Regulatory Affairs Officer

**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...

Job description **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...

Responsibilities As a regulatory affairs officer: ensure that a company's products comply with the regulations of the regions where they want to distribute them keep up to date with national and international legislation, guidelines and customer practices respond to queries from medical bodies like the Medicines and Pertaining to that Guidelines. collect,...

Looking for an Enthusiastic, Efficient & Trustworthy Senior Executive - Regulatory Affairs for a Leading MNC “**Ronak Group”** **Company: Ronak Group (MNC)** Position**:Executive / Senior Executive - Regulatory Affairs** Experience: 2 to 7 Years Location: Vadodara, India We are looking for Energetic & Goal Oriented **Executive / Senior Executive -...

**Vega Biotec Pvt Ltd** a part of Vega group of companies having global presence and state of the art manufacturing pharmaceutical factory is having an opening for the following post. Qualification - B.Pharm/ M. Pharm Experience - 3+ years of experience in regulatory affairs for ROW market (Rest of the world) **Job Summary**: The Regulatory Affairs...

**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...

Global Regulatory Affairs StrategistKey Responsibilities:Develop and direct global regulatory strategies covering clinical, non-clinical, and CMC aspects.Lead the preparation, review, and approval of submission dossiers for regulatory authorities including US FDA, EMA, Health Canada, Australia's TGA, and ANVISA (Brazil).Provide strategic guidance on...

**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,...

Job Title: Regulatory Affairs Specialist Department: Regulatory Affairs Location: HO Office, Gota Ahmedabad Company name : Noronic pharmaceutical Job Summary: The Regulatory Affairs Specialist is responsible for ensuring compliance with regulatory requirements, overseeing the preparation of technical documents, and supporting product registration and...

Job Overview:As a key member of our Regulatory Affairs team, you will be responsible for the compilation and submission of regulatory documents to various markets, including the US, EU, AU, Canada, IL, and Palestine. You will work closely with stakeholders to review and manage all aspects of dossier compilation, query response, and lifecycle management.About...