KPIs). Generate regular reports and provide insights for improvement. Identify trends and areas for enhancement. 4. Administrative Support: Provide administrative support, including scheduling meetings and pr...

Job Description: What are we looking for Analysts Consultants Senior Consultants We are looking for smart self driven high energy people with top notch communication skills intellectual curiosity and passion for excellence Our analysts have a blend of in depth domain expertise strong analytical and conceptual thinking skills and excellent soft skills We are looking for people who have demonstrated proven success in roles and through abilities in Computerized System Validation Risk Management and Audits2 14 years of professional experience in Life Sciences industry working for a consulting services organization and or industry experience Understanding of key pharmaceutical compliance regulati...

Your work days are brighter here. At Workday, it all began with a conversation over breakfast. When our founders met at a sunny California diner, they came up with an idea to revolutionize the enterprise software market. And when we began to rise, one thing that really set us apart was our culture. A culture which was driven by our value of putting our people first. And ever since, the happiness, development, and contribution of every Workmate is central to who we are. Our Workmates believe a healthy employee-centric, collaborative culture is the essential mix of ingredients for success in business. That s why we look after our people, communities and the planet while still being profitable....

As a Sr Doc Ctrl Assistant here at Honeywell, you will play a key role in managing and controlling documentation processes. You will be responsible for ensuring the accuracy, quality, and integrity of documents, maintaining document control systems, and supporting various departments with their documentation needs. Your attention to detail and organizational skills will be crucial in maintaining compliance with company policies and regulatory requirements. In this role, you will impact the efficiency and effectiveness of our documentation processes, ensuring that all documents are properly managed and accessible to relevant stakeholders. Your efforts will contribute to the smooth operation o...

Qualification : B.Sc, B.A, B.Com, BCA 12th + Computer Course Diploma (Civil/Mechanical) Candidate Requirement: Male only Experience: fresher Number of Openings: 5 Job Type: Full-time Location : Ambala Cantt, Haryana. Over time allowance Food allowance Leave encashment Job/soft skill training

Maintenance of document control procedures & systems to ensure accuracy, compliance, & accessibility of all organizational documents Establish procedures, lifecycle management, System Management, Compliance & Accuracy, Coordination & Communication

As a Regulatory Administrator at our company, you will play a vital role in providing administrative and operational support to the Regulatory Affairs department to ensure the smooth facilitation of the regulatory submissions process. Your responsibilities will include: - Uploading, organizing, and maintaining regulatory documents within various regulatory authority submissions portals such as CTIS, FDA eGateway, and CESP. - Coordinating the redaction of confidential information in regulatory documents and ensuring compliance with global standards. - Collaborating with external vendors for document redaction services and monitoring the progress of redaction processes. - Assisting in preparin...

As an Administrative Assistant at ADI Group in Mohali (WFO Only), you will play a crucial role in supporting the team with day-to-day administrative operations. Your attention to detail, strong communication skills, and ability to handle multiple priorities efficiently in a fast-paced environment will be key to your success. This internship opportunity is perfect for a recent graduate looking to kickstart their career in administrative support. Key Responsibilities: - Prepare and edit correspondence, reports, and presentations - Organize and maintain physical and digital filing systems - Assist in the preparation of regularly scheduled reports - Order office supplies and maintain inventory -...

Role Overview: As a Visa Documentation Executive at Migration Overseas, your primary responsibility will be to handle day-to-day tasks related to export documentation. This full-time on-site role, located in Vadodara, requires your attention to detail and excellent communication skills. You will be responsible for managing and preparing export documentation, ensuring compliance with regulations, communicating with clients and stakeholders, and organizing document management systems. Key Responsibilities: - Manage and prepare export documentation - Ensure compliance with documentation regulations - Communicate effectively with clients and stakeholders - Organize document management systems Qu...