Hays | Regulatory Affairs Officer | new delhi

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year , on-callKey Requirements :Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products .Regulatory Experience : Proven...

On-Call ContractorforRegulatory Affairs in Medical Device ComplianceWorkload:Approximately40-50 hoursper year , on-callKey Requirements :Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly forClass C and D products .Regulatory Experience : Proven experience in...

On-Call Contractor for Regulatory Affairs in Medical Device Compliance Workload: Approximately 40-50 hours per year , on-call Key Requirements : Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products . Regulatory Experience : Proven...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year , on-callKey Requirements :Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.Regulatory Experience : Proven...

On-Call Contractor for Regulatory Affairs in Medical Device Compliance Workload: Approximately 40-50 hours per year , on-call Key Requirements : Expertise in Indian Medical Device Regulations : Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products . Regulatory Experience : Proven...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year, on-callKey Requirements:Expertise in Indian Medical Device Regulations: Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.Regulatory Experience: Proven experience...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year, on-callKey Requirements:Expertise in Indian Medical Device Regulations: Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.Regulatory Experience: Proven experience...

On-Call Contractor for Regulatory Affairs in Medical Device ComplianceWorkload: Approximately 40-50 hours per year, on-callKey Requirements:- Expertise in Indian Medical Device Regulations: Comprehensive knowledge of Indian medical device legislation and regulatory requirements, particularly for Class C and D products.- Regulatory Experience: Proven...

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...

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,...

**Office Assistant - Regulatory Affairs** An Office Assistant is a professional who oversees clerical tasks, such as sorting and sending mail **Education**: Minimum Graduation in any stream. Excellent communication and interpersonal skills. **Job Profile**: - Good Knowledge of Microsoft Excel and Microsoft office for maintaining import database -...

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...

Job Description: Manager - Legal AffairsLocation: New Delhi, Delhi, India Industry: Import and Export Overview: We are hiring a Manager (Legal Affairs) to lead legal and compliance functions for a pioneering initiative under the Ministry of Cooperation. The role involves ensuring adherence to legal standards, managing corporate regulatory matters,...

Job Description: Manager - Legal AffairsLocation: New Delhi, Delhi, IndiaIndustry: Import and ExportOverview:We are hiring a Manager (Legal Affairs) to lead legal and compliance functions for a pioneering initiative under the Ministry of Cooperation. The role involves ensuring adherence to legal standards, managing corporate regulatory matters, overseeing...

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...

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: - **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...

The regulatory affairs consultant for Asia Pacific will provide regulatory strategic and tactical leadership for drug development projects, including health authority interactions, regulatory submissions, clinical trial applications and other regulatory requirements in line with GARDP objectives, timelines and budgets. This role requires a deep understanding...

The regulatory affairs consultant for Asia Pacific will provide regulatory strategic and tactical leadership for drug development projects, including health authority interactions, regulatory submissions, clinical trial applications and other regulatory requirements in line with GARDP objectives, timelines and budgets. This role requires a deep understanding...

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...