Drug Regulatory Affair

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...

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 -...

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...

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...

**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...

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...

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...

**Willing to relocate to Delhi.** **ONLY FEMALE CANDIDATES CAN APPLY.** **Informing strategic regulatory controls and providing the worldwide regulatory policy for product development, manufacturing, and registration: It aids the applicant **in advancing a universally accepted product**.** **Development of proper leaflets like a 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,...

The main role of a Drug Safety Associate is to monitor the safety of drugs and medical devices once they are on the market and ensure that they are being used safely. - Reviewing and evaluating adverse event reports (AERs) to determine if they meet regulatory reporting requirements. - Entering and maintaining adverse event information in safety databases -...

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...

Key Accountabilities:Project Execution:Regulatory Affairs LabelingMust have 4+ years of experience in drug development especially in labeling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality.Good working knowledge of key labeling regulations/guidance and past experience in label development (CCDS, USPI,...

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...

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...

Biocon Biologics, we are creating a model for the future of healthcare for all. We are a leading company in the biosimilars revolution where patients come first. Our ambition is to impact a billion lives and we do this by fostering a culture of affordable innovation, patient centricity and disruptive thinking. We are a multicultural global company where...

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...