3648 Data Integrity Jobs - Page 32

Job Title Salesforce Marketing Cloud Administrator (Hybrid) Job Description Overview We re seeking a Salesforce Marketing Cloud (SFMC) Administrator to play a central role in our Pathways IT team for our global marketing technology team. You ll ensure the platform is secure, reliable, and optimised for impact working at the intersection of marketing, CRM, and IT to enable data-driven engagement at scale. Reporting to the Head of CRM, you ll oversee platform administration, campaign execution, and data integrity, while championing best practices and innovation in marketing automation. Key Responsibilities Platform Administration & Governance Manage user roles, permissions, and platform config...

Conduct Risk Management by processing data for various asset classes from Custodians to third party risk analytics vendors. Partnering with IT and vendors to ensure accurate and complete data and risk analytics for Funds, Retail and Institutionally Managed accounts for around $700B of the $1 Trillion Assets Under Management/Advice Engaging with internal Risk SMEs and data operations team for resolving issues with source data, analysing and validating data and the end reports and fixing exceptions in both the daily and monthly risk process Managing data collection procedures, data processing, cleansing, and verifying data integrity to build robust risk management processes. Develop Tableau re...

Provide single point of co-ordination for all phases of International relocation activities, administering and policing client policy on behalf of client as outlined in their specific policies Provide impeccable customer service to assignee and their family Coordinate the delivery of services and manage vendors as dictated by client policy Counsel employees to the best utilization of program benefits Demonstrate sound knowledge of products and services Dealing with Client s employees on a day to day basis in accordance with their policy Deliver the International Relocation products and services to the employee Strive to maintain Cartus position as the Market Leader by continuing to deliver e...

Liaise with the employee, supplier providers and internal stakeholders andcoordinate the temporary housing throughout the booking process. Provide single point of co-ordination for all phases of International relocationactivities, administering and policing client policy on behalf of client as outlinedin their specific policies Provide impeccable customer service to assignee and their family Coordinate the delivery of services and manage vendors as dictated by clientpolicy Counsel employees to the best utilization of program benefits Demonstrate sound knowledge of products and services Dealing with Client s employees on a day to day basis in accordance with theirpolicy Deliver the Internatio...

Job Description Position: Database Administrator No of Vacancies: 2 Experience: 7 years Qualification: B Tech / BE/MCA. About Us: Kran Consulting Pvt Ltd, with Headquarters in Thiruvananthapuram, Kerala, is an innovative IT consulting company with almost 3 decades of industry presence with a primary focus on Public Administration. We have established ourselves as an organization delivering mission critical projects to Government Clients across the country. We confirm to Global Quality Standards including CMMI DEV/5, ISO 9001:2013, ISO 20000 and ISO 27001. Currently we are working on Government Projects in multiple states in the Country. Job Description: The Database Administrator is responsi...

Job Summary We are seeking a skilled Medical Coding Specialist with 2 to 3 years of experience in healthcare products and medical coding. The candidate will work in a hybrid model primarily during the day shift. This role involves ensuring accurate coding of medical records contributing to the efficiency and accuracy of healthcare data management and supporting the companys mission to enhance healthcare services. Responsibilities Ensure accurate coding of medical records to maintain data integrity and compliance with healthcare regulations. Collaborate with healthcare professionals to verify and clarify coding information for accuracy. Analyze medical records and assign appropriate codes to ...

We are seeking an experienced and highly skilled SAS Developer for an urgent 6-month contractual engagement. The successful candidate will be instrumental in ensuring the accuracy, efficiency, and completeness of our existing SAS data extract programs, with a particular focus on data integrity and performance optimization. Responsibilities : - Review and Analyze : Conduct thorough reviews and in-depth analysis of existing SAS data extract programs to assess their accuracy, efficiency, and completeness. - Data Remediation : Proactively identify, retrieve, and recode broken or non-performing data segments within SAS programs to restore functionality and data integrity. - Collaboration & Valida...

Data Management Accurately input and manage data in the company's backend systems Ensure data integrity/compliance with data entry standards Process Coordination Collaborate with different departments to ensure seamless backend operations Required Candidate profile Conduct regular checks to ensure the accuracy and quality of backend processes. Identify and rectify discrepancies or errors in a timely manner.

Key Responsibilities: Administer and maintain SQL Server databases, ensuring high availability (HA) and optimizing performance. Perform regular database backups, monitoring, and auditing to maintain data integrity and security. Utilize PowerShell scripting to automate routine database tasks, streamline processes, and improve operational efficiency. Perform performance tuning to optimize database systems for improved speed and responsiveness. Monitor and troubleshoot database-related issues, ensuring quick resolution of any operational problems. Implement and maintain disaster recovery procedures to ensure data availability and minimal downtime. Collaborate with other IT teams to ensure datab...

Data Management Accurately input and manage data in the company's backend systems Ensure data integrity/compliance with data entry standards Process Coordination Collaborate with different departments to ensure seamless backend operations Required Candidate profile Conduct regular checks to ensure the accuracy and quality of backend processes. Identify and rectify discrepancies or errors in a timely manner.

Data Management Accurately input and manage data in the company's backend systems Ensure data integrity/compliance with data entry standards Process Coordination Collaborate with different departments to ensure seamless backend operations Required Candidate profile Conduct regular checks to ensure the accuracy and quality of backend processes. Identify and rectify discrepancies or errors in a timely manner.

Data Management Accurately input and manage data in the company's backend systems Ensure data integrity/compliance with data entry standards Process Coordination Collaborate with different departments to ensure seamless backend operations Required Candidate profile Conduct regular checks to ensure the accuracy and quality of backend processes. Identify and rectify discrepancies or errors in a timely manner.

About The Opportunity : Operating at the forefront of the consulting and technology services sector, our client delivers transformative data management and business analytics solutions to a global clientele. Specializing in innovative approaches to data architecture and information management, they empower organizations to make data-driven decisions. We are seeking a seasoned professional to drive the evolution of our data infrastructure. This is an exciting chance to join a high-caliber team that values precision, efficiency, and strategic vision in a fully remote setting from anywhere in India. Role & Responsibilities : As a key member of our team, you will be instrumental in shaping our d...

Utility Operator HVAC / Water / Electrical (01 Position) based in Vapi, Gujarat. The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvemen...

The ideal candidate brings 15-20 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Plan resources, ensure statutory compliance, drive traini...

The ideal candidate brings 3- 8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Own production execution and shift supervision; ensure lin...

The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Own production execution and shift supervision; ensure line clea...

The ideal candidate brings 8 to 10 year and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Additional info: Key Skills: QMS (Change Control, Deviation...

The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Additional info: Key Skills: DMF Compilation, QA Coordinat...

The ideal candidate brings 10- 15 yrs exp and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility ...

The ideal candidate brings 15-20 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Plan resources, ensure statutory compliance, drive traini...

The ideal candidate brings 2 yrs exp and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Strengthen QMS: author/review SOPs, BMR/BPR, oversee IPQA/AQA,...

Production Executive based in Latur. The ideal candidate brings 0-1years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Own production executio...

Micro Head based in Kathua, Jammu & Kashmir. The ideal candidate brings 12 - 15 yrs exp. and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Lead mi...

Assistant Manager / Sr. Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improveme...