Regulatory Affairs Executive

**Job Description: Regulatory Affairs Executive (Fresher to 3 Years Experience)** **Position**: Regulatory Affairs Executive **Department**: Regulatory Affairs **#### **Key Responsibilities**: - **Regulatory Submissions**: - Prepare and submit regulatory documents to health authorities (FDA, EMA, TGA, etc.) for new products, amendments, and...

Regulatory Affairs Executive :(BKM) is seeking a Regulatory Affairs Executive to join our team. In this role, you will be responsible for getting new products approval from the regulated market. In-depth knowledge of US FDA, EMA, and ICH regulatory frameworks, eCTD/ACTD dossier preparation, compilation and submission. Familiar with regulatory tools like...

ONLY EXPERIENCE CANDIDATE CAN APPLYJob description: -We are looking for a Regulatory Affairs Executive with strong knowledge of pharmaceutical products. The candidatemust have experience in domestic regulatory compliance (FSSAI/CDSCO) and export documentation, specifically forLATAM & ROW. Responsibilities include dossier preparation, label review, and...

**West coast pharma is looking for Regulatory Affairs Head - Male preferred** Qualification: B.PHARM/M.PHARM Experience: 5 to 10 years only **Regulatory Affairs Head - Pharmaceuticals Job Role**: The Regulatory Affairs Head leads the regulatory strategy and compliance for pharmaceutical products. They oversee submission of dossiers to health authorities,...

**Company Description** Briyosis Soft Caps Pvt. Ltd. is a privately-owned contract manufacturer of custom dietary supplement formulations. Based in Vadodara, India, we are an FDA registered and WHO-GMP certified company. With our high-efficiency encapsulation lines operating 24/7, we have the capability to produce over 3 billion soft-gels annually. Our...

**Introduction**: We are seeking a Regulatory Affairs Executive to join our team. In this role, you will be responsible for getting new products approval from the regulated market. In-depth knowledge of US FDA, EMA, and ICH regulatory frameworks, eCTD/ACTD dossier preparation, compilation and submission. Familiar with regulatory tools like Extedo, Lorenz,...

To have a clear understanding of regulatory guidelines and data requirements for pesticide export. - Collect and coordinate information to prepare regulatory documentation for submission to regulatory agencies - To prepare a regulatory dossier on chemistry and residue, as per the company’s requirements and timelines. - To review PCP and other reports about...

**Position : Regulatory Affairs Officer/Executive (Female)** **Education : B Pharm (Preferably)** **Experience : 1-2 Years** **Work Profile**: 1. Preparation & Checking of Dossiers of formulation products for product registration in other countries. 2. Co-ordination with Manufacturer & our partner in country (With their regulatory person) 3. Travel may...

Vega Biotec Pvt Ltd forms part of Vega group companies involved in manufacturing and exporting of finished pharmaceutical products and having global presence in 20+ countries. We have an opening for the following post. 1. Regulatory Affairs Executive - Qualification - B.pharma/M.pharm Experience - 2-4 year's minimum in regulatory affairs Job profile: 1....

Regulatory Affairs ExpertThis position is responsible for managing regulatory submissions across multiple products and countries. The ideal candidate will have a strong understanding of global dossier formats, submission pathways, and lifecycle management.Key Responsibilities:Author and compile regulatory dossiers to global health authorities, including the...