Regulatory Affairs Executive

Sunrise Remedies Job Opening for Regulatory Affairs (RA). **Experience**: Minimum 2 Years **Industries**: Pharmaceutical Company **Education**: B.Sc. / M.Sc / B.Pharm / M.Pharm **Job Location**: Santej Ahmedabad. **Key Responsibilities**: - Regulatory Affairs Specialists assist in obtaining and maintaining government approval for drugs, medical devices,...

Job Title: Regulatory Affairs Junior ManagerLocation: At Ahmedabad Office , Near Thaltej CrossroadsDepartment: RAReports To: RA Head and Regulatory Department at HO /DirectorEmployment Type: Full TimeOffice hours : 9,30 AM to 6 PMWeek of: Sunday and Saturday Half DayPreferred Gender : M/FExperience: Minimum 2 yearsJob Summary:We are seeking a proactive and...

Regulatory Affairs Specialist">The Regulatory Affairs team is seeking a highly skilled and experienced specialist to support the management of regulatory submissions for healthcare products across diverse geographies.">Key Responsibilities:">Management and coordination with vendors of technical and legal requirements for obtaining marketing authorization...

We are seeking an experienced Clinical Trial Regulatory and Operations Manager based in Delhi/NCR who will ensure the timely initiation and successful execution of clinical trials. The ideal candidate will have extensive knowledge of India's clinical trial regulatory landscape, CDSCO submissions, import licensing, and operational oversight of clinical...

Job Title **:Expert Regulatory Affairs ( Contract for 18 months)** Job Type : Remote / WFH / Hybrid Location : India At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to...

**At Guerbet, we build lasting relationships so that to enable people to live better**. This is **Our Purpose.** We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 95...

Key Responsibilities:- Lead and manage CMC regulatory activities for USFDA submissions including ANDA preparation, review, and filing.- Oversee compilation and submission of Annual Reports, amendments, and deficiency responses.- Interface with cross-functional teams including Quality Assurance, Production, and R&D to gather required documentation and data.-...

Company Description Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can't Wait.We started in 1984 with a modest investment, 20...

Regulatory Intelligence CoordinatorWe are seeking a highly skilled and motivated individual to join our team as a Regulatory Intelligence Coordinator. This is an exciting opportunity for someone who is passionate about regulatory affairs, data management, and process improvement.Job DescriptionAs a Regulatory Intelligence Coordinator, you will play a...

Job DescriptionWe are seeking a highly motivated and detail-oriented Regulatory Intelligence Analyst to join our team. As a key member of the Regulatory Intelligence team, you will play a critical role in monitoring and analyzing the global regulatory landscape within the life sciences industry.You will actively participate in global regulatory intelligence...