RC-REGULATORY COMPLIANCE-REGULATORY COMPLIANCE-Senior - Bengaluru

We're seeking a Senior Veeva Vault RIM/PV Configuration Specialist to lead high-impact digital quality initiatives within the pharmaceutical domain.This opportunity is ideal for professionals who blend deep platform expertise with leadership and consulting acumen, and who thrive ...

We are seeking an experienced Business Analyst with strong consulting skills and domain knowledge in Life Sciences IT systems to support regulatory, clinical, safety, lab, and manufacturing-related technology implementations.At EY we help our clients build a better working world. ...

We are looking for an Kneat Developer to support the design, configuration, and implementation of Kneat Gx for validation and quality documentation management in regulated environments. · This role involves configuring Kneat Gx solutions using out-of-the-box capabilities, develop ...

+We are seeking a highly experienced Senior CSV/Quality lead Specialist to lead and manage validation activities for GxP-regulated computerized systems. · +Bachelor's or Master's degree in Life Sciences, Engineering, or related field. · 4-9 years of experience in CSV within the p ...

We're seeking a highly experienced Senior CSV/Quality lead Specialist to lead and manage validation activities for GxP-regulated computerized systems. · ...

+The opportunity · We are looking for a seasoned and strategic Veeva Vault Senior Configuration specialist with RIM and PV experience to lead high-impact digital quality initiatives within the pharmaceutical domain. · ...

We are seeking an experienced Senior Manager with strong consulting skills and deep industry expertise in Regulatory Affairs and Pharmacovigilance to lead IT implementation projects in regulated GxP environments. · The opportunity · We are seeking an experienced Senior Manager wi ...

We are seeking an experienced Senior Manager with strong consulting skills and deep industry expertise in Regulatory Affairs and Pharmacovigilance to lead IT implementation projects in regulated GxP environments. · Lead regulatory strategy/ pharmacovigilance (Safety) strategy dev ...

Global Compliance Employee Services (GCES) is responsible for overseeing employee-related compliance matters such as licensing and registrations; employee disclosures; review and approval of employees' outside brokerage accounts and the pre-clearance process for employees' person ...

We're seeking an experienced Manager – Regulatory Compliance to lead IT implementation projects in regulated GxP environments. · 8–12 years of hands-on experience in regulatory area · Proven experience in regulatory affairs, pharmacovigilance and RIMS implementation or management ...

We are looking for a seasoned and strategic Veeva Vault RIM Manager to lead high-impact digital quality initiatives within the pharmaceutical domain. · ...

We are seeking an experienced Manager with strong consulting skills and deep industry expertise in Regulatory Affairs and Pharmacovigilance to lead IT implementation projects in regulated GxP environments. · You will partner with clients to understand their business needs and tra ...

We are looking for a seasoned Regulatory Compliance professional with expertise in Veeva Vault RIM configuration and development who can lead high-impact digital quality initiatives within the pharmaceutical domain. · As part of our EY-ER-RAM team you will help clients by underst ...

We are looking for a seasoned and strategic Veeva Vault RIM Manager to lead high-impact digital quality initiatives within the pharmaceutical domain. This opportunity is ideal for professionals who blend deep platform expertise with leadership and consulting acumen, and who thriv ...

We are seeking an experienced Manager with strong consulting skills and deep industry expertise in Regulatory Affairs and Pharmacovigilance to lead IT implementation projects in regulated GxP environments. · Lead regulatory strategy/ pharmacovigilance (Safety) strategy developmen ...

RC-REGULATORY COMPLIANCE-REGULATORY COMPLIANCE-Senior - Veeva RIM/PV · At EY, we're all in to shape your future with confidence. · We'll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go. · Join EY and help to bui ...

Description · About IntertekIntertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices and over 46,000 people in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection an ...

Min yrs in regulatory affairs, pharmacovigilance and RIMS implementation or management. · Exp in CSV (Mandate) · knowledge of global regulatory frameworks, including FDA, EMA, PMDA, ICH guidelines, GVP Modules, & regional requirements. · Required Candidate profile · Expertise i ...

This role involves developing value-creating strategies and models for clients to innovate and increase their business profitability as an Actimize Consultant. · Develop value-creating strategies and models for clients · Assess the current processes and suggest technological sol ...

We are looking for a seasoned and strategic Veeva Vault RIM Manager to lead high-impact digital quality initiatives within the pharmaceutical domain. · Lead the configuration, customization, and deployment of Veeva Vault RIM (Registrations, Submissions, Submission Planning, Archi ...