jobs for regulatory affairs officer-Pharma industry-Delhi, India-3LPA

JOB DETAILS Preparation & Compilation of Dossiers in CTD/eCTD formats- good knowledge of Module Analysing and arranging the dossierArt work checkingKnowledge of ICH Guidelines- able to use Pharmacopoeia FUNCTIONAL AREA ich guideline, ctd, module 3, pharmacopoeia, Dossier, art work, analysis, Pharmaceutical industry jobs in Delhi, Pharmaceutical industry...

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 :...

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,...

**Regulatory Affairs Manager** **Benefits** JOB TYPE: Permanent EMPLOYMENT TYPE: Full-Time EXPERTISE: PHARMACEUTICAL REGULATORY AFFAIRS SALARY TYPE: Annually SALARY: Negotiable REPORTS TO: Managing Director VACATION LEAVE: paid LOCATION: Shimla, Himachal Pradesh, India. This role will be office-based or hybrid **REQUIRED: Direct experience working...

**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...

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 -...

**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 -...

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...

**Role** Regulatory Affairs Officer **Our Client** Our client has been declared as National Reference Lab (NRL) by the Ministry of Health & Family Welfare, Govt. of India. Our client is one of the largest Integrated Food, Pharma, Environment & Gas Quality Testing Service Providers with its Laboratory Operations Accredited for ISO 17025:2017 compliance...

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...

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...

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...

About Us: established player in the B2B Pharma raw material space has recently launched an exciting new E-commerce platform– CLYZOPosition- Regulatory Affairs AssociateJob Description:An organization with a reputed history of 10+ years in the Pharma raw material industry, dealing in excipient products is looking for Regulatory Affair Executive having...

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...

Job Description Copeland India is seeking a Director Public Affairs based in New Delhi. The individual will be instrumental in analysing and updating senior management on regulatory and legislative risks, opportunities and relevant laws and regulations. The individual will liaise with national, state and local government bodies, relevant industry...

We are looking for a Lead Regulatory Affairs who is specialized in Indian market regulatory affairs with good connections in DCGI for a Global Pharmaceutical MNC in Delhi / BangaloreJob Description:We are looking for a Regulatory Affairs Lead to lead regulatory processes for our assigned products, ensuring swift approvals and strict compliance with...

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...

Title/Designation:Senior Regulatory ExecutiveBased at:AhmedabadIndustry:Medical Devices manufacturing (Class III)Qualification:Postgraduate or equivalent in Pharma/Medical Devices domainExperience:5-6 years minReports to:Head of QA/RAAbout us:Aegis Lifesciences, established in 2008, is a distinguished manufacturer and exporter of medical devices,...