Senior Regulatory Affairs Associate

We are currently seeking a highly motivated and experienced professional in Regulatory Affairs specializing in Medical Devices Domain to join our team.Positions are: Senior Manager Regulatory AffairsExperience: 11 to 15 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) WFOResponsibilitiesLead regional team to ensure medical device product...

Regulatory Affairs Specialist - Legal Metrology and EPR India **Responsibilities**: Regulatory Compliance: Stay up-to-date with the latest Legal Metrology and EPR regulations in India. Ensure that all products and processes comply with these regulations. Documentation: Prepare and maintain all necessary documentation required for regulatory submissions,...

DESIGNATION/ TITLE Sr. Executive / Assistant Manager - Regulatory Affairs LOCATION NSP, Delhi YEAR OF EXP Minimum 3 yrs QUALIFICATION MSc (Toxicology/Agri/Chem) or similar BUDGET In b/w 8-10Lpa KEY RESPONSIBILITIES ROLES & RESPONSIBILITIES Manage the data gathering and compilation of studies (toxicology, chemical, efficacy) necessary for the...

Designation: RA Associate Department: Regulatory Affairs Work location: Delhi Working Days: Mon - Fri Work Timings: 9AM -5 PM **Salary**: Best in industry (On payroll of Talisman HR) Detailed Job description - **RA Associate**: - Preparation and submission of dossiers for product registrations, import licenses and other approvals from regulatory...

Greetings from Right Staff One of our client who are into Medical Devices Are looking for a Regulatory Affairs person at Delhi NCR Job Description - **Experience minimum 5 Years and above compulsory** Designation - Regulatory Affairs/QA Affairs Time - Day Shift Location - Delhi NCR **Responsibilities**: - 1. Identify regulatory and post market...

Senior Manager – Global Regulatory AffairsLocation – Head-Office, Bangalore, INAccountable for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products.12+ years experience is mandatoryResponsible for :Development and Implementation of regulatory strategies for global registrations...

Designation: - **Drug Regulatory Affairs-Male/Female** **JOB DESCRIPTION: -** - Delivery/Proper packing of goods for supplier - Maintaining the stock status at the back office - Settling of credit notes and following ups of payments from the parties - Coordinate with the vendors by keeping the track on purchase & delivery of orders sent - Maintaining the...

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

Responsibilities: - Develop and implement regulatory strategies for drug development, registration, and commercialization in compliance with local and international regulations. - Coordinate regulatory submissions and responses to regulatory agencies, ensuring accuracy, completeness, and timeliness. - Maintain up-to-date knowledge of regulatory...

Urgent Hiring for Drug Regulatory Affairs for Delhi Location Should have relevant expeirence in 3 to 8 years in DRA DRUG REGULATORY AFFAIRS (DRA) **Job Description**: Knowledge of Dossier Compilation as per the Country Guideline (CTD, ACTD, and Country Specific Format) Knowledge of COPP, FSC, Product Permission, and Summary of Product...

Urgent Hiring Drug Regulatory Affairs for Pharmaceutical Company in Delhi. DRUG REGULATORY AFFAIRS (DRA) **Job Description**: Knowledge of Dossier Compilation as per the Country Guideline (CTD, ACTD, and Country Specific Format) Knowledge of COPP, FSC, Product Permission, and Summary of Product Characteristics Knowledge of Technical Documents like -...

Regulatory affairs officers ensure that products such as foods, cosmetics, pharmaceuticals and veterinary medicines - and the steps involved in developing, testing and marketing them - meet legislative requirements. Typical duties include: studying scientific and legal documents to check they meet legal requirements Pay: ₹20,000.00 per...

**Job Role: International Regulatory Affairs** Responsible for compilation & submission of Dossier of a generic drug. Hand on experience in Filing dossiers to regulated, emerging and ROW markets. Experienced in CTD/ACTD and Regional Module. Experience in Filing in EU, ASEAN, MIDDLE EAST AND LATAM regions. To obtain approvals for relevant product...

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

We are currently seeking a proactive and dedicated Regulatory Affairs Specialist to join our team of business consultants. The primary responsibility of this role is to assist our clients in obtaining the necessary licenses and registrations from the Central Drugs Standard Control Organization (CDSCO) to establish and operate their pharmacy shops...

About Halma:Halma is a global group of life-saving technology companies, driven by a clear purpose. We are an FTSE 100 company with headquarters in the UK and operations in 23 countries, including regional hubs in India, China, Brazil, and the US.Our diverse group of nearly 50 global companies specialise in market leading technologies that push the...

Profile: Drug Regulatory Affairs (DRA) Location: Paschim Vihar, New Delhi **Salary**: Up to 50,000 5 Days Working Exp: 1 to 2 Years Yearly Bonus Office Timing: 9:30 to 5:30 **Roles and responsibilities -** - CDSCO Registration for Medical devices, Drugs and Cosmetics, WPC Approval, FDA Registration, Legal metrology Registration. - Must understand the...

Regulatory Affairs Consultant:Around 7-10 years of relevant experience in handling of pre and post approval life cycle management of drug products (small molecules as well as biologicals) in various markets.Good understanding of regulatory framework, including regional trends, for various types of applications and proceduresLead and / or contribute to the...

The primary role of the Regulatory Affairs function is to provide support and guidance with respect to regulatory environment, at all stages of the life cycle of ResMed's products. Key deliverables include adding value to business through ensuring compliance and delivery of optimal regulatory strategies for portfolio planning, active regulatory intelligence...