Regulatory submission B1/B2

Job descriptionFrench, Italian, Spanish Or German Certification - At least B1, B2 and aboveRequired Candidate profileInterested candidates can share the resumeswhitehorselanguage @ gmail .com Or call or Excellent Salary and Plus incentivesRequired Candidate profileGraduateResponsible for listening and precisely interpreting communication between two...

Job descriptionFrench, Italian, Spanish Or German Certification - At least B1, B2 and aboveRequired Candidate profileInterested candidates can share the resumeswhitehorselanguage @ gmail .com Or call or Excellent Salary and Plus incentivesRequired Candidate profileGraduateResponsible for listening and precisely interpreting communication between two...

Job descriptionFrench, Italian, Spanish Or German Certification - At least B1, B2 and aboveRequired Candidate profileInterested candidates can share the resumeswhitehorselanguage @ gmail .com Or call or Excellent Salary and Plus incentivesRequired Candidate profileGraduateResponsible for listening and precisely interpreting communication between two...

Hiring Polish B2 certified for an helpdesk - BangalorePFB JD Overall, 1 2 years of work experience in technical support environment Understanding of Windows Active directory to troubleshoot issues related to Account administration & access Good knowledge of O365 support Outlook, Intune, OneDrive, MFA configuration & troubleshooting Understanding of Windows...

Department: RA CMC Diabetes & ObesityAre you passionate about your work? Do you strive for process excellence in the most efficient way? Are you a change-maker with an innovative mindset, eager to shape the future? If you excel in what you do, then this role as a CMC Regulatory Professional II is an amazing opportunity for you at Novo Nordisk. Join us for a...

Looking to jump-start your career?We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most...

About the job Site Name: Bengaluru Luxor North Tower Key Responsibilities : Accountable to the GRL and Global Regulatory staff for the delivery of Marketing Application, pre-approval/investigational and lifecycle maintenance submissions to agreed timelines and in compliance with Regulatory Authority regulations and guidelines and in line with GSK SOPs and...

About the jobSite Name: Bengaluru Luxor North TowerKey Responsibilities :Accountable to the GRL and Global Regulatory staff for the delivery of Marketing Application, pre-approval/investigational and lifecycle maintenance submissions to agreed timelines and in compliance with Regulatory Authority regulations and guidelines and in line with GSK SOPs and...

We are hiring for dynamic individuals in Regulatory Affairs Department:Experience: 3 years up to 12 yearsDesignation: Senior Exec / Assistant Manager / Deputy ManagerQualification: M. Sc. / M. Pharma/ B.Pharma For Below Mentioned roles:Role 1: API Regulatory Affairs DMF filing / Submission. submission to global markets & handling health authority...

Looking to jump-start your career?We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most...

We are hiring for dynamic individuals in Regulatory Affairs Department: Experience: 3 years up to 12 years Designation: Senior Exec / Assistant Manager / Deputy Manager Qualification: M. Sc. / M. Pharma/ B.Pharma For Below Mentioned roles:Role 1: API Regulatory Affairs DMF filing / Submission. submission to global markets & handling health authority queries....

Job Description You will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions experts. Join our team and contribute to groundbreaking clinical research. Office-based in Bangalore Oversee preparation of clinical trial submission...

Job Description You will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions experts. Join our team and contribute to groundbreaking clinical research. Office-based in Bangalore or Remote in India Oversee preparation of clinical trial...

Department: RA CMC & Device Are you passionate about your work? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as "RA Specialist" with us....

Job DescriptionYou will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions experts. Join our team and contribute to groundbreaking clinical research. Office-based in Bangalore Oversee preparation of clinical trial submission dossiers for...

Job DescriptionYou will focus on leading regulatory services for global research projects of novel medicinal products in India while joining our global team of regulatory and ethics submissions experts. Join our team and contribute to groundbreaking clinical research. Office-based in Bangalore or Remote in IndiaOversee preparation of clinical trial...

Department: RA CMC Diabetes & Obesity Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for you as "CMC...

Regulatory Affairs Consultant.8 years' experience in handling life cycle management of approved drug products (small molecules) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute to the planning, preparation (including authoring where relevant) and...

Regulatory Affairs Consultant.8 years' experience in handling life cycle management of approved drug products (small molecules) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute to the planning, preparation (including authoring where relevant) and...

8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute to the planning, preparation...