Regulatory Affairs Officer

**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...

Bachelor's degree in Chemistry, Environmental Science, or related field. Advanced degree (e.g., MS, PhD) preferred. - 4+ years of experience in regulatory affairs within the agrochemical/pesticide. - In-depth knowledge of pesticide regulations (e.g., CIBRC/EPA, EU, other country etc.) and registration requirements. - Experience with regulatory submissions,...

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,...

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

**Role & responsibilities** - EU Dossier preparation and submission to Europe market. - EU ASMF and CEP preparation and submission to Europe with post-approval activities - Handling of EDQM Agency Queries. - Brazilian DMF Preparation and Deficiency response. - China DMF Preparation and Deficiency response. - eCTD publishing in EDUCE software with PDF...

**Roles and Responsibilities** - EU Dossier preparation and submission to Europe market - EU ASMF and CEP preparation and submission to Europe with post approval activities - Handling of EDQM Agency Queries - Brazilian DMF Preparation and Deficiency response - China DMF Preparation and Deficiency response - eCTD publishing in EDUCE software with PDF...

Job Title Executive - Regulatory Affairs Business Unit R D1 Regulatory Affairs Job Grade G12A Location Baroda At Sun Pharma we commit to helping you Create your own sunshine - by fostering an environment where you grow at every step take charge of your journey and thrive in a supportive community Are You Ready to Create Your Own Sunshine As...

**Job Opening: Regulatory Affairs Executive | Vital Group** Location: SG Highway, Ahmedabad **Experience**: 1-3 years (Pharma Industry) **Key Responsibilities**: - Preparation and submission of dossiers, CTD/ACTD, and regulatory documents. - Handling regulatory queries and compliance requirements. - Coordination with internal teams to ensure timely...

Job Title: Regulatory Affairs Junior ManagerLocation: At Ahmedabad Office , Near Thaltej Crossroads Department: RA Reports To: RA Head and Regulatory Department at HO /Director Employment Type: Full TimeOffice hours : 9,30 AM to 6 PMWeek of: Sunday and Saturday Half Day Preferred Gender : M/FExperience: Minimum 2 years Job Summary:We are seeking a...