Executive Regulatory Affairs

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 - Bsc. Chem/B.pharma/M.pharm Experience - 1 year minimum Job profile: 1. To assist manager...

Vega Biotec Pvt Ltd forms part of Vega group companies having state of the art manufacturing company in Vadodara and having presence in over 20 countries. Our export arm has an opening for the following post.1. Senior Regulatory affairs executive-Qualification- Bsc/Msc Chem,B.pharma/M.pharmaExperience- Minimum 4 years in RAJob Profile-1. CTD or ACTD dossier...

**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...

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...

Company OverviewRenown Pharmaceuticals Pvt. Ltd. is a reputable soft gelatin contract manufacturer with a state-of-the-art facility in Vadodara, India. The company upholds the highest quality standards and aims to be a top producer of soft gelatin capsules in India. Renown Pharma is known for its adherence to regulatory standards like MHRA, TGA, and WHO-GMP,...

Company Overview Renown Pharmaceuticals Pvt. Ltd. is a reputable soft gelatin contract manufacturer with a state-of-the-art facility in Vadodara, India. The company upholds the highest quality standards and aims to be a top producer of soft gelatin capsules in India. Renown Pharma is known for its adherence to regulatory standards like MHRA, TGA, and...

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 - Bsc. Chem/B.pharma/M.pharm Experience - 1 year minimum Job profile: 1. To assist manager...

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 -5 years minimum Job profile: 1. Dossier compilation for...

Job Description: Job Description: Experience in handling regulatory affairs for ROW market mainly Central and Latin American, African & Asian countries for Pharma Formulations. ? Preparation, Compilation & Review of Registration documents that include Administrative & Technical. ? Reviewing the technical documents provided by QA, QC,...

Collect and coordinate information and prepare regulatory documentation for submission to regulatory agencies or to commercial partners, advise on the submission strategy - Timely compile materials for license renewals, updates and registrations - Maintain regulatory files/database and chronologies in good order. Establish and maintain system for tracking...

**Qualification**: B. Pharm / M. Pharm-RA **Experience**: 2 to 3 Years **Description**: - Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority. - Well versed with the guidelines of ICH and other regulatory. - Preparation of documents for COPP, FSC, and other legal documents including product...

Qualification: B. Pharm / M. Pharm-RA Experience: 3 to 6 Years Description: - Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority. - Well versed with the guidelines of ICH and other regulatory. - Preparation of documents for COPP, FSC, and other legal documents including product permission -...

Job description: Q A Executive 1. Regulatory Excellence: - Ensure strict adherence to medical device industry regulatory standards. - Manage documentation for ISO 13485 and CE certification compliance. 2. Documentation Oversight: - Monitor and enforce documentation compliance across all departments. - Develop and implement standardized SOPs as...

From 2 to 3 year(s) of experience - ₹ 2,00,000 - 3,00,000 P.A. - Vadodara**Roles and Responsibilities** Job Opening for RA Officer having 2 to 3 Years of experience in any Pharma API Manufacturing Company near Vadodara. - To prepare and review of dossier in supervision of RA Head. - Collection, review and compilation of various QA and other department...

Vega Biotec Pvt.Ltd forms part of Vega group of companies having state of the art manufacturing pharmaceutical formulation factories and having global presence in 20+ countries. We have an opening in the export division. 1. QA/RA executive - Experience - Minimum 2 years in pharmaceutical formulation factory Qualification - B. Pharma/ M. Pharma Job...

PositionOverview: We are seeking ahighly skilled person to join the team. The ideal candidate willprovide technical expertise and guidance throughout the transferprocess focusing on process optimization scaleup and validationwithin the Analytical Method Developmentlab.KeyResponsibilities: Developand optimize analytical methods for the analysis of...

**Roles and Responsibilities** - Exhaustive literature search using various databases - To prepare API Landscape Report - To prepare Freedom to Operate (FTO) Report for API and their starting materials - To prepare Freedom to Operate (FTO) Report for Key starting material (KSM) of API [Inhouse or outsourced] - To prepared polymorph report for API - To...

Position : Exe / Sr. Exe (Regulatory Affairs, Baroda) Grade – G12A/G11B Education – B.Pharm / M. Pharm Experience – 4 to 6 years Location – R&D - Baroda Job Description: Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for submission to various...

Position : Exe / Sr. Exe (Regulatory Affairs, Baroda) Grade – G12A/G11B Education – B.Pharm / M. Pharm Experience – 4 to 6 years Location – R&D - Baroda Job Description: Review all data and documents related to product registrations for various health authorities. Compile registration dossiers for...

We areseeking a highly skilled person to join the team in thepharmaceutical industry. The ideal candidate will be responsiblefor method development and validation as well as routine andstability analysis utilizing a variety of analytical techniquesincluding HighPerformance Liquid Chromatography (HPLC) GasChromatography (GC) Dissolution testing and Karl...