Vacancy for Regulatory Affairs at Delhi Ncr

**Location**:Delhi NCR (Delhi/ Gurgaon)** **Experience: 1-2-year Experience in Medical devices (Fresher with interest in Medical devices may also apply)** **Qualifications: B. Pharma/ M Pharma only** **Job Profile**: - Regulatory and Quality Assurance for India Sub-continent to support the continuous development, implementation and maintenance of the...

**Job Title: Cosmetics Regulatory Affairs Specialist - Delhi** Key Responsibilities: - Conduct regulatory assessments of cosmetic products to ensure compliance with relevant regulations and guidelines - Prepare and submit regulatory dossiers to the appropriate authorities for import registration of cosmetics under COS 02 and COS 04 categories - Stay...

**Responsibilities**: Regulatory Compliance: Stay up-to-date with the latest CDSCO India guidelines and other relevant regulations pertaining to medical devices. Ensure that all products and processes adhere to these guidelines. Regulatory Strategy: Develop and implement regulatory strategies for the successful approval and launch of medical devices in...

Job Description - **Regulatory Affairs Executive Medical Devices** As a Manager - Regulatory and Government Affairs for Medical Devices, you would be expected to actively engage with government stakeholders and regulatory bodies to ensure crisp and effective representation on regulatory and policy matters and ensure continuity of license and permits as well...

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,...

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 -...

Profile: Regulatory Affairs (CDSCO) 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 **Job Descriptions**: - Proficient in English. - Must understand the regulatory requirements for medical devices in India. - Significant experience within the legislative and...

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...

Looking for person having experience in European CE Certification - documentation of Medical Device & InVitro Diagnostics. Designation : Regulatory Affairs Executive Dealing with licensioing work with CDSCO, ICMR & other Govt institution Education : DPharma / MPharma / Btech for Pharma regulatory / Medical device Experiance : 2-5 Yrs Job location :...

MAINTENANCE NOTICE - Due to maintenance work, our HR Management System might be inaccessible on - Monday, 26 February 2024, from 11:00 to 12:00 CET (UTC+01:00) **State Project Associate, Delhi NCR**: Vacancy #: 6748 Unit: India Programme Coordination Organisation: International Union for Conservation of Nature (IUCN) Location: India Country Office, New...

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 CharacteristicsKnowledge of Technical Documents like PVP-PVR, COA, FP...

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...

Apply for Project Vacancies Metabolic Engineering Group, Career Progress Consultants in Delhi ,Delhi/ NCR for 0 - 5 Year of Experience on

Apply for Project Vacancies Metabolic Engineering Group, Career Progress Consultants in Delhi ,Delhi/ NCR for 0 - 5 Year of Experience on

Apply for Project Vacancies Metabolic Engineering Group, Career Progress Consultants in Delhi ,Delhi/ NCR for 0 - 5 Year of Experience on

Apply for Project Vacancies Metabolic Engineering Group, Career Progress Consultants in Delhi ,Delhi/ NCR for 0 - 5 Year of Experience on TimesJobs.com.

Apply for Project Vacancies Metabolic Engineering Group, Career Progress Consultants in Delhi ,Delhi/ NCR for 0 - 5 Year of Experience on TimesJobs.com.

Job:Regulatory Affairs Specialist/SeniorSpecialist/Assistant Manager Experience:1012YearsSkills:The ideal candidate would have adiploma/degree in a scientific discipline such asBiology Microbiology Pharmacy pharmacology Biotechnologyengineering or medical technology. Minimum 5years of experience in Medical devices regulatory affairs and 78years of working...

**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 -...