Regulatory Specialist II - Chennai, Tamil Nadu

The Regulatory Information Specialist manages the intake, analysis, and archiving of official correspondence between the company and global Health Authorities. They ensure that the Regulatory Information Management (RIM) database remains accurate and compliant to support audit re ...

The Regulatory Specialist II supports the planning, preparation, and maintenance of essential regulatory documentation required for clinical research studies. This role ensures compliance with federal, state, and local regulations as well as KUR's internal policies and procedures ...

We aim to prevent stop and cure diseases ensuring everyone has access to healthcare today for generations to come Join Roche where every voice matters The Position Regulatory Information Specialist Roche India – Roche Services & Solutions Chennai/ Hyderabad A healthier future dri ...

Regulatory Affairs Specialist. Author, revise and maintain safety data sheets (SDSs) in compliance with regulations. · ...

We're an international bank working to make a positive difference for our clients communities and each other. · The role involves delivering regulatory reports adhering to SLA operating instructions quality requirements providing insightful analysis on variances commentaries on u ...

We are looking for an experienced Platform Control & Violation Management (PCVM) Team Leader to manage Investment Restrictions Monitoring and Compliance Operations across global teams.The role involves leading a high-performing team, ensuring strong compliance controls, overseein ...

We are seeking an experienced Regulatory Affairs Specialist to support U.S. and global regulatory activities for a growing biotech organization. · We are looking for someone with strong project management skills who can manage submission timelines and cross-functional coordinatio ...

Se busca especialista en configuración del Veeva Vault con experiencia en la configuración y mantenimiento del plataforma RIMSuite. · ...

4+ years of hands-on configuration experience in Veeva Vault Regulatory applications (RIM, Submissions, Submissions Archive, Registrations) · Familiarity with the regulatory submission lifecycle and global regulatory requirements. · ...

We are looking for an experienced Regulatory Affairs Specialist with strong exposure to medical device or IVD manufacturers in India who export their products to advanced regulated markets such as USA (FDA), Europe (EU MDR/IVDR), Japan (PMDA), Australia (TGA), India Regulatory an ...

We're seeking a highly experienced Senior CSV/Quality lead Specialist to lead and manage validation activities for GxP-regulated computerized systems.As part of our EY-ER-Regulatory Compliance team,you will help clients by understanding their business needsand delivering solution ...

The Clinical Data Repository (CDR) Specialist is responsible for the management, integration and maintenance of clinical data within the organization's data repository systems. · We are looking for an experienced CDR specialist who can ensure compliance with relevant regulations ...

We are looking for RA Specialist - Formulation Injectable for a leading pharma company at Chennai. · Greetings · , We are looking for RA Specialist - Formulation Injectable for a leading pharma company at Chennai.Preparation & review of regulatory documents. · ...

Job Description · MGM Healthcare is hiring a Purchase & Stores Specialist to manage inventory, ensure regulatory compliance, and support seamless coordination across hospital departments. · Receive and verify medical supplies against POs & invoices · Manage inventory: storage, ba ...

Teamware Solutions is seeking a skilled Risk Regulatory Compliance Analytics Specialist to join our team. This role is crucial for leveraging data and analytical techniques to ensure compliance with financial regulations and effectively manage risk. You will be responsible for de ...

The Associate Manager will supervise a team of specialists and ensure audit readiness. · Lead compliance activities across I-9, E-Verify, UI Claims. · ...

Manage daily operations for literature review biocuration regulatory services SDS authoring and PubMed research activities. · ...

We are hiring for Senior Data Governance Specialist. · ...

We are seeking a Dispute Package Specialist Technical Writer. This role is responsible for drafting, optimizing and maintaining Customer Dispute Packages (CDPs) in line with Visa Mastercard Amex Discover and other network rules. The specialist must stay ahead of card network rule ...

The position is responsible for managing device or pharmaceutical complaints and adverse events globally. · Duties include initial triage of complaint files, assessments of reportability, escalating customer advocacy events, · submitting regulatory reports in accordance with appl ...