Regulatory Affairs Officer

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...

Regulatory Affairs LeaderWe are seeking an experienced Regulatory Affairs professional to join our team.The ideal candidate will have extensive experience in managing regulatory affairs for pharmaceutical products, including dossier compilation, submission, and query response. This role requires strong leadership skills, attention to detail, and excellent...

**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...

**Regulatory Affairs Executive Job Description** **Job Summary**: The Regulatory Affairs Executive will work with product development and manufacturing management to ensure that the product development process meets all applicable regulatory requirements. **Duties/Responsibilities**: - Works in the regulatory affairs department on assigned projects. -...

Regulatory affairs executive - B Pharm or M Pharm with 2 years plus experience. **Job description**: - Preparing Dossiers for registration of products in various ROW markets and query response submission - Legalization of FDCA documents for respective country registration - Arrangement of Sample for registration submission from respective team - Prior...

Regulatory Affairs SpecialistWe are seeking a skilled Regulatory Affairs Specialist to join our team.About the Role:Develop and implement regulatory strategies to ensure compliance with laws and regulations.Collaborate with cross-functional teams to drive business growth and improve operational efficiency.Analyze complex data and information to inform...

**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...

**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 - Minimum 3 years in regulatory affairs for ROW market (Rest of the world) **Job Profile**: 1. Preparing dossiers as per country...

Job Title:Regulatory Affairs ManagerWe are seeking a seasoned Regulatory Affairs Manager to join our regulatory team. This role will be responsible for developing and directing global regulatory strategies, leading the preparation of submission dossiers, and collaborating with cross-functional teams.Key Responsibilities:Develop and direct global regulatory...

Position Regulatory Affairs Associates Location - Vadodara KRA: As a RA Sr. Officer Reviewing artwork, PRAC variations, CEP updates for EU market. Preparation of Regulatory Strategic documents for EU/UK market. Review and compilation of deficiencies response for ROW (specially MENA, LATAM market) Compilation and submission of renewal, variation for...