Regulatory

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...

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...

Job Req ID: 42140- Location: New Delhi, IN- Function: Other- About: - Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the large spectrum portfolio to support the growing demand for data...

Senior / Labelling SpecialistJob Description:We are seeking a highly skilled and experienced Senior Labelling Specialist to join our team and take on a pivotal role in the development and approval of labelling documents for our vaccine portfolio. As a Senior Labeling Specialist, you will be responsible for overseeing all aspects of labeling, from initial...

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 Specialist - CMC Variations/Submissions12 month contract - Immediate startOverview: Join our Regulatory Affairs team and contribute to the management of Chemistry, Manufacturing, and Controls (CMC) You’ll be pivotal in ensuring compliance and efficiency in our regulatory processes.Key Responsibilities:CMC Change Control Assessment: ...

**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...

About Us: ELT Consultants - Medical Law & Regulatory Consulting & Law Firm, operating its services amongst Hospital, Healthcare, Nutrition & Medical Industry, helps its clients for obtaining licensing, registrations, approvals, NOC’s from the Central and State Regulatory Authorities for the Drugs, Cosmetics, Medical Devices & AYUSH. In addition to that...

Job Req ID: 44054- Location: New Delhi, IN- Function: Other- About: - Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the large spectrum portfolio to support the growing demand for data...

Job Req ID: 41743- Location: New Delhi, IN- Function: Technology/ IOT/Cloud- About: - Vodafone Idea Limited is an Aditya Birla Group and Vodafone Group partnership. It is India’s leading telecom service provider. The Company provides pan India Voice and Data services across 2G, 3G and 4G platform. With the large spectrum portfolio to support the growing...

Key Skills:- MedWatch reports- 21CFR Part 803- Regulatory Reporting- Adverse events- Product problems- Complaint management- Assess complaints

Key Skills:MedWatch reports21CFR Part 803Regulatory ReportingAdverse eventsProduct problemsComplaint managementAssess complaints

Provide regulatory support to customers/ internal teams and assist in maintaining regulatory requirements at all levelsCoordinate for acquiring / renewal of FDA/FSSAI licenses, product approvals, chemist intimations/ approvals, maintain regulatory documentation and follow up on any Corrective action directed by the FDA officialsCoordinate with Global...

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 to join our team. Job Titles: Executive / Senior Executive / Assistant Manager Regulatory AffairsExperience: 3 to 9 yearsLocation: Andheri east, MumbaiWorking Days: 6 days (Mon-Sat) WFOResponsibilities:1. Dossier collation and...

**Position: Junior Associate - Regulatory Affairs (Medical Devices)** **Location**: **Delhi NCR (Delhi/ Gurgaon)** **Experience: 1-2-year Experience in Medical devices (Fresher with interest in medical devices may also apply)** **Qualifications: B. Pharmacy** **Job Profile**: - Regulatory and Quality Assurance for India Sub-continent to support the...

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 :...

Job Responsibilities: Compiling, organizing, and reviewing documentation required for regulatory submissions.Ensuring compliance with relevant regulations and guidelines, collaborating with cross-functional teams, and managing timelines to meet submission deadlines.Attention to detail, knowledge of regulatory requirements, and effective communication skills...

Organisation :USV, a top 15 pharmaceutical company in India, excels in the diabetes and cardio sectors. With a presence in over 65 countries, our dynamic team of over 7,000 spans generations. Our commitment to brand building is evident in our popular products like Glycomet GP, Ecosprin AV, Jalra, Tazloc, Glynase and more.Responsibilities:For the CMC RA...